TY  - JOUR
AU  - Aleksić, Katarina
AU  - Stojković Simatović, Ivana
AU  - Stanković, Ana
AU  - Veselinović, Ljiljana
AU  - Stojadinović, Stevan
AU  - Rac, Vladislav
AU  - Radmilović, Nadežda
AU  - Rajić, Vladimir
AU  - Škapin, Srečo Davor
AU  - Mančić, Lidija
AU  - Marković, Smilja
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/11080
AB  - Catalytic materials are the greatest challenge for the commercial application of water electrolysis (WEs) and fuel cells (FCs) as clean energy technologies. There is a need to find an alternative to expensive and unavailable platinum group metal (PGM) catalysts. This study aimed to reduce the cost of PGM materials by replacing Ru with RuO2 and lowering the amount of RuO2 by adding abundant and multifunctional ZnO. A ZnO@RuO2 composite in a 10:1 molar ratio was synthesized by microwave processing of a precipitate as a green, low-cost, and fast method, and then annealed at 300°C and 600°C to improve the catalytic properties. The physicochemical properties of the ZnO@RuO2 composites were investigated by X-ray powder diffraction (XRD), Raman and Fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), UV-Vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. The electrochemical activity of the samples was investigated by linear sweep voltammetry in acidic and alkaline electrolytes. We observed good bifunctional catalytic activity of the ZnO@RuO2 composites toward HER and OER in both electrolytes. The improved bifunctional catalytic activity of the ZnO@RuO2 composite by annealing was discussed and attributed to the reduced number of bulk oxygen vacancies and the increased number of established heterojunctions.
T2  - Frontiers in Chemistry
T1  - Enhancement of ZnO@RuO2 bifunctional photo-electro catalytic activity toward water splitting
VL  - 11
DO  - 10.3389/fchem.2023.1173910
ER  - 

@article{
author = "Aleksić, Katarina and Stojković Simatović, Ivana and Stanković, Ana and Veselinović, Ljiljana and Stojadinović, Stevan and Rac, Vladislav and Radmilović, Nadežda and Rajić, Vladimir and Škapin, Srečo Davor and Mančić, Lidija and Marković, Smilja",
year = "2023",
abstract = "Catalytic materials are the greatest challenge for the commercial application of water electrolysis (WEs) and fuel cells (FCs) as clean energy technologies. There is a need to find an alternative to expensive and unavailable platinum group metal (PGM) catalysts. This study aimed to reduce the cost of PGM materials by replacing Ru with RuO2 and lowering the amount of RuO2 by adding abundant and multifunctional ZnO. A ZnO@RuO2 composite in a 10:1 molar ratio was synthesized by microwave processing of a precipitate as a green, low-cost, and fast method, and then annealed at 300°C and 600°C to improve the catalytic properties. The physicochemical properties of the ZnO@RuO2 composites were investigated by X-ray powder diffraction (XRD), Raman and Fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), UV-Vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. The electrochemical activity of the samples was investigated by linear sweep voltammetry in acidic and alkaline electrolytes. We observed good bifunctional catalytic activity of the ZnO@RuO2 composites toward HER and OER in both electrolytes. The improved bifunctional catalytic activity of the ZnO@RuO2 composite by annealing was discussed and attributed to the reduced number of bulk oxygen vacancies and the increased number of established heterojunctions.",
journal = "Frontiers in Chemistry",
title = "Enhancement of ZnO@RuO2 bifunctional photo-electro catalytic activity toward water splitting",
volume = "11",
doi = "10.3389/fchem.2023.1173910"
}

Aleksić, K., Stojković Simatović, I., Stanković, A., Veselinović, L., Stojadinović, S., Rac, V., Radmilović, N., Rajić, V., Škapin, S. D., Mančić, L.,& Marković, S.. (2023). Enhancement of ZnO@RuO2 bifunctional photo-electro catalytic activity toward water splitting. in Frontiers in Chemistry, 11.
https://doi.org/10.3389/fchem.2023.1173910

Aleksić K, Stojković Simatović I, Stanković A, Veselinović L, Stojadinović S, Rac V, Radmilović N, Rajić V, Škapin SD, Mančić L, Marković S. Enhancement of ZnO@RuO2 bifunctional photo-electro catalytic activity toward water splitting. in Frontiers in Chemistry. 2023;11.
doi:10.3389/fchem.2023.1173910 .

Aleksić, Katarina, Stojković Simatović, Ivana, Stanković, Ana, Veselinović, Ljiljana, Stojadinović, Stevan, Rac, Vladislav, Radmilović, Nadežda, Rajić, Vladimir, Škapin, Srečo Davor, Mančić, Lidija, Marković, Smilja, "Enhancement of ZnO@RuO2 bifunctional photo-electro catalytic activity toward water splitting" in Frontiers in Chemistry, 11 (2023),
https://doi.org/10.3389/fchem.2023.1173910 . .

TY  - CONF
AU  - Rajić, Vladimir
AU  - Marković, Smilja
AU  - Popović, M.
AU  - Novaković, M.
AU  - Veselinović, Ljiljana
AU  - Stojković Simatović, Ivana
AU  - Škapin, Srečo Davor
AU  - Stojanović, S.
AU  - Rac, Vladislav
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/11554
AB  - Zink oxide-based materials have a great potential to be applied in photo and electro catalysts, opto-electronic (indoor illumination, LED), etc. Attractiveness of ZnO is attributed to wide bandgap energy at room temperature (3.37 eV), high electron mobility and transfer efficiency (115-155 cm2·V-1·s-1), large exciton binding energy (60 meV), intrinsic stability, nontoxicity, environmental compatibility and also, simple and not expensive synthesis procedure. A lot of different approaches can be used to modify the bandgap (i.e. optical absorption) of ZnO materials: metal and nonmetal ion doping, hydrogenation, the incorporation of crystalline defects in the form of V and I, modification of particles morphology and surface topology, etc. In this study, eco-friendly and rapid microwave processing of a precipitate was used to produce Fe-doped ZnO nanoparticles with 5, 10, 15 and 20 at.% of Fe (Zn1-xFeyO(1-x+1.5y)). The influence of different amount of Fe substituted Zn in ZnO on the crystal structure, morphological, textural, and optical properties as well as on functionality of ZnO particles was investigated. The crystal structure and phase purity of the Zn1-xFeyO(1-x+1.5y) particles were determined by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). Effects of the Fe3+ amount on particles morphology and texture properties were observed with field emission scanning electron microscopy (FE–SEM), transmission electron microscopy (TEM) and nitrogen adsorption–desorption isotherm, respectively. Optical properties were studied using UV-Vis diffuse reflectance and photoluminescence spectroscopy. Functionality of ZnO particles was studied due to their photocatalytic and electrochemical activities. Photocatalytic activity was examined via decolorization of methylene blue under direct sunlight irradiation. Electrochemical behavior of the ZnO samples as anode material was evaluated by linear sweep voltammetry in 0.5 M Na2SO4 electrolyte.
PB  - Belgrade : Vinča Institute of Nuclear Sciences
C3  - PHOTONICA2023 : 9th International School and Conference on Photonics : book of abstracts; August 28 - September 1, 2023; Belgrade
T1  - Crystal structure, optical properties and photo/electrocatalytic activity of nanostructured Zn1-xFeyO(1-x+1.5y)
SP  - 34
UR  - https://hdl.handle.net/21.15107/rcub_vinar_11554
ER  - 

@conference{
author = "Rajić, Vladimir and Marković, Smilja and Popović, M. and Novaković, M. and Veselinović, Ljiljana and Stojković Simatović, Ivana and Škapin, Srečo Davor and Stojanović, S. and Rac, Vladislav",
year = "2023",
abstract = "Zink oxide-based materials have a great potential to be applied in photo and electro catalysts, opto-electronic (indoor illumination, LED), etc. Attractiveness of ZnO is attributed to wide bandgap energy at room temperature (3.37 eV), high electron mobility and transfer efficiency (115-155 cm2·V-1·s-1), large exciton binding energy (60 meV), intrinsic stability, nontoxicity, environmental compatibility and also, simple and not expensive synthesis procedure. A lot of different approaches can be used to modify the bandgap (i.e. optical absorption) of ZnO materials: metal and nonmetal ion doping, hydrogenation, the incorporation of crystalline defects in the form of V and I, modification of particles morphology and surface topology, etc. In this study, eco-friendly and rapid microwave processing of a precipitate was used to produce Fe-doped ZnO nanoparticles with 5, 10, 15 and 20 at.% of Fe (Zn1-xFeyO(1-x+1.5y)). The influence of different amount of Fe substituted Zn in ZnO on the crystal structure, morphological, textural, and optical properties as well as on functionality of ZnO particles was investigated. The crystal structure and phase purity of the Zn1-xFeyO(1-x+1.5y) particles were determined by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). Effects of the Fe3+ amount on particles morphology and texture properties were observed with field emission scanning electron microscopy (FE–SEM), transmission electron microscopy (TEM) and nitrogen adsorption–desorption isotherm, respectively. Optical properties were studied using UV-Vis diffuse reflectance and photoluminescence spectroscopy. Functionality of ZnO particles was studied due to their photocatalytic and electrochemical activities. Photocatalytic activity was examined via decolorization of methylene blue under direct sunlight irradiation. Electrochemical behavior of the ZnO samples as anode material was evaluated by linear sweep voltammetry in 0.5 M Na2SO4 electrolyte.",
publisher = "Belgrade : Vinča Institute of Nuclear Sciences",
journal = "PHOTONICA2023 : 9th International School and Conference on Photonics : book of abstracts; August 28 - September 1, 2023; Belgrade",
title = "Crystal structure, optical properties and photo/electrocatalytic activity of nanostructured Zn1-xFeyO(1-x+1.5y)",
pages = "34",
url = "https://hdl.handle.net/21.15107/rcub_vinar_11554"
}

Rajić, V., Marković, S., Popović, M., Novaković, M., Veselinović, L., Stojković Simatović, I., Škapin, S. D., Stojanović, S.,& Rac, V.. (2023). Crystal structure, optical properties and photo/electrocatalytic activity of nanostructured Zn1-xFeyO(1-x+1.5y). in PHOTONICA2023 : 9th International School and Conference on Photonics : book of abstracts; August 28 - September 1, 2023; Belgrade
Belgrade : Vinča Institute of Nuclear Sciences., 34.
https://hdl.handle.net/21.15107/rcub_vinar_11554

Rajić V, Marković S, Popović M, Novaković M, Veselinović L, Stojković Simatović I, Škapin SD, Stojanović S, Rac V. Crystal structure, optical properties and photo/electrocatalytic activity of nanostructured Zn1-xFeyO(1-x+1.5y). in PHOTONICA2023 : 9th International School and Conference on Photonics : book of abstracts; August 28 - September 1, 2023; Belgrade. 2023;:34.
https://hdl.handle.net/21.15107/rcub_vinar_11554 .

Rajić, Vladimir, Marković, Smilja, Popović, M., Novaković, M., Veselinović, Ljiljana, Stojković Simatović, Ivana, Škapin, Srečo Davor, Stojanović, S., Rac, Vladislav, "Crystal structure, optical properties and photo/electrocatalytic activity of nanostructured Zn1-xFeyO(1-x+1.5y)" in PHOTONICA2023 : 9th International School and Conference on Photonics : book of abstracts; August 28 - September 1, 2023; Belgrade (2023):34,
https://hdl.handle.net/21.15107/rcub_vinar_11554 .

TY  - JOUR
AU  - Veselinović, Ljiljana
AU  - Mitrić, Miodrag
AU  - Mančić, Lidija
AU  - Jardim, Paula M.
AU  - Škapin, Srečo Davor
AU  - Cvjetićanin, Nikola
AU  - Milović, Miloš D.
AU  - Marković, Smilja
PY  - 2022
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/12382
AB  - This paper reports a detailed study of crystal structure and dielectric properties of ruthenium-substituted calcium-copper titanates (CaCu3Ti4−xRuxO12, CCTRO). A series of three samples with different stoichiometry was prepared: CaCu3Ti4−xRuxO12, x = 0, 1 and 4, abbreviated as CCTO, CCT3RO and CCRO, respectively. A detailed structural analysis of CCTRO samples was done by the Rietveld refinement of XRPD data. The results show that, regardless of whether Ti4+ or Ru4+ ions are placed in B crystallographic position in AA’3B4O12 (CaCu3Ti4−xRuxO12) unit cell, the crystal structure remains cubic with Im3¯ symmetry. Slight increases in the unit cell parameters, cell volume and interatomic distances indicate that Ru4+ ions with larger ionic radii (0.62 Å) than Ti4+ (0.605 Å) are incorporated in the CaCu3Ti4−xRuxO12 crystal lattice. The structural investigations were confirmed using TEM, HRTEM and ADF/STEM analyses, including EDXS elemental mapping. The effect of Ru atoms share in CaCu3Ti4−xRuxO12 samples on their electrical properties was determined by impedance and dielectric measurements. Results of dielectric measurements indicate that one atom of ruthenium per CaCu3Ti4−xRuxO12 unit cell transforms dielectric CCTO into conductive CCT3RO while preserving cubic crystal structure. Our findings about CCTO and CCT3RO ceramics promote them as ideal tandem to overcome the problem of stress on dielectric-electrode interfaces in capacitors.
T2  - Materials
T1  - Crystal Structure and Electrical Properties of Ruthenium-Substituted Calcium Copper Titanate
VL  - 15
IS  - 23
SP  - 8500
SP  - 8500
DO  - 10.3390/ma15238500
ER  - 

@article{
author = "Veselinović, Ljiljana and Mitrić, Miodrag and Mančić, Lidija and Jardim, Paula M. and Škapin, Srečo Davor and Cvjetićanin, Nikola and Milović, Miloš D. and Marković, Smilja",
year = "2022",
abstract = "This paper reports a detailed study of crystal structure and dielectric properties of ruthenium-substituted calcium-copper titanates (CaCu3Ti4−xRuxO12, CCTRO). A series of three samples with different stoichiometry was prepared: CaCu3Ti4−xRuxO12, x = 0, 1 and 4, abbreviated as CCTO, CCT3RO and CCRO, respectively. A detailed structural analysis of CCTRO samples was done by the Rietveld refinement of XRPD data. The results show that, regardless of whether Ti4+ or Ru4+ ions are placed in B crystallographic position in AA’3B4O12 (CaCu3Ti4−xRuxO12) unit cell, the crystal structure remains cubic with Im3¯ symmetry. Slight increases in the unit cell parameters, cell volume and interatomic distances indicate that Ru4+ ions with larger ionic radii (0.62 Å) than Ti4+ (0.605 Å) are incorporated in the CaCu3Ti4−xRuxO12 crystal lattice. The structural investigations were confirmed using TEM, HRTEM and ADF/STEM analyses, including EDXS elemental mapping. The effect of Ru atoms share in CaCu3Ti4−xRuxO12 samples on their electrical properties was determined by impedance and dielectric measurements. Results of dielectric measurements indicate that one atom of ruthenium per CaCu3Ti4−xRuxO12 unit cell transforms dielectric CCTO into conductive CCT3RO while preserving cubic crystal structure. Our findings about CCTO and CCT3RO ceramics promote them as ideal tandem to overcome the problem of stress on dielectric-electrode interfaces in capacitors.",
journal = "Materials",
title = "Crystal Structure and Electrical Properties of Ruthenium-Substituted Calcium Copper Titanate",
volume = "15",
number = "23",
pages = "8500-8500",
doi = "10.3390/ma15238500"
}

Veselinović, L., Mitrić, M., Mančić, L., Jardim, P. M., Škapin, S. D., Cvjetićanin, N., Milović, M. D.,& Marković, S.. (2022). Crystal Structure and Electrical Properties of Ruthenium-Substituted Calcium Copper Titanate. in Materials, 15(23), 8500.
https://doi.org/10.3390/ma15238500

Veselinović L, Mitrić M, Mančić L, Jardim PM, Škapin SD, Cvjetićanin N, Milović MD, Marković S. Crystal Structure and Electrical Properties of Ruthenium-Substituted Calcium Copper Titanate. in Materials. 2022;15(23):8500.
doi:10.3390/ma15238500 .

Veselinović, Ljiljana, Mitrić, Miodrag, Mančić, Lidija, Jardim, Paula M., Škapin, Srečo Davor, Cvjetićanin, Nikola, Milović, Miloš D., Marković, Smilja, "Crystal Structure and Electrical Properties of Ruthenium-Substituted Calcium Copper Titanate" in Materials, 15, no. 23 (2022):8500,
https://doi.org/10.3390/ma15238500 . .

TY  - JOUR
AU  - Marković, Smilja
AU  - Rau, Julietta V.
AU  - De Bonis, Angela
AU  - De Bellis, Giovanni
AU  - Stojanović, Zoran S.
AU  - Veselinović, Ljiljana M.
AU  - Mitrić, Miodrag
AU  - Ignjatović, Nenad L.
AU  - Škapin, Srečo Davor
AU  - Vengust, Damjan
PY  - 2022
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10206
AB  - Dense calcium phosphate-based ceramics were fabricated to be used as targets for pulsed laser deposition (PLD). Nanostructured cobalt-substituted hydroxyapatite (Co:HAP) was used as a starting powder. To vary phase composition and microstructure of targets, two sintering approaches were applied, conventional (CS) and two-step sintering (TSS). The obtained results show that in both cases biphasic calcium phosphate (BCP) ceramics (targets) were prepared, with slightly different HAP-to-β–TCP amount ratio and a significantly different microstructure. While the CS method yielded fully dense ceramics with an average grain size of 1.3 μm, the ceramics prepared by TSS had a density of 98.5%, with a predominant grain size below 100 nm. (Ca + Co)P coatings were prepared by PLD of (Ca + Co)P targets. The temperature of the Ti substrate was adjusted to be 25 and 500 °C. The results show that the phase composition of (Ca + Co)P coatings depended on the phase composition of targets as well as on the temperature of the Ti substrate. The coating prepared at 25 °C using CS target consisted of three calcium phosphate phases, HAP, β–TCP and α–TCP; when the TSS target was used, the coating was biphasic, containing HAP and β–TCP. When the substrate was heated to 500 °C, regardless of whether the CS or the TSS target was used, the deposited coatings were composed of HAP and α–TCP. Due to different phase compositions, the (Ca + Co)P coatings deposited at 25 °C showed an improved hardness compared to those deposited at 500 °C. The obtained results confirmed that the phase composition, morphology and mechanical properties of 0.3 μm thick (Ca + Co)P coatings on a Ti substrate can be tailored by employing (Ca + Co)P targets with different microstructures, and also by varying the temperature of the Ti substrate during deposition experiments.
T2  - Surface and Coatings Technology
T1  - Pathway to tailor the phase composition, microstructure and mechanical properties of pulsed laser deposited cobalt-substituted calcium phosphate coatings on titanium
VL  - 437
SP  - 128275
DO  - 10.1016/j.surfcoat.2022.128275
ER  - 

@article{
author = "Marković, Smilja and Rau, Julietta V. and De Bonis, Angela and De Bellis, Giovanni and Stojanović, Zoran S. and Veselinović, Ljiljana M. and Mitrić, Miodrag and Ignjatović, Nenad L. and Škapin, Srečo Davor and Vengust, Damjan",
year = "2022",
abstract = "Dense calcium phosphate-based ceramics were fabricated to be used as targets for pulsed laser deposition (PLD). Nanostructured cobalt-substituted hydroxyapatite (Co:HAP) was used as a starting powder. To vary phase composition and microstructure of targets, two sintering approaches were applied, conventional (CS) and two-step sintering (TSS). The obtained results show that in both cases biphasic calcium phosphate (BCP) ceramics (targets) were prepared, with slightly different HAP-to-β–TCP amount ratio and a significantly different microstructure. While the CS method yielded fully dense ceramics with an average grain size of 1.3 μm, the ceramics prepared by TSS had a density of 98.5%, with a predominant grain size below 100 nm. (Ca + Co)P coatings were prepared by PLD of (Ca + Co)P targets. The temperature of the Ti substrate was adjusted to be 25 and 500 °C. The results show that the phase composition of (Ca + Co)P coatings depended on the phase composition of targets as well as on the temperature of the Ti substrate. The coating prepared at 25 °C using CS target consisted of three calcium phosphate phases, HAP, β–TCP and α–TCP; when the TSS target was used, the coating was biphasic, containing HAP and β–TCP. When the substrate was heated to 500 °C, regardless of whether the CS or the TSS target was used, the deposited coatings were composed of HAP and α–TCP. Due to different phase compositions, the (Ca + Co)P coatings deposited at 25 °C showed an improved hardness compared to those deposited at 500 °C. The obtained results confirmed that the phase composition, morphology and mechanical properties of 0.3 μm thick (Ca + Co)P coatings on a Ti substrate can be tailored by employing (Ca + Co)P targets with different microstructures, and also by varying the temperature of the Ti substrate during deposition experiments.",
journal = "Surface and Coatings Technology",
title = "Pathway to tailor the phase composition, microstructure and mechanical properties of pulsed laser deposited cobalt-substituted calcium phosphate coatings on titanium",
volume = "437",
pages = "128275",
doi = "10.1016/j.surfcoat.2022.128275"
}

Marković, S., Rau, J. V., De Bonis, A., De Bellis, G., Stojanović, Z. S., Veselinović, L. M., Mitrić, M., Ignjatović, N. L., Škapin, S. D.,& Vengust, D.. (2022). Pathway to tailor the phase composition, microstructure and mechanical properties of pulsed laser deposited cobalt-substituted calcium phosphate coatings on titanium. in Surface and Coatings Technology, 437, 128275.
https://doi.org/10.1016/j.surfcoat.2022.128275

Marković S, Rau JV, De Bonis A, De Bellis G, Stojanović ZS, Veselinović LM, Mitrić M, Ignjatović NL, Škapin SD, Vengust D. Pathway to tailor the phase composition, microstructure and mechanical properties of pulsed laser deposited cobalt-substituted calcium phosphate coatings on titanium. in Surface and Coatings Technology. 2022;437:128275.
doi:10.1016/j.surfcoat.2022.128275 .

Marković, Smilja, Rau, Julietta V., De Bonis, Angela, De Bellis, Giovanni, Stojanović, Zoran S., Veselinović, Ljiljana M., Mitrić, Miodrag, Ignjatović, Nenad L., Škapin, Srečo Davor, Vengust, Damjan, "Pathway to tailor the phase composition, microstructure and mechanical properties of pulsed laser deposited cobalt-substituted calcium phosphate coatings on titanium" in Surface and Coatings Technology, 437 (2022):128275,
https://doi.org/10.1016/j.surfcoat.2022.128275 . .

TY  - CONF
AU  - Veselinović, Ljiljana
AU  - Mitrić, Miodrag
AU  - Mančić, Lidija
AU  - Jardim, Paula M.
AU  - Škapin, Srečo Davor
AU  - Cvjetićanin, N.
AU  - Marković, S.
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10779
AB  - The CaCu3 Ti 4 O12 belongs to the large ACu3B4 O12 family of materials. Crystallographic A site is most often occupied by alkaline-earth metals or lanthanides, while B site is occupied by transition metals. The type of cations that build up the structure strongly affects the properties of these. The CaCu 3 Ti 4 O12 has been extensively studied due to its high dielectric permittivity stable over a wide temperature and frequency range (up to 10 5 , for 100-600 K and 10 2 –105 Hz). Because of such characteristics, it has promising application in microelectronics. However, it has been shown that differences in the crystal structure and electrical properties of dielectric ceramics and metallic electrodes, may cause an energy barrier and occurrence of stress on the ceramic-electrode contact which reduces dielectric permittivity. Such stress can be prevented by using dielectric and electrode materials with as much as possible similar crystal structure, especially unit cell parameters. This investigation dealt with detailed structural (XRPD, HRTEM, SAED), dielectric and magnetic study of CaCu 3 Ti 4-xRuxO12 (CCTRO, x = 0, 1 and 4) materials. The results of structural refinement show that in cubic symmetry with space group 3Im , both titanium and ruthenium ions occupied crystallographic B site. Moreover, the variation in stoichiometry slightly affects the value of the unit cell parameters but changes electrical properties of studied material. Thus, substitution of even one atom of Ru in CaCu3 Ti 4-xRuxO12 unit cell is enough to change material properties from dielectric to conductor solving the problem of stress appearance on the contact layer of dielectric/electrode in capacitors.
PB  - Belgrade : Serbian Ceramic Society
C3  - Advanced Ceramics and Application : 9th Serbian Ceramic Society Conference : program and the book of abstracts; September 20-21, 2021; Belgrade
T1  - CaCu3Ti4-xRuxO12: Crystal structure, electrical and magnetic properties
SP  - 32
UR  - https://hdl.handle.net/21.15107/rcub_vinar_10779
ER  - 

@conference{
author = "Veselinović, Ljiljana and Mitrić, Miodrag and Mančić, Lidija and Jardim, Paula M. and Škapin, Srečo Davor and Cvjetićanin, N. and Marković, S.",
year = "2021",
abstract = "The CaCu3 Ti 4 O12 belongs to the large ACu3B4 O12 family of materials. Crystallographic A site is most often occupied by alkaline-earth metals or lanthanides, while B site is occupied by transition metals. The type of cations that build up the structure strongly affects the properties of these. The CaCu 3 Ti 4 O12 has been extensively studied due to its high dielectric permittivity stable over a wide temperature and frequency range (up to 10 5 , for 100-600 K and 10 2 –105 Hz). Because of such characteristics, it has promising application in microelectronics. However, it has been shown that differences in the crystal structure and electrical properties of dielectric ceramics and metallic electrodes, may cause an energy barrier and occurrence of stress on the ceramic-electrode contact which reduces dielectric permittivity. Such stress can be prevented by using dielectric and electrode materials with as much as possible similar crystal structure, especially unit cell parameters. This investigation dealt with detailed structural (XRPD, HRTEM, SAED), dielectric and magnetic study of CaCu 3 Ti 4-xRuxO12 (CCTRO, x = 0, 1 and 4) materials. The results of structural refinement show that in cubic symmetry with space group 3Im , both titanium and ruthenium ions occupied crystallographic B site. Moreover, the variation in stoichiometry slightly affects the value of the unit cell parameters but changes electrical properties of studied material. Thus, substitution of even one atom of Ru in CaCu3 Ti 4-xRuxO12 unit cell is enough to change material properties from dielectric to conductor solving the problem of stress appearance on the contact layer of dielectric/electrode in capacitors.",
publisher = "Belgrade : Serbian Ceramic Society",
journal = "Advanced Ceramics and Application : 9th Serbian Ceramic Society Conference : program and the book of abstracts; September 20-21, 2021; Belgrade",
title = "CaCu3Ti4-xRuxO12: Crystal structure, electrical and magnetic properties",
pages = "32",
url = "https://hdl.handle.net/21.15107/rcub_vinar_10779"
}

Veselinović, L., Mitrić, M., Mančić, L., Jardim, P. M., Škapin, S. D., Cvjetićanin, N.,& Marković, S.. (2021). CaCu3Ti4-xRuxO12: Crystal structure, electrical and magnetic properties. in Advanced Ceramics and Application : 9th Serbian Ceramic Society Conference : program and the book of abstracts; September 20-21, 2021; Belgrade
Belgrade : Serbian Ceramic Society., 32.
https://hdl.handle.net/21.15107/rcub_vinar_10779

Veselinović L, Mitrić M, Mančić L, Jardim PM, Škapin SD, Cvjetićanin N, Marković S. CaCu3Ti4-xRuxO12: Crystal structure, electrical and magnetic properties. in Advanced Ceramics and Application : 9th Serbian Ceramic Society Conference : program and the book of abstracts; September 20-21, 2021; Belgrade. 2021;:32.
https://hdl.handle.net/21.15107/rcub_vinar_10779 .

Veselinović, Ljiljana, Mitrić, Miodrag, Mančić, Lidija, Jardim, Paula M., Škapin, Srečo Davor, Cvjetićanin, N., Marković, S., "CaCu3Ti4-xRuxO12: Crystal structure, electrical and magnetic properties" in Advanced Ceramics and Application : 9th Serbian Ceramic Society Conference : program and the book of abstracts; September 20-21, 2021; Belgrade (2021):32,
https://hdl.handle.net/21.15107/rcub_vinar_10779 .

TY  - JOUR
AU  - Rajić, Vladimir
AU  - Simatović Stojković, Ivana
AU  - Veselinović, Ljiljana M.
AU  - Belošević-Čavor, Jelena
AU  - Novaković, Mirjana M.
AU  - Popović, Maja
AU  - Škapin, Srečo Davor
AU  - Mojović, Miloš
AU  - Stojadinović, Stevan
AU  - Rac, Vladislav
AU  - Častvan Janković, Ivona
AU  - Marković, Smilja
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9679
AB  - Eco-friendly and rapid microwave processing of a precipitate was used to produce Fe-doped zinc oxide (Zn1−xFexO, x = 0, 0.05, 0.1, 0.15 and 0.20; ZnO:Fe) nanoparticles, which were tested as catalysts toward the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in a moderately alkaline solution. The phase composition, crystal structure, morphology, textural properties, surface chemistry, optical properties and band structure were examined to comprehend the influence of Zn2+ partial substitution with Fe3+ on the catalytic activity of ZnO:Fe. Linear sweep voltammetry showed an improved catalytic activity of ZnO:5Fe toward the ORR, compared to pure ZnO, while with increased amounts of the Fe-dopant the activity decreased. The improvement was suggested by a more positive onset potential (0.394 V vs. RHE), current density (0.231 mA cm−2 at 0.150 V vs. RHE), and faster kinetics (Tafel slope, b = 248 mV dec−1), and it may be due to the synergistic effect of (1) a sufficient amount of surface oxygen vacancies, and (2) a certain amount of plate-like particles composed of crystallites with well developed (0001) and (000) facets. Quite the contrary, the OER study showed that the introduction of Fe3+ ions into the ZnO crystal structure resulted in enhanced catalytic activity of all ZnO:Fe samples, compared to pure ZnO, probably due to the modified binding energy and an optimized band structure. With the maximal current density of 1.066 mA cm−2 at 2.216 V vs. RHE, an onset potential of 1.856 V vs. RHE, and the smallest potential difference between the OER and ORR (ΔE = 1.58 V), ZnO:10Fe may be considered a promising bifunctional catalyst toward the OER/ORR in moderately alkaline solution. This study demonstrates that the electrocatalytic activity of ZnO:Fe strongly depends on the defect chemistry and consequently the band structure. Along with providing fundamental insight into the electrocatalytic activity of ZnO:Fe, the study also indicates an optimal stoichiometry for enhanced bifunctional activity toward the OER/ORR, compared to pure ZnO.
T2  - Physical Chemistry Chemical Physics
T1  - Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry
VL  - 22
IS  - 38
SP  - 22078
EP  - 22095
DO  - 10.1039/D0CP03377D
ER  - 

@article{
author = "Rajić, Vladimir and Simatović Stojković, Ivana and Veselinović, Ljiljana M. and Belošević-Čavor, Jelena and Novaković, Mirjana M. and Popović, Maja and Škapin, Srečo Davor and Mojović, Miloš and Stojadinović, Stevan and Rac, Vladislav and Častvan Janković, Ivona and Marković, Smilja",
year = "2020",
abstract = "Eco-friendly and rapid microwave processing of a precipitate was used to produce Fe-doped zinc oxide (Zn1−xFexO, x = 0, 0.05, 0.1, 0.15 and 0.20; ZnO:Fe) nanoparticles, which were tested as catalysts toward the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in a moderately alkaline solution. The phase composition, crystal structure, morphology, textural properties, surface chemistry, optical properties and band structure were examined to comprehend the influence of Zn2+ partial substitution with Fe3+ on the catalytic activity of ZnO:Fe. Linear sweep voltammetry showed an improved catalytic activity of ZnO:5Fe toward the ORR, compared to pure ZnO, while with increased amounts of the Fe-dopant the activity decreased. The improvement was suggested by a more positive onset potential (0.394 V vs. RHE), current density (0.231 mA cm−2 at 0.150 V vs. RHE), and faster kinetics (Tafel slope, b = 248 mV dec−1), and it may be due to the synergistic effect of (1) a sufficient amount of surface oxygen vacancies, and (2) a certain amount of plate-like particles composed of crystallites with well developed (0001) and (000) facets. Quite the contrary, the OER study showed that the introduction of Fe3+ ions into the ZnO crystal structure resulted in enhanced catalytic activity of all ZnO:Fe samples, compared to pure ZnO, probably due to the modified binding energy and an optimized band structure. With the maximal current density of 1.066 mA cm−2 at 2.216 V vs. RHE, an onset potential of 1.856 V vs. RHE, and the smallest potential difference between the OER and ORR (ΔE = 1.58 V), ZnO:10Fe may be considered a promising bifunctional catalyst toward the OER/ORR in moderately alkaline solution. This study demonstrates that the electrocatalytic activity of ZnO:Fe strongly depends on the defect chemistry and consequently the band structure. Along with providing fundamental insight into the electrocatalytic activity of ZnO:Fe, the study also indicates an optimal stoichiometry for enhanced bifunctional activity toward the OER/ORR, compared to pure ZnO.",
journal = "Physical Chemistry Chemical Physics",
title = "Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry",
volume = "22",
number = "38",
pages = "22078-22095",
doi = "10.1039/D0CP03377D"
}

Rajić, V., Simatović Stojković, I., Veselinović, L. M., Belošević-Čavor, J., Novaković, M. M., Popović, M., Škapin, S. D., Mojović, M., Stojadinović, S., Rac, V., Častvan Janković, I.,& Marković, S.. (2020). Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry. in Physical Chemistry Chemical Physics, 22(38), 22078-22095.
https://doi.org/10.1039/D0CP03377D

Rajić V, Simatović Stojković I, Veselinović LM, Belošević-Čavor J, Novaković MM, Popović M, Škapin SD, Mojović M, Stojadinović S, Rac V, Častvan Janković I, Marković S. Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry. in Physical Chemistry Chemical Physics. 2020;22(38):22078-22095.
doi:10.1039/D0CP03377D .

Rajić, Vladimir, Simatović Stojković, Ivana, Veselinović, Ljiljana M., Belošević-Čavor, Jelena, Novaković, Mirjana M., Popović, Maja, Škapin, Srečo Davor, Mojović, Miloš, Stojadinović, Stevan, Rac, Vladislav, Častvan Janković, Ivona, Marković, Smilja, "Bifunctional catalytic activity of Zn1−xFexO toward the OER/ORR: seeking an optimal stoichiometry" in Physical Chemistry Chemical Physics, 22, no. 38 (2020):22078-22095,
https://doi.org/10.1039/D0CP03377D . .

TY  - CONF
AU  - Marković, Smilja
AU  - Stojanović, Zoran S.
AU  - Veselinović, Ljiljana
AU  - Simić, Danica
AU  - Samolov, Aleksandra
AU  - Stojković Simatović, Ivana
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/11785
AB  - Radar-absorbent materials, used in stealth technology for defense aircrafts, vehicles, satellites, etc. from radar detection, are commonly based on graphite or semiconductive particles embedded in a polymer matrix. In this study, we employed Co2+ ion-substitution to improve Vis-NIR reflectivity of hydroxyapatite (Ca10(PO4)6(OH)2, HAP) powder. HAP:Co with nominally 5 at.% of Co was prepared with hydrothermal processing of a precipitate. Synthesized powder was characterized by XRD, Raman and ATR-FTIR spectroscopy, FE-SEM and TEM. Thermal stability of HAP:Co powder was examined by simultaneous TG-DTA analyzer. To modify its optical properties and obtain powders with a varietty of color tone, the HAP:Co powder was calcined at 800, 1000, and 1100 °C, in an air atmosphere, for 1 hour. Afterward, the calcined particles were used to prepare composites with poly(vinyl butyral), (PVB); the concentration range was 1 wt.% of the HAP:Co in PVB. The composite coatings, in the form of thin films on glass, were prepared by the solvent-casting technique, using ethanol as a fast evaporating solvent. Firstly, the HAP:Co particles were dispersed in ethanol, then PVB was added (Mowital B30H) and dissolved. To evaporate the solvent before spectrophotometric measurements, the coatings on glass were dried at room temperature for 72 hours. To comprehend optical properties of the coatings, diffuse reflection, transmission, and color coordinates were determined. We found that calcined HAP:Co particles have potential to be used in the formulation of coatings for camouflage protection.
PB  - Belgrade : Military Technical Institute
C3  - OTEH’20 : 9th International Scientific Conference on Defensive Technologies : the book of abstracts; Oct 15-16, Belgrade
T1  - HAp:Co as tunable VIS-NIR reflective pigment
SP  - 475
EP  - 480
UR  - https://hdl.handle.net/21.15107/rcub_vinar_11785
ER  - 

@conference{
author = "Marković, Smilja and Stojanović, Zoran S. and Veselinović, Ljiljana and Simić, Danica and Samolov, Aleksandra and Stojković Simatović, Ivana",
year = "2020",
abstract = "Radar-absorbent materials, used in stealth technology for defense aircrafts, vehicles, satellites, etc. from radar detection, are commonly based on graphite or semiconductive particles embedded in a polymer matrix. In this study, we employed Co2+ ion-substitution to improve Vis-NIR reflectivity of hydroxyapatite (Ca10(PO4)6(OH)2, HAP) powder. HAP:Co with nominally 5 at.% of Co was prepared with hydrothermal processing of a precipitate. Synthesized powder was characterized by XRD, Raman and ATR-FTIR spectroscopy, FE-SEM and TEM. Thermal stability of HAP:Co powder was examined by simultaneous TG-DTA analyzer. To modify its optical properties and obtain powders with a varietty of color tone, the HAP:Co powder was calcined at 800, 1000, and 1100 °C, in an air atmosphere, for 1 hour. Afterward, the calcined particles were used to prepare composites with poly(vinyl butyral), (PVB); the concentration range was 1 wt.% of the HAP:Co in PVB. The composite coatings, in the form of thin films on glass, were prepared by the solvent-casting technique, using ethanol as a fast evaporating solvent. Firstly, the HAP:Co particles were dispersed in ethanol, then PVB was added (Mowital B30H) and dissolved. To evaporate the solvent before spectrophotometric measurements, the coatings on glass were dried at room temperature for 72 hours. To comprehend optical properties of the coatings, diffuse reflection, transmission, and color coordinates were determined. We found that calcined HAP:Co particles have potential to be used in the formulation of coatings for camouflage protection.",
publisher = "Belgrade : Military Technical Institute",
journal = "OTEH’20 : 9th International Scientific Conference on Defensive Technologies : the book of abstracts; Oct 15-16, Belgrade",
title = "HAp:Co as tunable VIS-NIR reflective pigment",
pages = "475-480",
url = "https://hdl.handle.net/21.15107/rcub_vinar_11785"
}

Marković, S., Stojanović, Z. S., Veselinović, L., Simić, D., Samolov, A.,& Stojković Simatović, I.. (2020). HAp:Co as tunable VIS-NIR reflective pigment. in OTEH’20 : 9th International Scientific Conference on Defensive Technologies : the book of abstracts; Oct 15-16, Belgrade
Belgrade : Military Technical Institute., 475-480.
https://hdl.handle.net/21.15107/rcub_vinar_11785

Marković S, Stojanović ZS, Veselinović L, Simić D, Samolov A, Stojković Simatović I. HAp:Co as tunable VIS-NIR reflective pigment. in OTEH’20 : 9th International Scientific Conference on Defensive Technologies : the book of abstracts; Oct 15-16, Belgrade. 2020;:475-480.
https://hdl.handle.net/21.15107/rcub_vinar_11785 .

Marković, Smilja, Stojanović, Zoran S., Veselinović, Ljiljana, Simić, Danica, Samolov, Aleksandra, Stojković Simatović, Ivana, "HAp:Co as tunable VIS-NIR reflective pigment" in OTEH’20 : 9th International Scientific Conference on Defensive Technologies : the book of abstracts; Oct 15-16, Belgrade (2020):475-480,
https://hdl.handle.net/21.15107/rcub_vinar_11785 .

TY  - JOUR
AU  - Ignjatović, Nenad L.
AU  - Mančić, Lidija
AU  - Vuković, Marina
AU  - Stojanović, Zoran S.
AU  - Nikolić, Marko G.
AU  - Škapin, Srečo Davor
AU  - Jovanović, Sonja
AU  - Veselinović, Ljiljana M.
AU  - Uskoković, Vuk
AU  - Lazić, Snežana
AU  - Marković, Smilja
AU  - Lazarević, Miloš M.
AU  - Uskoković, Dragan
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8625
AB  - Taking advantage of the flexibility of the apatite structure, nano- and micro-particles of hydroxyapatite (HAp) were doped with different combinations of rare earth ions (RE3+ = Gd, Eu, Yb, Tm) to achieve a synergy among their magnetic and optical properties and to enable their application in preventive medicine, particularly diagnostics based on multimodal imaging. All powders were synthesized through hydrothermal processing at T ≤ 200 °C. An X-ray powder diffraction analysis showed that all powders crystallized in P63/m space group of the hexagonal crystal structure. The refined unit-cell parameters reflected a decrease in the unit cell volume as a result of the partial substitution of Ca2+ with smaller RE3+ ions at both cation positions. The FTIR analysis additionally suggested that a synergy may exist solely in the triply doped system, where the lattice symmetry and vibration modes become more coherent than in the singly or doubly doped systems. HAp:RE3+ optical characterization revealed a change in the energy band gap and the appearance of a weak blue luminescence (λex = 370 nm) due to an increased concentration of defects. The “up”- and the “down”-conversion spectra of HAp:Gd/Yb/Tm and HAp:Gd/Eu powders showed characteristic transitions of Tm3+ and Eu3+, respectively. Furthermore, in contrast to diamagnetic HAp, all HAp:RE3+ powders exhibited paramagnetic behavior. Cell viability tests of HAp:Gd/Yb/Tm and HAp:Gd/Eu powders in human dental pulp stem cell cultures indicated their good biocompatibility. © 2019, The Author(s).
T2  - Scientific Reports
T1  - Rare-earth (Gd3+,Yb3+/Tm3+, Eu3+) co-doped hydroxyapatite as magnetic, up-conversion and down-conversion materials for multimodal imaging
VL  - 9
IS  - 1
SP  - 16305
DO  - 10.1038/s41598-019-52885-0
ER  - 

@article{
author = "Ignjatović, Nenad L. and Mančić, Lidija and Vuković, Marina and Stojanović, Zoran S. and Nikolić, Marko G. and Škapin, Srečo Davor and Jovanović, Sonja and Veselinović, Ljiljana M. and Uskoković, Vuk and Lazić, Snežana and Marković, Smilja and Lazarević, Miloš M. and Uskoković, Dragan",
year = "2019",
abstract = "Taking advantage of the flexibility of the apatite structure, nano- and micro-particles of hydroxyapatite (HAp) were doped with different combinations of rare earth ions (RE3+ = Gd, Eu, Yb, Tm) to achieve a synergy among their magnetic and optical properties and to enable their application in preventive medicine, particularly diagnostics based on multimodal imaging. All powders were synthesized through hydrothermal processing at T ≤ 200 °C. An X-ray powder diffraction analysis showed that all powders crystallized in P63/m space group of the hexagonal crystal structure. The refined unit-cell parameters reflected a decrease in the unit cell volume as a result of the partial substitution of Ca2+ with smaller RE3+ ions at both cation positions. The FTIR analysis additionally suggested that a synergy may exist solely in the triply doped system, where the lattice symmetry and vibration modes become more coherent than in the singly or doubly doped systems. HAp:RE3+ optical characterization revealed a change in the energy band gap and the appearance of a weak blue luminescence (λex = 370 nm) due to an increased concentration of defects. The “up”- and the “down”-conversion spectra of HAp:Gd/Yb/Tm and HAp:Gd/Eu powders showed characteristic transitions of Tm3+ and Eu3+, respectively. Furthermore, in contrast to diamagnetic HAp, all HAp:RE3+ powders exhibited paramagnetic behavior. Cell viability tests of HAp:Gd/Yb/Tm and HAp:Gd/Eu powders in human dental pulp stem cell cultures indicated their good biocompatibility. © 2019, The Author(s).",
journal = "Scientific Reports",
title = "Rare-earth (Gd3+,Yb3+/Tm3+, Eu3+) co-doped hydroxyapatite as magnetic, up-conversion and down-conversion materials for multimodal imaging",
volume = "9",
number = "1",
pages = "16305",
doi = "10.1038/s41598-019-52885-0"
}

Ignjatović, N. L., Mančić, L., Vuković, M., Stojanović, Z. S., Nikolić, M. G., Škapin, S. D., Jovanović, S., Veselinović, L. M., Uskoković, V., Lazić, S., Marković, S., Lazarević, M. M.,& Uskoković, D.. (2019). Rare-earth (Gd3+,Yb3+/Tm3+, Eu3+) co-doped hydroxyapatite as magnetic, up-conversion and down-conversion materials for multimodal imaging. in Scientific Reports, 9(1), 16305.
https://doi.org/10.1038/s41598-019-52885-0

Ignjatović NL, Mančić L, Vuković M, Stojanović ZS, Nikolić MG, Škapin SD, Jovanović S, Veselinović LM, Uskoković V, Lazić S, Marković S, Lazarević MM, Uskoković D. Rare-earth (Gd3+,Yb3+/Tm3+, Eu3+) co-doped hydroxyapatite as magnetic, up-conversion and down-conversion materials for multimodal imaging. in Scientific Reports. 2019;9(1):16305.
doi:10.1038/s41598-019-52885-0 .

Ignjatović, Nenad L., Mančić, Lidija, Vuković, Marina, Stojanović, Zoran S., Nikolić, Marko G., Škapin, Srečo Davor, Jovanović, Sonja, Veselinović, Ljiljana M., Uskoković, Vuk, Lazić, Snežana, Marković, Smilja, Lazarević, Miloš M., Uskoković, Dragan, "Rare-earth (Gd3+,Yb3+/Tm3+, Eu3+) co-doped hydroxyapatite as magnetic, up-conversion and down-conversion materials for multimodal imaging" in Scientific Reports, 9, no. 1 (2019):16305,
https://doi.org/10.1038/s41598-019-52885-0 . .

TY  - JOUR
AU  - Milović, Miloš
AU  - Vasić Anićijević, Dragana D.
AU  - Jugović, Dragana
AU  - Anićijević, Vladan J.
AU  - Veselinović, Ljiljana M.
AU  - Mitrić, Miodrag
AU  - Uskoković, Dragan
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8017
AB  - Li2FeSiO4 material, which was prepared by a solid state method, crystallized as monoclinic P21/n polymorph. X-ray diffraction analysis with Rietveld structural refinement indicates specific occupation of Li2 crystallographic site by Fe2+ cation in the amount of 6 atom percents as a result of an antisite defect formation. The exclusive occupation of Li2 position, out of two crystallographic positions Li1 and Li2, by Fe2+ was discussed in relation to the differences that exist in the crystal environment of these positions and further investigated by DFT calculations. It was confirmed that Fe-Li2 substitution is energetically favorable compared to both Fe-Li1 substitution and the pristine crystal. In addition, changes of lattice geometry upon antisite defect formation were analyzed, and the obtained result is discussed in light of various factors (electronic, geometrical and enthropic) that contribute to the overall stability of the system. © 2018 Elsevier Masson SAS
T2  - Solid State Sciences
T1  - On the presence of antisite defect in monoclinic Li2FeSiO4 – A combined X-Ray diffraction and DFT study
VL  - 87
SP  - 81
EP  - 86
DO  - 10.1016/j.solidstatesciences.2018.11.008
ER  - 

@article{
author = "Milović, Miloš and Vasić Anićijević, Dragana D. and Jugović, Dragana and Anićijević, Vladan J. and Veselinović, Ljiljana M. and Mitrić, Miodrag and Uskoković, Dragan",
year = "2019",
abstract = "Li2FeSiO4 material, which was prepared by a solid state method, crystallized as monoclinic P21/n polymorph. X-ray diffraction analysis with Rietveld structural refinement indicates specific occupation of Li2 crystallographic site by Fe2+ cation in the amount of 6 atom percents as a result of an antisite defect formation. The exclusive occupation of Li2 position, out of two crystallographic positions Li1 and Li2, by Fe2+ was discussed in relation to the differences that exist in the crystal environment of these positions and further investigated by DFT calculations. It was confirmed that Fe-Li2 substitution is energetically favorable compared to both Fe-Li1 substitution and the pristine crystal. In addition, changes of lattice geometry upon antisite defect formation were analyzed, and the obtained result is discussed in light of various factors (electronic, geometrical and enthropic) that contribute to the overall stability of the system. © 2018 Elsevier Masson SAS",
journal = "Solid State Sciences",
title = "On the presence of antisite defect in monoclinic Li2FeSiO4 – A combined X-Ray diffraction and DFT study",
volume = "87",
pages = "81-86",
doi = "10.1016/j.solidstatesciences.2018.11.008"
}

Milović, M., Vasić Anićijević, D. D., Jugović, D., Anićijević, V. J., Veselinović, L. M., Mitrić, M.,& Uskoković, D.. (2019). On the presence of antisite defect in monoclinic Li2FeSiO4 – A combined X-Ray diffraction and DFT study. in Solid State Sciences, 87, 81-86.
https://doi.org/10.1016/j.solidstatesciences.2018.11.008

Milović M, Vasić Anićijević DD, Jugović D, Anićijević VJ, Veselinović LM, Mitrić M, Uskoković D. On the presence of antisite defect in monoclinic Li2FeSiO4 – A combined X-Ray diffraction and DFT study. in Solid State Sciences. 2019;87:81-86.
doi:10.1016/j.solidstatesciences.2018.11.008 .

Milović, Miloš, Vasić Anićijević, Dragana D., Jugović, Dragana, Anićijević, Vladan J., Veselinović, Ljiljana M., Mitrić, Miodrag, Uskoković, Dragan, "On the presence of antisite defect in monoclinic Li2FeSiO4 – A combined X-Ray diffraction and DFT study" in Solid State Sciences, 87 (2019):81-86,
https://doi.org/10.1016/j.solidstatesciences.2018.11.008 . .

TY  - JOUR
AU  - Milović, Miloš
AU  - Vasić Anićijević, Dragana D.
AU  - Jugović, Dragana
AU  - Anićijević, Vladan J.
AU  - Veselinović, Ljiljana M.
AU  - Mitrić, Miodrag
AU  - Uskoković, Dragan
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8021
AB  - Li2FeSiO4 material, which was prepared by a solid state method, crystallized as monoclinic P21/n polymorph. X-ray diffraction analysis with Rietveld structural refinement indicates specific occupation of Li2 crystallographic site by Fe2+ cation in the amount of 6 atom percents as a result of an antisite defect formation. The exclusive occupation of Li2 position, out of two crystallographic positions Li1 and Li2, by Fe2+ was discussed in relation to the differences that exist in the crystal environment of these positions and further investigated by DFT calculations. It was confirmed that Fe-Li2 substitution is energetically favorable compared to both Fe-Li1 substitution and the pristine crystal. In addition, changes of lattice geometry upon antisite defect formation were analyzed, and the obtained result is discussed in light of various factors (electronic, geometrical and enthropic) that contribute to the overall stability of the system. © 2018 Elsevier Masson SAS
T2  - Solid State Sciences
T1  - On the presence of antisite defect in monoclinic Li2FeSiO4 – A combined X-Ray diffraction and DFT study
VL  - 87
SP  - 81
EP  - 86
DO  - 10.1016/j.solidstatesciences.2018.11.008
ER  - 

@article{
author = "Milović, Miloš and Vasić Anićijević, Dragana D. and Jugović, Dragana and Anićijević, Vladan J. and Veselinović, Ljiljana M. and Mitrić, Miodrag and Uskoković, Dragan",
year = "2019",
abstract = "Li2FeSiO4 material, which was prepared by a solid state method, crystallized as monoclinic P21/n polymorph. X-ray diffraction analysis with Rietveld structural refinement indicates specific occupation of Li2 crystallographic site by Fe2+ cation in the amount of 6 atom percents as a result of an antisite defect formation. The exclusive occupation of Li2 position, out of two crystallographic positions Li1 and Li2, by Fe2+ was discussed in relation to the differences that exist in the crystal environment of these positions and further investigated by DFT calculations. It was confirmed that Fe-Li2 substitution is energetically favorable compared to both Fe-Li1 substitution and the pristine crystal. In addition, changes of lattice geometry upon antisite defect formation were analyzed, and the obtained result is discussed in light of various factors (electronic, geometrical and enthropic) that contribute to the overall stability of the system. © 2018 Elsevier Masson SAS",
journal = "Solid State Sciences",
title = "On the presence of antisite defect in monoclinic Li2FeSiO4 – A combined X-Ray diffraction and DFT study",
volume = "87",
pages = "81-86",
doi = "10.1016/j.solidstatesciences.2018.11.008"
}

Milović, M., Vasić Anićijević, D. D., Jugović, D., Anićijević, V. J., Veselinović, L. M., Mitrić, M.,& Uskoković, D.. (2019). On the presence of antisite defect in monoclinic Li2FeSiO4 – A combined X-Ray diffraction and DFT study. in Solid State Sciences, 87, 81-86.
https://doi.org/10.1016/j.solidstatesciences.2018.11.008

Milović M, Vasić Anićijević DD, Jugović D, Anićijević VJ, Veselinović LM, Mitrić M, Uskoković D. On the presence of antisite defect in monoclinic Li2FeSiO4 – A combined X-Ray diffraction and DFT study. in Solid State Sciences. 2019;87:81-86.
doi:10.1016/j.solidstatesciences.2018.11.008 .

Milović, Miloš, Vasić Anićijević, Dragana D., Jugović, Dragana, Anićijević, Vladan J., Veselinović, Ljiljana M., Mitrić, Miodrag, Uskoković, Dragan, "On the presence of antisite defect in monoclinic Li2FeSiO4 – A combined X-Ray diffraction and DFT study" in Solid State Sciences, 87 (2019):81-86,
https://doi.org/10.1016/j.solidstatesciences.2018.11.008 . .

TY  - JOUR
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7580
AB  - The present study describes sintering behaviour of hydroxyapatite (HAp) upon addition of lithium iron phosphate (LFP) (1-10 wt.%) system in inert (Ar) atmosphere. The interaction between materials and melting of LFP influenced early and intermediate stages of HAp sintering, shifting the densification curves towards low-temperature side. Analysis of densification process indicated significant differences upon LFP addition. The reaction mechanism that assumes the initial interaction between phosphates from LFP and calcium from HAp was proposed, generating calcium vacancies and contributing to HAp densification. Cross-sections of sintered samples showed changes in microstructural properties, with uniform atomic distribution and presence of Li2Fe3O4 spherical inclusions (200 nm) located at grain boundaries of calcium phosphate matrix. The Rietveld refinement analysis indicated changes in structural and microstructural parameters like crystallite size, anisotropy and microstructural strain of HAp upon LFP addition. Mechanical characterisation indicated improvements in fracture behaviour upon LFP addition.
T2  - Journal of the European Ceramic Society
T1  - Inert atmosphere processing of hydroxyapatite in the presence of lithium iron phosphate
VL  - 38
SP  - 2120
EP  - 2133
DO  - 10.1016/j.jeurceramsoc.2017.12.023
ER  - 

@article{
year = "2018",
abstract = "The present study describes sintering behaviour of hydroxyapatite (HAp) upon addition of lithium iron phosphate (LFP) (1-10 wt.%) system in inert (Ar) atmosphere. The interaction between materials and melting of LFP influenced early and intermediate stages of HAp sintering, shifting the densification curves towards low-temperature side. Analysis of densification process indicated significant differences upon LFP addition. The reaction mechanism that assumes the initial interaction between phosphates from LFP and calcium from HAp was proposed, generating calcium vacancies and contributing to HAp densification. Cross-sections of sintered samples showed changes in microstructural properties, with uniform atomic distribution and presence of Li2Fe3O4 spherical inclusions (200 nm) located at grain boundaries of calcium phosphate matrix. The Rietveld refinement analysis indicated changes in structural and microstructural parameters like crystallite size, anisotropy and microstructural strain of HAp upon LFP addition. Mechanical characterisation indicated improvements in fracture behaviour upon LFP addition.",
journal = "Journal of the European Ceramic Society",
title = "Inert atmosphere processing of hydroxyapatite in the presence of lithium iron phosphate",
volume = "38",
pages = "2120-2133",
doi = "10.1016/j.jeurceramsoc.2017.12.023"
}

(2018). Inert atmosphere processing of hydroxyapatite in the presence of lithium iron phosphate. in Journal of the European Ceramic Society, 38, 2120-2133.
https://doi.org/10.1016/j.jeurceramsoc.2017.12.023

Inert atmosphere processing of hydroxyapatite in the presence of lithium iron phosphate. in Journal of the European Ceramic Society. 2018;38:2120-2133.
doi:10.1016/j.jeurceramsoc.2017.12.023 .

"Inert atmosphere processing of hydroxyapatite in the presence of lithium iron phosphate" in Journal of the European Ceramic Society, 38 (2018):2120-2133,
https://doi.org/10.1016/j.jeurceramsoc.2017.12.023 . .

TY  - JOUR
AU  - Marković, Smilja
AU  - Rajić, Vladimir
AU  - Stanković, Ana
AU  - Veselinović, Ljiljana M.
AU  - Belošević-Čavor, Jelena
AU  - Batalović, Katarina
AU  - Abazović, Nadica
AU  - Škapin, Srečo Davor
AU  - Uskoković, Dragan
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/963
AB  - ZnO spheroidal nanoparticles, synthesized by microwave processing, were used for preparation of composites with polyethylene oxide (PEO). The phase purity and crystal structure of the composites were investigated by X-ray diffraction (XRD) and Raman spectroscopy. The composites particles morphology and size distributions were studied by FE-SEM and laser diffraction particle size analyzer, respectively. The optical properties were studied using UV Vis diffuse reflectance and photoluminescence spectroscopy. It is found that in the wavelength range 550-800 nm, ZnO and ZnO/PEO composites absorb about 50% of the incident light intensity. Also red-shift of band gap energy (0.12-0.15 eV) compared to bulk ZnO was determined. The effect of PEO molecular weights, 200,000, 600,000 and 900,000 g/mol, on photocatalytic activity of ZnO/PEO composites were examined via de-colorization of methylene blue (MB) under direct sunlight irradiation. A large efficiency of MB de-colorization was found after 6 h of irradiation. The enhanced photocatalytic activity of ZnO/PEO composites is attributed to the: (1) lattice defects introduced in ZnO crystal structure by rapid microwave processing, and (2) presence of PEO as a source of oxygen interstitials. In order to confirm and further clarify the experimental results ab initio calculations based on density functional theory (DFT) were performed. (C) 2016 Elsevier Ltd. All rights reserved.
PB  - Elsevier
T2  - Solar Energy
T1  - Effect of PEO molecular weight on sunlight induced photocatalytic activity of ZnO/PEO composites
VL  - 127
SP  - 124
EP  - 135
DO  - 10.1016/j.solener.2016.01.026
ER  - 

@article{
author = "Marković, Smilja and Rajić, Vladimir and Stanković, Ana and Veselinović, Ljiljana M. and Belošević-Čavor, Jelena and Batalović, Katarina and Abazović, Nadica and Škapin, Srečo Davor and Uskoković, Dragan",
year = "2016",
abstract = "ZnO spheroidal nanoparticles, synthesized by microwave processing, were used for preparation of composites with polyethylene oxide (PEO). The phase purity and crystal structure of the composites were investigated by X-ray diffraction (XRD) and Raman spectroscopy. The composites particles morphology and size distributions were studied by FE-SEM and laser diffraction particle size analyzer, respectively. The optical properties were studied using UV Vis diffuse reflectance and photoluminescence spectroscopy. It is found that in the wavelength range 550-800 nm, ZnO and ZnO/PEO composites absorb about 50% of the incident light intensity. Also red-shift of band gap energy (0.12-0.15 eV) compared to bulk ZnO was determined. The effect of PEO molecular weights, 200,000, 600,000 and 900,000 g/mol, on photocatalytic activity of ZnO/PEO composites were examined via de-colorization of methylene blue (MB) under direct sunlight irradiation. A large efficiency of MB de-colorization was found after 6 h of irradiation. The enhanced photocatalytic activity of ZnO/PEO composites is attributed to the: (1) lattice defects introduced in ZnO crystal structure by rapid microwave processing, and (2) presence of PEO as a source of oxygen interstitials. In order to confirm and further clarify the experimental results ab initio calculations based on density functional theory (DFT) were performed. (C) 2016 Elsevier Ltd. All rights reserved.",
publisher = "Elsevier",
journal = "Solar Energy",
title = "Effect of PEO molecular weight on sunlight induced photocatalytic activity of ZnO/PEO composites",
volume = "127",
pages = "124-135",
doi = "10.1016/j.solener.2016.01.026"
}

Marković, S., Rajić, V., Stanković, A., Veselinović, L. M., Belošević-Čavor, J., Batalović, K., Abazović, N., Škapin, S. D.,& Uskoković, D.. (2016). Effect of PEO molecular weight on sunlight induced photocatalytic activity of ZnO/PEO composites. in Solar Energy
Elsevier., 127, 124-135.
https://doi.org/10.1016/j.solener.2016.01.026

Marković S, Rajić V, Stanković A, Veselinović LM, Belošević-Čavor J, Batalović K, Abazović N, Škapin SD, Uskoković D. Effect of PEO molecular weight on sunlight induced photocatalytic activity of ZnO/PEO composites. in Solar Energy. 2016;127:124-135.
doi:10.1016/j.solener.2016.01.026 .

Marković, Smilja, Rajić, Vladimir, Stanković, Ana, Veselinović, Ljiljana M., Belošević-Čavor, Jelena, Batalović, Katarina, Abazović, Nadica, Škapin, Srečo Davor, Uskoković, Dragan, "Effect of PEO molecular weight on sunlight induced photocatalytic activity of ZnO/PEO composites" in Solar Energy, 127 (2016):124-135,
https://doi.org/10.1016/j.solener.2016.01.026 . .

TY  - JOUR
AU  - Stojanović, Zoran S.
AU  - Ignjatović, Nenad L.
AU  - Wu, Victoria
AU  - Žunič, Vojka
AU  - Veselinović, Ljiljana M.
AU  - Škapin, Srečo Davor
AU  - Miljković, Miroslav
AU  - Uskoković, Vuk
AU  - Uskoković, Dragan
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7575
AB  - Recent developments in bone tissue engineering have led to an increased interest in one-dimensional (1D) hydroxyapatite (HA) nano- and micro-structures such as wires, ribbons and tubes. They have been proposed for use as cell substrates, reinforcing phases in composites and carriers for biologically active substances. Here we demonstrate the synthesis of 1D HA structures using an optimized, urea-assisted, high-yield hydrothermal batch process. The one-pot process, yielding HA structures composed of bundles of ribbons and wires, was typified by the simultaneous occurrence of a multitude of intermediate reactions, failing to meet the uniformity criteria over particle morphology and size. To overcome these issues, the preparation procedure was divided to two stages: dicalcium phosphate platelets synthesized in the first step were used as a precursor for the synthesis of 1D HA in the second stage. Despite the elongated particle morphologies, both the precursor and the final product exhibited excellent biocompatibility and caused no reduction of viability when tested against osteoblastic MC3T3-E1 cells in 2D culture up to the concentration of 2.6 mg/cm2. X-ray powder diffraction combined with a range of electron microscopies and laser diffraction analyses was used to elucidate the formation mechanism and the microstructure of the final particles. The two-step synthesis involved a more direct transformation of DCP to 1D HA with the average diameter of 37 nm and the aspect ratio exceeding 100:1. The comparison of crystalline domain sizes along different crystallographic directions showed no signs of significant anisotropy, while indicating that individual nanowires are ordered in bundles in the b crystallographic direction of the P63/m space group of HA. Intermediate processes, e.g., dehydration of dicalcium phosphate, are critical for the formation of 1D HA alongside other key aspects of this phase transformation, it must be investigated in more detail in the continuous design of smart HA micro- and nano-structures with advanced therapeutic potentials.
T2  - Materials Science and Engineering: C
T1  - Hydrothermally processed 1D hydroxyapatite: Mechanism of formation and biocompatibility studies
VL  - 68
SP  - 746
EP  - 757
DO  - 10.1016/j.msec.2016.06.047
ER  - 

@article{
author = "Stojanović, Zoran S. and Ignjatović, Nenad L. and Wu, Victoria and Žunič, Vojka and Veselinović, Ljiljana M. and Škapin, Srečo Davor and Miljković, Miroslav and Uskoković, Vuk and Uskoković, Dragan",
year = "2016",
abstract = "Recent developments in bone tissue engineering have led to an increased interest in one-dimensional (1D) hydroxyapatite (HA) nano- and micro-structures such as wires, ribbons and tubes. They have been proposed for use as cell substrates, reinforcing phases in composites and carriers for biologically active substances. Here we demonstrate the synthesis of 1D HA structures using an optimized, urea-assisted, high-yield hydrothermal batch process. The one-pot process, yielding HA structures composed of bundles of ribbons and wires, was typified by the simultaneous occurrence of a multitude of intermediate reactions, failing to meet the uniformity criteria over particle morphology and size. To overcome these issues, the preparation procedure was divided to two stages: dicalcium phosphate platelets synthesized in the first step were used as a precursor for the synthesis of 1D HA in the second stage. Despite the elongated particle morphologies, both the precursor and the final product exhibited excellent biocompatibility and caused no reduction of viability when tested against osteoblastic MC3T3-E1 cells in 2D culture up to the concentration of 2.6 mg/cm2. X-ray powder diffraction combined with a range of electron microscopies and laser diffraction analyses was used to elucidate the formation mechanism and the microstructure of the final particles. The two-step synthesis involved a more direct transformation of DCP to 1D HA with the average diameter of 37 nm and the aspect ratio exceeding 100:1. The comparison of crystalline domain sizes along different crystallographic directions showed no signs of significant anisotropy, while indicating that individual nanowires are ordered in bundles in the b crystallographic direction of the P63/m space group of HA. Intermediate processes, e.g., dehydration of dicalcium phosphate, are critical for the formation of 1D HA alongside other key aspects of this phase transformation, it must be investigated in more detail in the continuous design of smart HA micro- and nano-structures with advanced therapeutic potentials.",
journal = "Materials Science and Engineering: C",
title = "Hydrothermally processed 1D hydroxyapatite: Mechanism of formation and biocompatibility studies",
volume = "68",
pages = "746-757",
doi = "10.1016/j.msec.2016.06.047"
}

Stojanović, Z. S., Ignjatović, N. L., Wu, V., Žunič, V., Veselinović, L. M., Škapin, S. D., Miljković, M., Uskoković, V.,& Uskoković, D.. (2016). Hydrothermally processed 1D hydroxyapatite: Mechanism of formation and biocompatibility studies. in Materials Science and Engineering: C, 68, 746-757.
https://doi.org/10.1016/j.msec.2016.06.047

Stojanović ZS, Ignjatović NL, Wu V, Žunič V, Veselinović LM, Škapin SD, Miljković M, Uskoković V, Uskoković D. Hydrothermally processed 1D hydroxyapatite: Mechanism of formation and biocompatibility studies. in Materials Science and Engineering: C. 2016;68:746-757.
doi:10.1016/j.msec.2016.06.047 .

Stojanović, Zoran S., Ignjatović, Nenad L., Wu, Victoria, Žunič, Vojka, Veselinović, Ljiljana M., Škapin, Srečo Davor, Miljković, Miroslav, Uskoković, Vuk, Uskoković, Dragan, "Hydrothermally processed 1D hydroxyapatite: Mechanism of formation and biocompatibility studies" in Materials Science and Engineering: C, 68 (2016):746-757,
https://doi.org/10.1016/j.msec.2016.06.047 . .

TY  - JOUR
AU  - Stojanović, Zoran S.
AU  - Ignjatović, Nenad L.
AU  - Wu, Victoria
AU  - Žunič, Vojka
AU  - Veselinović, Ljiljana M.
AU  - Škapin, Srečo Davor
AU  - Miljković, Miroslav
AU  - Uskoković, Vuk
AU  - Uskoković, Dragan
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7576
AB  - Recent developments in bone tissue engineering have led to an increased interest in one-dimensional (1D) hydroxyapatite (HA) nano- and micro-structures such as wires, ribbons and tubes. They have been proposed for use as cell substrates, reinforcing phases in composites and carriers for biologically active substances. Here we demonstrate the synthesis of 1D HA structures using an optimized, urea-assisted, high-yield hydrothermal batch process. The one-pot process, yielding HA structures composed of bundles of ribbons and wires, was typified by the simultaneous occurrence of a multitude of intermediate reactions, failing to meet the uniformity criteria over particle morphology and size. To overcome these issues, the preparation procedure was divided to two stages: dicalcium phosphate platelets synthesized in the first step were used as a precursor for the synthesis of 1D HA in the second stage. Despite the elongated particle morphologies, both the precursor and the final product exhibited excellent biocompatibility and caused no reduction of viability when tested against osteoblastic MC3T3-E1 cells in 2D culture up to the concentration of 2.6 mg/cm2. X-ray powder diffraction combined with a range of electron microscopies and laser diffraction analyses was used to elucidate the formation mechanism and the microstructure of the final particles. The two-step synthesis involved a more direct transformation of DCP to 1D HA with the average diameter of 37 nm and the aspect ratio exceeding 100:1. The comparison of crystalline domain sizes along different crystallographic directions showed no signs of significant anisotropy, while indicating that individual nanowires are ordered in bundles in the b crystallographic direction of the P63/m space group of HA. Intermediate processes, e.g., dehydration of dicalcium phosphate, are critical for the formation of 1D HA alongside other key aspects of this phase transformation, it must be investigated in more detail in the continuous design of smart HA micro- and nano-structures with advanced therapeutic potentials.
PB  - Elsevier
T2  - Materials Science and Engineering: C
T1  - Hydrothermally processed 1D hydroxyapatite: Mechanism of formation and biocompatibility studies
VL  - 68
SP  - 746
EP  - 757
DO  - 10.1016/j.msec.2016.06.047
ER  - 

@article{
author = "Stojanović, Zoran S. and Ignjatović, Nenad L. and Wu, Victoria and Žunič, Vojka and Veselinović, Ljiljana M. and Škapin, Srečo Davor and Miljković, Miroslav and Uskoković, Vuk and Uskoković, Dragan",
year = "2016",
abstract = "Recent developments in bone tissue engineering have led to an increased interest in one-dimensional (1D) hydroxyapatite (HA) nano- and micro-structures such as wires, ribbons and tubes. They have been proposed for use as cell substrates, reinforcing phases in composites and carriers for biologically active substances. Here we demonstrate the synthesis of 1D HA structures using an optimized, urea-assisted, high-yield hydrothermal batch process. The one-pot process, yielding HA structures composed of bundles of ribbons and wires, was typified by the simultaneous occurrence of a multitude of intermediate reactions, failing to meet the uniformity criteria over particle morphology and size. To overcome these issues, the preparation procedure was divided to two stages: dicalcium phosphate platelets synthesized in the first step were used as a precursor for the synthesis of 1D HA in the second stage. Despite the elongated particle morphologies, both the precursor and the final product exhibited excellent biocompatibility and caused no reduction of viability when tested against osteoblastic MC3T3-E1 cells in 2D culture up to the concentration of 2.6 mg/cm2. X-ray powder diffraction combined with a range of electron microscopies and laser diffraction analyses was used to elucidate the formation mechanism and the microstructure of the final particles. The two-step synthesis involved a more direct transformation of DCP to 1D HA with the average diameter of 37 nm and the aspect ratio exceeding 100:1. The comparison of crystalline domain sizes along different crystallographic directions showed no signs of significant anisotropy, while indicating that individual nanowires are ordered in bundles in the b crystallographic direction of the P63/m space group of HA. Intermediate processes, e.g., dehydration of dicalcium phosphate, are critical for the formation of 1D HA alongside other key aspects of this phase transformation, it must be investigated in more detail in the continuous design of smart HA micro- and nano-structures with advanced therapeutic potentials.",
publisher = "Elsevier",
journal = "Materials Science and Engineering: C",
title = "Hydrothermally processed 1D hydroxyapatite: Mechanism of formation and biocompatibility studies",
volume = "68",
pages = "746-757",
doi = "10.1016/j.msec.2016.06.047"
}

Stojanović, Z. S., Ignjatović, N. L., Wu, V., Žunič, V., Veselinović, L. M., Škapin, S. D., Miljković, M., Uskoković, V.,& Uskoković, D.. (2016). Hydrothermally processed 1D hydroxyapatite: Mechanism of formation and biocompatibility studies. in Materials Science and Engineering: C
Elsevier., 68, 746-757.
https://doi.org/10.1016/j.msec.2016.06.047

Stojanović ZS, Ignjatović NL, Wu V, Žunič V, Veselinović LM, Škapin SD, Miljković M, Uskoković V, Uskoković D. Hydrothermally processed 1D hydroxyapatite: Mechanism of formation and biocompatibility studies. in Materials Science and Engineering: C. 2016;68:746-757.
doi:10.1016/j.msec.2016.06.047 .

Stojanović, Zoran S., Ignjatović, Nenad L., Wu, Victoria, Žunič, Vojka, Veselinović, Ljiljana M., Škapin, Srečo Davor, Miljković, Miroslav, Uskoković, Vuk, Uskoković, Dragan, "Hydrothermally processed 1D hydroxyapatite: Mechanism of formation and biocompatibility studies" in Materials Science and Engineering: C, 68 (2016):746-757,
https://doi.org/10.1016/j.msec.2016.06.047 . .

TY  - JOUR
AU  - Veselinović, Ljiljana M.
AU  - Mitrić, Miodrag
AU  - Avdeev, Maxim
AU  - Marković, Smilja
AU  - Uskoković, Dragan
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1312
AB  - Neutron powder diffraction (NPD) was employed to further investigate the BaTi1-xSnxO3 (BTS) system previously studied by X-ray diffraction. The room-temperature phase compositions and crystal structures of BTS samples with x = 0, 0.025, 0.05, 0.07, 0.10, 0.12, 0.15 and 0.20 were refined by the Rietveld method using NPD data. It is well known that barium titanate powder (x = 0) crystallizes in the tetragonal P4mm space group. The crystal structures of the samples with 0.025 LT = x LT = 0.07 were refined as mixtures of P4mm and Amm2 phases; those with x = 0.1 and 0.12 show the coexistence of rhombohedral R3m and cubic phases, while the samples with x = 0.15 and 0.20 crystallize in a single cubic Pm (3) over barm phase. Temperature-dependent NPD was used to characterize the BaTi0.95Sn0.05O3 sample at 273, 333 and 373 K, and it was found to form single-phase Amm2, P4mm and Pm (3) over barm structures at these respective temperatures. The NPD results are in agreement with data obtained by differential scanning calorimetry and dielectric permittivity measurements, which show a para-electric-ferroelectric transition (associated with structural transition) from Pm (3) over barm to P4mm at about 353 K followed by a P4mm to Amm2 phase transition at about 303 K.
T2  - Journal of Applied Crystallography
T1  - New insights into BaTi1-xSnxO3 (0 LT = x LT = 0.20) phase diagram from neutron diffraction data
VL  - 49
SP  - 1726
EP  - 1733
DO  - 10.1107/S1600576716013157
ER  - 

@article{
author = "Veselinović, Ljiljana M. and Mitrić, Miodrag and Avdeev, Maxim and Marković, Smilja and Uskoković, Dragan",
year = "2016",
abstract = "Neutron powder diffraction (NPD) was employed to further investigate the BaTi1-xSnxO3 (BTS) system previously studied by X-ray diffraction. The room-temperature phase compositions and crystal structures of BTS samples with x = 0, 0.025, 0.05, 0.07, 0.10, 0.12, 0.15 and 0.20 were refined by the Rietveld method using NPD data. It is well known that barium titanate powder (x = 0) crystallizes in the tetragonal P4mm space group. The crystal structures of the samples with 0.025 LT = x LT = 0.07 were refined as mixtures of P4mm and Amm2 phases; those with x = 0.1 and 0.12 show the coexistence of rhombohedral R3m and cubic phases, while the samples with x = 0.15 and 0.20 crystallize in a single cubic Pm (3) over barm phase. Temperature-dependent NPD was used to characterize the BaTi0.95Sn0.05O3 sample at 273, 333 and 373 K, and it was found to form single-phase Amm2, P4mm and Pm (3) over barm structures at these respective temperatures. The NPD results are in agreement with data obtained by differential scanning calorimetry and dielectric permittivity measurements, which show a para-electric-ferroelectric transition (associated with structural transition) from Pm (3) over barm to P4mm at about 353 K followed by a P4mm to Amm2 phase transition at about 303 K.",
journal = "Journal of Applied Crystallography",
title = "New insights into BaTi1-xSnxO3 (0 LT = x LT = 0.20) phase diagram from neutron diffraction data",
volume = "49",
pages = "1726-1733",
doi = "10.1107/S1600576716013157"
}

Veselinović, L. M., Mitrić, M., Avdeev, M., Marković, S.,& Uskoković, D.. (2016). New insights into BaTi1-xSnxO3 (0 LT = x LT = 0.20) phase diagram from neutron diffraction data. in Journal of Applied Crystallography, 49, 1726-1733.
https://doi.org/10.1107/S1600576716013157

Veselinović LM, Mitrić M, Avdeev M, Marković S, Uskoković D. New insights into BaTi1-xSnxO3 (0 LT = x LT = 0.20) phase diagram from neutron diffraction data. in Journal of Applied Crystallography. 2016;49:1726-1733.
doi:10.1107/S1600576716013157 .

Veselinović, Ljiljana M., Mitrić, Miodrag, Avdeev, Maxim, Marković, Smilja, Uskoković, Dragan, "New insights into BaTi1-xSnxO3 (0 LT = x LT = 0.20) phase diagram from neutron diffraction data" in Journal of Applied Crystallography, 49 (2016):1726-1733,
https://doi.org/10.1107/S1600576716013157 . .

TY  - CONF
AU  - Stojanović, Zoran S.
AU  - Veselinović, Ljiljana M.
AU  - Ignjatović, Nenad L.
AU  - Miljković, Miroslav
AU  - Uskoković, Dragan
PY  - 2014
UR  - http://dais.sanu.ac.rs/123456789/576
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7482
AB  - Poster presented at the 16th Annual Conference of the Materials Research Society of Serbia - YUCOMAT 2014, Herceg Novi, Montenegro, September 1–5, 2014
T1  - The Hydrothermal Synthesis of 1D Biomedical Hydroxyapatite Nanostructures
UR  - https://hdl.handle.net/21.15107/rcub_vinar_7482
ER  - 

@conference{
author = "Stojanović, Zoran S. and Veselinović, Ljiljana M. and Ignjatović, Nenad L. and Miljković, Miroslav and Uskoković, Dragan",
year = "2014",
abstract = "Poster presented at the 16th Annual Conference of the Materials Research Society of Serbia - YUCOMAT 2014, Herceg Novi, Montenegro, September 1–5, 2014",
title = "The Hydrothermal Synthesis of 1D Biomedical Hydroxyapatite Nanostructures",
url = "https://hdl.handle.net/21.15107/rcub_vinar_7482"
}

Stojanović, Z. S., Veselinović, L. M., Ignjatović, N. L., Miljković, M.,& Uskoković, D.. (2014). The Hydrothermal Synthesis of 1D Biomedical Hydroxyapatite Nanostructures. .
https://hdl.handle.net/21.15107/rcub_vinar_7482

Stojanović ZS, Veselinović LM, Ignjatović NL, Miljković M, Uskoković D. The Hydrothermal Synthesis of 1D Biomedical Hydroxyapatite Nanostructures. 2014;.
https://hdl.handle.net/21.15107/rcub_vinar_7482 .

Stojanović, Zoran S., Veselinović, Ljiljana M., Ignjatović, Nenad L., Miljković, Miroslav, Uskoković, Dragan, "The Hydrothermal Synthesis of 1D Biomedical Hydroxyapatite Nanostructures" (2014),
https://hdl.handle.net/21.15107/rcub_vinar_7482 .

TY  - CONF
AU  - Stojanović, Zoran S.
AU  - Veselinović, Ljiljana M.
AU  - Ignjatović, Nenad L.
AU  - Miljković, Miroslav
AU  - Uskoković, Dragan
PY  - 2014
UR  - http://dais.sanu.ac.rs/123456789/581
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7484
AB  - 1D hydroxyapatite nanostructures such as nanotubes, ultra long nanowires and other morphological varieties have been promising material for bone reconstruction and therapy. Advantages like high specific surface, packing properties and mechanical properties make those nanostructures excellent candidates for scaffolds. This work is focused on soft hydrothermal routes for preparing different 1D nanostructures. Using hydroxyapatite formation mechanisms in hydrothermal and solvothermal systems, various chemical parameters, i.e. precursor chemical composition, are investigated for obtaining these 1D materials on gram scale. The synthesized materials are characterized by X – ray diffraction, scanning electron microscopy and laser diffraction methods.
PB  - Belgrade : Materials Research Society of Serbia
C3  - The Sixteenth Annual Conference YUCOMAT 2014: Programme and the Book of Abstracts
T1  - The hydrothermal synthesis of 1d biomedical hydroxyapatite nanostructures
SP  - 63
EP  - 63
UR  - https://hdl.handle.net/21.15107/rcub_vinar_7484
ER  - 

@conference{
author = "Stojanović, Zoran S. and Veselinović, Ljiljana M. and Ignjatović, Nenad L. and Miljković, Miroslav and Uskoković, Dragan",
year = "2014",
abstract = "1D hydroxyapatite nanostructures such as nanotubes, ultra long nanowires and other morphological varieties have been promising material for bone reconstruction and therapy. Advantages like high specific surface, packing properties and mechanical properties make those nanostructures excellent candidates for scaffolds. This work is focused on soft hydrothermal routes for preparing different 1D nanostructures. Using hydroxyapatite formation mechanisms in hydrothermal and solvothermal systems, various chemical parameters, i.e. precursor chemical composition, are investigated for obtaining these 1D materials on gram scale. The synthesized materials are characterized by X – ray diffraction, scanning electron microscopy and laser diffraction methods.",
publisher = "Belgrade : Materials Research Society of Serbia",
journal = "The Sixteenth Annual Conference YUCOMAT 2014: Programme and the Book of Abstracts",
title = "The hydrothermal synthesis of 1d biomedical hydroxyapatite nanostructures",
pages = "63-63",
url = "https://hdl.handle.net/21.15107/rcub_vinar_7484"
}

Stojanović, Z. S., Veselinović, L. M., Ignjatović, N. L., Miljković, M.,& Uskoković, D.. (2014). The hydrothermal synthesis of 1d biomedical hydroxyapatite nanostructures. in The Sixteenth Annual Conference YUCOMAT 2014: Programme and the Book of Abstracts
Belgrade : Materials Research Society of Serbia., 63-63.
https://hdl.handle.net/21.15107/rcub_vinar_7484

Stojanović ZS, Veselinović LM, Ignjatović NL, Miljković M, Uskoković D. The hydrothermal synthesis of 1d biomedical hydroxyapatite nanostructures. in The Sixteenth Annual Conference YUCOMAT 2014: Programme and the Book of Abstracts. 2014;:63-63.
https://hdl.handle.net/21.15107/rcub_vinar_7484 .

Stojanović, Zoran S., Veselinović, Ljiljana M., Ignjatović, Nenad L., Miljković, Miroslav, Uskoković, Dragan, "The hydrothermal synthesis of 1d biomedical hydroxyapatite nanostructures" in The Sixteenth Annual Conference YUCOMAT 2014: Programme and the Book of Abstracts (2014):63-63,
https://hdl.handle.net/21.15107/rcub_vinar_7484 .

TY  - JOUR
AU  - Veselinović, Ljiljana M.
AU  - Mitrić, Miodrag
AU  - Mančić, Lidija
AU  - Vukomanovic, Marija
AU  - Hadžić, Branka B.
AU  - Marković, Smilja
AU  - Uskoković, Dragan
PY  - 2014
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6022
AB  - The effect of Sn for Ti substitution on the crystal structure of a perovskite, barium titanate stannate (BTS), BaTi1-xSnxO3 for x = 0, 0.025, 0.05, 0.07, 0.10, 0.12, 0.15 and 0.20, was investigated. The powders were prepared by the conventional solid-state reaction technique. The structural investigations of the BTS powders were done at room temperature by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), selected-area electron diffraction (SAED) and Raman spectroscopy analyses. Rietveld refinement of XRD data indicates that gradual replacement of titanium by tin in BaTiO3 provokes a phase transition from tetragonal for 0 LT = x LT = 0.07 to cubic for x = 0.12, 0.15 and 0.20. The coexistence of tetragonal (P4mm) and cubic (Pm (3) over barm) crystal phases was established in powder with nominal composition BaTi0.9Sn0.1O3. The crystal phases determined by Rietveld refinement were confirmed by HRTEM and SAED analyses. The crystal structures of the BTS powders at short-range scale were studied by Raman spectroscopy, which shows tetragonal (P4mm) and a small fraction of orthorhombic (Pmm2) crystal phases for all the examined BTS powders, implying a lower local ordering when compared to the average symmetry.
T2  - Journal of Applied Crystallography
T1  - The effect of Sn for Ti substitution on the average and local crystal structure of BaTi1-xSnxO3 (0 LT = x LT = 0.20)
VL  - 47
SP  - 999
EP  - 1007
DO  - 10.1107/S1600576714007584
ER  - 

@article{
author = "Veselinović, Ljiljana M. and Mitrić, Miodrag and Mančić, Lidija and Vukomanovic, Marija and Hadžić, Branka B. and Marković, Smilja and Uskoković, Dragan",
year = "2014",
abstract = "The effect of Sn for Ti substitution on the crystal structure of a perovskite, barium titanate stannate (BTS), BaTi1-xSnxO3 for x = 0, 0.025, 0.05, 0.07, 0.10, 0.12, 0.15 and 0.20, was investigated. The powders were prepared by the conventional solid-state reaction technique. The structural investigations of the BTS powders were done at room temperature by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), selected-area electron diffraction (SAED) and Raman spectroscopy analyses. Rietveld refinement of XRD data indicates that gradual replacement of titanium by tin in BaTiO3 provokes a phase transition from tetragonal for 0 LT = x LT = 0.07 to cubic for x = 0.12, 0.15 and 0.20. The coexistence of tetragonal (P4mm) and cubic (Pm (3) over barm) crystal phases was established in powder with nominal composition BaTi0.9Sn0.1O3. The crystal phases determined by Rietveld refinement were confirmed by HRTEM and SAED analyses. The crystal structures of the BTS powders at short-range scale were studied by Raman spectroscopy, which shows tetragonal (P4mm) and a small fraction of orthorhombic (Pmm2) crystal phases for all the examined BTS powders, implying a lower local ordering when compared to the average symmetry.",
journal = "Journal of Applied Crystallography",
title = "The effect of Sn for Ti substitution on the average and local crystal structure of BaTi1-xSnxO3 (0 LT = x LT = 0.20)",
volume = "47",
pages = "999-1007",
doi = "10.1107/S1600576714007584"
}

Veselinović, L. M., Mitrić, M., Mančić, L., Vukomanovic, M., Hadžić, B. B., Marković, S.,& Uskoković, D.. (2014). The effect of Sn for Ti substitution on the average and local crystal structure of BaTi1-xSnxO3 (0 LT = x LT = 0.20). in Journal of Applied Crystallography, 47, 999-1007.
https://doi.org/10.1107/S1600576714007584

Veselinović LM, Mitrić M, Mančić L, Vukomanovic M, Hadžić BB, Marković S, Uskoković D. The effect of Sn for Ti substitution on the average and local crystal structure of BaTi1-xSnxO3 (0 LT = x LT = 0.20). in Journal of Applied Crystallography. 2014;47:999-1007.
doi:10.1107/S1600576714007584 .

Veselinović, Ljiljana M., Mitrić, Miodrag, Mančić, Lidija, Vukomanovic, Marija, Hadžić, Branka B., Marković, Smilja, Uskoković, Dragan, "The effect of Sn for Ti substitution on the average and local crystal structure of BaTi1-xSnxO3 (0 LT = x LT = 0.20)" in Journal of Applied Crystallography, 47 (2014):999-1007,
https://doi.org/10.1107/S1600576714007584 . .

TY  - CONF
AU  - Veselinović, Ljiljana M.
AU  - Marković, Smilja
AU  - Lukić, Miodrag
AU  - Mančić, Lidija
AU  - Škapin, Srečo Davor
AU  - Mitrić, Miodrag
AU  - Uskoković, Dragan
PY  - 2014
UR  - http://dais.sanu.ac.rs/123456789/562
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7478
AB  - Perovskite-related materials with the general formula AC3B4O12 have great technological significance due to their specific physical properties. The crystal structure of AC3B4O12 compounds is cubic with Im3 symmetry. Different cations can occupy A and B sites, while the C site is commonly occupied by Cu2+ or Mn3+ ions. It has been found that the nature of B cation changes the physical properties of the material. In our previous studies we dealt with CaCu3Ti4O12 (CCTO) and CaCu3Ru4O12 (CCRO) compounds. CCTO has the gigantic permittivity of 104105 in the kilohertz region and good stability over the temperature range from -170 to 330 °C. While Ti-compound is semiconductor, the Ru one is conductive oxide and could be used as interfaces between CCTO and metallic electrodes. Thus, CCTO and CCRO have potential application for preparation of layer capacitors with CCRO as the electrode and CCTO as the dielectric material. Since the oxygen vacancies and/or intrinsic defects in perovskites have a crucial role in the physical properties it is important to determine crystal structure of ceramic materials. In this work, a detailed structural investigation of CCTO and CCRO perovskites was performed. The powders were prepared by precipitation and successive calcination at 1100 °C with 3 h dwell time to obtained single phased materials. The phase composition and crystal structure of synthesized powders were studied by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), selected-area electron diffraction (SAED) and Raman spectroscopy analyses. Rietveld refinement of XRD data was used to calculate the powders stoichiometry. Furthermore, since the XRD method is not adequate for determination of oxygen atoms due to their small scattering factors, to confirm the (oxygen-) stoichiometry of the ceramic powders, thermogravimetric (TG) measurements were employed. Two sets of experiments were performed; powders were heated in a flowing: (1) air atmosphere, and (2) reducing atmosphere (mixture of 5% H2 with Ar; 20 ml/min), to 1100 °C with a heating rate 10 °C/min with 3 h dwell time. TG measurements were performed on system coupled to a quadrupole mass spectrometer used for determination of volatile compounds. The weight losses measured by TG, in two different atmospheres, were compared; minor deviations in stoichiometries of CaCu3B4O12 compounds determined by Rietveld refinement were corrected.
PB  - Belgrade : Materials Research Society of Serbia
C3  - The Sixteenth Annual Conference YUCOMAT 2014: Programme and the Book of Abstracts
T1  - Structural investigation of CaCu3B4O12 (B = Ti, Ru)
SP  - 67
EP  - 67
UR  - https://hdl.handle.net/21.15107/rcub_vinar_7478
ER  - 

@conference{
author = "Veselinović, Ljiljana M. and Marković, Smilja and Lukić, Miodrag and Mančić, Lidija and Škapin, Srečo Davor and Mitrić, Miodrag and Uskoković, Dragan",
year = "2014",
abstract = "Perovskite-related materials with the general formula AC3B4O12 have great technological significance due to their specific physical properties. The crystal structure of AC3B4O12 compounds is cubic with Im3 symmetry. Different cations can occupy A and B sites, while the C site is commonly occupied by Cu2+ or Mn3+ ions. It has been found that the nature of B cation changes the physical properties of the material. In our previous studies we dealt with CaCu3Ti4O12 (CCTO) and CaCu3Ru4O12 (CCRO) compounds. CCTO has the gigantic permittivity of 104105 in the kilohertz region and good stability over the temperature range from -170 to 330 °C. While Ti-compound is semiconductor, the Ru one is conductive oxide and could be used as interfaces between CCTO and metallic electrodes. Thus, CCTO and CCRO have potential application for preparation of layer capacitors with CCRO as the electrode and CCTO as the dielectric material. Since the oxygen vacancies and/or intrinsic defects in perovskites have a crucial role in the physical properties it is important to determine crystal structure of ceramic materials. In this work, a detailed structural investigation of CCTO and CCRO perovskites was performed. The powders were prepared by precipitation and successive calcination at 1100 °C with 3 h dwell time to obtained single phased materials. The phase composition and crystal structure of synthesized powders were studied by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), selected-area electron diffraction (SAED) and Raman spectroscopy analyses. Rietveld refinement of XRD data was used to calculate the powders stoichiometry. Furthermore, since the XRD method is not adequate for determination of oxygen atoms due to their small scattering factors, to confirm the (oxygen-) stoichiometry of the ceramic powders, thermogravimetric (TG) measurements were employed. Two sets of experiments were performed; powders were heated in a flowing: (1) air atmosphere, and (2) reducing atmosphere (mixture of 5% H2 with Ar; 20 ml/min), to 1100 °C with a heating rate 10 °C/min with 3 h dwell time. TG measurements were performed on system coupled to a quadrupole mass spectrometer used for determination of volatile compounds. The weight losses measured by TG, in two different atmospheres, were compared; minor deviations in stoichiometries of CaCu3B4O12 compounds determined by Rietveld refinement were corrected.",
publisher = "Belgrade : Materials Research Society of Serbia",
journal = "The Sixteenth Annual Conference YUCOMAT 2014: Programme and the Book of Abstracts",
title = "Structural investigation of CaCu3B4O12 (B = Ti, Ru)",
pages = "67-67",
url = "https://hdl.handle.net/21.15107/rcub_vinar_7478"
}

Veselinović, L. M., Marković, S., Lukić, M., Mančić, L., Škapin, S. D., Mitrić, M.,& Uskoković, D.. (2014). Structural investigation of CaCu3B4O12 (B = Ti, Ru). in The Sixteenth Annual Conference YUCOMAT 2014: Programme and the Book of Abstracts
Belgrade : Materials Research Society of Serbia., 67-67.
https://hdl.handle.net/21.15107/rcub_vinar_7478

Veselinović LM, Marković S, Lukić M, Mančić L, Škapin SD, Mitrić M, Uskoković D. Structural investigation of CaCu3B4O12 (B = Ti, Ru). in The Sixteenth Annual Conference YUCOMAT 2014: Programme and the Book of Abstracts. 2014;:67-67.
https://hdl.handle.net/21.15107/rcub_vinar_7478 .

Veselinović, Ljiljana M., Marković, Smilja, Lukić, Miodrag, Mančić, Lidija, Škapin, Srečo Davor, Mitrić, Miodrag, Uskoković, Dragan, "Structural investigation of CaCu3B4O12 (B = Ti, Ru)" in The Sixteenth Annual Conference YUCOMAT 2014: Programme and the Book of Abstracts (2014):67-67,
https://hdl.handle.net/21.15107/rcub_vinar_7478 .

TY  - CONF
AU  - Stanković, Ana
AU  - Stojanović, Zoran S.
AU  - Veselinović, Ljiljana M.
AU  - Abazović, Nadica
AU  - Škapin, Srečo Davor
AU  - Marković, Smilja
AU  - Uskoković, Dragan
PY  - 2012
UR  - http://dais.sanu.ac.rs/123456789/529
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7471
AB  - In this work we present details of different synthesis procedures for preparation of ZnO powders and a possibility to create various particles morphology and average size; from micrometer rods to nanometer spherical particles. We studied two synthesis methods, low temperature hydrothermal processing (HT) and ultrasound processing (US). The morphology and average particle size of the ZnO particles were modified by adjusting the mole ratio of [Zn2+]/[OH] in the reactants solution. Agglomeration of the particles was prevented using a polyvinyl pyrrolidone (PVP) as a capping agent. The synthesized powders were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (FESEM) and UV-Vis - diffusion reflection spectroscopy (UV-Vis DRS). Based on the results of the scanning electron microscopy we proposed a possible growth mechanism of the ZnO particles depending on the mole ratio of [Zn2+]/[OH]. Also, we considered the influence of particle size and morphology on the optical properties of the prepared powders. The observed results sowed that the size and morphology of ZnO particles greatly affect the absorption of visible light (%) and the shift of the energy gap (eV).
PB  - Belgrade : Serbian Ceramic Society
C3  - Joint Event of the 11th Young Researchers’ Conference: Materials Science and Engineering and the 1st European Early Stage Researches’ Conference on Hydrogen Storage: Program and the Book of Abstracts
T1  - Influence of particle size and morphology of ZnO powders on their optical properties
SP  - 60
EP  - 60
UR  - https://hdl.handle.net/21.15107/rcub_vinar_7471
ER  - 

@conference{
author = "Stanković, Ana and Stojanović, Zoran S. and Veselinović, Ljiljana M. and Abazović, Nadica and Škapin, Srečo Davor and Marković, Smilja and Uskoković, Dragan",
year = "2012",
abstract = "In this work we present details of different synthesis procedures for preparation of ZnO powders and a possibility to create various particles morphology and average size; from micrometer rods to nanometer spherical particles. We studied two synthesis methods, low temperature hydrothermal processing (HT) and ultrasound processing (US). The morphology and average particle size of the ZnO particles were modified by adjusting the mole ratio of [Zn2+]/[OH] in the reactants solution. Agglomeration of the particles was prevented using a polyvinyl pyrrolidone (PVP) as a capping agent. The synthesized powders were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (FESEM) and UV-Vis - diffusion reflection spectroscopy (UV-Vis DRS). Based on the results of the scanning electron microscopy we proposed a possible growth mechanism of the ZnO particles depending on the mole ratio of [Zn2+]/[OH]. Also, we considered the influence of particle size and morphology on the optical properties of the prepared powders. The observed results sowed that the size and morphology of ZnO particles greatly affect the absorption of visible light (%) and the shift of the energy gap (eV).",
publisher = "Belgrade : Serbian Ceramic Society",
journal = "Joint Event of the 11th Young Researchers’ Conference: Materials Science and Engineering and the 1st European Early Stage Researches’ Conference on Hydrogen Storage: Program and the Book of Abstracts",
title = "Influence of particle size and morphology of ZnO powders on their optical properties",
pages = "60-60",
url = "https://hdl.handle.net/21.15107/rcub_vinar_7471"
}

Stanković, A., Stojanović, Z. S., Veselinović, L. M., Abazović, N., Škapin, S. D., Marković, S.,& Uskoković, D.. (2012). Influence of particle size and morphology of ZnO powders on their optical properties. in Joint Event of the 11th Young Researchers’ Conference: Materials Science and Engineering and the 1st European Early Stage Researches’ Conference on Hydrogen Storage: Program and the Book of Abstracts
Belgrade : Serbian Ceramic Society., 60-60.
https://hdl.handle.net/21.15107/rcub_vinar_7471

Stanković A, Stojanović ZS, Veselinović LM, Abazović N, Škapin SD, Marković S, Uskoković D. Influence of particle size and morphology of ZnO powders on their optical properties. in Joint Event of the 11th Young Researchers’ Conference: Materials Science and Engineering and the 1st European Early Stage Researches’ Conference on Hydrogen Storage: Program and the Book of Abstracts. 2012;:60-60.
https://hdl.handle.net/21.15107/rcub_vinar_7471 .

Stanković, Ana, Stojanović, Zoran S., Veselinović, Ljiljana M., Abazović, Nadica, Škapin, Srečo Davor, Marković, Smilja, Uskoković, Dragan, "Influence of particle size and morphology of ZnO powders on their optical properties" in Joint Event of the 11th Young Researchers’ Conference: Materials Science and Engineering and the 1st European Early Stage Researches’ Conference on Hydrogen Storage: Program and the Book of Abstracts (2012):60-60,
https://hdl.handle.net/21.15107/rcub_vinar_7471 .

TY  - CONF
AU  - Stanković, Ana
AU  - Stojanović, Zoran S.
AU  - Veselinović, Ljiljana M.
AU  - Bračko, Ines
AU  - Škapin, Srečo Davor
AU  - Marković, Smilja
AU  - Uskoković, Dragan
PY  - 2012
UR  - http://dais.sanu.ac.rs/123456789/435
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7437
AB  - ZnO represent one of the most important multifunctional materials. Its properties are well known and confirmed in different application areas such as: gas sensors, UV lasers, solar cells, electroluminescent and optoelectronic devices, piezoelectric transducers, hydrogen-storages, rubber industry and plastic processing, cosmetics and pharmacy, and it is also used as an antibacterial agent. In this work, we propose a low-temperature hydrothermal method for the synthesis of phase-pure ZnO powders with a controlled morphology and narrow particle size distribution. This simple and low-cost method allows tailoring of the shape and size of ZnO particles, from micro-rods via hexagonal prism-like to nano-spheres, by choosing the appropriate pH of the reaction solution, tuned by the varying of [Na+]:[Zn2+] molar ratio. The agglomeration of the powders was prevented with the assistance of PVP as a capping agent. The synthesized powders were characterized by XRD, TEM, SEAD and HRTEM methods to examine the phase purity and crystallinity. FE-SEM measurements were used for the morphology characterization, while the results of Raman and UV-Vis DRS measurements were used for the study of optical properties. The relationship between the particle size and morphology and the optical properties is discussed. Diffuse reflectance spectra of ZnO powders with different size and morphology revealed characteristic R curves with the absorption edge near 380 nm, but with obvious difference in the absorption in the visible region. The micro-sized powder ZnO8 revealed the lowest reflectance (∼70%), compared to submicro- (∼80%) and nano-sized (ZnO12 and ZnO13, ∼90%) powders. Thus, the reflectance of the ZnO powders decreases with the increase in the average particle size.
PB  - Belgrade : Materials Research Society of Serbia
C3  - The Fourteenth Annual Conference YUCOMAT 2012: Programme and the Book of Abstracts
T1  - Hydrothermal synthesis of ZnO powders with a tailored particle morphology and improved optical characteristics
SP  - 47
EP  - 47
UR  - https://hdl.handle.net/21.15107/rcub_vinar_7437
ER  - 

@conference{
author = "Stanković, Ana and Stojanović, Zoran S. and Veselinović, Ljiljana M. and Bračko, Ines and Škapin, Srečo Davor and Marković, Smilja and Uskoković, Dragan",
year = "2012",
abstract = "ZnO represent one of the most important multifunctional materials. Its properties are well known and confirmed in different application areas such as: gas sensors, UV lasers, solar cells, electroluminescent and optoelectronic devices, piezoelectric transducers, hydrogen-storages, rubber industry and plastic processing, cosmetics and pharmacy, and it is also used as an antibacterial agent. In this work, we propose a low-temperature hydrothermal method for the synthesis of phase-pure ZnO powders with a controlled morphology and narrow particle size distribution. This simple and low-cost method allows tailoring of the shape and size of ZnO particles, from micro-rods via hexagonal prism-like to nano-spheres, by choosing the appropriate pH of the reaction solution, tuned by the varying of [Na+]:[Zn2+] molar ratio. The agglomeration of the powders was prevented with the assistance of PVP as a capping agent. The synthesized powders were characterized by XRD, TEM, SEAD and HRTEM methods to examine the phase purity and crystallinity. FE-SEM measurements were used for the morphology characterization, while the results of Raman and UV-Vis DRS measurements were used for the study of optical properties. The relationship between the particle size and morphology and the optical properties is discussed. Diffuse reflectance spectra of ZnO powders with different size and morphology revealed characteristic R curves with the absorption edge near 380 nm, but with obvious difference in the absorption in the visible region. The micro-sized powder ZnO8 revealed the lowest reflectance (∼70%), compared to submicro- (∼80%) and nano-sized (ZnO12 and ZnO13, ∼90%) powders. Thus, the reflectance of the ZnO powders decreases with the increase in the average particle size.",
publisher = "Belgrade : Materials Research Society of Serbia",
journal = "The Fourteenth Annual Conference YUCOMAT 2012: Programme and the Book of Abstracts",
title = "Hydrothermal synthesis of ZnO powders with a tailored particle morphology and improved optical characteristics",
pages = "47-47",
url = "https://hdl.handle.net/21.15107/rcub_vinar_7437"
}

Stanković, A., Stojanović, Z. S., Veselinović, L. M., Bračko, I., Škapin, S. D., Marković, S.,& Uskoković, D.. (2012). Hydrothermal synthesis of ZnO powders with a tailored particle morphology and improved optical characteristics. in The Fourteenth Annual Conference YUCOMAT 2012: Programme and the Book of Abstracts
Belgrade : Materials Research Society of Serbia., 47-47.
https://hdl.handle.net/21.15107/rcub_vinar_7437

Stanković A, Stojanović ZS, Veselinović LM, Bračko I, Škapin SD, Marković S, Uskoković D. Hydrothermal synthesis of ZnO powders with a tailored particle morphology and improved optical characteristics. in The Fourteenth Annual Conference YUCOMAT 2012: Programme and the Book of Abstracts. 2012;:47-47.
https://hdl.handle.net/21.15107/rcub_vinar_7437 .

Stanković, Ana, Stojanović, Zoran S., Veselinović, Ljiljana M., Bračko, Ines, Škapin, Srečo Davor, Marković, Smilja, Uskoković, Dragan, "Hydrothermal synthesis of ZnO powders with a tailored particle morphology and improved optical characteristics" in The Fourteenth Annual Conference YUCOMAT 2012: Programme and the Book of Abstracts (2012):47-47,
https://hdl.handle.net/21.15107/rcub_vinar_7437 .

TY  - JOUR
AU  - Lukić, Miodrag
AU  - Veselinović, Ljiljana M.
AU  - Stojanović, Zoran S.
AU  - Maček Kržmanc, Marjeta
AU  - Bračko, Ines
AU  - Škapin, Srečo Davor
AU  - Marković, Smilja
AU  - Uskoković, Dragan
PY  - 2012
UR  - http://dais.sanu.ac.rs/123456789/476
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7447
AB  - We report unusual sintering behavior of Ca-deficient hydroxyapatite processed with different heating rates; particularly, faster heating resulted in higher densification. We hypothesize that faster heating delays formation of β-tricalcium phosphate which yields to unobstructed densification in intermediate sintering stage, allowing further tailoring of both microstructure and phase composition (hydroxyapatite/tricalcium phosphate).
PB  - Elsevier
T2  - Materials Letters
T1  - Peculiarities in sintering behavior of Ca-deficient hydroxyapatite nanopowders
SP  - 331
EP  - 335
DO  - 10.1016/j.matlet.2011.10.085
ER  - 

@article{
author = "Lukić, Miodrag and Veselinović, Ljiljana M. and Stojanović, Zoran S. and Maček Kržmanc, Marjeta and Bračko, Ines and Škapin, Srečo Davor and Marković, Smilja and Uskoković, Dragan",
year = "2012",
abstract = "We report unusual sintering behavior of Ca-deficient hydroxyapatite processed with different heating rates; particularly, faster heating resulted in higher densification. We hypothesize that faster heating delays formation of β-tricalcium phosphate which yields to unobstructed densification in intermediate sintering stage, allowing further tailoring of both microstructure and phase composition (hydroxyapatite/tricalcium phosphate).",
publisher = "Elsevier",
journal = "Materials Letters",
title = "Peculiarities in sintering behavior of Ca-deficient hydroxyapatite nanopowders",
pages = "331-335",
doi = "10.1016/j.matlet.2011.10.085"
}

Lukić, M., Veselinović, L. M., Stojanović, Z. S., Maček Kržmanc, M., Bračko, I., Škapin, S. D., Marković, S.,& Uskoković, D.. (2012). Peculiarities in sintering behavior of Ca-deficient hydroxyapatite nanopowders. in Materials Letters
Elsevier., 331-335.
https://doi.org/10.1016/j.matlet.2011.10.085

Lukić M, Veselinović LM, Stojanović ZS, Maček Kržmanc M, Bračko I, Škapin SD, Marković S, Uskoković D. Peculiarities in sintering behavior of Ca-deficient hydroxyapatite nanopowders. in Materials Letters. 2012;:331-335.
doi:10.1016/j.matlet.2011.10.085 .

Lukić, Miodrag, Veselinović, Ljiljana M., Stojanović, Zoran S., Maček Kržmanc, Marjeta, Bračko, Ines, Škapin, Srečo Davor, Marković, Smilja, Uskoković, Dragan, "Peculiarities in sintering behavior of Ca-deficient hydroxyapatite nanopowders" in Materials Letters (2012):331-335,
https://doi.org/10.1016/j.matlet.2011.10.085 . .

TY  - JOUR
AU  - Marković, Smilja
AU  - Stanković, Ana
AU  - Veselinović, Ljiljana M.
AU  - Stojanović, Zoran S.
AU  - Uskoković, Dragan
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7449
AB  - U ovom tekstu objašnjeni su postupci sinteze prahova ZnO i mogućnosti da se tim sintezama morfologija i srednja veličina čestica kreiraju od mikrometarskih štapića do nanometarskih sfernih čestica. Primenjene su dve metode sinteze, niskotemperatursko hidrotermalno (HT) procesiranje i ultrazvučno (UZ) procesiranje. Morfologija i srednja veličina čestica su kreirane podešavanjem molskog odnosa [Zn2+]/[OH-] polaznog (prekurskorskog) rastvora. Aglomeracija čestica je sprečena upotrebom polivinil pirolidona (PVP). Sintetisani prahovi su karakterisani metodom rendgenske difrakcije na prahu (XRD), skanirajuće elektronske mikroskopije (FESEM) i UV-Vis difuzione refleksione spektroskopije (UV-Vis DRS). Na osnovu skanirajućih elektronskih mikrografija predložen je mehanizam rasta čestica ZnO u zavisnosti od molskog odnosa [Zn2+]/[OH-] polaznog rastvora. Takođe, ispitan je i uticaj veličine i morfologije čestica na optičke karakteristike prahova ZnO; uočeno je da veličina i morfologija čestica utiču kako na apsorpciju vidljive svetlosti (%) tako i na pomeraj energetskog procepa (eV).
AB  - Different ZnO powders synthesis methods as well as possibilities to obtain particles with controlled morphology and average particle size from micro- to nano-level were discussed. Two synthesis methods were applied, low-temperature hydrothermal (HT) and ultrasound processing (UZ). Morphology and average particle size were tailored by adjusting of initial solution [Zn2+]/[OH-]molar ratio. Particles agglomeration is suppressed by polyvinylpyrrolidone (PVP). Synthesized powders were characterized by X-ray diffraction method (XRD), field emission scanning electron microscopy (FESEM) and UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS). Considering FESEM micrographs the ZnO particles growth mechanism depending on initial solution [Zn2+]/[OH-] molar ratio is proposed. Furthermore, influence of average particle size and morphology on ZnO optical properties is studied; it is observed that both average particle size and morphology affect visible light absorption (%) as well as shift of Ebg (eV).
PB  - Beograd : Savez inženjera i tehničara Srbije
T2  - Tehnika - Novi materijali
T1  - Kreiranje morfologije i veličine čestica ZnO prahova
SP  - 685
EP  - 691
UR  - https://hdl.handle.net/21.15107/rcub_vinar_7449
ER  - 

@article{
author = "Marković, Smilja and Stanković, Ana and Veselinović, Ljiljana M. and Stojanović, Zoran S. and Uskoković, Dragan",
year = "2012",
abstract = "U ovom tekstu objašnjeni su postupci sinteze prahova ZnO i mogućnosti da se tim sintezama morfologija i srednja veličina čestica kreiraju od mikrometarskih štapića do nanometarskih sfernih čestica. Primenjene su dve metode sinteze, niskotemperatursko hidrotermalno (HT) procesiranje i ultrazvučno (UZ) procesiranje. Morfologija i srednja veličina čestica su kreirane podešavanjem molskog odnosa [Zn2+]/[OH-] polaznog (prekurskorskog) rastvora. Aglomeracija čestica je sprečena upotrebom polivinil pirolidona (PVP). Sintetisani prahovi su karakterisani metodom rendgenske difrakcije na prahu (XRD), skanirajuće elektronske mikroskopije (FESEM) i UV-Vis difuzione refleksione spektroskopije (UV-Vis DRS). Na osnovu skanirajućih elektronskih mikrografija predložen je mehanizam rasta čestica ZnO u zavisnosti od molskog odnosa [Zn2+]/[OH-] polaznog rastvora. Takođe, ispitan je i uticaj veličine i morfologije čestica na optičke karakteristike prahova ZnO; uočeno je da veličina i morfologija čestica utiču kako na apsorpciju vidljive svetlosti (%) tako i na pomeraj energetskog procepa (eV)., Different ZnO powders synthesis methods as well as possibilities to obtain particles with controlled morphology and average particle size from micro- to nano-level were discussed. Two synthesis methods were applied, low-temperature hydrothermal (HT) and ultrasound processing (UZ). Morphology and average particle size were tailored by adjusting of initial solution [Zn2+]/[OH-]molar ratio. Particles agglomeration is suppressed by polyvinylpyrrolidone (PVP). Synthesized powders were characterized by X-ray diffraction method (XRD), field emission scanning electron microscopy (FESEM) and UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS). Considering FESEM micrographs the ZnO particles growth mechanism depending on initial solution [Zn2+]/[OH-] molar ratio is proposed. Furthermore, influence of average particle size and morphology on ZnO optical properties is studied; it is observed that both average particle size and morphology affect visible light absorption (%) as well as shift of Ebg (eV).",
publisher = "Beograd : Savez inženjera i tehničara Srbije",
journal = "Tehnika - Novi materijali",
title = "Kreiranje morfologije i veličine čestica ZnO prahova",
pages = "685-691",
url = "https://hdl.handle.net/21.15107/rcub_vinar_7449"
}

Marković, S., Stanković, A., Veselinović, L. M., Stojanović, Z. S.,& Uskoković, D.. (2012). Kreiranje morfologije i veličine čestica ZnO prahova. in Tehnika - Novi materijali
Beograd : Savez inženjera i tehničara Srbije., 685-691.
https://hdl.handle.net/21.15107/rcub_vinar_7449

Marković S, Stanković A, Veselinović LM, Stojanović ZS, Uskoković D. Kreiranje morfologije i veličine čestica ZnO prahova. in Tehnika - Novi materijali. 2012;:685-691.
https://hdl.handle.net/21.15107/rcub_vinar_7449 .

Marković, Smilja, Stanković, Ana, Veselinović, Ljiljana M., Stojanović, Zoran S., Uskoković, Dragan, "Kreiranje morfologije i veličine čestica ZnO prahova" in Tehnika - Novi materijali (2012):685-691,
https://hdl.handle.net/21.15107/rcub_vinar_7449 .

TY  - JOUR
AU  - Stanković, Ana
AU  - Stojanović, Zoran S.
AU  - Veselinović, Ljiljana M.
AU  - Škapin, Srečo Davor
AU  - Bračko, Ines
AU  - Marković, Smilja
AU  - Uskoković, Dragan
PY  - 2012
UR  - http://dais.sanu.ac.rs/123456789/486
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7450
AB  - In this paper, we investigate the effect of the particle size and morphology on the optical properties of ZnO. A series of ZnO micro and nanocrystals were synthesized by the hydrothermal processing of zinc acetate dihydrate and sodium hydroxide as the starting materials, and polyvinylpyrrolidone (PVP) as the polymer surfactant. The particle size and morphology were tailored by adjusting the reactant molar ratios [Zn2+]/[OH−], while the reaction temperature and the time remained unchanged. X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SAED) and high-resolution TEM (HRTEM) have shown that the micro and nanocrystals have a high crystalline pure wurtzite-type hexagonal structure with nanosized crystallites. The size and morphology of the ZnO micro and nanocrystals were investigated by field emission scanning electron microscopy (FE-SEM), which showed a modification from micro-rods via hexagonal-faceted prismatic morphology to nanospheres, caused by simple adjustment of the reactant molar ratio [Zn2+]/[OH−] from 1:1 to 1:5. The optical properties of the ZnO micro and nanocrystals, as well as their dependence on the particle size and morphology were investigated by Raman and ultraviolet–visible (UV–vis) diffuse reflectance spectroscopy (DRS). The UV–vis spectra showed that the modification of the particle size and morphology from nanospheres to micro-rods resulted in increased absorption, and a slight red-shift of the absorption edge (0.06 eV). Besides, the band gap energy of the synthesized ZnO micro and nanocrystals showed the red shift (∼0.20 eV) compared to bulk ZnO. According to the results of a Raman spectroscopy, the enhanced visible light absorption of the ZnO micro and nanocrystals is related to two phenomena: (1) the existence of lattice defects (oxygen vacancies and zinc interstitials), and (2) the particle surface sensitization by PVP.
PB  - Elsevier
T2  - Materials Science and Engineering: B
T1  - ZnO micro and nanocrystals with enhanced visible light absorption
SP  - 1038
EP  - 1045
DO  - 10.1016/j.mseb.2012.05.013
ER  - 

@article{
author = "Stanković, Ana and Stojanović, Zoran S. and Veselinović, Ljiljana M. and Škapin, Srečo Davor and Bračko, Ines and Marković, Smilja and Uskoković, Dragan",
year = "2012",
abstract = "In this paper, we investigate the effect of the particle size and morphology on the optical properties of ZnO. A series of ZnO micro and nanocrystals were synthesized by the hydrothermal processing of zinc acetate dihydrate and sodium hydroxide as the starting materials, and polyvinylpyrrolidone (PVP) as the polymer surfactant. The particle size and morphology were tailored by adjusting the reactant molar ratios [Zn2+]/[OH−], while the reaction temperature and the time remained unchanged. X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SAED) and high-resolution TEM (HRTEM) have shown that the micro and nanocrystals have a high crystalline pure wurtzite-type hexagonal structure with nanosized crystallites. The size and morphology of the ZnO micro and nanocrystals were investigated by field emission scanning electron microscopy (FE-SEM), which showed a modification from micro-rods via hexagonal-faceted prismatic morphology to nanospheres, caused by simple adjustment of the reactant molar ratio [Zn2+]/[OH−] from 1:1 to 1:5. The optical properties of the ZnO micro and nanocrystals, as well as their dependence on the particle size and morphology were investigated by Raman and ultraviolet–visible (UV–vis) diffuse reflectance spectroscopy (DRS). The UV–vis spectra showed that the modification of the particle size and morphology from nanospheres to micro-rods resulted in increased absorption, and a slight red-shift of the absorption edge (0.06 eV). Besides, the band gap energy of the synthesized ZnO micro and nanocrystals showed the red shift (∼0.20 eV) compared to bulk ZnO. According to the results of a Raman spectroscopy, the enhanced visible light absorption of the ZnO micro and nanocrystals is related to two phenomena: (1) the existence of lattice defects (oxygen vacancies and zinc interstitials), and (2) the particle surface sensitization by PVP.",
publisher = "Elsevier",
journal = "Materials Science and Engineering: B",
title = "ZnO micro and nanocrystals with enhanced visible light absorption",
pages = "1038-1045",
doi = "10.1016/j.mseb.2012.05.013"
}

Stanković, A., Stojanović, Z. S., Veselinović, L. M., Škapin, S. D., Bračko, I., Marković, S.,& Uskoković, D.. (2012). ZnO micro and nanocrystals with enhanced visible light absorption. in Materials Science and Engineering: B
Elsevier., 1038-1045.
https://doi.org/10.1016/j.mseb.2012.05.013

Stanković A, Stojanović ZS, Veselinović LM, Škapin SD, Bračko I, Marković S, Uskoković D. ZnO micro and nanocrystals with enhanced visible light absorption. in Materials Science and Engineering: B. 2012;:1038-1045.
doi:10.1016/j.mseb.2012.05.013 .

Stanković, Ana, Stojanović, Zoran S., Veselinović, Ljiljana M., Škapin, Srečo Davor, Bračko, Ines, Marković, Smilja, Uskoković, Dragan, "ZnO micro and nanocrystals with enhanced visible light absorption" in Materials Science and Engineering: B (2012):1038-1045,
https://doi.org/10.1016/j.mseb.2012.05.013 . .

TY  - CONF
AU  - Stanković, Ana
AU  - Stojanović, Zoran S.
AU  - Veselinović, Ljiljana M.
AU  - Marković, Smilja
AU  - Uskoković, Dragan
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7472
AB  - In this study low-temperature hydrothermal processing was used for synthesis of ZnO powders with controlled morphology, from micro rods, via hexagonal prism-like to nano-spheres, by varying [Zn2+]/[OH-] molar ratio. The synthesized powders were characterized using XRPD, FE-SEM, UV-Vis diffuse reflectance and Raman spectroscopy. It is noticed that the modification of the particle size and morphology from nanospheres to micro-rods resulted in increased visible light absorption. Besides, the band gap energy of the synthesized ZnO powders showed the red shift (-0.20eV) compared to bulk ZnO. The enhanced visible light absorption of the ZnO powders is related to the existence of lattice defects and the particle surface sensitization by PVP.
PB  - Society of Physical Chemists of Serbia
C3  - Physical chemistry 2012 : 11th international conference on fundamental and applied aspects of physical chemistry
T1  - Controlled hydrothermal processing of ZnO powders in the presence of PVP
SP  - 431
EP  - 433
UR  - https://hdl.handle.net/21.15107/rcub_vinar_7472
ER  - 

@conference{
author = "Stanković, Ana and Stojanović, Zoran S. and Veselinović, Ljiljana M. and Marković, Smilja and Uskoković, Dragan",
year = "2012",
abstract = "In this study low-temperature hydrothermal processing was used for synthesis of ZnO powders with controlled morphology, from micro rods, via hexagonal prism-like to nano-spheres, by varying [Zn2+]/[OH-] molar ratio. The synthesized powders were characterized using XRPD, FE-SEM, UV-Vis diffuse reflectance and Raman spectroscopy. It is noticed that the modification of the particle size and morphology from nanospheres to micro-rods resulted in increased visible light absorption. Besides, the band gap energy of the synthesized ZnO powders showed the red shift (-0.20eV) compared to bulk ZnO. The enhanced visible light absorption of the ZnO powders is related to the existence of lattice defects and the particle surface sensitization by PVP.",
publisher = "Society of Physical Chemists of Serbia",
journal = "Physical chemistry 2012 : 11th international conference on fundamental and applied aspects of physical chemistry",
title = "Controlled hydrothermal processing of ZnO powders in the presence of PVP",
pages = "431-433",
url = "https://hdl.handle.net/21.15107/rcub_vinar_7472"
}

Stanković, A., Stojanović, Z. S., Veselinović, L. M., Marković, S.,& Uskoković, D.. (2012). Controlled hydrothermal processing of ZnO powders in the presence of PVP. in Physical chemistry 2012 : 11th international conference on fundamental and applied aspects of physical chemistry
Society of Physical Chemists of Serbia., 431-433.
https://hdl.handle.net/21.15107/rcub_vinar_7472

Stanković A, Stojanović ZS, Veselinović LM, Marković S, Uskoković D. Controlled hydrothermal processing of ZnO powders in the presence of PVP. in Physical chemistry 2012 : 11th international conference on fundamental and applied aspects of physical chemistry. 2012;:431-433.
https://hdl.handle.net/21.15107/rcub_vinar_7472 .

Stanković, Ana, Stojanović, Zoran S., Veselinović, Ljiljana M., Marković, Smilja, Uskoković, Dragan, "Controlled hydrothermal processing of ZnO powders in the presence of PVP" in Physical chemistry 2012 : 11th international conference on fundamental and applied aspects of physical chemistry (2012):431-433,
https://hdl.handle.net/21.15107/rcub_vinar_7472 .