Krstić, Jugoslav B.

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Authority KeyName Variants
orcid::0000-0003-0321-0698
  • Krstić, Jugoslav B. (46)
  • Krstić, Jugoslav (18)
Projects
Lithium-ion batteries and fuel cells - research and development Nanostructured Functional and Composite Materials in Catalytic and Sorption Processes
Physics and Chemistry with Ion Beams Synthesis, processing and characterization of nanostructured materials for application in the field of energy, mechanical engineering, environmental protection and biomedicine
Electroconducting and redox-active polymers and oligomers: synthesis, structure, properties and applications ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, European Union, ERC, European Union, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Canton of Bern, Switzerland, Canton of Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA
COST Action [CM1206] ICREA
Development of Methods of Monitoring and Removal of Biologically Actives Substances Aimed at Improving the Quality of the Environment Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200017 (University of Belgrade, Institute of Nuclear Sciences 'Vinča', Belgrade-Vinča)
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200026 (University of Belgrade, Institute of Chemistry, Technology and Metallurgy - IChTM) Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200146 (University of Belgrade, Faculty of Physical Chemistry)
ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, ANAS, Azerbaijan, SSTC, Belarus, CNPq, FAPESP, Brazil, BMWF, FWF, Austria, NSERC, NRC, CFI, Canada, CERN, CONICYT, Chile, CAS, MOST, NSFC, China, COL-CIENCIAS, Colombia, MSMT CR, MPO CR, VSC CR, Czech Republic, DNRF, DNSRC, Lundbeck Foundation, Denmark, EPLANET, ERC, NSRF, European Union, IN2P3-CNRS, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, HGF, MPG, AvH Foundation, Germany, GSRT, NSRF, Greece, ISF, MINERVA, GIF, DIP, Benoziyo Center, Israel, INFN, Italy, MEXT, JSPS, Japan, CNRST, Morocco, FOM, NWO, Netherlands, BRF, RCN, Norway, MNiSW, Poland, GRICES, FCT, Portugal, MERYS (MECTS), Romania, MES of Russia, ROSATOM, Russian Federation, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, MIZS, Slovenia, DST/NRF, South Africa, MICINN, Spain, SRC, Wallenberg Foundation, Sweden, SER, SNSF, Cantons of Bern and Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, Royal Society and Leverhulme Trust, United Kingdom, DOE, NSF, United States of America, ICREA ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, Chile, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, European Union, ERC, European Union, NSRF, European Union, IN2P3-CNRS, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, DIP, Israel, Benoziyo Center, Israel, INEN, Italy, MEXT, Japan, ISPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, GRICES, Portugal, FCT, Portugal, MERYS (MECTS), Romania, MES of Russia, ROSATOM, Russian Federation, JINR, Serbia, MSTD, Serbia, MSSR, Slovakia, (MECTS), Romania, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MICINN, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Geneva, Switzerland, SNSF, Geneva, Switzerland, Cantons of Bern, Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA
ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, ERC, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES , Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Canton of Bern, Switzerland, Canton of Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, Chile, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, European Union, ERC, European Union, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, Russian Federation, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern, Switzerland, Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA
ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, Chile, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, European Union, ERC, European Union, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, Russian Federation, ROSATOM, Russian Federation, JINR, Serbia, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern, Switzerland, Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, European Union, ERC, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, DIP, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, GRICES, Portugal, FCT, Portugal, MERYS (MECTS), Romania, MES of Russia, Russian Federation, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MVZT, Slovenia, DST/NRF, South Africa, MICINN, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern and Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA
ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, ERC, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MIN-ERVA, Israe, GIF, Israe, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portuga, FCT, Portugal, MNE/IFA, Romania, MES of Russia, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Geneva, Switzerland, SNSF, Geneva, Switzerland, Cantons of Bern and Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, the Royal Society and Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, ERC, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, ROSATOM, Russian Federation, JINR, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern and Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, USA, NSF, USA
ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, ERC, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Canton of Bern, Switzerland, Canton of Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COL-CIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, ERC, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern and Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States, NSF, United States, ICREA
ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, ERC, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern and Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, ERC, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern, Switzerland, Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE United States of America, NSF, United States of America, ATLAS Tier-1 facilities at TRIUMF (Canada), NDGF (Denmark, Norway, Sweden), CC-IN2P3 (France), KIT/GridKA (Germany), INFN-CNAF (Italy), NL-T1 (Netherlands), PIC (Spain), ASGC (Taiwan), RAL (U.K.), BNL (USA), ICREA
ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, ERC, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern, Switzerland, Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIEN-CIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, ERC, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, Russian Federation, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Canton of Bern, Switzerland, Canton of Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA
ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPE SP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, ERC, NSRF, European Un ion, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portuga l, FCT, Portuga l, MNE/IFA, Romania, MES of Russia, Russian Federation, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZ. S, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern and Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society and Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, European Union, ERC, European Union, NSRF, European Union, IN2P3-CNRS, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern and Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, the Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA
ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COLCIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, European Union, ERC, European Union, NSRF, European Union, IN2P3-CNRS, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, Russian Federation, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern and Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, USA, NSF, USA, ICREA ANPCyT, Argentina, YerPhI, Armenia, ARC, Australia, BMWF, Austria, FWF, Austria, ANAS, Azerbaijan, SSTC, Belarus, CNPq, Brazil, FAPESP, Brazil, NSERC, Canada, NRC, Canada, CFI, Canada, CERN, CONICYT, Chile, CAS, China, MOST, China, NSFC, China, COL-CIENCIAS, Colombia, MSMT CR, Czech Republic, MPO CR, Czech Republic, VSC CR, Czech Republic, DNRF, Denmark, DNSRC, Denmark, Lundbeck Foundation, Denmark, EPLANET, European Union, ERC, European Union, NSRF, European Union, IN2P3-CNRS, France, CEA-DSM/IRFU, France, GNSF, Georgia, BMBF, Germany, DFG, Germany, HGF, Germany, MPG, Germany, AvH Foundation, Germany, GSRT, Greece, NSRF, Greece, ISF, Israel, MINERVA, Israel, GIF, Israel, I-CORE, Israel, Benoziyo Center, Israel, INFN, Italy, MEXT, Japan, JSPS, Japan, CNRST, Morocco, FOM, Netherlands, NWO, Netherlands, BRF, Norway, RCN, Norway, MNiSW, Poland, NCN, Poland, GRICES, Portugal, FCT, Portugal, MNE/IFA, Romania, MES of Russia, ROSATOM, Russian Federation, JINR, MSTD, Serbia, MSSR, Slovakia, ARRS, Slovenia, MIZS, Slovenia, DST/NRF, South Africa, MINECO, Spain, SRC, Sweden, Wallenberg Foundation, Sweden, SER, Switzerland, SNSF, Switzerland, Cantons of Bern, Switzerland, Geneva, Switzerland, NSC, Taiwan, TAEK, Turkey, STFC, United Kingdom, Royal Society, United Kingdom, Leverhulme Trust, United Kingdom, DOE, United States of America, NSF, United States of America, ICREA

Author's Bibliography

Carbonization of MOF-5/Polyaniline Composites to N,O-Doped Carbon/ZnO/ZnS and N,O-Doped Carbon/ZnO Composites with High Specific Capacitance, Specific Surface Area and Electrical Conductivity

Savić, Marjetka; Janošević Ležaić, Aleksandra; Gavrilov, Nemanja; Pašti, Igor; Nedić Vasiljević, Bojana; Krstić, Jugoslav; Ćirić-Marjanović, Gordana

(2023)

TY  - JOUR
AU  - Savić, Marjetka
AU  - Janošević Ležaić, Aleksandra
AU  - Gavrilov, Nemanja
AU  - Pašti, Igor
AU  - Nedić Vasiljević, Bojana
AU  - Krstić, Jugoslav
AU  - Ćirić-Marjanović, Gordana
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10645
AB  - Composites of carbons with metal oxides and metal sulfides have attracted a lot of interestas materials for energy conversion and storage applications. Herein, we report on novel N,O-dopedcarbon/ZnO/ZnS and N,O-doped carbon/ZnO composites (generally named C-(MOF-5/PANI)),synthesized by the carbonization of metal–organic framework MOF-5/polyaniline (PANI) composites.The produced C-(MOF-5/PANI)s are comprehensively characterized in terms of composition,molecular and crystalline structure, morphology, electrical conductivity, surface area, and electrochemicalbehavior. The composition and properties of C-(MOF-5/PANI) composites are dictated bythe composition of MOF-5/PANI precursors and the form of PANI (conducting emeraldine salt (ES)or nonconducting emeraldine base). The ZnS phase is formed only with the PANI-ES form due toS-containing counter-ions. XRPD revealed that ZnO and ZnS existed as pure wurtzite crystallinephases. PANI and MOF-5 acted synergistically to produce C-(MOF-5/PANI)s with high SBET (up to609 m2 g−1), electrical conductivity (up to 0.24 S cm−1), and specific capacitance, Cspec, (up to 238.2 Fg−1 at 10 mV s−1). Values of Cspec commensurated with N content in C-(MOF-5/PANI) composites (1–10 wt.%) and overcame Cspec of carbonized individual components PANI and MOF-5. By acid etchingtreatment of C-(MOF-5/PANI), SBET and Cspec increased to 1148 m2 g−1 and 341 F g−1, respectively.The developed composites represent promising electrode materials for supercapacitors.
T2  - Materials
T1  - Carbonization of MOF-5/Polyaniline Composites to N,O-Doped Carbon/ZnO/ZnS and N,O-Doped Carbon/ZnO Composites with High Specific Capacitance, Specific Surface Area and Electrical Conductivity
VL  - 16
IS  - 3
SP  - 1018
DO  - 10.3390/ma16031018
ER  - 
@article{
author = "Savić, Marjetka and Janošević Ležaić, Aleksandra and Gavrilov, Nemanja and Pašti, Igor and Nedić Vasiljević, Bojana and Krstić, Jugoslav and Ćirić-Marjanović, Gordana",
year = "2023",
abstract = "Composites of carbons with metal oxides and metal sulfides have attracted a lot of interestas materials for energy conversion and storage applications. Herein, we report on novel N,O-dopedcarbon/ZnO/ZnS and N,O-doped carbon/ZnO composites (generally named C-(MOF-5/PANI)),synthesized by the carbonization of metal–organic framework MOF-5/polyaniline (PANI) composites.The produced C-(MOF-5/PANI)s are comprehensively characterized in terms of composition,molecular and crystalline structure, morphology, electrical conductivity, surface area, and electrochemicalbehavior. The composition and properties of C-(MOF-5/PANI) composites are dictated bythe composition of MOF-5/PANI precursors and the form of PANI (conducting emeraldine salt (ES)or nonconducting emeraldine base). The ZnS phase is formed only with the PANI-ES form due toS-containing counter-ions. XRPD revealed that ZnO and ZnS existed as pure wurtzite crystallinephases. PANI and MOF-5 acted synergistically to produce C-(MOF-5/PANI)s with high SBET (up to609 m2 g−1), electrical conductivity (up to 0.24 S cm−1), and specific capacitance, Cspec, (up to 238.2 Fg−1 at 10 mV s−1). Values of Cspec commensurated with N content in C-(MOF-5/PANI) composites (1–10 wt.%) and overcame Cspec of carbonized individual components PANI and MOF-5. By acid etchingtreatment of C-(MOF-5/PANI), SBET and Cspec increased to 1148 m2 g−1 and 341 F g−1, respectively.The developed composites represent promising electrode materials for supercapacitors.",
journal = "Materials",
title = "Carbonization of MOF-5/Polyaniline Composites to N,O-Doped Carbon/ZnO/ZnS and N,O-Doped Carbon/ZnO Composites with High Specific Capacitance, Specific Surface Area and Electrical Conductivity",
volume = "16",
number = "3",
pages = "1018",
doi = "10.3390/ma16031018"
}
Savić, M., Janošević Ležaić, A., Gavrilov, N., Pašti, I., Nedić Vasiljević, B., Krstić, J.,& Ćirić-Marjanović, G.. (2023). Carbonization of MOF-5/Polyaniline Composites to N,O-Doped Carbon/ZnO/ZnS and N,O-Doped Carbon/ZnO Composites with High Specific Capacitance, Specific Surface Area and Electrical Conductivity. in Materials, 16(3), 1018.
https://doi.org/10.3390/ma16031018
Savić M, Janošević Ležaić A, Gavrilov N, Pašti I, Nedić Vasiljević B, Krstić J, Ćirić-Marjanović G. Carbonization of MOF-5/Polyaniline Composites to N,O-Doped Carbon/ZnO/ZnS and N,O-Doped Carbon/ZnO Composites with High Specific Capacitance, Specific Surface Area and Electrical Conductivity. in Materials. 2023;16(3):1018.
doi:10.3390/ma16031018 .
Savić, Marjetka, Janošević Ležaić, Aleksandra, Gavrilov, Nemanja, Pašti, Igor, Nedić Vasiljević, Bojana, Krstić, Jugoslav, Ćirić-Marjanović, Gordana, "Carbonization of MOF-5/Polyaniline Composites to N,O-Doped Carbon/ZnO/ZnS and N,O-Doped Carbon/ZnO Composites with High Specific Capacitance, Specific Surface Area and Electrical Conductivity" in Materials, 16, no. 3 (2023):1018,
https://doi.org/10.3390/ma16031018 . .
3
2

Characterization and photocatalytic application of SrGd2O4 doped with rare earth Sm3+ and Dy3+ ions

Stamenković, Tijana; Pjević, Dejan J.; Krstić, Jugoslav; Popović, Maja; Rajić, Vladimir; Lojpur, Vesna

(2023)

TY  - JOUR
AU  - Stamenković, Tijana
AU  - Pjević, Dejan J.
AU  - Krstić, Jugoslav
AU  - Popović, Maja
AU  - Rajić, Vladimir
AU  - Lojpur, Vesna
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10684
AB  - A set of samples of SrGd2O4 doped with Sm3+ and Dy3+with different concentrations was prepared via glycine-assisted combustion synthesis. All of the diffraction peaks are related to the pure orthorhombic lattice SrGd2O4, according to X-ray Powder Diffraction investigation. The Energy Dispersive X-ray Spectroscopy chemical characterization revealed that the structure included all desired elements. Field Emission Scanning Electron Microscopy was used to capture the morphology, which showed porous aggregated particles consisting of roughly 50 nm-sized spherical particles. The Mercury Intrusion Porosimetry was used to establish where voids originated, and the results showed that samples have a real permanent 3D pore structure. X-ray Photoelectron Spectroscopy verified the successful incorporation of Dy3+ and Sm3+ ions in the matrix. Down-conversion luminescence spectra were recorded and typical emission transitions were found for either Sm3+ (4G5/2→6H5/2, 4G5/2→6H7/2, 4G5/2→6H9/2) or Dy3+ (4F9/2→6H15/2 and 4F9/2→6H13/2) ions. Calculation of the energy band gap using UV-VIS Diffuse Reflectance Spectroscopy yielded values of 4.3 eV for both doped samples. Using UV-VIS Absorption Spectroscopy, the photocatalytic degradation process was observed. After 4 h of simulating Sun exposure, an analysis of the photocatalytic properties revealed that approximately 50% of the Rhodamine B had been mineralized.
T2  - Surfaces and Interfaces
T1  - Characterization and photocatalytic application of SrGd2O4 doped with rare earth Sm3+ and Dy3+ ions
VL  - 37
SP  - 102755
DO  - 10.1016/j.surfin.2023.102755
ER  - 
@article{
author = "Stamenković, Tijana and Pjević, Dejan J. and Krstić, Jugoslav and Popović, Maja and Rajić, Vladimir and Lojpur, Vesna",
year = "2023",
abstract = "A set of samples of SrGd2O4 doped with Sm3+ and Dy3+with different concentrations was prepared via glycine-assisted combustion synthesis. All of the diffraction peaks are related to the pure orthorhombic lattice SrGd2O4, according to X-ray Powder Diffraction investigation. The Energy Dispersive X-ray Spectroscopy chemical characterization revealed that the structure included all desired elements. Field Emission Scanning Electron Microscopy was used to capture the morphology, which showed porous aggregated particles consisting of roughly 50 nm-sized spherical particles. The Mercury Intrusion Porosimetry was used to establish where voids originated, and the results showed that samples have a real permanent 3D pore structure. X-ray Photoelectron Spectroscopy verified the successful incorporation of Dy3+ and Sm3+ ions in the matrix. Down-conversion luminescence spectra were recorded and typical emission transitions were found for either Sm3+ (4G5/2→6H5/2, 4G5/2→6H7/2, 4G5/2→6H9/2) or Dy3+ (4F9/2→6H15/2 and 4F9/2→6H13/2) ions. Calculation of the energy band gap using UV-VIS Diffuse Reflectance Spectroscopy yielded values of 4.3 eV for both doped samples. Using UV-VIS Absorption Spectroscopy, the photocatalytic degradation process was observed. After 4 h of simulating Sun exposure, an analysis of the photocatalytic properties revealed that approximately 50% of the Rhodamine B had been mineralized.",
journal = "Surfaces and Interfaces",
title = "Characterization and photocatalytic application of SrGd2O4 doped with rare earth Sm3+ and Dy3+ ions",
volume = "37",
pages = "102755",
doi = "10.1016/j.surfin.2023.102755"
}
Stamenković, T., Pjević, D. J., Krstić, J., Popović, M., Rajić, V.,& Lojpur, V.. (2023). Characterization and photocatalytic application of SrGd2O4 doped with rare earth Sm3+ and Dy3+ ions. in Surfaces and Interfaces, 37, 102755.
https://doi.org/10.1016/j.surfin.2023.102755
Stamenković T, Pjević DJ, Krstić J, Popović M, Rajić V, Lojpur V. Characterization and photocatalytic application of SrGd2O4 doped with rare earth Sm3+ and Dy3+ ions. in Surfaces and Interfaces. 2023;37:102755.
doi:10.1016/j.surfin.2023.102755 .
Stamenković, Tijana, Pjević, Dejan J., Krstić, Jugoslav, Popović, Maja, Rajić, Vladimir, Lojpur, Vesna, "Characterization and photocatalytic application of SrGd2O4 doped with rare earth Sm3+ and Dy3+ ions" in Surfaces and Interfaces, 37 (2023):102755,
https://doi.org/10.1016/j.surfin.2023.102755 . .
6
5

What role does carbonized tannic acid play in energy storage composites?

Janošević-Ležaić, Aleksandra; Bajuk-Bogdanović, Danica V.; Krstić, Jugoslav B.; Jovanović, Zoran; Mravik, Željko; Kovač, Janez; Gavrilov, Nemanja

(2022)

TY  - JOUR
AU  - Janošević-Ležaić, Aleksandra
AU  - Bajuk-Bogdanović, Danica V.
AU  - Krstić, Jugoslav B.
AU  - Jovanović, Zoran
AU  - Mravik, Željko
AU  - Kovač, Janez
AU  - Gavrilov, Nemanja
PY  - 2022
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10213
AB  - Transformation of tannic acid (TA), a cheap, abundant and environmentally friendly (by)product, upon carbonization at various temperatures was examined as it is extensively being used in energy storing devices. In addition of reviling what is happening with TA upon carbonization, a step further has been taken to scrutinize the role of carbonized TA (CTA) playing in energy storage composites. Increasing the carbonization temperature from 500 ◦C to 800 ◦C led to a nine orders of magnitude increase in conductivity, from 9⋅10–9 S cm
T2  - Fuel
T1  - What role does carbonized tannic acid play in energy storage composites?
VL  - 312
DO  - 10.1016/j.fuel.2021.122930
ER  - 
@article{
author = "Janošević-Ležaić, Aleksandra and Bajuk-Bogdanović, Danica V. and Krstić, Jugoslav B. and Jovanović, Zoran and Mravik, Željko and Kovač, Janez and Gavrilov, Nemanja",
year = "2022",
abstract = "Transformation of tannic acid (TA), a cheap, abundant and environmentally friendly (by)product, upon carbonization at various temperatures was examined as it is extensively being used in energy storing devices. In addition of reviling what is happening with TA upon carbonization, a step further has been taken to scrutinize the role of carbonized TA (CTA) playing in energy storage composites. Increasing the carbonization temperature from 500 ◦C to 800 ◦C led to a nine orders of magnitude increase in conductivity, from 9⋅10–9 S cm",
journal = "Fuel",
title = "What role does carbonized tannic acid play in energy storage composites?",
volume = "312",
doi = "10.1016/j.fuel.2021.122930"
}
Janošević-Ležaić, A., Bajuk-Bogdanović, D. V., Krstić, J. B., Jovanović, Z., Mravik, Ž., Kovač, J.,& Gavrilov, N.. (2022). What role does carbonized tannic acid play in energy storage composites?. in Fuel, 312.
https://doi.org/10.1016/j.fuel.2021.122930
Janošević-Ležaić A, Bajuk-Bogdanović DV, Krstić JB, Jovanović Z, Mravik Ž, Kovač J, Gavrilov N. What role does carbonized tannic acid play in energy storage composites?. in Fuel. 2022;312.
doi:10.1016/j.fuel.2021.122930 .
Janošević-Ležaić, Aleksandra, Bajuk-Bogdanović, Danica V., Krstić, Jugoslav B., Jovanović, Zoran, Mravik, Željko, Kovač, Janez, Gavrilov, Nemanja, "What role does carbonized tannic acid play in energy storage composites?" in Fuel, 312 (2022),
https://doi.org/10.1016/j.fuel.2021.122930 . .
7
6

Deep Eutectic Solvent (DES) for In Situ Templating Carbon Material: Carbon Characterization and Application in Supercapacitors Containing Multivalent Ions

Zdolšek, Nikola; Janković, Bojan Ž.; Milović, Miloš; Brković, Snežana M.; Krstić, Jugoslav B.; Perović, Ivana M.; Vujković, Milica

(2022)

TY  - JOUR
AU  - Zdolšek, Nikola
AU  - Janković, Bojan Ž.
AU  - Milović, Miloš
AU  - Brković, Snežana M.
AU  - Krstić, Jugoslav B.
AU  - Perović, Ivana M.
AU  - Vujković, Milica
PY  - 2022
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10571
AB  - The development of carbon materials with desirable textures and new aqueous electrolytes is the key strategy to improve the performance of supercapacitors. Herein, a deep eutectic solvent (DES) was used for in situ templating of a carbon material. A carbon material was characterized (XRD, N2-physisorption, FTIR, SEM and EDS) and used as an electrode material for the first time in multivalent-based supercapacitors. In situ templating of carbon was performed using a novel DES, which serves as a precursor for carbon and for in situ generation of MgO. The generation of MgO and its roles in templating of carbon were discussed. Templating of carbon with MgO lead to an increase in surface area and a microporous texture. The obtained carbon was tested in multivalent-ion (Al3+ and Mg2+) electrolytes and compared with H2SO4. The charge-storage mechanism was investigated and elaborated. The highest specific capacitance was obtained for the Al(NO3)3 electrolyte, while the operating voltage follows the order: Mg(NO3)2 > Al(NO3)3 > H2SO4. Electrical double-layer capacitance (versus pseudocapacitance) was dominant in all investigated electrolytes. The larger operating voltage in multivalent electrolytes is a consequence of the lower fraction of free water, which suppresses hydrogen evolution (when compared with H2SO4). The GCD was experimentally performed on the Al(NO3)3 electrolyte, which showed good cyclic stability, with an energy density of 22.3 Wh kg−1 at 65 W kg−1.
T2  - Batteries
T1  - Deep Eutectic Solvent (DES) for In Situ Templating Carbon Material: Carbon Characterization and Application in Supercapacitors Containing Multivalent Ions
VL  - 8
IS  - 12
SP  - 284
DO  - 10.3390/batteries8120284
ER  - 
@article{
author = "Zdolšek, Nikola and Janković, Bojan Ž. and Milović, Miloš and Brković, Snežana M. and Krstić, Jugoslav B. and Perović, Ivana M. and Vujković, Milica",
year = "2022",
abstract = "The development of carbon materials with desirable textures and new aqueous electrolytes is the key strategy to improve the performance of supercapacitors. Herein, a deep eutectic solvent (DES) was used for in situ templating of a carbon material. A carbon material was characterized (XRD, N2-physisorption, FTIR, SEM and EDS) and used as an electrode material for the first time in multivalent-based supercapacitors. In situ templating of carbon was performed using a novel DES, which serves as a precursor for carbon and for in situ generation of MgO. The generation of MgO and its roles in templating of carbon were discussed. Templating of carbon with MgO lead to an increase in surface area and a microporous texture. The obtained carbon was tested in multivalent-ion (Al3+ and Mg2+) electrolytes and compared with H2SO4. The charge-storage mechanism was investigated and elaborated. The highest specific capacitance was obtained for the Al(NO3)3 electrolyte, while the operating voltage follows the order: Mg(NO3)2 > Al(NO3)3 > H2SO4. Electrical double-layer capacitance (versus pseudocapacitance) was dominant in all investigated electrolytes. The larger operating voltage in multivalent electrolytes is a consequence of the lower fraction of free water, which suppresses hydrogen evolution (when compared with H2SO4). The GCD was experimentally performed on the Al(NO3)3 electrolyte, which showed good cyclic stability, with an energy density of 22.3 Wh kg−1 at 65 W kg−1.",
journal = "Batteries",
title = "Deep Eutectic Solvent (DES) for In Situ Templating Carbon Material: Carbon Characterization and Application in Supercapacitors Containing Multivalent Ions",
volume = "8",
number = "12",
pages = "284",
doi = "10.3390/batteries8120284"
}
Zdolšek, N., Janković, B. Ž., Milović, M., Brković, S. M., Krstić, J. B., Perović, I. M.,& Vujković, M.. (2022). Deep Eutectic Solvent (DES) for In Situ Templating Carbon Material: Carbon Characterization and Application in Supercapacitors Containing Multivalent Ions. in Batteries, 8(12), 284.
https://doi.org/10.3390/batteries8120284
Zdolšek N, Janković BŽ, Milović M, Brković SM, Krstić JB, Perović IM, Vujković M. Deep Eutectic Solvent (DES) for In Situ Templating Carbon Material: Carbon Characterization and Application in Supercapacitors Containing Multivalent Ions. in Batteries. 2022;8(12):284.
doi:10.3390/batteries8120284 .
Zdolšek, Nikola, Janković, Bojan Ž., Milović, Miloš, Brković, Snežana M., Krstić, Jugoslav B., Perović, Ivana M., Vujković, Milica, "Deep Eutectic Solvent (DES) for In Situ Templating Carbon Material: Carbon Characterization and Application in Supercapacitors Containing Multivalent Ions" in Batteries, 8, no. 12 (2022):284,
https://doi.org/10.3390/batteries8120284 . .

Novel composite based on zirconia and graphite. First results of application for synthetic dyes removal

Stepić, Katarina; Ljupković, Radomir; Zarubica, Aleksandra R.; Đorđijevski, Stefan; Matović, Branko; Krstić, Jugoslav B.; Bojić, Aleksandar

(2022)

TY  - JOUR
AU  - Stepić, Katarina
AU  - Ljupković, Radomir
AU  - Zarubica, Aleksandra R.
AU  - Đorđijevski, Stefan
AU  - Matović, Branko
AU  - Krstić, Jugoslav B.
AU  - Bojić, Aleksandar
PY  - 2022
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10361
AB  - In this research composite based on zirconia and graphite was synthesized using the sol-gel method. Aim of this research is to activate and increase the photocatalytic activity of ZrO2 by combining with graphite-based material. Our results show that we obtained material that can remove both cationic and anionic dyes by sorption and photocatalytic processes. Obtained composite is very effective in sorption of RB19 with up to 100% removal. Photocatalytic activity of composite is higher than pristine GO and goes up to 100% for RB19 degradation and about 50% degradation of MB. These results are promising and present an excellent base for further research. © 2022, Universitatea Babes-Bolyai, Catedra de Filosofie Sistematica. All rights reserved.
T2  - Studia Universitatis Babes-Bolyai Chemia
T1  - Novel composite based on zirconia and graphite. First results of application for synthetic dyes removal
VL  - 67
IS  - 2
SP  - 23
EP  - 43
DO  - 10.24193/subbchem.2022.2.02
ER  - 
@article{
author = "Stepić, Katarina and Ljupković, Radomir and Zarubica, Aleksandra R. and Đorđijevski, Stefan and Matović, Branko and Krstić, Jugoslav B. and Bojić, Aleksandar",
year = "2022",
abstract = "In this research composite based on zirconia and graphite was synthesized using the sol-gel method. Aim of this research is to activate and increase the photocatalytic activity of ZrO2 by combining with graphite-based material. Our results show that we obtained material that can remove both cationic and anionic dyes by sorption and photocatalytic processes. Obtained composite is very effective in sorption of RB19 with up to 100% removal. Photocatalytic activity of composite is higher than pristine GO and goes up to 100% for RB19 degradation and about 50% degradation of MB. These results are promising and present an excellent base for further research. © 2022, Universitatea Babes-Bolyai, Catedra de Filosofie Sistematica. All rights reserved.",
journal = "Studia Universitatis Babes-Bolyai Chemia",
title = "Novel composite based on zirconia and graphite. First results of application for synthetic dyes removal",
volume = "67",
number = "2",
pages = "23-43",
doi = "10.24193/subbchem.2022.2.02"
}
Stepić, K., Ljupković, R., Zarubica, A. R., Đorđijevski, S., Matović, B., Krstić, J. B.,& Bojić, A.. (2022). Novel composite based on zirconia and graphite. First results of application for synthetic dyes removal. in Studia Universitatis Babes-Bolyai Chemia, 67(2), 23-43.
https://doi.org/10.24193/subbchem.2022.2.02
Stepić K, Ljupković R, Zarubica AR, Đorđijevski S, Matović B, Krstić JB, Bojić A. Novel composite based on zirconia and graphite. First results of application for synthetic dyes removal. in Studia Universitatis Babes-Bolyai Chemia. 2022;67(2):23-43.
doi:10.24193/subbchem.2022.2.02 .
Stepić, Katarina, Ljupković, Radomir, Zarubica, Aleksandra R., Đorđijevski, Stefan, Matović, Branko, Krstić, Jugoslav B., Bojić, Aleksandar, "Novel composite based on zirconia and graphite. First results of application for synthetic dyes removal" in Studia Universitatis Babes-Bolyai Chemia, 67, no. 2 (2022):23-43,
https://doi.org/10.24193/subbchem.2022.2.02 . .

Electromagnetic characterization of Ni0.5Zn0.3Co0.2Fe2O4 bulk ceramics in the 1 MHz-12 GHz frequency range

Zarubica, Aleksandra R.; Krstić, Jugoslav B.; Popović, Dejan; Krstić, Aleksandra; Ljupković, Radomir; Ranđelović, Marjan S.; Matović, Branko

(2021)

TY  - JOUR
AU  - Zarubica, Aleksandra R.
AU  - Krstić, Jugoslav B.
AU  - Popović, Dejan
AU  - Krstić, Aleksandra
AU  - Ljupković, Radomir
AU  - Ranđelović, Marjan S.
AU  - Matović, Branko
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9900
AB  - In this paper, NiZnCo ferrite was produced by solid state synthesis, calcination at 1000 °C and sintering at 1250 °C in air atmosphere. The microstructure and phases of the sintered sample were analysed by scanning electron microscopy and X-ray diffraction, respectively. The magnetic properties of the ferrite were evaluated by magnetization and magnetostriction measurements. The complex magnetic permeability and complex permittivity were also measured between 1 MHz-12 GHz and the reflection loss (RL) was calculated in the 100 MHz-12 GHz frequency range. The results show that the ferrite sample presents magnetostrictive behaviour and a saturation magnetization of 71 Am2/kg. Complex permittivity measurements indicate that the material has dielectric behaviour in the whole frequency range studied, with ε′ varying between 7-40, and magnetic behaviour in frequencies between 1 MHz-5 GHz. The minimum RL was found at frequencies between 2.4-3.3 GHz and the calculated RL value for a thickness of 3 mm was lower than −10 dB in frequencies between 2.3-7.3 GHz. These results indicate potential application as microwave absorber in the S band.
T2  - Processing and Application of Ceramics
T1  - Electromagnetic characterization of Ni0.5Zn0.3Co0.2Fe2O4 bulk ceramics in the 1 MHz-12 GHz frequency range
VL  - 15
IS  - 2
SP  - 136
DO  - 10.2298/PAC2102111Z
ER  - 
@article{
author = "Zarubica, Aleksandra R. and Krstić, Jugoslav B. and Popović, Dejan and Krstić, Aleksandra and Ljupković, Radomir and Ranđelović, Marjan S. and Matović, Branko",
year = "2021",
abstract = "In this paper, NiZnCo ferrite was produced by solid state synthesis, calcination at 1000 °C and sintering at 1250 °C in air atmosphere. The microstructure and phases of the sintered sample were analysed by scanning electron microscopy and X-ray diffraction, respectively. The magnetic properties of the ferrite were evaluated by magnetization and magnetostriction measurements. The complex magnetic permeability and complex permittivity were also measured between 1 MHz-12 GHz and the reflection loss (RL) was calculated in the 100 MHz-12 GHz frequency range. The results show that the ferrite sample presents magnetostrictive behaviour and a saturation magnetization of 71 Am2/kg. Complex permittivity measurements indicate that the material has dielectric behaviour in the whole frequency range studied, with ε′ varying between 7-40, and magnetic behaviour in frequencies between 1 MHz-5 GHz. The minimum RL was found at frequencies between 2.4-3.3 GHz and the calculated RL value for a thickness of 3 mm was lower than −10 dB in frequencies between 2.3-7.3 GHz. These results indicate potential application as microwave absorber in the S band.",
journal = "Processing and Application of Ceramics",
title = "Electromagnetic characterization of Ni0.5Zn0.3Co0.2Fe2O4 bulk ceramics in the 1 MHz-12 GHz frequency range",
volume = "15",
number = "2",
pages = "136",
doi = "10.2298/PAC2102111Z"
}
Zarubica, A. R., Krstić, J. B., Popović, D., Krstić, A., Ljupković, R., Ranđelović, M. S.,& Matović, B.. (2021). Electromagnetic characterization of Ni0.5Zn0.3Co0.2Fe2O4 bulk ceramics in the 1 MHz-12 GHz frequency range. in Processing and Application of Ceramics, 15(2), 136.
https://doi.org/10.2298/PAC2102111Z
Zarubica AR, Krstić JB, Popović D, Krstić A, Ljupković R, Ranđelović MS, Matović B. Electromagnetic characterization of Ni0.5Zn0.3Co0.2Fe2O4 bulk ceramics in the 1 MHz-12 GHz frequency range. in Processing and Application of Ceramics. 2021;15(2):136.
doi:10.2298/PAC2102111Z .
Zarubica, Aleksandra R., Krstić, Jugoslav B., Popović, Dejan, Krstić, Aleksandra, Ljupković, Radomir, Ranđelović, Marjan S., Matović, Branko, "Electromagnetic characterization of Ni0.5Zn0.3Co0.2Fe2O4 bulk ceramics in the 1 MHz-12 GHz frequency range" in Processing and Application of Ceramics, 15, no. 2 (2021):136,
https://doi.org/10.2298/PAC2102111Z . .
1

Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I—Physical–Chemical and Physical–Mechanical Characterization of Slag

Nedeljković, Andrijana; Stojmenović, Marija; Gulicovski, Jelena J.; Ristić, Nenad; Milićević, Sonja; Krstić, Jugoslav B.; Kragović, Milan M.

(MDPI, 2020)

TY  - JOUR
AU  - Nedeljković, Andrijana
AU  - Stojmenović, Marija
AU  - Gulicovski, Jelena J.
AU  - Ristić, Nenad
AU  - Milićević, Sonja
AU  - Krstić, Jugoslav B.
AU  - Kragović, Milan M.
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9730
AB  - Numerous factors influence the complexity of environmental and waste management problems, and the most significant goal is the reuse of materials that have completed their “life cycle” and the reduction in the use of new resources. In order to reduce impact of waste slag on the environment, in the present study, waste slag, generated in heating plants after lignite combustion, was characterized in detail and tested for application as a replacement for cement in mortar or concrete production. For physical–chemical characterization of slag, different experimental and instrumental techniques were used such as chemical composition and determination of the content of heavy metals, investigation of morphological and textural properties, thermal analysis, X-ray, and infrared spectroscopy. Physical–mechanical characterization of slag was also performed and included determination of activity index, water requirement, setting time and soundness. A leaching test was also performed. Presented results show that waste slag may be used in mortar and concrete production as a partial cement replacement, but after additional combustion at 650 °C and partial replacement of slag with silica fume in the minimal amount of 12%. The maximal obtained cement replacement was 20% (17.8% slag and 2.2% of silica fume).
PB  - MDPI
T2  - Minerals
T1  - Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I—Physical–Chemical and Physical–Mechanical Characterization of Slag
VL  - 10
IS  - 11
SP  - 992
DO  - 10.3390/min10110992
ER  - 
@article{
author = "Nedeljković, Andrijana and Stojmenović, Marija and Gulicovski, Jelena J. and Ristić, Nenad and Milićević, Sonja and Krstić, Jugoslav B. and Kragović, Milan M.",
year = "2020",
abstract = "Numerous factors influence the complexity of environmental and waste management problems, and the most significant goal is the reuse of materials that have completed their “life cycle” and the reduction in the use of new resources. In order to reduce impact of waste slag on the environment, in the present study, waste slag, generated in heating plants after lignite combustion, was characterized in detail and tested for application as a replacement for cement in mortar or concrete production. For physical–chemical characterization of slag, different experimental and instrumental techniques were used such as chemical composition and determination of the content of heavy metals, investigation of morphological and textural properties, thermal analysis, X-ray, and infrared spectroscopy. Physical–mechanical characterization of slag was also performed and included determination of activity index, water requirement, setting time and soundness. A leaching test was also performed. Presented results show that waste slag may be used in mortar and concrete production as a partial cement replacement, but after additional combustion at 650 °C and partial replacement of slag with silica fume in the minimal amount of 12%. The maximal obtained cement replacement was 20% (17.8% slag and 2.2% of silica fume).",
publisher = "MDPI",
journal = "Minerals",
title = "Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I—Physical–Chemical and Physical–Mechanical Characterization of Slag",
volume = "10",
number = "11",
pages = "992",
doi = "10.3390/min10110992"
}
Nedeljković, A., Stojmenović, M., Gulicovski, J. J., Ristić, N., Milićević, S., Krstić, J. B.,& Kragović, M. M.. (2020). Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I—Physical–Chemical and Physical–Mechanical Characterization of Slag. in Minerals
MDPI., 10(11), 992.
https://doi.org/10.3390/min10110992
Nedeljković A, Stojmenović M, Gulicovski JJ, Ristić N, Milićević S, Krstić JB, Kragović MM. Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I—Physical–Chemical and Physical–Mechanical Characterization of Slag. in Minerals. 2020;10(11):992.
doi:10.3390/min10110992 .
Nedeljković, Andrijana, Stojmenović, Marija, Gulicovski, Jelena J., Ristić, Nenad, Milićević, Sonja, Krstić, Jugoslav B., Kragović, Milan M., "Waste Slag from Heating Plants as a Partial Replacement for Cement in Mortar and Concrete Production. Part I—Physical–Chemical and Physical–Mechanical Characterization of Slag" in Minerals, 10, no. 11 (2020):992,
https://doi.org/10.3390/min10110992 . .
8
2
8

Synthesis and antibacterial activity of iron manganite (FeMnO3) particles against the environmental bacterium Bacillus subtilis

Vasiljević, Zorka; Dojčinović, Milena; Krstić, Jugoslav B.; Ribić, Vesna; Tadić, Nenad B.; Ognjanović, Miloš; Auger, Sandrine; Vidić, Jasmina; Nikolić, Maria Vesna

(2020)

TY  - JOUR
AU  - Vasiljević, Zorka
AU  - Dojčinović, Milena
AU  - Krstić, Jugoslav B.
AU  - Ribić, Vesna
AU  - Tadić, Nenad B.
AU  - Ognjanović, Miloš
AU  - Auger, Sandrine
AU  - Vidić, Jasmina
AU  - Nikolić, Maria Vesna
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8941
AB  - Nanocrystalline iron manganite powder was synthesized using the sol–gel combustion process, with glycine as fuel. It was further calcined at 900 °C for 8 h, resulting in the formation of a loose cubic FeMnO3 powder with a small specific surface area, net-like structure and plate-like particles as confirmed by XRD, N2 physisorption, FESEM and TEM analyses. The metal ion release was studied by ICP-OES and showed that less than 10 ppb of Fe or Mn ions were released by leaching in water, but 0.36 ppm Fe and 3.69 ppm Mn was found in LB (Luria–Bertani) bacterial medium. The generation of reactive oxygen species (ROS) was monitored in distilled water and bacterial medium and showed that FeMnO3 particles do not generate O2˙− ions with or without UV irradiation, but synthesize H2O2 and show an antioxidative effect. Besides the higher stability of FeMnO3 particles in aqueous solution they showed an inhibitory effect on Bacillus subtilis growth in LB medium even at low concentrations (0.01 mg ml−1), but not in BHI medium even at 1 mg ml−1. This study points out that the mechanism of antibacterial action of engineered metal oxides needs continued investigation and specific experimental controls.
T2  - RSC Advances
T1  - Synthesis and antibacterial activity of iron manganite (FeMnO3) particles against the environmental bacterium Bacillus subtilis
VL  - 10
IS  - 23
SP  - 13879
EP  - 13888
DO  - 10.1039/D0RA01809K
ER  - 
@article{
author = "Vasiljević, Zorka and Dojčinović, Milena and Krstić, Jugoslav B. and Ribić, Vesna and Tadić, Nenad B. and Ognjanović, Miloš and Auger, Sandrine and Vidić, Jasmina and Nikolić, Maria Vesna",
year = "2020",
abstract = "Nanocrystalline iron manganite powder was synthesized using the sol–gel combustion process, with glycine as fuel. It was further calcined at 900 °C for 8 h, resulting in the formation of a loose cubic FeMnO3 powder with a small specific surface area, net-like structure and plate-like particles as confirmed by XRD, N2 physisorption, FESEM and TEM analyses. The metal ion release was studied by ICP-OES and showed that less than 10 ppb of Fe or Mn ions were released by leaching in water, but 0.36 ppm Fe and 3.69 ppm Mn was found in LB (Luria–Bertani) bacterial medium. The generation of reactive oxygen species (ROS) was monitored in distilled water and bacterial medium and showed that FeMnO3 particles do not generate O2˙− ions with or without UV irradiation, but synthesize H2O2 and show an antioxidative effect. Besides the higher stability of FeMnO3 particles in aqueous solution they showed an inhibitory effect on Bacillus subtilis growth in LB medium even at low concentrations (0.01 mg ml−1), but not in BHI medium even at 1 mg ml−1. This study points out that the mechanism of antibacterial action of engineered metal oxides needs continued investigation and specific experimental controls.",
journal = "RSC Advances",
title = "Synthesis and antibacterial activity of iron manganite (FeMnO3) particles against the environmental bacterium Bacillus subtilis",
volume = "10",
number = "23",
pages = "13879-13888",
doi = "10.1039/D0RA01809K"
}
Vasiljević, Z., Dojčinović, M., Krstić, J. B., Ribić, V., Tadić, N. B., Ognjanović, M., Auger, S., Vidić, J.,& Nikolić, M. V.. (2020). Synthesis and antibacterial activity of iron manganite (FeMnO3) particles against the environmental bacterium Bacillus subtilis. in RSC Advances, 10(23), 13879-13888.
https://doi.org/10.1039/D0RA01809K
Vasiljević Z, Dojčinović M, Krstić JB, Ribić V, Tadić NB, Ognjanović M, Auger S, Vidić J, Nikolić MV. Synthesis and antibacterial activity of iron manganite (FeMnO3) particles against the environmental bacterium Bacillus subtilis. in RSC Advances. 2020;10(23):13879-13888.
doi:10.1039/D0RA01809K .
Vasiljević, Zorka, Dojčinović, Milena, Krstić, Jugoslav B., Ribić, Vesna, Tadić, Nenad B., Ognjanović, Miloš, Auger, Sandrine, Vidić, Jasmina, Nikolić, Maria Vesna, "Synthesis and antibacterial activity of iron manganite (FeMnO3) particles against the environmental bacterium Bacillus subtilis" in RSC Advances, 10, no. 23 (2020):13879-13888,
https://doi.org/10.1039/D0RA01809K . .
17
11
17

Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?

Bajuk-Bogdanović, Danica V.; Holclajtner-Antunović, Ivanka D.; Jovanović, Zoran M.; Mravik, Željko; Krstić, Jugoslav B.; Uskoković-Marković, Snežana; Vujković, Milica

(2019)

TY  - JOUR
AU  - Bajuk-Bogdanović, Danica V.
AU  - Holclajtner-Antunović, Ivanka D.
AU  - Jovanović, Zoran M.
AU  - Mravik, Željko
AU  - Krstić, Jugoslav B.
AU  - Uskoković-Marković, Snežana
AU  - Vujković, Milica
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8500
AB  - The synergistic effects between two Keggin-type heteropoly acids (HPAs) and carbon surface were examined and elucidated. An improved high rate capability (and potential high capacitor electrode for supercapacitors) of the hybrid materials, obtained by anchoring of α-dodecamolybdophosphoric (MoPA), α-dodecatungstophosphoric (WPA), and their mixture to activated carbon (AC), was achieved through the different mechanism of interaction. In order to elaborate this, a detailed analysis of AC-HPA composites has been performed by scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) analysis, temperature-programmed desorption (TPD), Fourier-transform infrared spectroscopy (FTIR), micro Raman spectroscopy, and zeta potential measurements. The zeta potential measurements revealed positive charge of carbon surface thus indicating attractive interactions with negatively charged Keggin anion. The surface analysis has shown that WPA spontaneously reduces the carbon surface, while interaction with MoPA leads to its oxidation. As the consequence of the tailoring of the functional groups at carbon surface through HPAs’ action, the distortion of cyclic voltammograms (CVs) decreased in the following order: AC-MoPA, AC-MoPA-WPA, and AC-WPA. A prominent rectangular shape of AC-WPA, even at an extremely high scan rate of 400 mVs−1, was measured, which is rarely demonstrated for carbon-based composites. By applying the theory of electrode potentials, the HPA-AC synergistic effect was explained and discussed in terms of charge storage improvement of HPA-modified carbon. © 2019, Springer-Verlag GmbH Germany, part of Springer Nature.
T2  - Journal of Solid State Electrochemistry
T1  - Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?
VL  - 23
IS  - 9
SP  - 2747
EP  - 2758
DO  - 10.1007/s10008-019-04369-4
ER  - 
@article{
author = "Bajuk-Bogdanović, Danica V. and Holclajtner-Antunović, Ivanka D. and Jovanović, Zoran M. and Mravik, Željko and Krstić, Jugoslav B. and Uskoković-Marković, Snežana and Vujković, Milica",
year = "2019",
abstract = "The synergistic effects between two Keggin-type heteropoly acids (HPAs) and carbon surface were examined and elucidated. An improved high rate capability (and potential high capacitor electrode for supercapacitors) of the hybrid materials, obtained by anchoring of α-dodecamolybdophosphoric (MoPA), α-dodecatungstophosphoric (WPA), and their mixture to activated carbon (AC), was achieved through the different mechanism of interaction. In order to elaborate this, a detailed analysis of AC-HPA composites has been performed by scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) analysis, temperature-programmed desorption (TPD), Fourier-transform infrared spectroscopy (FTIR), micro Raman spectroscopy, and zeta potential measurements. The zeta potential measurements revealed positive charge of carbon surface thus indicating attractive interactions with negatively charged Keggin anion. The surface analysis has shown that WPA spontaneously reduces the carbon surface, while interaction with MoPA leads to its oxidation. As the consequence of the tailoring of the functional groups at carbon surface through HPAs’ action, the distortion of cyclic voltammograms (CVs) decreased in the following order: AC-MoPA, AC-MoPA-WPA, and AC-WPA. A prominent rectangular shape of AC-WPA, even at an extremely high scan rate of 400 mVs−1, was measured, which is rarely demonstrated for carbon-based composites. By applying the theory of electrode potentials, the HPA-AC synergistic effect was explained and discussed in terms of charge storage improvement of HPA-modified carbon. © 2019, Springer-Verlag GmbH Germany, part of Springer Nature.",
journal = "Journal of Solid State Electrochemistry",
title = "Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?",
volume = "23",
number = "9",
pages = "2747-2758",
doi = "10.1007/s10008-019-04369-4"
}
Bajuk-Bogdanović, D. V., Holclajtner-Antunović, I. D., Jovanović, Z. M., Mravik, Ž., Krstić, J. B., Uskoković-Marković, S.,& Vujković, M.. (2019). Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?. in Journal of Solid State Electrochemistry, 23(9), 2747-2758.
https://doi.org/10.1007/s10008-019-04369-4
Bajuk-Bogdanović DV, Holclajtner-Antunović ID, Jovanović ZM, Mravik Ž, Krstić JB, Uskoković-Marković S, Vujković M. Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?. in Journal of Solid State Electrochemistry. 2019;23(9):2747-2758.
doi:10.1007/s10008-019-04369-4 .
Bajuk-Bogdanović, Danica V., Holclajtner-Antunović, Ivanka D., Jovanović, Zoran M., Mravik, Željko, Krstić, Jugoslav B., Uskoković-Marković, Snežana, Vujković, Milica, "Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?" in Journal of Solid State Electrochemistry, 23, no. 9 (2019):2747-2758,
https://doi.org/10.1007/s10008-019-04369-4 . .
3
2
3

Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer

Zdolšek, Nikola; Rocha, Raquel P.; Krstić, Jugoslav B.; Trtić-Petrović, Tatjana M.; Šljukić, Biljana; Figueiredo, Jose L.; Vujković, Milica

(2019)

TY  - JOUR
AU  - Zdolšek, Nikola
AU  - Rocha, Raquel P.
AU  - Krstić, Jugoslav B.
AU  - Trtić-Petrović, Tatjana M.
AU  - Šljukić, Biljana
AU  - Figueiredo, Jose L.
AU  - Vujković, Milica
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0013468618328482
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8023
AB  - This work shows the potential application of carbon materials prepared by three different ionic liquid-based methods, using 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3], for electrochemical supercapacitors. The effects of [bmim][MeSO3] on morphology, texture and surface chemistry of prepared materials has been explored by SEM/TEM, N2/CO2 adsorption measurements and XPS. The results indicate the possibility of synthesis of carbon materials with tunable physicochemical properties using ionic liquid based methods. The charge storage behavior of all materials was studied in three different pH aqueous electrolytes. The pseudocapacitive and double layer contributions were estimated and discussed from the aspect of the textural changes and the changes of the chemical composition of surface functional groups containing heteroatoms. C[dbnd]O type functional groups, with the contribution of COOH groups, were found to be responsible for a different amount of charge, which could be stored in alkaline and acidic electrolytic solution. The material prepared by direct carbonization of [bmim][MeSO3], showed the best electrochemical performance in alkaline electrolyte with a capacitance of 187 F g−1 at 5 mV s−1 (or 148 F g−1 at 1 A g−1), due to the contribution of both electric-double layer capacitance and pseudocapacitance which arises from oxygen, nitrogen and sulfur functional groups. © 2018 Elsevier Ltd
T2  - Electrochimica Acta
T1  - Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer
VL  - 298
SP  - 541
EP  - 551
DO  - 10.1016/j.electacta.2018.12.129
ER  - 
@article{
author = "Zdolšek, Nikola and Rocha, Raquel P. and Krstić, Jugoslav B. and Trtić-Petrović, Tatjana M. and Šljukić, Biljana and Figueiredo, Jose L. and Vujković, Milica",
year = "2019",
abstract = "This work shows the potential application of carbon materials prepared by three different ionic liquid-based methods, using 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3], for electrochemical supercapacitors. The effects of [bmim][MeSO3] on morphology, texture and surface chemistry of prepared materials has been explored by SEM/TEM, N2/CO2 adsorption measurements and XPS. The results indicate the possibility of synthesis of carbon materials with tunable physicochemical properties using ionic liquid based methods. The charge storage behavior of all materials was studied in three different pH aqueous electrolytes. The pseudocapacitive and double layer contributions were estimated and discussed from the aspect of the textural changes and the changes of the chemical composition of surface functional groups containing heteroatoms. C[dbnd]O type functional groups, with the contribution of COOH groups, were found to be responsible for a different amount of charge, which could be stored in alkaline and acidic electrolytic solution. The material prepared by direct carbonization of [bmim][MeSO3], showed the best electrochemical performance in alkaline electrolyte with a capacitance of 187 F g−1 at 5 mV s−1 (or 148 F g−1 at 1 A g−1), due to the contribution of both electric-double layer capacitance and pseudocapacitance which arises from oxygen, nitrogen and sulfur functional groups. © 2018 Elsevier Ltd",
journal = "Electrochimica Acta",
title = "Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer",
volume = "298",
pages = "541-551",
doi = "10.1016/j.electacta.2018.12.129"
}
Zdolšek, N., Rocha, R. P., Krstić, J. B., Trtić-Petrović, T. M., Šljukić, B., Figueiredo, J. L.,& Vujković, M.. (2019). Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer. in Electrochimica Acta, 298, 541-551.
https://doi.org/10.1016/j.electacta.2018.12.129
Zdolšek N, Rocha RP, Krstić JB, Trtić-Petrović TM, Šljukić B, Figueiredo JL, Vujković M. Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer. in Electrochimica Acta. 2019;298:541-551.
doi:10.1016/j.electacta.2018.12.129 .
Zdolšek, Nikola, Rocha, Raquel P., Krstić, Jugoslav B., Trtić-Petrović, Tatjana M., Šljukić, Biljana, Figueiredo, Jose L., Vujković, Milica, "Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer" in Electrochimica Acta, 298 (2019):541-551,
https://doi.org/10.1016/j.electacta.2018.12.129 . .
32
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32

Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]

Zdolšek, Nikola; Rocha, Raquel P.; Krstić, Jugoslav B.; Trtić-Petrović, Tatjana M.; Šljukić, Biljana; Figueiredo, José L.; Vujković, Milica

(2019)

TY  - JOUR
AU  - Zdolšek, Nikola
AU  - Rocha, Raquel P.
AU  - Krstić, Jugoslav B.
AU  - Trtić-Petrović, Tatjana M.
AU  - Šljukić, Biljana
AU  - Figueiredo, José L.
AU  - Vujković, Milica
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0013468619307960
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8159
AB  - The authors regret errors in the above mentioned article in the equation (2)as well as in the Fig. 10a. In the equation (2)the number 2 was accidently omitted, whereas the values for the x-axis of Fig. 10a were doubled by accident. The authors would like to apologise for any inconvenience caused. The corrected equation (2)and Fig. 10 are shown below. [Formula presented][Figure presented]Fig. 10. a)Galvanostatic charge-discharge curves for Carb-IL at different current densities in 6 M KOH and b)dependence of the discharge specific capacitance of Carb-IL on the number of cycles, at 5 A g −1 . © 2018 Elsevier Ltd
T2  - Electrochimica Acta
T1  - Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]
VL  - 310
SP  - 221
DO  - 10.1016/j.electacta.2019.04.108
ER  - 
@article{
author = "Zdolšek, Nikola and Rocha, Raquel P. and Krstić, Jugoslav B. and Trtić-Petrović, Tatjana M. and Šljukić, Biljana and Figueiredo, José L. and Vujković, Milica",
year = "2019",
abstract = "The authors regret errors in the above mentioned article in the equation (2)as well as in the Fig. 10a. In the equation (2)the number 2 was accidently omitted, whereas the values for the x-axis of Fig. 10a were doubled by accident. The authors would like to apologise for any inconvenience caused. The corrected equation (2)and Fig. 10 are shown below. [Formula presented][Figure presented]Fig. 10. a)Galvanostatic charge-discharge curves for Carb-IL at different current densities in 6 M KOH and b)dependence of the discharge specific capacitance of Carb-IL on the number of cycles, at 5 A g −1 . © 2018 Elsevier Ltd",
journal = "Electrochimica Acta",
title = "Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]",
volume = "310",
pages = "221",
doi = "10.1016/j.electacta.2019.04.108"
}
Zdolšek, N., Rocha, R. P., Krstić, J. B., Trtić-Petrović, T. M., Šljukić, B., Figueiredo, J. L.,& Vujković, M.. (2019). Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]. in Electrochimica Acta, 310, 221.
https://doi.org/10.1016/j.electacta.2019.04.108
Zdolšek N, Rocha RP, Krstić JB, Trtić-Petrović TM, Šljukić B, Figueiredo JL, Vujković M. Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]. in Electrochimica Acta. 2019;310:221.
doi:10.1016/j.electacta.2019.04.108 .
Zdolšek, Nikola, Rocha, Raquel P., Krstić, Jugoslav B., Trtić-Petrović, Tatjana M., Šljukić, Biljana, Figueiredo, José L., Vujković, Milica, "Corrigendum to “Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: Pseudocapacitance versus electrical double layer” [Electrochim. Acta 298 (2019) 541–551]" in Electrochimica Acta, 310 (2019):221,
https://doi.org/10.1016/j.electacta.2019.04.108 . .

Novel WO3/Fe3O4 magnetic photocatalysts: Preparation, characterization and thiacloprid photodegradation

Banić, Nemanja D.; Abramović, Biljana F.; Krstić, Jugoslav B.; Šojić Merkulov, Daniela V.; Finčur, Nina L.; Mitrić, Miodrag

(2019)

TY  - JOUR
AU  - Banić, Nemanja D.
AU  - Abramović, Biljana F.
AU  - Krstić, Jugoslav B.
AU  - Šojić Merkulov, Daniela V.
AU  - Finčur, Nina L.
AU  - Mitrić, Miodrag
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8446
AB  - This work presents the characterization of novel synthesized WO3/Fe3O4 catalysts and investigates their photocatalytic activity for thiacloprid decomposition under UV and simulated sunlight radiation. Four WO3/Fe3O4 nanopowders with different amounts of WO3 were synthesized by chemical co-precipitation method. XRD analysis showed the presence of hematite and magnetite nano-dimensional phases of Fe3O4 in the catalysts. The magnetite phase content increased with increasing WO3 content. Degradation efficiency of thiacloprid in the presence of 6.1WO3/Fe3O4/H2O2 under simulated solar radiation was 2.2 times higher compared to Fe3O4. Under an external magnetic field, a significant increase in the catalysts separation from reaction mixture was observed. © 2018 The Korean Society of Industrial and Engineering Chemistry
T2  - Journal of Industrial and Engineering Chemistry
T1  - Novel WO3/Fe3O4 magnetic photocatalysts: Preparation, characterization and thiacloprid photodegradation
VL  - 70
SP  - 264
EP  - 275
DO  - 10.1016/j.jiec.2018.10.025
ER  - 
@article{
author = "Banić, Nemanja D. and Abramović, Biljana F. and Krstić, Jugoslav B. and Šojić Merkulov, Daniela V. and Finčur, Nina L. and Mitrić, Miodrag",
year = "2019",
abstract = "This work presents the characterization of novel synthesized WO3/Fe3O4 catalysts and investigates their photocatalytic activity for thiacloprid decomposition under UV and simulated sunlight radiation. Four WO3/Fe3O4 nanopowders with different amounts of WO3 were synthesized by chemical co-precipitation method. XRD analysis showed the presence of hematite and magnetite nano-dimensional phases of Fe3O4 in the catalysts. The magnetite phase content increased with increasing WO3 content. Degradation efficiency of thiacloprid in the presence of 6.1WO3/Fe3O4/H2O2 under simulated solar radiation was 2.2 times higher compared to Fe3O4. Under an external magnetic field, a significant increase in the catalysts separation from reaction mixture was observed. © 2018 The Korean Society of Industrial and Engineering Chemistry",
journal = "Journal of Industrial and Engineering Chemistry",
title = "Novel WO3/Fe3O4 magnetic photocatalysts: Preparation, characterization and thiacloprid photodegradation",
volume = "70",
pages = "264-275",
doi = "10.1016/j.jiec.2018.10.025"
}
Banić, N. D., Abramović, B. F., Krstić, J. B., Šojić Merkulov, D. V., Finčur, N. L.,& Mitrić, M.. (2019). Novel WO3/Fe3O4 magnetic photocatalysts: Preparation, characterization and thiacloprid photodegradation. in Journal of Industrial and Engineering Chemistry, 70, 264-275.
https://doi.org/10.1016/j.jiec.2018.10.025
Banić ND, Abramović BF, Krstić JB, Šojić Merkulov DV, Finčur NL, Mitrić M. Novel WO3/Fe3O4 magnetic photocatalysts: Preparation, characterization and thiacloprid photodegradation. in Journal of Industrial and Engineering Chemistry. 2019;70:264-275.
doi:10.1016/j.jiec.2018.10.025 .
Banić, Nemanja D., Abramović, Biljana F., Krstić, Jugoslav B., Šojić Merkulov, Daniela V., Finčur, Nina L., Mitrić, Miodrag, "Novel WO3/Fe3O4 magnetic photocatalysts: Preparation, characterization and thiacloprid photodegradation" in Journal of Industrial and Engineering Chemistry, 70 (2019):264-275,
https://doi.org/10.1016/j.jiec.2018.10.025 . .
31
16
29

Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction

Zdolšek, Nikola; Dimitrijević, Aleksandra; Bendova, Magdalena; Krstić, Jugoslav B.; Rocha, Raquel P.; Figueiredo, Jose L.; Bajuk-Bogdanović, Danica V.; Trtić-Petrović, Tatjana M.; Šljukić, Biljana

(2018)

TY  - JOUR
AU  - Zdolšek, Nikola
AU  - Dimitrijević, Aleksandra
AU  - Bendova, Magdalena
AU  - Krstić, Jugoslav B.
AU  - Rocha, Raquel P.
AU  - Figueiredo, Jose L.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Trtić-Petrović, Tatjana M.
AU  - Šljukić, Biljana
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9881
AB  - Carbon materials, prepared by using different methods with ionic liquids, are compared as electrocatalysts for the oxygen reduction reaction (ORR). Materials were synthesized through the hydrothermal carbonization of glucose and by using the same method in the presence of 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3] as an additive. Another two carbon-based materials were prepared by using ionic-liquid-based methods: ionothermal carbonization of glucose using [bmim][MeSO3] as a recyclable medium for the carbonization reaction and by direct carbonization of the ionic liquid in a one-step method using [bmim][MeSO3] as the precursor for N- and S-doped porous carbon (Carb-IL). Characterization results showed the possibility of morphology and porosity control by using [bmim][MeSO3]. All materials were subsequently tested for the ORR in alkaline media. Carb-IL showed enhanced and stable electrocatalytic ORR activity, even in the presence of methanol, ethanol, and borohydride, opening the possibility for its application in fuel cells.
T2  - ChemElectroChem
T1  - Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction
VL  - 5
IS  - 7
SP  - 1037
EP  - 1046
DO  - 10.1002/celc.201701369
ER  - 
@article{
author = "Zdolšek, Nikola and Dimitrijević, Aleksandra and Bendova, Magdalena and Krstić, Jugoslav B. and Rocha, Raquel P. and Figueiredo, Jose L. and Bajuk-Bogdanović, Danica V. and Trtić-Petrović, Tatjana M. and Šljukić, Biljana",
year = "2018",
abstract = "Carbon materials, prepared by using different methods with ionic liquids, are compared as electrocatalysts for the oxygen reduction reaction (ORR). Materials were synthesized through the hydrothermal carbonization of glucose and by using the same method in the presence of 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3] as an additive. Another two carbon-based materials were prepared by using ionic-liquid-based methods: ionothermal carbonization of glucose using [bmim][MeSO3] as a recyclable medium for the carbonization reaction and by direct carbonization of the ionic liquid in a one-step method using [bmim][MeSO3] as the precursor for N- and S-doped porous carbon (Carb-IL). Characterization results showed the possibility of morphology and porosity control by using [bmim][MeSO3]. All materials were subsequently tested for the ORR in alkaline media. Carb-IL showed enhanced and stable electrocatalytic ORR activity, even in the presence of methanol, ethanol, and borohydride, opening the possibility for its application in fuel cells.",
journal = "ChemElectroChem",
title = "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction",
volume = "5",
number = "7",
pages = "1037-1046",
doi = "10.1002/celc.201701369"
}
Zdolšek, N., Dimitrijević, A., Bendova, M., Krstić, J. B., Rocha, R. P., Figueiredo, J. L., Bajuk-Bogdanović, D. V., Trtić-Petrović, T. M.,& Šljukić, B.. (2018). Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in ChemElectroChem, 5(7), 1037-1046.
https://doi.org/10.1002/celc.201701369
Zdolšek N, Dimitrijević A, Bendova M, Krstić JB, Rocha RP, Figueiredo JL, Bajuk-Bogdanović DV, Trtić-Petrović TM, Šljukić B. Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in ChemElectroChem. 2018;5(7):1037-1046.
doi:10.1002/celc.201701369 .
Zdolšek, Nikola, Dimitrijević, Aleksandra, Bendova, Magdalena, Krstić, Jugoslav B., Rocha, Raquel P., Figueiredo, Jose L., Bajuk-Bogdanović, Danica V., Trtić-Petrović, Tatjana M., Šljukić, Biljana, "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction" in ChemElectroChem, 5, no. 7 (2018):1037-1046,
https://doi.org/10.1002/celc.201701369 . .
1
22
16
22

Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction

Zdolšek, Nikola; Dimitrijević, Aleksandra; Bendova, Magdalena; Krstić, Jugoslav B.; Rocha, Raquel P.; Figueiredo, Jose L.; Bajuk-Bogdanović, Danica V.; Trtić-Petrović, Tatjana M.; Šljukić, Biljana

(2018)

TY  - JOUR
AU  - Zdolšek, Nikola
AU  - Dimitrijević, Aleksandra
AU  - Bendova, Magdalena
AU  - Krstić, Jugoslav B.
AU  - Rocha, Raquel P.
AU  - Figueiredo, Jose L.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Trtić-Petrović, Tatjana M.
AU  - Šljukić, Biljana
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7672
AB  - Carbon materials, prepared by using different methods with ionicliquids, are compared as electrocatalysts for the oxygen reductionreaction (ORR). Materials were synthesized through the hydrothermalcarbonization of glucose and by using the same method in the presence of1-butyl-3-methylimidazolium methanesulfonate {[}bmim]{[}MeSO3] as anadditive. Another two carbon-based materials were prepared by usingionic-liquid-based methods: ionothermal carbonization of glucose using{[}bmim]{[}MeSO3] as a recyclable medium for the carbonization reactionand by direct carbonization of the ionic liquid in a one-step methodusing {[}bmim]{[}MeSO3] as the precursor for N- and S-doped porouscarbon (Carb-IL). Characterization results showed the possibility ofmorphology and porosity control by using {[}bmim]{[}MeSO3]. Allmaterials were subsequently tested for the ORR in alkaline media.Carb-IL showed enhanced and stable electrocatalytic ORR activity, evenin the presence of methanol, ethanol, and borohydride, opening thepossibility for its application in fuel cells.
T2  - ChemElectroChem
T1  - Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction
VL  - 5
IS  - 7
SP  - 1037
EP  - 1046
DO  - 10.1002/celc.201701369
ER  - 
@article{
author = "Zdolšek, Nikola and Dimitrijević, Aleksandra and Bendova, Magdalena and Krstić, Jugoslav B. and Rocha, Raquel P. and Figueiredo, Jose L. and Bajuk-Bogdanović, Danica V. and Trtić-Petrović, Tatjana M. and Šljukić, Biljana",
year = "2018",
abstract = "Carbon materials, prepared by using different methods with ionicliquids, are compared as electrocatalysts for the oxygen reductionreaction (ORR). Materials were synthesized through the hydrothermalcarbonization of glucose and by using the same method in the presence of1-butyl-3-methylimidazolium methanesulfonate {[}bmim]{[}MeSO3] as anadditive. Another two carbon-based materials were prepared by usingionic-liquid-based methods: ionothermal carbonization of glucose using{[}bmim]{[}MeSO3] as a recyclable medium for the carbonization reactionand by direct carbonization of the ionic liquid in a one-step methodusing {[}bmim]{[}MeSO3] as the precursor for N- and S-doped porouscarbon (Carb-IL). Characterization results showed the possibility ofmorphology and porosity control by using {[}bmim]{[}MeSO3]. Allmaterials were subsequently tested for the ORR in alkaline media.Carb-IL showed enhanced and stable electrocatalytic ORR activity, evenin the presence of methanol, ethanol, and borohydride, opening thepossibility for its application in fuel cells.",
journal = "ChemElectroChem",
title = "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction",
volume = "5",
number = "7",
pages = "1037-1046",
doi = "10.1002/celc.201701369"
}
Zdolšek, N., Dimitrijević, A., Bendova, M., Krstić, J. B., Rocha, R. P., Figueiredo, J. L., Bajuk-Bogdanović, D. V., Trtić-Petrović, T. M.,& Šljukić, B.. (2018). Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in ChemElectroChem, 5(7), 1037-1046.
https://doi.org/10.1002/celc.201701369
Zdolšek N, Dimitrijević A, Bendova M, Krstić JB, Rocha RP, Figueiredo JL, Bajuk-Bogdanović DV, Trtić-Petrović TM, Šljukić B. Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in ChemElectroChem. 2018;5(7):1037-1046.
doi:10.1002/celc.201701369 .
Zdolšek, Nikola, Dimitrijević, Aleksandra, Bendova, Magdalena, Krstić, Jugoslav B., Rocha, Raquel P., Figueiredo, Jose L., Bajuk-Bogdanović, Danica V., Trtić-Petrović, Tatjana M., Šljukić, Biljana, "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction" in ChemElectroChem, 5, no. 7 (2018):1037-1046,
https://doi.org/10.1002/celc.201701369 . .
1
22
16
22

Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions

Vujković, Milica; Matović, Ljiljana; Krstić, Jugoslav B.; Stojmenović, Marija; Đukić, Anđelka B.; Babić, Biljana M.; Mentus, Slavko V.

(2017)

TY  - JOUR
AU  - Vujković, Milica
AU  - Matović, Ljiljana
AU  - Krstić, Jugoslav B.
AU  - Stojmenović, Marija
AU  - Đukić, Anđelka B.
AU  - Babić, Biljana M.
AU  - Mentus, Slavko V.
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1661
AB  - The activated carbon cloth (ACC), obtained by chemical/physical activation of carbonized rayon fibers, was grinded in a ball mill and studied from the aspect of double layer capacitance. The changes in pore structure, morphology and acid/basic properties caused by ball milling were studied by means of N-2 adsorption/desorption, Fourier-transformed infrared spectrometry, Boehms titration and Scanning Electron Microscopy. Both potentiodynamic and galvanostatic cycling were used to evaluate the double layer capacitance in three alkaline, acidic and neutral aqueous solutions (KOH, H2SO4 and Na2SO4). While double layer capacitance of original ACC was found to be negligible, ball milled material (ACCm) displayed capacitance in the range of supercapacitors. In order to explain this huge capacitance improvement, we found that ball milling substantially increased the concentration of lactone, phenolic and quinone groups on the surface. We suggest that these groups, through improved hydrophilicity, enable faster ion diffusion into carbon micropores. The energy density stored by double layer was highest in neutral sodium sulphate solution. Namely, operational voltage of similar to 2 V and double layer capacitance of 220 F g(-1) at 1A g(-1), enable the energy density of ACCm/Na2SO4/ACCm capacitor of 31.7 Wh kg(-1) at 2000 W kg(-1), much higher than that of commercial EDLC carbon capacitors. According to the here presented literature survey in a tabular form, the energy density of the studied sample is also higher from that of numerous thus far published aqueous carbon capacitors. (C) 2017 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions
VL  - 245
SP  - 796
EP  - 806
DO  - 10.1016/j.electacta.2017.06.018
ER  - 
@article{
author = "Vujković, Milica and Matović, Ljiljana and Krstić, Jugoslav B. and Stojmenović, Marija and Đukić, Anđelka B. and Babić, Biljana M. and Mentus, Slavko V.",
year = "2017",
abstract = "The activated carbon cloth (ACC), obtained by chemical/physical activation of carbonized rayon fibers, was grinded in a ball mill and studied from the aspect of double layer capacitance. The changes in pore structure, morphology and acid/basic properties caused by ball milling were studied by means of N-2 adsorption/desorption, Fourier-transformed infrared spectrometry, Boehms titration and Scanning Electron Microscopy. Both potentiodynamic and galvanostatic cycling were used to evaluate the double layer capacitance in three alkaline, acidic and neutral aqueous solutions (KOH, H2SO4 and Na2SO4). While double layer capacitance of original ACC was found to be negligible, ball milled material (ACCm) displayed capacitance in the range of supercapacitors. In order to explain this huge capacitance improvement, we found that ball milling substantially increased the concentration of lactone, phenolic and quinone groups on the surface. We suggest that these groups, through improved hydrophilicity, enable faster ion diffusion into carbon micropores. The energy density stored by double layer was highest in neutral sodium sulphate solution. Namely, operational voltage of similar to 2 V and double layer capacitance of 220 F g(-1) at 1A g(-1), enable the energy density of ACCm/Na2SO4/ACCm capacitor of 31.7 Wh kg(-1) at 2000 W kg(-1), much higher than that of commercial EDLC carbon capacitors. According to the here presented literature survey in a tabular form, the energy density of the studied sample is also higher from that of numerous thus far published aqueous carbon capacitors. (C) 2017 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions",
volume = "245",
pages = "796-806",
doi = "10.1016/j.electacta.2017.06.018"
}
Vujković, M., Matović, L., Krstić, J. B., Stojmenović, M., Đukić, A. B., Babić, B. M.,& Mentus, S. V.. (2017). Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions. in Electrochimica Acta, 245, 796-806.
https://doi.org/10.1016/j.electacta.2017.06.018
Vujković M, Matović L, Krstić JB, Stojmenović M, Đukić AB, Babić BM, Mentus SV. Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions. in Electrochimica Acta. 2017;245:796-806.
doi:10.1016/j.electacta.2017.06.018 .
Vujković, Milica, Matović, Ljiljana, Krstić, Jugoslav B., Stojmenović, Marija, Đukić, Anđelka B., Babić, Biljana M., Mentus, Slavko V., "Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions" in Electrochimica Acta, 245 (2017):796-806,
https://doi.org/10.1016/j.electacta.2017.06.018 . .
27
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27

Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template

Stojmenović, Marija; Vujković, Milica; Matović, Ljiljana; Krstić, Jugoslav B.; Đukić, Anđelka B.; Dodevski, Vladimir; Živković, Sanja; Mentus, Slavko V.

(Elsevier, 2016)

TY  - JOUR
AU  - Stojmenović, Marija
AU  - Vujković, Milica
AU  - Matović, Ljiljana
AU  - Krstić, Jugoslav B.
AU  - Đukić, Anđelka B.
AU  - Dodevski, Vladimir
AU  - Živković, Sanja
AU  - Mentus, Slavko V.
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1096
AB  - Microporous zeolite templated carbon (ZTC) was synthesized by impregnation method using zeolite Y (Na-form) as a template, and furfuryl alcohol as a carbon precursor. The characterization was carried out by X-ray diffractometry, Raman spectroscopy, scanning electron microscopy, nitrogen physisorption, elemental analysis and electrochemical methods. Physisorption measurements evidenced high micro pore volume of obtained material (similar to 0.43 cm(3) g(-1)). The charge storage ability in aqueous KOH, H2SO4 and Na2SO4 solutions was systematically studied by cyclic voltammetry, galvanostatic charging/discharging and complex impedance measurements. Specific coulombic capacitance, the hydrogen storage, H-ZTC bonding and relaxation time of adsorption were found to be dependent on the type of electrolyte. Neutral Na2SO4 aqueous solution was found to be the best for supercapacitor application, thanks to: i) the highest available voltage window ii) lowest corrosion and iii) highest capacitance amounting to 123 F g(-1) at 1 A g(-1) (C) 2016 Elsevier Inc. All rights reserved.
PB  - Elsevier
T2  - Microporous and Mesoporous Materials
T1  - Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template
VL  - 228
SP  - 94
EP  - 106
DO  - 10.1016/j.micromeso.2016.03.029
ER  - 
@article{
author = "Stojmenović, Marija and Vujković, Milica and Matović, Ljiljana and Krstić, Jugoslav B. and Đukić, Anđelka B. and Dodevski, Vladimir and Živković, Sanja and Mentus, Slavko V.",
year = "2016",
abstract = "Microporous zeolite templated carbon (ZTC) was synthesized by impregnation method using zeolite Y (Na-form) as a template, and furfuryl alcohol as a carbon precursor. The characterization was carried out by X-ray diffractometry, Raman spectroscopy, scanning electron microscopy, nitrogen physisorption, elemental analysis and electrochemical methods. Physisorption measurements evidenced high micro pore volume of obtained material (similar to 0.43 cm(3) g(-1)). The charge storage ability in aqueous KOH, H2SO4 and Na2SO4 solutions was systematically studied by cyclic voltammetry, galvanostatic charging/discharging and complex impedance measurements. Specific coulombic capacitance, the hydrogen storage, H-ZTC bonding and relaxation time of adsorption were found to be dependent on the type of electrolyte. Neutral Na2SO4 aqueous solution was found to be the best for supercapacitor application, thanks to: i) the highest available voltage window ii) lowest corrosion and iii) highest capacitance amounting to 123 F g(-1) at 1 A g(-1) (C) 2016 Elsevier Inc. All rights reserved.",
publisher = "Elsevier",
journal = "Microporous and Mesoporous Materials",
title = "Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template",
volume = "228",
pages = "94-106",
doi = "10.1016/j.micromeso.2016.03.029"
}
Stojmenović, M., Vujković, M., Matović, L., Krstić, J. B., Đukić, A. B., Dodevski, V., Živković, S.,& Mentus, S. V.. (2016). Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template. in Microporous and Mesoporous Materials
Elsevier., 228, 94-106.
https://doi.org/10.1016/j.micromeso.2016.03.029
Stojmenović M, Vujković M, Matović L, Krstić JB, Đukić AB, Dodevski V, Živković S, Mentus SV. Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template. in Microporous and Mesoporous Materials. 2016;228:94-106.
doi:10.1016/j.micromeso.2016.03.029 .
Stojmenović, Marija, Vujković, Milica, Matović, Ljiljana, Krstić, Jugoslav B., Đukić, Anđelka B., Dodevski, Vladimir, Živković, Sanja, Mentus, Slavko V., "Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template" in Microporous and Mesoporous Materials, 228 (2016):94-106,
https://doi.org/10.1016/j.micromeso.2016.03.029 . .
19
13
18

Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed

Dodevski, Vladimir; Stojmenović, Marija; Vujković, Milica; Krstić, Jugoslav B.; Krstić, Sanja S.; Bajuk-Bogdanović, Danica V.; Kuzmanović, Bojana; Kaluđerović, Branka V.; Mentus, Slavko V.

(2016)

TY  - JOUR
AU  - Dodevski, Vladimir
AU  - Stojmenović, Marija
AU  - Vujković, Milica
AU  - Krstić, Jugoslav B.
AU  - Krstić, Sanja S.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Kuzmanović, Bojana
AU  - Kaluđerović, Branka V.
AU  - Mentus, Slavko V.
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1396
AB  - Activated carbon was prepared using plane tree seed as a cheap and renewable raw material. The samples were prepared by carbonization under N-2 atmosphere up to 850 degrees C, and activation in CO2 atmosphere at different both temperatures (750 and 850 degrees C) and times of activation (0.3,1 and 2 h). The influence of activation parameters on physicochemical properties was studied by XRPD, Raman spectroscopy, FTIR, N-2 physisorption, SEM and electrochemical methods. The pore structure was correlated to the specific capacitance and the amount of hydrogen stored, in alkaline, neutral and acidic electrolyte solution. The relationship of asymmetrical shape of CV curves with the porosity of samples has served to better understand some unclear issues related to the complex mechanism of charge storage. The sample activated at 850 degrees C for 2 h displayed the best behavior. At a high scan rate of 300 mV s(-1), its capacitance, amounted to similar to 26.8 mu F cm(-2) 19.69 mu F cm(-2) and 25.8 mu Fcm(-2) in KOH, Na2SO4, and H2SO4 solutions, respectively. (C) 2016 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed
VL  - 222
SP  - 156
EP  - 171
DO  - 10.1016/j.electacta.2016.10.182
ER  - 
@article{
author = "Dodevski, Vladimir and Stojmenović, Marija and Vujković, Milica and Krstić, Jugoslav B. and Krstić, Sanja S. and Bajuk-Bogdanović, Danica V. and Kuzmanović, Bojana and Kaluđerović, Branka V. and Mentus, Slavko V.",
year = "2016",
abstract = "Activated carbon was prepared using plane tree seed as a cheap and renewable raw material. The samples were prepared by carbonization under N-2 atmosphere up to 850 degrees C, and activation in CO2 atmosphere at different both temperatures (750 and 850 degrees C) and times of activation (0.3,1 and 2 h). The influence of activation parameters on physicochemical properties was studied by XRPD, Raman spectroscopy, FTIR, N-2 physisorption, SEM and electrochemical methods. The pore structure was correlated to the specific capacitance and the amount of hydrogen stored, in alkaline, neutral and acidic electrolyte solution. The relationship of asymmetrical shape of CV curves with the porosity of samples has served to better understand some unclear issues related to the complex mechanism of charge storage. The sample activated at 850 degrees C for 2 h displayed the best behavior. At a high scan rate of 300 mV s(-1), its capacitance, amounted to similar to 26.8 mu F cm(-2) 19.69 mu F cm(-2) and 25.8 mu Fcm(-2) in KOH, Na2SO4, and H2SO4 solutions, respectively. (C) 2016 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed",
volume = "222",
pages = "156-171",
doi = "10.1016/j.electacta.2016.10.182"
}
Dodevski, V., Stojmenović, M., Vujković, M., Krstić, J. B., Krstić, S. S., Bajuk-Bogdanović, D. V., Kuzmanović, B., Kaluđerović, B. V.,& Mentus, S. V.. (2016). Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed. in Electrochimica Acta, 222, 156-171.
https://doi.org/10.1016/j.electacta.2016.10.182
Dodevski V, Stojmenović M, Vujković M, Krstić JB, Krstić SS, Bajuk-Bogdanović DV, Kuzmanović B, Kaluđerović BV, Mentus SV. Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed. in Electrochimica Acta. 2016;222:156-171.
doi:10.1016/j.electacta.2016.10.182 .
Dodevski, Vladimir, Stojmenović, Marija, Vujković, Milica, Krstić, Jugoslav B., Krstić, Sanja S., Bajuk-Bogdanović, Danica V., Kuzmanović, Bojana, Kaluđerović, Branka V., Mentus, Slavko V., "Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed" in Electrochimica Acta, 222 (2016):156-171,
https://doi.org/10.1016/j.electacta.2016.10.182 . .
13
12
14

Measurements of the Total and Differential Higgs Boson Production Cross Sections Combining the H - GT gamma gamma and H - GT ZZ* - GT 4l Decay Channels at root s=8 TeV with the ATLAS Detector

Aad, G.; Agatonović-Jovin, Tatjana; Bozic, I.; Dimitrievska, A.; Krstić, Jugoslav B.; Mamužić, Judita; Marjanović, M.; Popović, D. S.; Sijacki, Dj.; Simić, Lj.; Vranješ, Nenad; Vranješ Milosavljević, Marija; Živković, Lada

(2015)

TY  - JOUR
AU  - Aad, G.
AU  - Agatonović-Jovin, Tatjana
AU  - Bozic, I.
AU  - Dimitrievska, A.
AU  - Krstić, Jugoslav B.
AU  - Mamužić, Judita
AU  - Marjanović, M.
AU  - Popović, D. S.
AU  - Sijacki, Dj.
AU  - Simić, Lj.
AU  - Vranješ, Nenad
AU  - Vranješ Milosavljević, Marija
AU  - Živković, Lada
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/258
AB  - Measurements of the total and differential cross sections of Higgs boson production are performed using 20.3 fb(-1) of pp collisions produced by the Large Hadron Collider at a center-of-mass energy of root s = 8 TeV and recorded by the ATLAS detector. Cross sections are obtained from measured H - GT gamma gamma and H - GT ZZ*. 4l event yields, which are combined accounting for detector efficiencies, fiducial acceptances, and branching fractions. Differential cross sections are reported as a function of Higgs boson transverse momentum, Higgs boson rapidity, number of jets in the event, and transverse momentum of the leading jet. The total production cross section is determined to be sigma(pp - GT H) = 33.0 +/- 5.3 (stat) +/- 1.6 (syst) pb. The measurements are compared to state-of-the-art predictions.
T2  - Physical Review Letters
T1  - Measurements of the Total and Differential Higgs Boson Production Cross Sections Combining the H - GT gamma gamma and H - GT ZZ* - GT 4l Decay Channels at root s=8 TeV with the ATLAS Detector
VL  - 115
IS  - 9
DO  - 10.1103/PhysRevLett.115.091801
ER  - 
@article{
author = "Aad, G. and Agatonović-Jovin, Tatjana and Bozic, I. and Dimitrievska, A. and Krstić, Jugoslav B. and Mamužić, Judita and Marjanović, M. and Popović, D. S. and Sijacki, Dj. and Simić, Lj. and Vranješ, Nenad and Vranješ Milosavljević, Marija and Živković, Lada",
year = "2015",
abstract = "Measurements of the total and differential cross sections of Higgs boson production are performed using 20.3 fb(-1) of pp collisions produced by the Large Hadron Collider at a center-of-mass energy of root s = 8 TeV and recorded by the ATLAS detector. Cross sections are obtained from measured H - GT gamma gamma and H - GT ZZ*. 4l event yields, which are combined accounting for detector efficiencies, fiducial acceptances, and branching fractions. Differential cross sections are reported as a function of Higgs boson transverse momentum, Higgs boson rapidity, number of jets in the event, and transverse momentum of the leading jet. The total production cross section is determined to be sigma(pp - GT H) = 33.0 +/- 5.3 (stat) +/- 1.6 (syst) pb. The measurements are compared to state-of-the-art predictions.",
journal = "Physical Review Letters",
title = "Measurements of the Total and Differential Higgs Boson Production Cross Sections Combining the H - GT gamma gamma and H - GT ZZ* - GT 4l Decay Channels at root s=8 TeV with the ATLAS Detector",
volume = "115",
number = "9",
doi = "10.1103/PhysRevLett.115.091801"
}
Aad, G., Agatonović-Jovin, T., Bozic, I., Dimitrievska, A., Krstić, J. B., Mamužić, J., Marjanović, M., Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, N., Vranješ Milosavljević, M.,& Živković, L.. (2015). Measurements of the Total and Differential Higgs Boson Production Cross Sections Combining the H - GT gamma gamma and H - GT ZZ* - GT 4l Decay Channels at root s=8 TeV with the ATLAS Detector. in Physical Review Letters, 115(9).
https://doi.org/10.1103/PhysRevLett.115.091801
Aad G, Agatonović-Jovin T, Bozic I, Dimitrievska A, Krstić JB, Mamužić J, Marjanović M, Popović DS, Sijacki D, Simić L, Vranješ N, Vranješ Milosavljević M, Živković L. Measurements of the Total and Differential Higgs Boson Production Cross Sections Combining the H - GT gamma gamma and H - GT ZZ* - GT 4l Decay Channels at root s=8 TeV with the ATLAS Detector. in Physical Review Letters. 2015;115(9).
doi:10.1103/PhysRevLett.115.091801 .
Aad, G., Agatonović-Jovin, Tatjana, Bozic, I., Dimitrievska, A., Krstić, Jugoslav B., Mamužić, Judita, Marjanović, M., Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, Nenad, Vranješ Milosavljević, Marija, Živković, Lada, "Measurements of the Total and Differential Higgs Boson Production Cross Sections Combining the H - GT gamma gamma and H - GT ZZ* - GT 4l Decay Channels at root s=8 TeV with the ATLAS Detector" in Physical Review Letters, 115, no. 9 (2015),
https://doi.org/10.1103/PhysRevLett.115.091801 . .
7
51
18
59

Photocatalytic degradation of alprazolam in water suspension of brookite type TiO2 nanopowders prepared using hydrothermal route

Tomić, Nataša; Grujić-Brojčin, Mirjana; Finčur, Nina L.; Abramović, Biljana F.; Simović, Bojana; Krstić, Jugoslav B.; Matović, Branko; Šćepanović, Maja

(Elsevier, 2015)

TY  - JOUR
AU  - Tomić, Nataša
AU  - Grujić-Brojčin, Mirjana
AU  - Finčur, Nina L.
AU  - Abramović, Biljana F.
AU  - Simović, Bojana
AU  - Krstić, Jugoslav B.
AU  - Matović, Branko
AU  - Šćepanović, Maja
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/821
AB  - Two series of nanocrystalline brookite-type powders have been synthesized by using combined sal gel hydrothermal method with titanium tetrachloride (TiCI4) as a precursor and hydrothermal temperature and reaction time varied in the range of 120-200 degrees C and 12-48 h, respectively. The effects of chosen synthesis parameters on structural, morphological and optical properties of synthesized powders have been investigated by the XRPD, SEM, EDS and BET measurements, as well Raman spectroscopy and spectroscopic ellipsometry. The XRPD results have shown that pure brookite phase, with mean crystallite size of -33 nm, has been obtained only in the sample synthesized at 200 degrees C, after 24 h of hydrothermal process. In all other samples anatase phase also appears, whereas rutile and sodium titanate phases have been noticed in the samples synthesized at lower temperatures. The presence of different titania phases has also been confirmed and analyzed by Raman scattering measurements. The SEM measurements have shown spindle-like particles in brookite-rich samples synthesized at 200 degrees C, whereas BET measurements have detected mesoporous structure in these samples. The properties of synthesized powders have been correlated to their photocatalytic efficiency, tested in degradation of alprazolam, one of the 5th generation benzodiazepines. The sample consisted of pure brookite has shown the highest efficiency in the photodegradation of alprazolam, practically equal to the activity of Degussa P25. (C) 2015 Elsevier B.V. All rights reserved.
PB  - Elsevier
T2  - Materials Chemistry and Physics
T1  - Photocatalytic degradation of alprazolam in water suspension of brookite type TiO2 nanopowders prepared using hydrothermal route
VL  - 163
SP  - 518
EP  - 528
DO  - 10.1016/j.matchemphys.2015.08.008
ER  - 
@article{
author = "Tomić, Nataša and Grujić-Brojčin, Mirjana and Finčur, Nina L. and Abramović, Biljana F. and Simović, Bojana and Krstić, Jugoslav B. and Matović, Branko and Šćepanović, Maja",
year = "2015",
abstract = "Two series of nanocrystalline brookite-type powders have been synthesized by using combined sal gel hydrothermal method with titanium tetrachloride (TiCI4) as a precursor and hydrothermal temperature and reaction time varied in the range of 120-200 degrees C and 12-48 h, respectively. The effects of chosen synthesis parameters on structural, morphological and optical properties of synthesized powders have been investigated by the XRPD, SEM, EDS and BET measurements, as well Raman spectroscopy and spectroscopic ellipsometry. The XRPD results have shown that pure brookite phase, with mean crystallite size of -33 nm, has been obtained only in the sample synthesized at 200 degrees C, after 24 h of hydrothermal process. In all other samples anatase phase also appears, whereas rutile and sodium titanate phases have been noticed in the samples synthesized at lower temperatures. The presence of different titania phases has also been confirmed and analyzed by Raman scattering measurements. The SEM measurements have shown spindle-like particles in brookite-rich samples synthesized at 200 degrees C, whereas BET measurements have detected mesoporous structure in these samples. The properties of synthesized powders have been correlated to their photocatalytic efficiency, tested in degradation of alprazolam, one of the 5th generation benzodiazepines. The sample consisted of pure brookite has shown the highest efficiency in the photodegradation of alprazolam, practically equal to the activity of Degussa P25. (C) 2015 Elsevier B.V. All rights reserved.",
publisher = "Elsevier",
journal = "Materials Chemistry and Physics",
title = "Photocatalytic degradation of alprazolam in water suspension of brookite type TiO2 nanopowders prepared using hydrothermal route",
volume = "163",
pages = "518-528",
doi = "10.1016/j.matchemphys.2015.08.008"
}
Tomić, N., Grujić-Brojčin, M., Finčur, N. L., Abramović, B. F., Simović, B., Krstić, J. B., Matović, B.,& Šćepanović, M.. (2015). Photocatalytic degradation of alprazolam in water suspension of brookite type TiO2 nanopowders prepared using hydrothermal route. in Materials Chemistry and Physics
Elsevier., 163, 518-528.
https://doi.org/10.1016/j.matchemphys.2015.08.008
Tomić N, Grujić-Brojčin M, Finčur NL, Abramović BF, Simović B, Krstić JB, Matović B, Šćepanović M. Photocatalytic degradation of alprazolam in water suspension of brookite type TiO2 nanopowders prepared using hydrothermal route. in Materials Chemistry and Physics. 2015;163:518-528.
doi:10.1016/j.matchemphys.2015.08.008 .
Tomić, Nataša, Grujić-Brojčin, Mirjana, Finčur, Nina L., Abramović, Biljana F., Simović, Bojana, Krstić, Jugoslav B., Matović, Branko, Šćepanović, Maja, "Photocatalytic degradation of alprazolam in water suspension of brookite type TiO2 nanopowders prepared using hydrothermal route" in Materials Chemistry and Physics, 163 (2015):518-528,
https://doi.org/10.1016/j.matchemphys.2015.08.008 . .
35
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36

Erratum: Search for new phenomena in final states with large jet multiplicities and missing transverse momentum at root s = 8 TeV proton-proton collisions using the ATLAS experiment (vol 10, pg 130, 2013)

Aad, G.; Agatonović-Jovin, Tatjana; Božović-Jelisavčić, Ivanka; Ćirković, Predrag; Krstić, Jugoslav B.; Mamužić, Judita; Popović, D. S.; Sijacki, Dj.; Simić, Lj.; Vranješ, Nenad; Vranješ Milosavljević, Marija; Živković, Lada

(2014)

TY  - JOUR
AU  - Aad, G.
AU  - Agatonović-Jovin, Tatjana
AU  - Božović-Jelisavčić, Ivanka
AU  - Ćirković, Predrag
AU  - Krstić, Jugoslav B.
AU  - Mamužić, Judita
AU  - Popović, D. S.
AU  - Sijacki, Dj.
AU  - Simić, Lj.
AU  - Vranješ, Nenad
AU  - Vranješ Milosavljević, Marija
AU  - Živković, Lada
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/289
T2  - Journal of High Energy Physics
T1  - Erratum: Search for new phenomena in final states with large jet multiplicities and missing transverse momentum at root s = 8 TeV proton-proton collisions using the ATLAS experiment (vol 10, pg 130, 2013)
IS  - 1
DO  - 10.1007/JHEP01(2014)109
ER  - 
@article{
author = "Aad, G. and Agatonović-Jovin, Tatjana and Božović-Jelisavčić, Ivanka and Ćirković, Predrag and Krstić, Jugoslav B. and Mamužić, Judita and Popović, D. S. and Sijacki, Dj. and Simić, Lj. and Vranješ, Nenad and Vranješ Milosavljević, Marija and Živković, Lada",
year = "2014",
journal = "Journal of High Energy Physics",
title = "Erratum: Search for new phenomena in final states with large jet multiplicities and missing transverse momentum at root s = 8 TeV proton-proton collisions using the ATLAS experiment (vol 10, pg 130, 2013)",
number = "1",
doi = "10.1007/JHEP01(2014)109"
}
Aad, G., Agatonović-Jovin, T., Božović-Jelisavčić, I., Ćirković, P., Krstić, J. B., Mamužić, J., Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, N., Vranješ Milosavljević, M.,& Živković, L.. (2014). Erratum: Search for new phenomena in final states with large jet multiplicities and missing transverse momentum at root s = 8 TeV proton-proton collisions using the ATLAS experiment (vol 10, pg 130, 2013). in Journal of High Energy Physics(1).
https://doi.org/10.1007/JHEP01(2014)109
Aad G, Agatonović-Jovin T, Božović-Jelisavčić I, Ćirković P, Krstić JB, Mamužić J, Popović DS, Sijacki D, Simić L, Vranješ N, Vranješ Milosavljević M, Živković L. Erratum: Search for new phenomena in final states with large jet multiplicities and missing transverse momentum at root s = 8 TeV proton-proton collisions using the ATLAS experiment (vol 10, pg 130, 2013). in Journal of High Energy Physics. 2014;(1).
doi:10.1007/JHEP01(2014)109 .
Aad, G., Agatonović-Jovin, Tatjana, Božović-Jelisavčić, Ivanka, Ćirković, Predrag, Krstić, Jugoslav B., Mamužić, Judita, Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, Nenad, Vranješ Milosavljević, Marija, Živković, Lada, "Erratum: Search for new phenomena in final states with large jet multiplicities and missing transverse momentum at root s = 8 TeV proton-proton collisions using the ATLAS experiment (vol 10, pg 130, 2013)" in Journal of High Energy Physics, no. 1 (2014),
https://doi.org/10.1007/JHEP01(2014)109 . .
8
9
14

Design and photocatalytic ability of ordered mesoporous TiO2 thin films

Zarubica, Aleksandra R.; Vučinić-Vasić, Milica; Antonijević, Milan D.; Ranđelović, Marjan S.; Momčilović, Milan Z.; Krstić, Jugoslav B.; Nedeljković, Jovan

(2014)

TY  - JOUR
AU  - Zarubica, Aleksandra R.
AU  - Vučinić-Vasić, Milica
AU  - Antonijević, Milan D.
AU  - Ranđelović, Marjan S.
AU  - Momčilović, Milan Z.
AU  - Krstić, Jugoslav B.
AU  - Nedeljković, Jovan
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/95
AB  - Homogeneous and crack-free TiO2 films with templated mesoporosity were prepared by the dip coating technique using an evaporation-induced, self-assembly method. The synthesized mesoporous TiO2 films were characterized using SEM/TEM, BET and XRD techniques. Degradation reactions of methylene blue and crystal violet dyes were used to test the photocatalytic capability of mesoporous TiO2 films. The degradation kinetics of methylene blue and crystal violet were investigated over a broad range of initial concentrations of the organic dyes. The kinetic data were correlated with the specific surface area and thickness of mesoporous TiO2 films, as well as number of reaction cycles. (C) 2014 Elsevier Ltd. All rights reserved.
T2  - Materials Research Bulletin
T1  - Design and photocatalytic ability of ordered mesoporous TiO2 thin films
VL  - 57
SP  - 146
EP  - 151
DO  - 10.1016/j.materresbull.2014.03.015
ER  - 
@article{
author = "Zarubica, Aleksandra R. and Vučinić-Vasić, Milica and Antonijević, Milan D. and Ranđelović, Marjan S. and Momčilović, Milan Z. and Krstić, Jugoslav B. and Nedeljković, Jovan",
year = "2014",
abstract = "Homogeneous and crack-free TiO2 films with templated mesoporosity were prepared by the dip coating technique using an evaporation-induced, self-assembly method. The synthesized mesoporous TiO2 films were characterized using SEM/TEM, BET and XRD techniques. Degradation reactions of methylene blue and crystal violet dyes were used to test the photocatalytic capability of mesoporous TiO2 films. The degradation kinetics of methylene blue and crystal violet were investigated over a broad range of initial concentrations of the organic dyes. The kinetic data were correlated with the specific surface area and thickness of mesoporous TiO2 films, as well as number of reaction cycles. (C) 2014 Elsevier Ltd. All rights reserved.",
journal = "Materials Research Bulletin",
title = "Design and photocatalytic ability of ordered mesoporous TiO2 thin films",
volume = "57",
pages = "146-151",
doi = "10.1016/j.materresbull.2014.03.015"
}
Zarubica, A. R., Vučinić-Vasić, M., Antonijević, M. D., Ranđelović, M. S., Momčilović, M. Z., Krstić, J. B.,& Nedeljković, J.. (2014). Design and photocatalytic ability of ordered mesoporous TiO2 thin films. in Materials Research Bulletin, 57, 146-151.
https://doi.org/10.1016/j.materresbull.2014.03.015
Zarubica AR, Vučinić-Vasić M, Antonijević MD, Ranđelović MS, Momčilović MZ, Krstić JB, Nedeljković J. Design and photocatalytic ability of ordered mesoporous TiO2 thin films. in Materials Research Bulletin. 2014;57:146-151.
doi:10.1016/j.materresbull.2014.03.015 .
Zarubica, Aleksandra R., Vučinić-Vasić, Milica, Antonijević, Milan D., Ranđelović, Marjan S., Momčilović, Milan Z., Krstić, Jugoslav B., Nedeljković, Jovan, "Design and photocatalytic ability of ordered mesoporous TiO2 thin films" in Materials Research Bulletin, 57 (2014):146-151,
https://doi.org/10.1016/j.materresbull.2014.03.015 . .
1
14
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14

Search for nonpointing and delayed photons in the diphoton and missing transverse momentum final state in 8 TeV pp collisions at the LHC using the ATLAS detector

Aad, G.; Agatonović-Jovin, Tatjana; Bozic, I.; Dimitrievska, A.; Krstić, Jugoslav B.; Mamužić, Judita; Marjanović, M.; Popović, D. S.; Sijacki, Dj.; Simić, Lj.; Vranješ, Nenad; Vranješ Milosavljević, Marija

(2014)

TY  - JOUR
AU  - Aad, G.
AU  - Agatonović-Jovin, Tatjana
AU  - Bozic, I.
AU  - Dimitrievska, A.
AU  - Krstić, Jugoslav B.
AU  - Mamužić, Judita
AU  - Marjanović, M.
AU  - Popović, D. S.
AU  - Sijacki, Dj.
AU  - Simić, Lj.
AU  - Vranješ, Nenad
AU  - Vranješ Milosavljević, Marija
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/283
AB  - A search has been performed, using the full 20.3 fb(-1) data sample of 8 TeV proton-proton collisions collected in 2012 with the ATLAS detector at the LHC, for photons originating from a displaced vertex due to the decay of a neutral long-lived particle into a photon and an invisible particle. The analysis investigates the diphoton plus missing transverse momentum final state, and is therefore most sensitive to pair production of long-lived particles. The analysis technique exploits the capabilities of the ATLAS electromagnetic calorimeter to make precise measurements of the flight direction, as well as the time of flight, of photons. No excess is observed over the Standard Model predictions for background. Exclusion limits are set within the context of gauge mediated supersymmetry breaking models, with the lightest neutralino being the next-to-lightest supersymmetric particle and decaying into a photon and gravitino with a lifetime in the range from 250 ps to about 100 ns.
T2  - Physical Review D
T1  - Search for nonpointing and delayed photons in the diphoton and missing transverse momentum final state in 8 TeV pp collisions at the LHC using the ATLAS detector
VL  - 90
IS  - 11
DO  - 10.1103/PhysRevD.90.112005
ER  - 
@article{
author = "Aad, G. and Agatonović-Jovin, Tatjana and Bozic, I. and Dimitrievska, A. and Krstić, Jugoslav B. and Mamužić, Judita and Marjanović, M. and Popović, D. S. and Sijacki, Dj. and Simić, Lj. and Vranješ, Nenad and Vranješ Milosavljević, Marija",
year = "2014",
abstract = "A search has been performed, using the full 20.3 fb(-1) data sample of 8 TeV proton-proton collisions collected in 2012 with the ATLAS detector at the LHC, for photons originating from a displaced vertex due to the decay of a neutral long-lived particle into a photon and an invisible particle. The analysis investigates the diphoton plus missing transverse momentum final state, and is therefore most sensitive to pair production of long-lived particles. The analysis technique exploits the capabilities of the ATLAS electromagnetic calorimeter to make precise measurements of the flight direction, as well as the time of flight, of photons. No excess is observed over the Standard Model predictions for background. Exclusion limits are set within the context of gauge mediated supersymmetry breaking models, with the lightest neutralino being the next-to-lightest supersymmetric particle and decaying into a photon and gravitino with a lifetime in the range from 250 ps to about 100 ns.",
journal = "Physical Review D",
title = "Search for nonpointing and delayed photons in the diphoton and missing transverse momentum final state in 8 TeV pp collisions at the LHC using the ATLAS detector",
volume = "90",
number = "11",
doi = "10.1103/PhysRevD.90.112005"
}
Aad, G., Agatonović-Jovin, T., Bozic, I., Dimitrievska, A., Krstić, J. B., Mamužić, J., Marjanović, M., Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, N.,& Vranješ Milosavljević, M.. (2014). Search for nonpointing and delayed photons in the diphoton and missing transverse momentum final state in 8 TeV pp collisions at the LHC using the ATLAS detector. in Physical Review D, 90(11).
https://doi.org/10.1103/PhysRevD.90.112005
Aad G, Agatonović-Jovin T, Bozic I, Dimitrievska A, Krstić JB, Mamužić J, Marjanović M, Popović DS, Sijacki D, Simić L, Vranješ N, Vranješ Milosavljević M. Search for nonpointing and delayed photons in the diphoton and missing transverse momentum final state in 8 TeV pp collisions at the LHC using the ATLAS detector. in Physical Review D. 2014;90(11).
doi:10.1103/PhysRevD.90.112005 .
Aad, G., Agatonović-Jovin, Tatjana, Bozic, I., Dimitrievska, A., Krstić, Jugoslav B., Mamužić, Judita, Marjanović, M., Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, Nenad, Vranješ Milosavljević, Marija, "Search for nonpointing and delayed photons in the diphoton and missing transverse momentum final state in 8 TeV pp collisions at the LHC using the ATLAS detector" in Physical Review D, 90, no. 11 (2014),
https://doi.org/10.1103/PhysRevD.90.112005 . .
2
41
52
60

Measurement of inclusive jet charged-particle fragmentation functions in Pb plus Pb collisions at root S-NN=2.76 TeV with the ATLAS detector

Aad, G.; Agatonović-Jovin, Tatjana; Ćirković, Predrag; Dimitrievska, A.; Krstić, Jugoslav B.; Mamužić, Judita; Marjanović, M.; Popović, D. S.; Sijacki, Dj.; Simić, Lj.; Vranješ, Nenad; Vranješ Milosavljević, Marija

(2014)

TY  - JOUR
AU  - Aad, G.
AU  - Agatonović-Jovin, Tatjana
AU  - Ćirković, Predrag
AU  - Dimitrievska, A.
AU  - Krstić, Jugoslav B.
AU  - Mamužić, Judita
AU  - Marjanović, M.
AU  - Popović, D. S.
AU  - Sijacki, Dj.
AU  - Simić, Lj.
AU  - Vranješ, Nenad
AU  - Vranješ Milosavljević, Marija
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/280
AB  - Measurements of charged-particle fragmentation functions of jets produced in ultra-relativistic nuclear collisions can provide insight into the modification of parton showers in the hot, dense medium created in the collisions. ATLAS has measured jets in root S-NN = 2.76 TeV Pb+Pb collisions at the LHC using a data set recorded in 2011 with an integrated luminosity of 0.14 nb(-1). Jets were reconstructed using the anti-k(t) algorithm with distance parameter values R = 0.2, 0.3, and 0.4. Distributions of charged-particle transverse momentum and longitudinal momentum fraction are reported for seven bins in collision centrality for R = 0.4 jets with p(T)(jet) GT 100 GeV. Commensurate minimum p(T) values are used for the other radii. Ratios of fragment distributions in each centrality bin to those measured in the most peripheral bin are presented. These ratios show a reduction of fragment yield in central collisions relative to peripheral collisions at intermediate z values, 0.04 less than or similar to z less than or similar to 0.2, and an enhancement in fragment yield for z less than or similar to 0.04. A smaller, less significant enhancement is observed at large z and large p(T) in central collisions. (C) 2014 The Authors. Published by Elsevier B.V.
T2  - Physics Letters B
T1  - Measurement of inclusive jet charged-particle fragmentation functions in Pb plus Pb collisions at root S-NN=2.76 TeV with the ATLAS detector
VL  - 739
SP  - 320
EP  - 342
DO  - 10.1016/j.physletb.2014.10.065
ER  - 
@article{
author = "Aad, G. and Agatonović-Jovin, Tatjana and Ćirković, Predrag and Dimitrievska, A. and Krstić, Jugoslav B. and Mamužić, Judita and Marjanović, M. and Popović, D. S. and Sijacki, Dj. and Simić, Lj. and Vranješ, Nenad and Vranješ Milosavljević, Marija",
year = "2014",
abstract = "Measurements of charged-particle fragmentation functions of jets produced in ultra-relativistic nuclear collisions can provide insight into the modification of parton showers in the hot, dense medium created in the collisions. ATLAS has measured jets in root S-NN = 2.76 TeV Pb+Pb collisions at the LHC using a data set recorded in 2011 with an integrated luminosity of 0.14 nb(-1). Jets were reconstructed using the anti-k(t) algorithm with distance parameter values R = 0.2, 0.3, and 0.4. Distributions of charged-particle transverse momentum and longitudinal momentum fraction are reported for seven bins in collision centrality for R = 0.4 jets with p(T)(jet) GT 100 GeV. Commensurate minimum p(T) values are used for the other radii. Ratios of fragment distributions in each centrality bin to those measured in the most peripheral bin are presented. These ratios show a reduction of fragment yield in central collisions relative to peripheral collisions at intermediate z values, 0.04 less than or similar to z less than or similar to 0.2, and an enhancement in fragment yield for z less than or similar to 0.04. A smaller, less significant enhancement is observed at large z and large p(T) in central collisions. (C) 2014 The Authors. Published by Elsevier B.V.",
journal = "Physics Letters B",
title = "Measurement of inclusive jet charged-particle fragmentation functions in Pb plus Pb collisions at root S-NN=2.76 TeV with the ATLAS detector",
volume = "739",
pages = "320-342",
doi = "10.1016/j.physletb.2014.10.065"
}
Aad, G., Agatonović-Jovin, T., Ćirković, P., Dimitrievska, A., Krstić, J. B., Mamužić, J., Marjanović, M., Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, N.,& Vranješ Milosavljević, M.. (2014). Measurement of inclusive jet charged-particle fragmentation functions in Pb plus Pb collisions at root S-NN=2.76 TeV with the ATLAS detector. in Physics Letters B, 739, 320-342.
https://doi.org/10.1016/j.physletb.2014.10.065
Aad G, Agatonović-Jovin T, Ćirković P, Dimitrievska A, Krstić JB, Mamužić J, Marjanović M, Popović DS, Sijacki D, Simić L, Vranješ N, Vranješ Milosavljević M. Measurement of inclusive jet charged-particle fragmentation functions in Pb plus Pb collisions at root S-NN=2.76 TeV with the ATLAS detector. in Physics Letters B. 2014;739:320-342.
doi:10.1016/j.physletb.2014.10.065 .
Aad, G., Agatonović-Jovin, Tatjana, Ćirković, Predrag, Dimitrievska, A., Krstić, Jugoslav B., Mamužić, Judita, Marjanović, M., Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, Nenad, Vranješ Milosavljević, Marija, "Measurement of inclusive jet charged-particle fragmentation functions in Pb plus Pb collisions at root S-NN=2.76 TeV with the ATLAS detector" in Physics Letters B, 739 (2014):320-342,
https://doi.org/10.1016/j.physletb.2014.10.065 . .
2
123
115
143

Observation of an Excited B-c(+/-) Meson State with the ATLAS Detector

Aad, G.; Agatonović-Jovin, Tatjana; Ćirković, Predrag; Dimitrievska, A.; Krstić, Jugoslav B.; Mamužić, Judita; Marjanović, M.; Popović, D. S.; Sijacki, Dj.; Simić, Lj.; Vranješ, Nenad; Vranješ Milosavljević, Marija

(2014)

TY  - JOUR
AU  - Aad, G.
AU  - Agatonović-Jovin, Tatjana
AU  - Ćirković, Predrag
AU  - Dimitrievska, A.
AU  - Krstić, Jugoslav B.
AU  - Mamužić, Judita
AU  - Marjanović, M.
AU  - Popović, D. S.
AU  - Sijacki, Dj.
AU  - Simić, Lj.
AU  - Vranješ, Nenad
AU  - Vranješ Milosavljević, Marija
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/247
AB  - A search for excited states of the B-c(+/-) meson is performed using 4.9 fb(-1) of 7 TeV and 19.2 fb(-1) of 8 TeV pp collision data collected by the ATLAS experiment at the LHC. A new state is observed through its hadronic transition to the ground state, with the latter detected in the decayB(c)(+/-) - GT J/psi pi(+/-). The state appears in the m(B-c(+/-)pi(+)pi(-)) - m(B-c(+/-)) - 2m(pi(+/-)) mass difference distribution with a significance of 5.2 standard deviations. The mass of the observed state is 6842 +/- 4 +/- 5 MeV, where the first error is statistical and the second is systematic. The mass and decay of this state are consistent with expectations for the second S-wave state of the B-c(+/-) meson, B-c(+/-)(2S).
T2  - Physical Review Letters
T1  - Observation of an Excited B-c(+/-) Meson State with the ATLAS Detector
VL  - 113
IS  - 21
DO  - 10.1103/PhysRevLett.113.212004
ER  - 
@article{
author = "Aad, G. and Agatonović-Jovin, Tatjana and Ćirković, Predrag and Dimitrievska, A. and Krstić, Jugoslav B. and Mamužić, Judita and Marjanović, M. and Popović, D. S. and Sijacki, Dj. and Simić, Lj. and Vranješ, Nenad and Vranješ Milosavljević, Marija",
year = "2014",
abstract = "A search for excited states of the B-c(+/-) meson is performed using 4.9 fb(-1) of 7 TeV and 19.2 fb(-1) of 8 TeV pp collision data collected by the ATLAS experiment at the LHC. A new state is observed through its hadronic transition to the ground state, with the latter detected in the decayB(c)(+/-) - GT J/psi pi(+/-). The state appears in the m(B-c(+/-)pi(+)pi(-)) - m(B-c(+/-)) - 2m(pi(+/-)) mass difference distribution with a significance of 5.2 standard deviations. The mass of the observed state is 6842 +/- 4 +/- 5 MeV, where the first error is statistical and the second is systematic. The mass and decay of this state are consistent with expectations for the second S-wave state of the B-c(+/-) meson, B-c(+/-)(2S).",
journal = "Physical Review Letters",
title = "Observation of an Excited B-c(+/-) Meson State with the ATLAS Detector",
volume = "113",
number = "21",
doi = "10.1103/PhysRevLett.113.212004"
}
Aad, G., Agatonović-Jovin, T., Ćirković, P., Dimitrievska, A., Krstić, J. B., Mamužić, J., Marjanović, M., Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, N.,& Vranješ Milosavljević, M.. (2014). Observation of an Excited B-c(+/-) Meson State with the ATLAS Detector. in Physical Review Letters, 113(21).
https://doi.org/10.1103/PhysRevLett.113.212004
Aad G, Agatonović-Jovin T, Ćirković P, Dimitrievska A, Krstić JB, Mamužić J, Marjanović M, Popović DS, Sijacki D, Simić L, Vranješ N, Vranješ Milosavljević M. Observation of an Excited B-c(+/-) Meson State with the ATLAS Detector. in Physical Review Letters. 2014;113(21).
doi:10.1103/PhysRevLett.113.212004 .
Aad, G., Agatonović-Jovin, Tatjana, Ćirković, Predrag, Dimitrievska, A., Krstić, Jugoslav B., Mamužić, Judita, Marjanović, M., Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, Nenad, Vranješ Milosavljević, Marija, "Observation of an Excited B-c(+/-) Meson State with the ATLAS Detector" in Physical Review Letters, 113, no. 21 (2014),
https://doi.org/10.1103/PhysRevLett.113.212004 . .
22
75
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108

Search for long-lived neutral particles decaying into lepton jets in proton-proton collisions at root s=8 Tev with the ATLAS detector

Aad, G.; Agatonović-Jovin, Tatjana; Bozic, I.; Ćirković, Predrag; Dimitrievska, A.; Krstić, Jugoslav B.; Mamužić, Judita; Marjanović, M.; Popović, D. S.; Sijacki, Dj.; Simić, Lj.; Vranješ, Nenad; Vranješ Milosavljević, Marija

(2014)

TY  - JOUR
AU  - Aad, G.
AU  - Agatonović-Jovin, Tatjana
AU  - Bozic, I.
AU  - Ćirković, Predrag
AU  - Dimitrievska, A.
AU  - Krstić, Jugoslav B.
AU  - Mamužić, Judita
AU  - Marjanović, M.
AU  - Popović, D. S.
AU  - Sijacki, Dj.
AU  - Simić, Lj.
AU  - Vranješ, Nenad
AU  - Vranješ Milosavljević, Marija
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/237
AB  - Several models of physics beyond the Standard Model predict neutral particles that decay into final states consisting of collimated jets of light leptons and hadrons (so-called lepton jets). These particles can also be long-lived with decay length comparable to, or even larger than, the LHC detectors linear dimensions. This paper presents the results of a search for lepton jets in proton-proton collisions at the centre-of-mass energy of root s = 8 TeV in a sample of 20.3 fb(-1) collected during 2012 with the ATLAS detector at the LHC. Limits on models predicting Higgs boson decays to neutral long-lived lepton jets are derived as a function of the particles proper decay length.
T2  - Journal of High Energy Physics
T1  - Search for long-lived neutral particles decaying into lepton jets in proton-proton collisions at root s=8 Tev with the ATLAS detector
IS  - 11
DO  - 10.1007/JHEP11(2014)088
ER  - 
@article{
author = "Aad, G. and Agatonović-Jovin, Tatjana and Bozic, I. and Ćirković, Predrag and Dimitrievska, A. and Krstić, Jugoslav B. and Mamužić, Judita and Marjanović, M. and Popović, D. S. and Sijacki, Dj. and Simić, Lj. and Vranješ, Nenad and Vranješ Milosavljević, Marija",
year = "2014",
abstract = "Several models of physics beyond the Standard Model predict neutral particles that decay into final states consisting of collimated jets of light leptons and hadrons (so-called lepton jets). These particles can also be long-lived with decay length comparable to, or even larger than, the LHC detectors linear dimensions. This paper presents the results of a search for lepton jets in proton-proton collisions at the centre-of-mass energy of root s = 8 TeV in a sample of 20.3 fb(-1) collected during 2012 with the ATLAS detector at the LHC. Limits on models predicting Higgs boson decays to neutral long-lived lepton jets are derived as a function of the particles proper decay length.",
journal = "Journal of High Energy Physics",
title = "Search for long-lived neutral particles decaying into lepton jets in proton-proton collisions at root s=8 Tev with the ATLAS detector",
number = "11",
doi = "10.1007/JHEP11(2014)088"
}
Aad, G., Agatonović-Jovin, T., Bozic, I., Ćirković, P., Dimitrievska, A., Krstić, J. B., Mamužić, J., Marjanović, M., Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, N.,& Vranješ Milosavljević, M.. (2014). Search for long-lived neutral particles decaying into lepton jets in proton-proton collisions at root s=8 Tev with the ATLAS detector. in Journal of High Energy Physics(11).
https://doi.org/10.1007/JHEP11(2014)088
Aad G, Agatonović-Jovin T, Bozic I, Ćirković P, Dimitrievska A, Krstić JB, Mamužić J, Marjanović M, Popović DS, Sijacki D, Simić L, Vranješ N, Vranješ Milosavljević M. Search for long-lived neutral particles decaying into lepton jets in proton-proton collisions at root s=8 Tev with the ATLAS detector. in Journal of High Energy Physics. 2014;(11).
doi:10.1007/JHEP11(2014)088 .
Aad, G., Agatonović-Jovin, Tatjana, Bozic, I., Ćirković, Predrag, Dimitrievska, A., Krstić, Jugoslav B., Mamužić, Judita, Marjanović, M., Popović, D. S., Sijacki, Dj., Simić, Lj., Vranješ, Nenad, Vranješ Milosavljević, Marija, "Search for long-lived neutral particles decaying into lepton jets in proton-proton collisions at root s=8 Tev with the ATLAS detector" in Journal of High Energy Physics, no. 11 (2014),
https://doi.org/10.1007/JHEP11(2014)088 . .
14
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