Vujković, Milica

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Authority KeyName Variants
orcid::0000-0002-0518-8837
  • Vujković, Milica (20)
Projects
Lithium-ion batteries and fuel cells - research and development Electroconducting and redox-active polymers and oligomers: synthesis, structure, properties and applications
Physics and Chemistry with Ion Beams Synthesis, processing and characterization of nanostructured materials for application in the field of energy, mechanical engineering, environmental protection and biomedicine
Molecular designing of nanoparticles with controlled morphological and physicochemical characteristics and functional materials based on them Magnetic and radionuclide labeled nanostructured materials for medical applications
Bilateral project Serbia-Slovenia “Developments of novel materials for alkaline-ion batteries” SASPRO - Mobility Programme of Slovak Academy of Sciences: Supportive Fund for Excellent Scientists
Thin films of single wall carbon nanotubes and graphene for electronic application Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200175 (Institute of Technical Sciences of SASA, Belgrade)
Nanostructured Functional and Composite Materials in Catalytic and Sorption Processes Optoelectronics nanodimension systems - the rout towards applications
Functional, Functionalized and Advanced Nanomaterials Fabrication and characterization of nano-photonic functional structrues in biomedicine and informatics
Nanostructured multifunctional materials and nanocomposites Synthesis, processing and applications of nanostructured multifunctional materials with defined properties
HiSuperBat - High-Capacity Electrodes for Aqueous Rechargeable Multivalent-Ion Batteries and Supercapacitors: Next Step Towards a Hybrid Model NATO [EAP.SFPP 984925-DURAPEM]
NATO through the Science for Peace Project [EAP.SFPP 984925-DURAPEM] Project "AIProc-Mat@N2020-Advanced Industrial Processes and Materials for a Sustainable Northern Region of Portugal 2020" - Norte Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (ERDF) (NORTE-01-0145-FEDER-000006)
Project POCI-01-0145-FEDER-006984 - Associate Laboratory LSRE-LCM funded by ERDF through COMPETE2020-Programa Operacional Competitividade e Internacionalizacao (POCI) Project Serbia-Montenegro entitled ''Development of ecological Li-ion batteries''
Project Serbia-Slovenia entitled ''Developments of novel materials for alkaline-ion batteries'' Serbian Academy of Science and Arts
Serbian Academy of Sciences and Arts Serbian Academy of Sciences and Arts Electrocatalysis in the contemporary processes of energy conversion, NATO through the Science for Peace Project [EAP. SFPP 984925-DURAPEM]
Serbian Academy of Sciences and Arts “Electrocatalysis in the contemporary process of energy conversion” Serbian Academy of Sciences and Arts ["Electrocatalysis in the contemporary process of energy conversion"]
Serbian Academy of Sciences and Arts (F-190) Serbian Academy of Sciences and Arts, Portuguese Foundaton for science and Technology (Fundacao para a Ciencia e a Tecnologia, FCT)

Author's Bibliography

Electrochemical and structural study on cycling performance of γ-LiV2O5 cathode

Milović, Miloš; Vujković, Milica; Jugović, Dragana; Mitrić, Miodrag

(2021)

TY  - JOUR
AU  - Milović, Miloš
AU  - Vujković, Milica
AU  - Jugović, Dragana
AU  - Mitrić, Miodrag
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9148
AB  - Electrochemical and structural properties of LiV2O5 cathode were investigated. Obtained by solid state reaction at high temperature the material crystallized as gamma polymorph phase, γ-LiV2O5. The gamma structure provides two crystallographic sites to accommodate lithium ions, Li1 and Li2 position. Lithium insertion at these two sites occurs at two respective voltages versus lithium metal: ~3.6 V (Li1) and ~2.4 V (Li2). Intercalation at Li1 position is reversible in both organic and aqueous electrolyte and provides stable cycling performance at the high voltage. On the contrary, sluggish insertion/removal of Li+ at Li2 sites causes unstable performance and significant storage capacity fade at lower voltages. Lithium diffusion 3d landscape was determined by bond valence calculations applied on the γ-LiV2O5 phase, as well as on the metastable phases of γ′-V2O5 and ζ-Li2V2O5 that exist at high and low voltages respectively. The model was proposed based on inactivity of Li2 position of the metastable ζ-Li2V2O5 phase which provides explanation for the observed storage capacity loss at low voltages. © 2021 Elsevier Ltd and Techna Group S.r.l.
T2  - Ceramics International
T1  - Electrochemical and structural study on cycling performance of γ-LiV2O5 cathode
VL  - 47
IS  - 12
SP  - 17077
EP  - 17083
DO  - 10.1016/j.ceramint.2021.03.016
ER  - 
@article{
author = "Milović, Miloš and Vujković, Milica and Jugović, Dragana and Mitrić, Miodrag",
year = "2021",
url = "https://vinar.vin.bg.ac.rs/handle/123456789/9148",
abstract = "Electrochemical and structural properties of LiV2O5 cathode were investigated. Obtained by solid state reaction at high temperature the material crystallized as gamma polymorph phase, γ-LiV2O5. The gamma structure provides two crystallographic sites to accommodate lithium ions, Li1 and Li2 position. Lithium insertion at these two sites occurs at two respective voltages versus lithium metal: ~3.6 V (Li1) and ~2.4 V (Li2). Intercalation at Li1 position is reversible in both organic and aqueous electrolyte and provides stable cycling performance at the high voltage. On the contrary, sluggish insertion/removal of Li+ at Li2 sites causes unstable performance and significant storage capacity fade at lower voltages. Lithium diffusion 3d landscape was determined by bond valence calculations applied on the γ-LiV2O5 phase, as well as on the metastable phases of γ′-V2O5 and ζ-Li2V2O5 that exist at high and low voltages respectively. The model was proposed based on inactivity of Li2 position of the metastable ζ-Li2V2O5 phase which provides explanation for the observed storage capacity loss at low voltages. © 2021 Elsevier Ltd and Techna Group S.r.l.",
journal = "Ceramics International",
title = "Electrochemical and structural study on cycling performance of γ-LiV2O5 cathode",
volume = "47",
number = "12",
pages = "17077-17083",
doi = "10.1016/j.ceramint.2021.03.016"
}
Milović, M., Vujković, M., Jugović, D.,& Mitrić, M. (2021). Electrochemical and structural study on cycling performance of γ-LiV2O5 cathode.
Ceramics International, 47(12), 17077-17083.
https://doi.org/10.1016/j.ceramint.2021.03.016
Milović M, Vujković M, Jugović D, Mitrić M. Electrochemical and structural study on cycling performance of γ-LiV2O5 cathode. Ceramics International. 2021;47(12):17077-17083
Milović Miloš, Vujković Milica, Jugović Dragana, Mitrić Miodrag, "Electrochemical and structural study on cycling performance of γ-LiV2O5 cathode" Ceramics International, 47, no. 12 (2021):17077-17083,
https://doi.org/10.1016/j.ceramint.2021.03.016 .

Self-limiting interactions in 2D–0D systems: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite

Jovanović, Zoran M.; Mravik, Željko; Bajuk-Bogdanović, Danica V.; Jovanović, Sonja; Marković, Smilja; Vujković, Milica; Kovač, Janez; Vengust, Damjan; Uskoković-Marković, Snežana; Holclajtner-Antunović, Ivanka D.

(2020)

TY  - JOUR
AU  - Jovanović, Zoran M.
AU  - Mravik, Željko
AU  - Bajuk-Bogdanović, Danica V.
AU  - Jovanović, Sonja
AU  - Marković, Smilja
AU  - Vujković, Milica
AU  - Kovač, Janez
AU  - Vengust, Damjan
AU  - Uskoković-Marković, Snežana
AU  - Holclajtner-Antunović, Ivanka D.
PY  - 2020
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8520
AB  - In the present study we investigated the interaction between 12-tungstophosphoric acid (WPA) and graphene oxide (GO) in their nanocomposite by utilizing the loading of WPA as an intrinsic parameter for interaction tuning. The Fourier-transform infrared spectroscopy, temperature-programmed desorption, X-ray photoelectron spectroscopy, zeta-potential measurements, thermogravimetric analysis, X-ray diffraction, Raman spectroscopy and transmission electron microscopy methods revealed that ∼5–13 wt% of WPA represents critical loading that separates two distinct contributions to GO-WPA interaction. This was explained by the self-limiting nature of GO-WPA interaction, initially controlled by high dispersion of WPA on GO (up to 13 wt%), that is eventually overpowered by WPA-WPA interaction as loading increases. As a result, the WPA agglomerates are being formed because of which the hybrid character of the nanocomposite diminishes, i.e., the properties of independent components start to be manifested to greater extent. The obtained results provide an important framework for considering possible outcomes in other 2D-0D systems, whose interaction is relevant both from fundamental and applicative point of view. Thus, the GO/WPA nanocomposite illustrates how the interactions between the components can be used for tuning the properties of nanocomposite as a whole. © 2019 Elsevier Ltd
T2  - Carbon
T1  - Self-limiting interactions in 2D–0D systems: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite
VL  - 156
SP  - 166
EP  - 178
DO  - 10.1016/j.carbon.2019.09.072
ER  - 
@article{
author = "Jovanović, Zoran M. and Mravik, Željko and Bajuk-Bogdanović, Danica V. and Jovanović, Sonja and Marković, Smilja and Vujković, Milica and Kovač, Janez and Vengust, Damjan and Uskoković-Marković, Snežana and Holclajtner-Antunović, Ivanka D.",
year = "2020",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8520",
abstract = "In the present study we investigated the interaction between 12-tungstophosphoric acid (WPA) and graphene oxide (GO) in their nanocomposite by utilizing the loading of WPA as an intrinsic parameter for interaction tuning. The Fourier-transform infrared spectroscopy, temperature-programmed desorption, X-ray photoelectron spectroscopy, zeta-potential measurements, thermogravimetric analysis, X-ray diffraction, Raman spectroscopy and transmission electron microscopy methods revealed that ∼5–13 wt% of WPA represents critical loading that separates two distinct contributions to GO-WPA interaction. This was explained by the self-limiting nature of GO-WPA interaction, initially controlled by high dispersion of WPA on GO (up to 13 wt%), that is eventually overpowered by WPA-WPA interaction as loading increases. As a result, the WPA agglomerates are being formed because of which the hybrid character of the nanocomposite diminishes, i.e., the properties of independent components start to be manifested to greater extent. The obtained results provide an important framework for considering possible outcomes in other 2D-0D systems, whose interaction is relevant both from fundamental and applicative point of view. Thus, the GO/WPA nanocomposite illustrates how the interactions between the components can be used for tuning the properties of nanocomposite as a whole. © 2019 Elsevier Ltd",
journal = "Carbon",
title = "Self-limiting interactions in 2D–0D systems: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite",
volume = "156",
pages = "166-178",
doi = "10.1016/j.carbon.2019.09.072"
}
Jovanović, Z. M., Mravik, Ž., Bajuk-Bogdanović, D. V., Jovanović, S., Marković, S., Vujković, M., Kovač, J., Vengust, D., Uskoković-Marković, S.,& Holclajtner-Antunović, I. D. (2020). Self-limiting interactions in 2D–0D systems: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite.
Carbon, 156, 166-178.
https://doi.org/10.1016/j.carbon.2019.09.072
Jovanović ZM, Mravik Ž, Bajuk-Bogdanović DV, Jovanović S, Marković S, Vujković M, Kovač J, Vengust D, Uskoković-Marković S, Holclajtner-Antunović ID. Self-limiting interactions in 2D–0D systems: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite. Carbon. 2020;156:166-178
Jovanović Zoran M., Mravik Željko, Bajuk-Bogdanović Danica V., Jovanović Sonja, Marković Smilja, Vujković Milica, Kovač Janez, Vengust Damjan, Uskoković-Marković Snežana, Holclajtner-Antunović Ivanka D., "Self-limiting interactions in 2D–0D systems: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite" Carbon, 156 (2020):166-178,
https://doi.org/10.1016/j.carbon.2019.09.072 .
4
3

The influence of synthesis conditions on the redox behaviour of LiFePO4 in aqueous solution

Georgijević, Radovan; Vujković, Milica; Gutić, Sanjin J.; Aliefendić, Meho; Jugović, Dragana; Mitrić, Miodrag; Đokić, Veljko R.; Mentus, Slavko V.

(2019)

TY  - JOUR
AU  - Georgijević, Radovan
AU  - Vujković, Milica
AU  - Gutić, Sanjin J.
AU  - Aliefendić, Meho
AU  - Jugović, Dragana
AU  - Mitrić, Miodrag
AU  - Đokić, Veljko R.
AU  - Mentus, Slavko V.
PY  - 2019
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7936
AB  - To contribute to the knowledge on the influence of synthesis procedure on the intercalation kinetics of lithium ions into phospho-olivines, LiFePO4/C composite samples (LFPC) were synthesized in two ways, the first one in a sol-gel procedure (SG), and the other in a solid-state reaction (SS). The X-ray diffractograms (XRD) of both samples overlapped with that of pure LiFePO4, taken from the crystallographic database. Scanning electron microscopy pictures indicated the high degree of interparticle sintering, which caused a considerable agglomerate growth. The results of potentiodynamic measurements in aqueous LiNO3 solution revealed that for SS sample, three times higher initial capacity from that of SG one, (amounting to 74 mAh g−1 at 5 mV s−1). However, capacity fade on rising scan rate is much more expressed for SS sample than for SG one. We suggest that a different degree of material utilization due to the incomplete coverage of olivine particles by carbon explains this difference. The technique of separation of diffusion and capacitance currents was applied in a kinetic analysis, but it was shown to be inappropriate. We suggest the inapplicability of classic CV theory to the intercalation system accompanied by phase transition. Instead, a model of ohmic resistance determination of process kinetics was considered. LFPC-SS sample delivers three times larger capacity in LiNO3, amounting to 74 mAh g−1 at 1 mV s−1.
T2  - Journal of Alloys and Compounds
T1  - The influence of synthesis conditions on the redox behaviour of LiFePO4 in aqueous solution
VL  - 776
SP  - 475
EP  - 485
DO  - 10.1016/j.jallcom.2018.10.246
ER  - 
@article{
author = "Georgijević, Radovan and Vujković, Milica and Gutić, Sanjin J. and Aliefendić, Meho and Jugović, Dragana and Mitrić, Miodrag and Đokić, Veljko R. and Mentus, Slavko V.",
year = "2019",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/7936",
abstract = "To contribute to the knowledge on the influence of synthesis procedure on the intercalation kinetics of lithium ions into phospho-olivines, LiFePO4/C composite samples (LFPC) were synthesized in two ways, the first one in a sol-gel procedure (SG), and the other in a solid-state reaction (SS). The X-ray diffractograms (XRD) of both samples overlapped with that of pure LiFePO4, taken from the crystallographic database. Scanning electron microscopy pictures indicated the high degree of interparticle sintering, which caused a considerable agglomerate growth. The results of potentiodynamic measurements in aqueous LiNO3 solution revealed that for SS sample, three times higher initial capacity from that of SG one, (amounting to 74 mAh g−1 at 5 mV s−1). However, capacity fade on rising scan rate is much more expressed for SS sample than for SG one. We suggest that a different degree of material utilization due to the incomplete coverage of olivine particles by carbon explains this difference. The technique of separation of diffusion and capacitance currents was applied in a kinetic analysis, but it was shown to be inappropriate. We suggest the inapplicability of classic CV theory to the intercalation system accompanied by phase transition. Instead, a model of ohmic resistance determination of process kinetics was considered. LFPC-SS sample delivers three times larger capacity in LiNO3, amounting to 74 mAh g−1 at 1 mV s−1.",
journal = "Journal of Alloys and Compounds",
title = "The influence of synthesis conditions on the redox behaviour of LiFePO4 in aqueous solution",
volume = "776",
pages = "475-485",
doi = "10.1016/j.jallcom.2018.10.246"
}
Georgijević, R., Vujković, M., Gutić, S. J., Aliefendić, M., Jugović, D., Mitrić, M., Đokić, V. R.,& Mentus, S. V. (2019). The influence of synthesis conditions on the redox behaviour of LiFePO4 in aqueous solution.
Journal of Alloys and Compounds, 776, 475-485.
https://doi.org/10.1016/j.jallcom.2018.10.246
Georgijević R, Vujković M, Gutić SJ, Aliefendić M, Jugović D, Mitrić M, Đokić VR, Mentus SV. The influence of synthesis conditions on the redox behaviour of LiFePO4 in aqueous solution. Journal of Alloys and Compounds. 2019;776:475-485
Georgijević Radovan, Vujković Milica, Gutić Sanjin J., Aliefendić Meho, Jugović Dragana, Mitrić Miodrag, Đokić Veljko R., Mentus Slavko V., "The influence of synthesis conditions on the redox behaviour of LiFePO4 in aqueous solution" Journal of Alloys and Compounds, 776 (2019):475-485,
https://doi.org/10.1016/j.jallcom.2018.10.246 .
5
6
6

The influence of oxygen vacancy concentration in nanodispersed non-stoichiometric CeO2-δ oxides on the physico-chemical properties of conducting polyaniline/CeO2 composites

Kuzmanović, Bojana; Vujković, Milica; Tomić, Nataša M.; Bajuk-Bogdanović, Danica V.; Lazović, Vladimir M.; Šljukić, Biljana; Ivanović, Nenad; Mentus, Slavko V.

(2019)

TY  - JOUR
AU  - Kuzmanović, Bojana
AU  - Vujković, Milica
AU  - Tomić, Nataša M.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Lazović, Vladimir M.
AU  - Šljukić, Biljana
AU  - Ivanović, Nenad
AU  - Mentus, Slavko V.
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0013468619305584
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8135
AB  - Cerium oxide (CeO 2-δ ) ultrafine nanoparticles, with the lower (CeO 2-δ -HT) and higher (CeO 2-δ -SS) fraction of oxygen vacancies, were used as anchoring sites for the polymerization of aniline in acidic medium. As a result, polyaniline-emeraldine salt (PANI-ES)-based composites (PANI-ES@CeO 2-δ -HT and PANI-ES@CeO 2-δ -SS) were obtained. The interaction between CeO 2-δ and PANI was examined by FTIR and Raman spectroscopy. The PANI polymerization is initiated via electrostatic interaction of anilinium cation and Cl − ions (adsorbed at the protonated hydroxyl groups of CeO 2-δ ), and proceeds with hydrogen and nitrogen interaction with oxide nanoparticles. Tailoring the oxygen vacancy population of oxide offers the possibility to control the type of PANI-cerium oxide interaction, and consequently structural, electrical, thermal, electronic and charge storage properties of composite. A high capacitance of synthesized materials, reaching ∼294 F g −1 (PANI-ES), ∼299 F g −1 (PANI-ES@CeO 2-δ -HT) and ∼314 F g −1 (PANI-ES@CeO 2-δ -SS), was measured in 1 M HCl, at a common scan rate of 20 mV s −1 . The high adhesion of PANI with cerium oxide prevents the oxide from its slow dissolution in 1MHCl thus providing the stability of this composite in an acidic solution. The rate of electrochemical oxidation of emeraldine salt into pernigraniline was also found to depend on CeO 2-δ characteristics. © 2019 Elsevier Ltd
T2  - Electrochimica Acta
T1  - The influence of oxygen vacancy concentration in nanodispersed non-stoichiometric CeO2-δ oxides on the physico-chemical properties of conducting polyaniline/CeO2 composites
VL  - 306
SP  - 506
EP  - 515
DO  - 10.1016/j.electacta.2019.03.135
ER  - 
@article{
author = "Kuzmanović, Bojana and Vujković, Milica and Tomić, Nataša M. and Bajuk-Bogdanović, Danica V. and Lazović, Vladimir M. and Šljukić, Biljana and Ivanović, Nenad and Mentus, Slavko V.",
year = "2019",
url = "https://linkinghub.elsevier.com/retrieve/pii/S0013468619305584, http://vinar.vin.bg.ac.rs/handle/123456789/8135",
abstract = "Cerium oxide (CeO 2-δ ) ultrafine nanoparticles, with the lower (CeO 2-δ -HT) and higher (CeO 2-δ -SS) fraction of oxygen vacancies, were used as anchoring sites for the polymerization of aniline in acidic medium. As a result, polyaniline-emeraldine salt (PANI-ES)-based composites (PANI-ES@CeO 2-δ -HT and PANI-ES@CeO 2-δ -SS) were obtained. The interaction between CeO 2-δ and PANI was examined by FTIR and Raman spectroscopy. The PANI polymerization is initiated via electrostatic interaction of anilinium cation and Cl − ions (adsorbed at the protonated hydroxyl groups of CeO 2-δ ), and proceeds with hydrogen and nitrogen interaction with oxide nanoparticles. Tailoring the oxygen vacancy population of oxide offers the possibility to control the type of PANI-cerium oxide interaction, and consequently structural, electrical, thermal, electronic and charge storage properties of composite. A high capacitance of synthesized materials, reaching ∼294 F g −1 (PANI-ES), ∼299 F g −1 (PANI-ES@CeO 2-δ -HT) and ∼314 F g −1 (PANI-ES@CeO 2-δ -SS), was measured in 1 M HCl, at a common scan rate of 20 mV s −1 . The high adhesion of PANI with cerium oxide prevents the oxide from its slow dissolution in 1MHCl thus providing the stability of this composite in an acidic solution. The rate of electrochemical oxidation of emeraldine salt into pernigraniline was also found to depend on CeO 2-δ characteristics. © 2019 Elsevier Ltd",
journal = "Electrochimica Acta",
title = "The influence of oxygen vacancy concentration in nanodispersed non-stoichiometric CeO2-δ oxides on the physico-chemical properties of conducting polyaniline/CeO2 composites",
volume = "306",
pages = "506-515",
doi = "10.1016/j.electacta.2019.03.135"
}
Kuzmanović, B., Vujković, M., Tomić, N. M., Bajuk-Bogdanović, D. V., Lazović, V. M., Šljukić, B., Ivanović, N.,& Mentus, S. V. (2019). The influence of oxygen vacancy concentration in nanodispersed non-stoichiometric CeO2-δ oxides on the physico-chemical properties of conducting polyaniline/CeO2 composites.
Electrochimica Acta, 306, 506-515.
https://doi.org/10.1016/j.electacta.2019.03.135
Kuzmanović B, Vujković M, Tomić NM, Bajuk-Bogdanović DV, Lazović VM, Šljukić B, Ivanović N, Mentus SV. The influence of oxygen vacancy concentration in nanodispersed non-stoichiometric CeO2-δ oxides on the physico-chemical properties of conducting polyaniline/CeO2 composites. Electrochimica Acta. 2019;306:506-515
Kuzmanović Bojana, Vujković Milica, Tomić Nataša M., Bajuk-Bogdanović Danica V., Lazović Vladimir M., Šljukić Biljana, Ivanović Nenad, Mentus Slavko V., "The influence of oxygen vacancy concentration in nanodispersed non-stoichiometric CeO2-δ oxides on the physico-chemical properties of conducting polyaniline/CeO2 composites" Electrochimica Acta, 306 (2019):506-515,
https://doi.org/10.1016/j.electacta.2019.03.135 .
4
2
4

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

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

(2019)

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

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

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

(2019)

TY  - JOUR
AU  - Zdolšek, Nikola
AU  - Rocha, Raquel P.
AU  - Krstić, Jugoslav B.
AU  - Trtić-Petrović, Tatjana M.
AU  - Šljukić, Biljana
AU  - Figueiredo, Jose L.
AU  - Vujković, Milica
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0013468618328482
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8023
AB  - This work shows the potential application of carbon materials prepared by three different ionic liquid-based methods, using 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3], for electrochemical supercapacitors. The effects of [bmim][MeSO3] on morphology, texture and surface chemistry of prepared materials has been explored by SEM/TEM, N2/CO2 adsorption measurements and XPS. The results indicate the possibility of synthesis of carbon materials with tunable physicochemical properties using ionic liquid based methods. The charge storage behavior of all materials was studied in three different pH aqueous electrolytes. The pseudocapacitive and double layer contributions were estimated and discussed from the aspect of the textural changes and the changes of the chemical composition of surface functional groups containing heteroatoms. C[dbnd]O type functional groups, with the contribution of COOH groups, were found to be responsible for a different amount of charge, which could be stored in alkaline and acidic electrolytic solution. The material prepared by direct carbonization of [bmim][MeSO3], showed the best electrochemical performance in alkaline electrolyte with a capacitance of 187 F g−1 at 5 mV s−1 (or 148 F g−1 at 1 A g−1), due to the contribution of both electric-double layer capacitance and pseudocapacitance which arises from oxygen, nitrogen and sulfur functional groups. © 2018 Elsevier Ltd
T2  - Electrochimica Acta
T1  - Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer
VL  - 298
SP  - 541
EP  - 551
DO  - 10.1016/j.electacta.2018.12.129
ER  - 
@article{
author = "Zdolšek, Nikola and Rocha, Raquel P. and Krstić, Jugoslav B. and Trtić-Petrović, Tatjana M. and Šljukić, Biljana and Figueiredo, Jose L. and Vujković, Milica",
year = "2019",
url = "https://linkinghub.elsevier.com/retrieve/pii/S0013468618328482, http://vinar.vin.bg.ac.rs/handle/123456789/8023",
abstract = "This work shows the potential application of carbon materials prepared by three different ionic liquid-based methods, using 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3], for electrochemical supercapacitors. The effects of [bmim][MeSO3] on morphology, texture and surface chemistry of prepared materials has been explored by SEM/TEM, N2/CO2 adsorption measurements and XPS. The results indicate the possibility of synthesis of carbon materials with tunable physicochemical properties using ionic liquid based methods. The charge storage behavior of all materials was studied in three different pH aqueous electrolytes. The pseudocapacitive and double layer contributions were estimated and discussed from the aspect of the textural changes and the changes of the chemical composition of surface functional groups containing heteroatoms. C[dbnd]O type functional groups, with the contribution of COOH groups, were found to be responsible for a different amount of charge, which could be stored in alkaline and acidic electrolytic solution. The material prepared by direct carbonization of [bmim][MeSO3], showed the best electrochemical performance in alkaline electrolyte with a capacitance of 187 F g−1 at 5 mV s−1 (or 148 F g−1 at 1 A g−1), due to the contribution of both electric-double layer capacitance and pseudocapacitance which arises from oxygen, nitrogen and sulfur functional groups. © 2018 Elsevier Ltd",
journal = "Electrochimica Acta",
title = "Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer",
volume = "298",
pages = "541-551",
doi = "10.1016/j.electacta.2018.12.129"
}
Zdolšek, N., Rocha, R. P., Krstić, J. B., Trtić-Petrović, T. M., Šljukić, B., Figueiredo, J. L.,& Vujković, M. (2019). Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer.
Electrochimica Acta, 298, 541-551.
https://doi.org/10.1016/j.electacta.2018.12.129
Zdolšek N, Rocha RP, Krstić JB, Trtić-Petrović TM, Šljukić B, Figueiredo JL, Vujković M. Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer. Electrochimica Acta. 2019;298:541-551
Zdolšek Nikola, Rocha Raquel P., Krstić Jugoslav B., Trtić-Petrović Tatjana M., Šljukić Biljana, Figueiredo Jose L., Vujković Milica, "Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer" Electrochimica Acta, 298 (2019):541-551,
https://doi.org/10.1016/j.electacta.2018.12.129 .
15
13
14

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

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

(2019)

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

Mild electrochemical oxidation of zeolite templated carbon in acidic solutions, as a way to boost its charge storage properties in alkaline solutions

Vujković, Milica; Bajuk-Bogdanović, Danica V.; Matović, Ljiljana; Stojmenović, Marija; Mentus, Slavko V.

(2018)

TY  - JOUR
AU  - Vujković, Milica
AU  - Bajuk-Bogdanović, Danica V.
AU  - Matović, Ljiljana
AU  - Stojmenović, Marija
AU  - Mentus, Slavko V.
PY  - 2018
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0008622318307036
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7872
AB  - Coulombic capacity of zeolite-templated carbon (ZTC) measured in alkaline solution was roughly doubled by a previous potentiodynamic treatment in sulfuric acidic solution. In order to explain the reasons of this capacity improvement, the changes in chemical composition of ZTC surface during its pretreatment in sulfuric acid either by simple immersion, or by potentiodynamic polarization, and during subsequent potentiodynamic polarization in KOH solutions, were studied by means of TG/DTA, FTIR spectroscopy and Raman spectroscopy. The results of this study open some novel insights in understanding of very peculiar carbon electrochemistry. The observed changes in surface chemistry include i) fast adsorption of H2O and formation of OH− and epoxide groups on immersion in sulfuric acid, ii) the multiplication of concentration of H2O/OH− and epoxide groups during potentiodynamic cycling in sulfuric acid and iii) the ring-opening of epoxide groups (formed during potentiodynamic cycling in acidic solution) upon its potentiodynamic cycling in alkaline solution, according to a SN2 type mechanism, which results in the formation of aromatic OH-containing diol compounds. © 2018 Elsevier Ltd
T2  - Carbon
T1  - Mild electrochemical oxidation of zeolite templated carbon in acidic solutions, as a way to boost its charge storage properties in alkaline solutions
VL  - 138
SP  - 369
EP  - 378
DO  - 10.1016/j.carbon.2018.07.053
ER  - 
@article{
author = "Vujković, Milica and Bajuk-Bogdanović, Danica V. and Matović, Ljiljana and Stojmenović, Marija and Mentus, Slavko V.",
year = "2018",
url = "https://linkinghub.elsevier.com/retrieve/pii/S0008622318307036, http://vinar.vin.bg.ac.rs/handle/123456789/7872",
abstract = "Coulombic capacity of zeolite-templated carbon (ZTC) measured in alkaline solution was roughly doubled by a previous potentiodynamic treatment in sulfuric acidic solution. In order to explain the reasons of this capacity improvement, the changes in chemical composition of ZTC surface during its pretreatment in sulfuric acid either by simple immersion, or by potentiodynamic polarization, and during subsequent potentiodynamic polarization in KOH solutions, were studied by means of TG/DTA, FTIR spectroscopy and Raman spectroscopy. The results of this study open some novel insights in understanding of very peculiar carbon electrochemistry. The observed changes in surface chemistry include i) fast adsorption of H2O and formation of OH− and epoxide groups on immersion in sulfuric acid, ii) the multiplication of concentration of H2O/OH− and epoxide groups during potentiodynamic cycling in sulfuric acid and iii) the ring-opening of epoxide groups (formed during potentiodynamic cycling in acidic solution) upon its potentiodynamic cycling in alkaline solution, according to a SN2 type mechanism, which results in the formation of aromatic OH-containing diol compounds. © 2018 Elsevier Ltd",
journal = "Carbon",
title = "Mild electrochemical oxidation of zeolite templated carbon in acidic solutions, as a way to boost its charge storage properties in alkaline solutions",
volume = "138",
pages = "369-378",
doi = "10.1016/j.carbon.2018.07.053"
}
Vujković, M., Bajuk-Bogdanović, D. V., Matović, L., Stojmenović, M.,& Mentus, S. V. (2018). Mild electrochemical oxidation of zeolite templated carbon in acidic solutions, as a way to boost its charge storage properties in alkaline solutions.
Carbon, 138, 369-378.
https://doi.org/10.1016/j.carbon.2018.07.053
Vujković M, Bajuk-Bogdanović DV, Matović L, Stojmenović M, Mentus SV. Mild electrochemical oxidation of zeolite templated carbon in acidic solutions, as a way to boost its charge storage properties in alkaline solutions. Carbon. 2018;138:369-378
Vujković Milica, Bajuk-Bogdanović Danica V., Matović Ljiljana, Stojmenović Marija, Mentus Slavko V., "Mild electrochemical oxidation of zeolite templated carbon in acidic solutions, as a way to boost its charge storage properties in alkaline solutions" Carbon, 138 (2018):369-378,
https://doi.org/10.1016/j.carbon.2018.07.053 .
7
7
7

The synthesis of Li(Co-Mn-Ni)O-2 cathode material from spent-Li ion batteries and the proof of its functionality in aqueous lithium and sodium electrolytic solutions

Senćanski, Jelena; Bajuk-Bogdanović, Danica V.; Majstorović, Divna M.; Tchernychova, Elena; Papan, Jelena; Vujković, Milica

(2017)

TY  - JOUR
AU  - Senćanski, Jelena
AU  - Bajuk-Bogdanović, Danica V.
AU  - Majstorović, Divna M.
AU  - Tchernychova, Elena
AU  - Papan, Jelena
AU  - Vujković, Milica
PY  - 2017
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/1457
AB  - Several spent Li-ion batteries were manually dismantled and their components were uncurled and separated. The chemical composition of each batterys component was determined by atomic absorption spectroscopy. Among several ways to separate cathode material from the collector, the alkali dissolution treatment was selected as the most effective one. After both complete separation and acid leaching steps, the co-precipitation method, followed by a thermal treatment (700 degrees C or 850 degrees C), was used to resynthesize cathode material LiCo0.415Mn0.435Ni0.15O2. Its structure and morphology were characterized by XRD, Raman spectroscopy and SEM-EDS methods. The electrochemical behavior of recycled cathode materials was examined by cyclic voltammetry and chronopotentiometry in both LiNO3 and NaNO3 aqueous solutions. High sodium storage capacity, amounting to 93 mAh g(-1), was measured galvanostatically at a relatively high current of 100 mA g(-1). Initial lithium intercalation capacity of 64 mAh was determined potentiodynamically at very high scan rate of 20 mV s(-1) (similar to 40 C). Somewhat lower initial capacity of 30 mAh g(-1), but much lower capacity fade on cycling, was found for sodium intercalation at the same scan rate. The differences in the Li and Na charge storage capability were explained in terms of ion rearrangement during charging/discharging processes. (C) 2017 Elsevier B.V. All rights reserved.
T2  - Journal of Power Sources
T1  - The synthesis of Li(Co-Mn-Ni)O-2 cathode material from spent-Li ion batteries and the proof of its functionality in aqueous lithium and sodium electrolytic solutions
VL  - 342
SP  - 690
EP  - 703
DO  - 10.1016/j.jpowsour.2016.12.115
ER  - 
@article{
author = "Senćanski, Jelena and Bajuk-Bogdanović, Danica V. and Majstorović, Divna M. and Tchernychova, Elena and Papan, Jelena and Vujković, Milica",
year = "2017",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/1457",
abstract = "Several spent Li-ion batteries were manually dismantled and their components were uncurled and separated. The chemical composition of each batterys component was determined by atomic absorption spectroscopy. Among several ways to separate cathode material from the collector, the alkali dissolution treatment was selected as the most effective one. After both complete separation and acid leaching steps, the co-precipitation method, followed by a thermal treatment (700 degrees C or 850 degrees C), was used to resynthesize cathode material LiCo0.415Mn0.435Ni0.15O2. Its structure and morphology were characterized by XRD, Raman spectroscopy and SEM-EDS methods. The electrochemical behavior of recycled cathode materials was examined by cyclic voltammetry and chronopotentiometry in both LiNO3 and NaNO3 aqueous solutions. High sodium storage capacity, amounting to 93 mAh g(-1), was measured galvanostatically at a relatively high current of 100 mA g(-1). Initial lithium intercalation capacity of 64 mAh was determined potentiodynamically at very high scan rate of 20 mV s(-1) (similar to 40 C). Somewhat lower initial capacity of 30 mAh g(-1), but much lower capacity fade on cycling, was found for sodium intercalation at the same scan rate. The differences in the Li and Na charge storage capability were explained in terms of ion rearrangement during charging/discharging processes. (C) 2017 Elsevier B.V. All rights reserved.",
journal = "Journal of Power Sources",
title = "The synthesis of Li(Co-Mn-Ni)O-2 cathode material from spent-Li ion batteries and the proof of its functionality in aqueous lithium and sodium electrolytic solutions",
volume = "342",
pages = "690-703",
doi = "10.1016/j.jpowsour.2016.12.115"
}
Senćanski, J., Bajuk-Bogdanović, D. V., Majstorović, D. M., Tchernychova, E., Papan, J.,& Vujković, M. (2017). The synthesis of Li(Co-Mn-Ni)O-2 cathode material from spent-Li ion batteries and the proof of its functionality in aqueous lithium and sodium electrolytic solutions.
Journal of Power Sources, 342, 690-703.
https://doi.org/10.1016/j.jpowsour.2016.12.115
Senćanski J, Bajuk-Bogdanović DV, Majstorović DM, Tchernychova E, Papan J, Vujković M. The synthesis of Li(Co-Mn-Ni)O-2 cathode material from spent-Li ion batteries and the proof of its functionality in aqueous lithium and sodium electrolytic solutions. Journal of Power Sources. 2017;342:690-703
Senćanski Jelena, Bajuk-Bogdanović Danica V., Majstorović Divna M., Tchernychova Elena, Papan Jelena, Vujković Milica, "The synthesis of Li(Co-Mn-Ni)O-2 cathode material from spent-Li ion batteries and the proof of its functionality in aqueous lithium and sodium electrolytic solutions" Journal of Power Sources, 342 (2017):690-703,
https://doi.org/10.1016/j.jpowsour.2016.12.115 .
30
22
34

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

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

(2017)

TY  - JOUR
AU  - Vujković, Milica
AU  - Matović, Ljiljana
AU  - Krstić, Jugoslav B.
AU  - Stojmenović, Marija
AU  - Đukić, Anđelka B.
AU  - Babić, Biljana M.
AU  - Mentus, Slavko V.
PY  - 2017
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/1661
AB  - The activated carbon cloth (ACC), obtained by chemical/physical activation of carbonized rayon fibers, was grinded in a ball mill and studied from the aspect of double layer capacitance. The changes in pore structure, morphology and acid/basic properties caused by ball milling were studied by means of N-2 adsorption/desorption, Fourier-transformed infrared spectrometry, Boehms titration and Scanning Electron Microscopy. Both potentiodynamic and galvanostatic cycling were used to evaluate the double layer capacitance in three alkaline, acidic and neutral aqueous solutions (KOH, H2SO4 and Na2SO4). While double layer capacitance of original ACC was found to be negligible, ball milled material (ACCm) displayed capacitance in the range of supercapacitors. In order to explain this huge capacitance improvement, we found that ball milling substantially increased the concentration of lactone, phenolic and quinone groups on the surface. We suggest that these groups, through improved hydrophilicity, enable faster ion diffusion into carbon micropores. The energy density stored by double layer was highest in neutral sodium sulphate solution. Namely, operational voltage of similar to 2 V and double layer capacitance of 220 F g(-1) at 1A g(-1), enable the energy density of ACCm/Na2SO4/ACCm capacitor of 31.7 Wh kg(-1) at 2000 W kg(-1), much higher than that of commercial EDLC carbon capacitors. According to the here presented literature survey in a tabular form, the energy density of the studied sample is also higher from that of numerous thus far published aqueous carbon capacitors. (C) 2017 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions
VL  - 245
SP  - 796
EP  - 806
DO  - 10.1016/j.electacta.2017.06.018
ER  - 
@article{
author = "Vujković, Milica and Matović, Ljiljana and Krstić, Jugoslav B. and Stojmenović, Marija and Đukić, Anđelka B. and Babić, Biljana M. and Mentus, Slavko V.",
year = "2017",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/1661",
abstract = "The activated carbon cloth (ACC), obtained by chemical/physical activation of carbonized rayon fibers, was grinded in a ball mill and studied from the aspect of double layer capacitance. The changes in pore structure, morphology and acid/basic properties caused by ball milling were studied by means of N-2 adsorption/desorption, Fourier-transformed infrared spectrometry, Boehms titration and Scanning Electron Microscopy. Both potentiodynamic and galvanostatic cycling were used to evaluate the double layer capacitance in three alkaline, acidic and neutral aqueous solutions (KOH, H2SO4 and Na2SO4). While double layer capacitance of original ACC was found to be negligible, ball milled material (ACCm) displayed capacitance in the range of supercapacitors. In order to explain this huge capacitance improvement, we found that ball milling substantially increased the concentration of lactone, phenolic and quinone groups on the surface. We suggest that these groups, through improved hydrophilicity, enable faster ion diffusion into carbon micropores. The energy density stored by double layer was highest in neutral sodium sulphate solution. Namely, operational voltage of similar to 2 V and double layer capacitance of 220 F g(-1) at 1A g(-1), enable the energy density of ACCm/Na2SO4/ACCm capacitor of 31.7 Wh kg(-1) at 2000 W kg(-1), much higher than that of commercial EDLC carbon capacitors. According to the here presented literature survey in a tabular form, the energy density of the studied sample is also higher from that of numerous thus far published aqueous carbon capacitors. (C) 2017 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions",
volume = "245",
pages = "796-806",
doi = "10.1016/j.electacta.2017.06.018"
}
Vujković, M., Matović, L., Krstić, J. B., Stojmenović, M., Đukić, A. B., Babić, B. M.,& Mentus, S. V. (2017). Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions.
Electrochimica Acta, 245, 796-806.
https://doi.org/10.1016/j.electacta.2017.06.018
Vujković M, Matović L, Krstić JB, Stojmenović M, Đukić AB, Babić BM, Mentus SV. Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions. Electrochimica Acta. 2017;245:796-806
Vujković Milica, Matović Ljiljana, Krstić Jugoslav B., Stojmenović Marija, Đukić Anđelka B., Babić Biljana M., Mentus Slavko V., "Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions" Electrochimica Acta, 245 (2017):796-806,
https://doi.org/10.1016/j.electacta.2017.06.018 .
17
16
16

Effect of thermal treatment on the charge storage properties of graphene oxide/12-tungstophosphoric acid nanocomposite

Jovanović, Zoran M.; Holclajtner-Antunović, Ivanka D.; Bajuk-Bogdanović, Danica V.; Jovanović, Sonja; Mravik, Željko; Vujković, Milica

(2017)

TY  - JOUR
AU  - Jovanović, Zoran M.
AU  - Holclajtner-Antunović, Ivanka D.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Jovanović, Sonja
AU  - Mravik, Željko
AU  - Vujković, Milica
PY  - 2017
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/1737
AB  - The influence of thermal treatment in an inert atmosphere on the charge storage properties of graphene oxide (GO)/12-tungstophosphoric acid (WPA) nanocomposite was examined. The transmission electron microscopy analysis revealed high dispersion of WPA on GO matrix, while the surface analysis showed thermal activation of structural changes of WPA and desorption of oxygen functional groups from GO and GO/WPA nanocomposite. Initial GO/WPA nanocomposite had approximately two times higher capacitance compared to initial GO. The thermal treatment of initial GO and GO/WPA to 500 degrees C induced twofold increase of capacitance of GO and 40% increase of GO/WPA, accompanied with significant increase of operating voltage compared to GO (for 300 mV). Above 500 degrees C, a decrease of capacitance of both GO and GO/WPA was observed. The results suggest that understanding of structural changes of components and their interaction is crucial for improvement of electrochemical properties of considered composite.
T2  - Electrochemistry Communications
T1  - Effect of thermal treatment on the charge storage properties of graphene oxide/12-tungstophosphoric acid nanocomposite
VL  - 83
SP  - 36
EP  - 40
DO  - 10.1016/j.elecom.2017.08.017
ER  - 
@article{
author = "Jovanović, Zoran M. and Holclajtner-Antunović, Ivanka D. and Bajuk-Bogdanović, Danica V. and Jovanović, Sonja and Mravik, Željko and Vujković, Milica",
year = "2017",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/1737",
abstract = "The influence of thermal treatment in an inert atmosphere on the charge storage properties of graphene oxide (GO)/12-tungstophosphoric acid (WPA) nanocomposite was examined. The transmission electron microscopy analysis revealed high dispersion of WPA on GO matrix, while the surface analysis showed thermal activation of structural changes of WPA and desorption of oxygen functional groups from GO and GO/WPA nanocomposite. Initial GO/WPA nanocomposite had approximately two times higher capacitance compared to initial GO. The thermal treatment of initial GO and GO/WPA to 500 degrees C induced twofold increase of capacitance of GO and 40% increase of GO/WPA, accompanied with significant increase of operating voltage compared to GO (for 300 mV). Above 500 degrees C, a decrease of capacitance of both GO and GO/WPA was observed. The results suggest that understanding of structural changes of components and their interaction is crucial for improvement of electrochemical properties of considered composite.",
journal = "Electrochemistry Communications",
title = "Effect of thermal treatment on the charge storage properties of graphene oxide/12-tungstophosphoric acid nanocomposite",
volume = "83",
pages = "36-40",
doi = "10.1016/j.elecom.2017.08.017"
}
Jovanović, Z. M., Holclajtner-Antunović, I. D., Bajuk-Bogdanović, D. V., Jovanović, S., Mravik, Ž.,& Vujković, M. (2017). Effect of thermal treatment on the charge storage properties of graphene oxide/12-tungstophosphoric acid nanocomposite.
Electrochemistry Communications, 83, 36-40.
https://doi.org/10.1016/j.elecom.2017.08.017
Jovanović ZM, Holclajtner-Antunović ID, Bajuk-Bogdanović DV, Jovanović S, Mravik Ž, Vujković M. Effect of thermal treatment on the charge storage properties of graphene oxide/12-tungstophosphoric acid nanocomposite. Electrochemistry Communications. 2017;83:36-40
Jovanović Zoran M., Holclajtner-Antunović Ivanka D., Bajuk-Bogdanović Danica V., Jovanović Sonja, Mravik Željko, Vujković Milica, "Effect of thermal treatment on the charge storage properties of graphene oxide/12-tungstophosphoric acid nanocomposite" Electrochemistry Communications, 83 (2017):36-40,
https://doi.org/10.1016/j.elecom.2017.08.017 .
9
8
8

The role of surface chemistry in the charge storage properties of graphene oxide

Jovanović, Zoran M.; Bajuk-Bogdanović, Danica V.; Jovanović, Sonja; Mravik, Željko; Kovač, Janez; Holclajtner-Antunović, Ivanka D.; Vujković, Milica

(2017)

TY  - JOUR
AU  - Jovanović, Zoran M.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Jovanović, Sonja
AU  - Mravik, Željko
AU  - Kovač, Janez
AU  - Holclajtner-Antunović, Ivanka D.
AU  - Vujković, Milica
PY  - 2017
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/1879
AB  - In the present study we have evaluated the contribution of particular oxygen functional groups in the charge storage properties of graphene oxide (GO). This was achieved by a gradual thermal reduction of GO in an inert atmosphere (up to 800 degrees C) and thorough examination of functional groups which remained after each de-functionalization step. After identification of functional groups, the character of additional cyclovoltammetric peak, less pronounced than the main redox quinone/hydroquinone pair, and overall charge storage properties of GO were discussed from the perspective of different thermal stability of its surface groups. The results indicated three-stage deoxidation process of GO, each comprising of specific surface chemistry, structural changes and electrochemical behavior. The low capacitance, similar to 50 F g(-1), at T LT = 300 degrees C was attributed to the presence of epoxy and carboxyl groups. The highest capacitance (120-130 F g(-1)) was observed in the case of GO reduced at 400 and 500 degrees C, which we attributed to positive effects of phenol and carbonyl/quinone groups, while at high temperatures (T GT = 600 degrees C, similar to 30 F g(-1)) the extensive desorption of functional groups and structural changes were emphasized as the main reasons for additional decrease of capacitance. Our results highlight the cases where the duality of interpretation of surface functional groups is likely to happen and indicate that not all functional groups play a positive role in charge storage behavior of graphene oxide. (C) 2017 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - The role of surface chemistry in the charge storage properties of graphene oxide
VL  - 258
SP  - 1228
EP  - 1243
DO  - 10.1016/j.electacta.2017.11.178
ER  - 
@article{
author = "Jovanović, Zoran M. and Bajuk-Bogdanović, Danica V. and Jovanović, Sonja and Mravik, Željko and Kovač, Janez and Holclajtner-Antunović, Ivanka D. and Vujković, Milica",
year = "2017",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/1879",
abstract = "In the present study we have evaluated the contribution of particular oxygen functional groups in the charge storage properties of graphene oxide (GO). This was achieved by a gradual thermal reduction of GO in an inert atmosphere (up to 800 degrees C) and thorough examination of functional groups which remained after each de-functionalization step. After identification of functional groups, the character of additional cyclovoltammetric peak, less pronounced than the main redox quinone/hydroquinone pair, and overall charge storage properties of GO were discussed from the perspective of different thermal stability of its surface groups. The results indicated three-stage deoxidation process of GO, each comprising of specific surface chemistry, structural changes and electrochemical behavior. The low capacitance, similar to 50 F g(-1), at T LT = 300 degrees C was attributed to the presence of epoxy and carboxyl groups. The highest capacitance (120-130 F g(-1)) was observed in the case of GO reduced at 400 and 500 degrees C, which we attributed to positive effects of phenol and carbonyl/quinone groups, while at high temperatures (T GT = 600 degrees C, similar to 30 F g(-1)) the extensive desorption of functional groups and structural changes were emphasized as the main reasons for additional decrease of capacitance. Our results highlight the cases where the duality of interpretation of surface functional groups is likely to happen and indicate that not all functional groups play a positive role in charge storage behavior of graphene oxide. (C) 2017 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "The role of surface chemistry in the charge storage properties of graphene oxide",
volume = "258",
pages = "1228-1243",
doi = "10.1016/j.electacta.2017.11.178"
}
Jovanović, Z. M., Bajuk-Bogdanović, D. V., Jovanović, S., Mravik, Ž., Kovač, J., Holclajtner-Antunović, I. D.,& Vujković, M. (2017). The role of surface chemistry in the charge storage properties of graphene oxide.
Electrochimica Acta, 258, 1228-1243.
https://doi.org/10.1016/j.electacta.2017.11.178
Jovanović ZM, Bajuk-Bogdanović DV, Jovanović S, Mravik Ž, Kovač J, Holclajtner-Antunović ID, Vujković M. The role of surface chemistry in the charge storage properties of graphene oxide. Electrochimica Acta. 2017;258:1228-1243
Jovanović Zoran M., Bajuk-Bogdanović Danica V., Jovanović Sonja, Mravik Željko, Kovač Janez, Holclajtner-Antunović Ivanka D., Vujković Milica, "The role of surface chemistry in the charge storage properties of graphene oxide" Electrochimica Acta, 258 (2017):1228-1243,
https://doi.org/10.1016/j.electacta.2017.11.178 .
18
15
17

Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices

Vujković, Milica; Vidoeski, Bojan; Jovanović, Svetlana P.; Bajuk-Bogdanović, Danica V.; Budimir, Milica; Marković, Zoran M.; Pavlović, Vladimir B.; Todorović-Marković, Biljana; Holclajtner-Antunović, Ivanka D.

(2016)

TY  - JOUR
AU  - Vujković, Milica
AU  - Vidoeski, Bojan
AU  - Jovanović, Svetlana P.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Budimir, Milica
AU  - Marković, Zoran M.
AU  - Pavlović, Vladimir B.
AU  - Todorović-Marković, Biljana
AU  - Holclajtner-Antunović, Ivanka D.
PY  - 2016
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/1274
AB  - A novel electrochemically exfoliated graphene-molybdophosphoric acid nanohybride (EG-MoPA) was prepared via a simple method. Both scanning electron (SEM) and atomic force microscopy (AFM) results show that MoPA clusters are attached to the surfaces of graphene sheets. By changing the mass ratio of EG-MoPA, the morphology of nanohybrid itself can be significantly modulated, from mostly flat graphene like structure at low amount of MoPA to very uneven, wavy surfaces when MoPA is present in higher concentration. The Raman and Fourier transform infra red (FTIR) spectra in conjunction with electrochemical results indicate that strong interaction exists between the components of nanohybride based on charge transfer and electrostatic interaction of graphene sheets and MoPA. The electrochemical performances are improved by synergetic effect of reversible redox properties of MoPA and the double layer capacitance of a high-surface area of the obtained nanohybrides. The higher current capability of EG was achieved by anchoring the small MoPA concentration on the graphene support. The strong bonding of EG with the MoPA prevents acid to dissolve in the electrolyte upon cycling, enabling the stable capacitance behaviour of the low-doped EG sample. The capacitance for the EG doped with the high amount of MoPA was found to be much larger than for EG. However, the obtained capacitance decreases at the beginning of cycling due to the dissolution of excessive amount of surface MoPA, weakly bonded to the graphene support. (C) 2016 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices
VL  - 217
SP  - 34
EP  - 46
DO  - 10.1016/j.electacta.2016.09.067
ER  - 
@article{
author = "Vujković, Milica and Vidoeski, Bojan and Jovanović, Svetlana P. and Bajuk-Bogdanović, Danica V. and Budimir, Milica and Marković, Zoran M. and Pavlović, Vladimir B. and Todorović-Marković, Biljana and Holclajtner-Antunović, Ivanka D.",
year = "2016",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/1274",
abstract = "A novel electrochemically exfoliated graphene-molybdophosphoric acid nanohybride (EG-MoPA) was prepared via a simple method. Both scanning electron (SEM) and atomic force microscopy (AFM) results show that MoPA clusters are attached to the surfaces of graphene sheets. By changing the mass ratio of EG-MoPA, the morphology of nanohybrid itself can be significantly modulated, from mostly flat graphene like structure at low amount of MoPA to very uneven, wavy surfaces when MoPA is present in higher concentration. The Raman and Fourier transform infra red (FTIR) spectra in conjunction with electrochemical results indicate that strong interaction exists between the components of nanohybride based on charge transfer and electrostatic interaction of graphene sheets and MoPA. The electrochemical performances are improved by synergetic effect of reversible redox properties of MoPA and the double layer capacitance of a high-surface area of the obtained nanohybrides. The higher current capability of EG was achieved by anchoring the small MoPA concentration on the graphene support. The strong bonding of EG with the MoPA prevents acid to dissolve in the electrolyte upon cycling, enabling the stable capacitance behaviour of the low-doped EG sample. The capacitance for the EG doped with the high amount of MoPA was found to be much larger than for EG. However, the obtained capacitance decreases at the beginning of cycling due to the dissolution of excessive amount of surface MoPA, weakly bonded to the graphene support. (C) 2016 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices",
volume = "217",
pages = "34-46",
doi = "10.1016/j.electacta.2016.09.067"
}
Vujković, M., Vidoeski, B., Jovanović, S. P., Bajuk-Bogdanović, D. V., Budimir, M., Marković, Z. M., Pavlović, V. B., Todorović-Marković, B.,& Holclajtner-Antunović, I. D. (2016). Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices.
Electrochimica Acta, 217, 34-46.
https://doi.org/10.1016/j.electacta.2016.09.067
Vujković M, Vidoeski B, Jovanović SP, Bajuk-Bogdanović DV, Budimir M, Marković ZM, Pavlović VB, Todorović-Marković B, Holclajtner-Antunović ID. Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices. Electrochimica Acta. 2016;217:34-46
Vujković Milica, Vidoeski Bojan, Jovanović Svetlana P., Bajuk-Bogdanović Danica V., Budimir Milica, Marković Zoran M., Pavlović Vladimir B., Todorović-Marković Biljana, Holclajtner-Antunović Ivanka D., "Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices" Electrochimica Acta, 217 (2016):34-46,
https://doi.org/10.1016/j.electacta.2016.09.067 .
5
5
5

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

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

(2016)

TY  - JOUR
AU  - Dodevski, Vladimir
AU  - Stojmenović, Marija
AU  - Vujković, Milica
AU  - Krstić, Jugoslav B.
AU  - Krstić, Sanja S.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Kuzmanović, Bojana
AU  - Kaluđerović, Branka V.
AU  - Mentus, Slavko V.
PY  - 2016
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/1396
AB  - Activated carbon was prepared using plane tree seed as a cheap and renewable raw material. The samples were prepared by carbonization under N-2 atmosphere up to 850 degrees C, and activation in CO2 atmosphere at different both temperatures (750 and 850 degrees C) and times of activation (0.3,1 and 2 h). The influence of activation parameters on physicochemical properties was studied by XRPD, Raman spectroscopy, FTIR, N-2 physisorption, SEM and electrochemical methods. The pore structure was correlated to the specific capacitance and the amount of hydrogen stored, in alkaline, neutral and acidic electrolyte solution. The relationship of asymmetrical shape of CV curves with the porosity of samples has served to better understand some unclear issues related to the complex mechanism of charge storage. The sample activated at 850 degrees C for 2 h displayed the best behavior. At a high scan rate of 300 mV s(-1), its capacitance, amounted to similar to 26.8 mu F cm(-2) 19.69 mu F cm(-2) and 25.8 mu Fcm(-2) in KOH, Na2SO4, and H2SO4 solutions, respectively. (C) 2016 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed
VL  - 222
SP  - 156
EP  - 171
DO  - 10.1016/j.electacta.2016.10.182
ER  - 
@article{
author = "Dodevski, Vladimir and Stojmenović, Marija and Vujković, Milica and Krstić, Jugoslav B. and Krstić, Sanja S. and Bajuk-Bogdanović, Danica V. and Kuzmanović, Bojana and Kaluđerović, Branka V. and Mentus, Slavko V.",
year = "2016",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/1396",
abstract = "Activated carbon was prepared using plane tree seed as a cheap and renewable raw material. The samples were prepared by carbonization under N-2 atmosphere up to 850 degrees C, and activation in CO2 atmosphere at different both temperatures (750 and 850 degrees C) and times of activation (0.3,1 and 2 h). The influence of activation parameters on physicochemical properties was studied by XRPD, Raman spectroscopy, FTIR, N-2 physisorption, SEM and electrochemical methods. The pore structure was correlated to the specific capacitance and the amount of hydrogen stored, in alkaline, neutral and acidic electrolyte solution. The relationship of asymmetrical shape of CV curves with the porosity of samples has served to better understand some unclear issues related to the complex mechanism of charge storage. The sample activated at 850 degrees C for 2 h displayed the best behavior. At a high scan rate of 300 mV s(-1), its capacitance, amounted to similar to 26.8 mu F cm(-2) 19.69 mu F cm(-2) and 25.8 mu Fcm(-2) in KOH, Na2SO4, and H2SO4 solutions, respectively. (C) 2016 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed",
volume = "222",
pages = "156-171",
doi = "10.1016/j.electacta.2016.10.182"
}
Dodevski, V., Stojmenović, M., Vujković, M., Krstić, J. B., Krstić, S. S., Bajuk-Bogdanović, D. V., Kuzmanović, B., Kaluđerović, B. V.,& Mentus, S. V. (2016). Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed.
Electrochimica Acta, 222, 156-171.
https://doi.org/10.1016/j.electacta.2016.10.182
Dodevski V, Stojmenović M, Vujković M, Krstić JB, Krstić SS, Bajuk-Bogdanović DV, Kuzmanović B, Kaluđerović BV, Mentus SV. Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed. Electrochimica Acta. 2016;222:156-171
Dodevski Vladimir, Stojmenović Marija, Vujković Milica, Krstić Jugoslav B., Krstić Sanja S., Bajuk-Bogdanović Danica V., Kuzmanović Bojana, Kaluđerović Branka V., Mentus Slavko V., "Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed" Electrochimica Acta, 222 (2016):156-171,
https://doi.org/10.1016/j.electacta.2016.10.182 .
10
11
10

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

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

(2016)

TY  - JOUR
AU  - Stojmenović, Marija
AU  - Vujković, Milica
AU  - Matović, Ljiljana
AU  - Krstić, Jugoslav B.
AU  - Đukić, Anđelka B.
AU  - Dodevski, Vladimir
AU  - Živković, Sanja
AU  - Mentus, Slavko V.
PY  - 2016
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/1096
AB  - Microporous zeolite templated carbon (ZTC) was synthesized by impregnation method using zeolite Y (Na-form) as a template, and furfuryl alcohol as a carbon precursor. The characterization was carried out by X-ray diffractometry, Raman spectroscopy, scanning electron microscopy, nitrogen physisorption, elemental analysis and electrochemical methods. Physisorption measurements evidenced high micro pore volume of obtained material (similar to 0.43 cm(3) g(-1)). The charge storage ability in aqueous KOH, H2SO4 and Na2SO4 solutions was systematically studied by cyclic voltammetry, galvanostatic charging/discharging and complex impedance measurements. Specific coulombic capacitance, the hydrogen storage, H-ZTC bonding and relaxation time of adsorption were found to be dependent on the type of electrolyte. Neutral Na2SO4 aqueous solution was found to be the best for supercapacitor application, thanks to: i) the highest available voltage window ii) lowest corrosion and iii) highest capacitance amounting to 123 F g(-1) at 1 A g(-1) (C) 2016 Elsevier Inc. All rights reserved.
T2  - Microporous and Mesoporous Materials
T1  - Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template
VL  - 228
SP  - 94
EP  - 106
DO  - 10.1016/j.micromeso.2016.03.029
ER  - 
@article{
author = "Stojmenović, Marija and Vujković, Milica and Matović, Ljiljana and Krstić, Jugoslav B. and Đukić, Anđelka B. and Dodevski, Vladimir and Živković, Sanja and Mentus, Slavko V.",
year = "2016",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/1096",
abstract = "Microporous zeolite templated carbon (ZTC) was synthesized by impregnation method using zeolite Y (Na-form) as a template, and furfuryl alcohol as a carbon precursor. The characterization was carried out by X-ray diffractometry, Raman spectroscopy, scanning electron microscopy, nitrogen physisorption, elemental analysis and electrochemical methods. Physisorption measurements evidenced high micro pore volume of obtained material (similar to 0.43 cm(3) g(-1)). The charge storage ability in aqueous KOH, H2SO4 and Na2SO4 solutions was systematically studied by cyclic voltammetry, galvanostatic charging/discharging and complex impedance measurements. Specific coulombic capacitance, the hydrogen storage, H-ZTC bonding and relaxation time of adsorption were found to be dependent on the type of electrolyte. Neutral Na2SO4 aqueous solution was found to be the best for supercapacitor application, thanks to: i) the highest available voltage window ii) lowest corrosion and iii) highest capacitance amounting to 123 F g(-1) at 1 A g(-1) (C) 2016 Elsevier Inc. All rights reserved.",
journal = "Microporous and Mesoporous Materials",
title = "Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template",
volume = "228",
pages = "94-106",
doi = "10.1016/j.micromeso.2016.03.029"
}
Stojmenović, M., Vujković, M., Matović, L., Krstić, J. B., Đukić, A. B., Dodevski, V., Živković, S.,& Mentus, S. V. (2016). Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template.
Microporous and Mesoporous Materials, 228, 94-106.
https://doi.org/10.1016/j.micromeso.2016.03.029
Stojmenović M, Vujković M, Matović L, Krstić JB, Đukić AB, Dodevski V, Živković S, Mentus SV. Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template. Microporous and Mesoporous Materials. 2016;228:94-106
Stojmenović Marija, Vujković Milica, Matović Ljiljana, Krstić Jugoslav B., Đukić Anđelka B., Dodevski Vladimir, Živković Sanja, Mentus Slavko V., "Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template" Microporous and Mesoporous Materials, 228 (2016):94-106,
https://doi.org/10.1016/j.micromeso.2016.03.029 .
14
13
13

High-rate intercalation capability of NaTi2(PO4)(3)/C composite in aqueous lithium and sodium nitrate solutions

Vujković, Milica; Mitrić, Miodrag; Mentus, Slavko V.

(2015)

TY  - JOUR
AU  - Vujković, Milica
AU  - Mitrić, Miodrag
AU  - Mentus, Slavko V.
PY  - 2015
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/599
AB  - The nanodispersed NaTi2(PO4)(3)/C composite containing 20-25 wt.% of in-situ formed carbon, was synthesized by gel combustion procedure followed by a heat treatment at 650, 700 and 750 degrees C. The samples calcined at 700 and 750 degrees C displayed crystalline nasicon structure. They were subjected to the investigation of intercalation/deintercalation kinetics in aqueous NaNO3 and LiNO3 solutions, using cyclic voltammetry and galvanostatic charging/discharging measurements. As regards to the effect of electrolyte composition, the reactions were evidenced to be roughly twice faster in sodium nitrate than in lithium nitrate solution. Among the samples treated at 700 and 750 degrees C, better performance was evidenced for the sample treated at lower temperature. Coulombic capacity in NaNO3 solution at charging rate 1C amounted to similar to 70 mAh g(-1) and similar to 55 mAh g(-1) for the sample calcined at 700 and 750 degrees C, respectively, and displayed surprisingly slight dependence on charging rate up to even 100C. (c) 2015 Elsevier B.V. All rights reserved.
T2  - Journal of Power Sources
T1  - High-rate intercalation capability of NaTi2(PO4)(3)/C composite in aqueous lithium and sodium nitrate solutions
VL  - 288
SP  - 176
EP  - 186
DO  - 10.1016/j.jpowsour.2015.04.132
ER  - 
@article{
author = "Vujković, Milica and Mitrić, Miodrag and Mentus, Slavko V.",
year = "2015",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/599",
abstract = "The nanodispersed NaTi2(PO4)(3)/C composite containing 20-25 wt.% of in-situ formed carbon, was synthesized by gel combustion procedure followed by a heat treatment at 650, 700 and 750 degrees C. The samples calcined at 700 and 750 degrees C displayed crystalline nasicon structure. They were subjected to the investigation of intercalation/deintercalation kinetics in aqueous NaNO3 and LiNO3 solutions, using cyclic voltammetry and galvanostatic charging/discharging measurements. As regards to the effect of electrolyte composition, the reactions were evidenced to be roughly twice faster in sodium nitrate than in lithium nitrate solution. Among the samples treated at 700 and 750 degrees C, better performance was evidenced for the sample treated at lower temperature. Coulombic capacity in NaNO3 solution at charging rate 1C amounted to similar to 70 mAh g(-1) and similar to 55 mAh g(-1) for the sample calcined at 700 and 750 degrees C, respectively, and displayed surprisingly slight dependence on charging rate up to even 100C. (c) 2015 Elsevier B.V. All rights reserved.",
journal = "Journal of Power Sources",
title = "High-rate intercalation capability of NaTi2(PO4)(3)/C composite in aqueous lithium and sodium nitrate solutions",
volume = "288",
pages = "176-186",
doi = "10.1016/j.jpowsour.2015.04.132"
}
Vujković, M., Mitrić, M.,& Mentus, S. V. (2015). High-rate intercalation capability of NaTi2(PO4)(3)/C composite in aqueous lithium and sodium nitrate solutions.
Journal of Power Sources, 288, 176-186.
https://doi.org/10.1016/j.jpowsour.2015.04.132
Vujković M, Mitrić M, Mentus SV. High-rate intercalation capability of NaTi2(PO4)(3)/C composite in aqueous lithium and sodium nitrate solutions. Journal of Power Sources. 2015;288:176-186
Vujković Milica, Mitrić Miodrag, Mentus Slavko V., "High-rate intercalation capability of NaTi2(PO4)(3)/C composite in aqueous lithium and sodium nitrate solutions" Journal of Power Sources, 288 (2015):176-186,
https://doi.org/10.1016/j.jpowsour.2015.04.132 .
59
57
59

Versatile insertion capability of Na1.2V3O8 nanobelts in aqueous electrolyte solutions

Vujković, Milica; Šljukić-Paunković, Biljana; Stojković-Simatović, Ivana; Mitrić, Miodrag; Sequeira, C. A. C.; Mentus, Slavko V.

(2014)

TY  - JOUR
AU  - Vujković, Milica
AU  - Šljukić-Paunković, Biljana
AU  - Stojković-Simatović, Ivana
AU  - Mitrić, Miodrag
AU  - Sequeira, C. A. C.
AU  - Mentus, Slavko V.
PY  - 2014
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/285
AB  - Single phase nanobelt-like Na1.2V3O8 was synthesized by precipitation from aqueous solution of V2O5, H2O2 and NaOH, and subsequent annealing at 400 degrees C. The product was characterized by X-ray diffraction, scanning electron microscopy and transmission electron microscopy. As measured by both galvanostatic charging/discharging and cyclic voltammetry methods, in air-equilibrated equeous electrolyte solutions containing nitrates of lithium, sodium and magnesium, this compound displayed fast inter- calation/deintercalation reactions. The galvanostatic charging and discharging curves observed at rates ranging 500-7000 mA g(-1), did not display clear plateaus characteristic of phase changes. The discharging capacities were found to range 101-35, 55-17 and 67-22 mAh g(-1) for Li, Na and Mg intercalation, respectively. By cyclic voltammetry, for the sweep rates increasing in the range 5-400 mV s(-1) (roughly 9-700 C), the capacity was found to decrease within the limits 63-35 mAh g(-1) for Li+ intercalation, and 40 -11 mAh g(-1) for Na+ and Mg2+ intercalation, respectively. By analyzing the dependence log (current) versus log (sweep rate), the interval of potentials corresponding to preferably diffusion control of intercalation/deintercalation processes was determined. (C) 2014 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Versatile insertion capability of Na1.2V3O8 nanobelts in aqueous electrolyte solutions
VL  - 147
SP  - 167
EP  - 175
DO  - 10.1016/j.electacta.2014.08.137
ER  - 
@article{
author = "Vujković, Milica and Šljukić-Paunković, Biljana and Stojković-Simatović, Ivana and Mitrić, Miodrag and Sequeira, C. A. C. and Mentus, Slavko V.",
year = "2014",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/285",
abstract = "Single phase nanobelt-like Na1.2V3O8 was synthesized by precipitation from aqueous solution of V2O5, H2O2 and NaOH, and subsequent annealing at 400 degrees C. The product was characterized by X-ray diffraction, scanning electron microscopy and transmission electron microscopy. As measured by both galvanostatic charging/discharging and cyclic voltammetry methods, in air-equilibrated equeous electrolyte solutions containing nitrates of lithium, sodium and magnesium, this compound displayed fast inter- calation/deintercalation reactions. The galvanostatic charging and discharging curves observed at rates ranging 500-7000 mA g(-1), did not display clear plateaus characteristic of phase changes. The discharging capacities were found to range 101-35, 55-17 and 67-22 mAh g(-1) for Li, Na and Mg intercalation, respectively. By cyclic voltammetry, for the sweep rates increasing in the range 5-400 mV s(-1) (roughly 9-700 C), the capacity was found to decrease within the limits 63-35 mAh g(-1) for Li+ intercalation, and 40 -11 mAh g(-1) for Na+ and Mg2+ intercalation, respectively. By analyzing the dependence log (current) versus log (sweep rate), the interval of potentials corresponding to preferably diffusion control of intercalation/deintercalation processes was determined. (C) 2014 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Versatile insertion capability of Na1.2V3O8 nanobelts in aqueous electrolyte solutions",
volume = "147",
pages = "167-175",
doi = "10.1016/j.electacta.2014.08.137"
}
Vujković, M., Šljukić-Paunković, B., Stojković-Simatović, I., Mitrić, M., Sequeira, C. A. C.,& Mentus, S. V. (2014). Versatile insertion capability of Na1.2V3O8 nanobelts in aqueous electrolyte solutions.
Electrochimica Acta, 147, 167-175.
https://doi.org/10.1016/j.electacta.2014.08.137
Vujković M, Šljukić-Paunković B, Stojković-Simatović I, Mitrić M, Sequeira CAC, Mentus SV. Versatile insertion capability of Na1.2V3O8 nanobelts in aqueous electrolyte solutions. Electrochimica Acta. 2014;147:167-175
Vujković Milica, Šljukić-Paunković Biljana, Stojković-Simatović Ivana, Mitrić Miodrag, Sequeira C. A. C., Mentus Slavko V., "Versatile insertion capability of Na1.2V3O8 nanobelts in aqueous electrolyte solutions" Electrochimica Acta, 147 (2014):167-175,
https://doi.org/10.1016/j.electacta.2014.08.137 .
9
11
13

Hydrothermal synthesis of Li4Ti5O12/C nanostructured composites: Morphology and electrochemical performance

Vujković, Milica; Stojković, Ivana; Mitrić, Miodrag; Mentus, Slavko V.; Cvjeticanin, Nikola

(2013)

TY  - JOUR
AU  - Vujković, Milica
AU  - Stojković, Ivana
AU  - Mitrić, Miodrag
AU  - Mentus, Slavko V.
AU  - Cvjeticanin, Nikola
PY  - 2013
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/5356
AB  - Li4Ti5O12/C composites with low (3 wt.%) and high (33 wt.%) carbon black content as well as carbon-free Li4Ti5O12 were prepared in two steps under identical conditions: hydrothermal reaction at 130 degrees C and post-calcination at 400 degrees C. The X-ray diffraction experiments confirmed the spinet structure of Li4Ti5O12 in all samples. The carbon content altered significantly the morphology of obtained micro/nanoparticles. The Li4Ti5O12/C composite with the high carbon content showed the highest electrical conductivity (2.0 S cm(-1)), and displayed also extraordinary electrochemical performance: the cyclovoltammograms consisted of well defined reversible redox peaks at a scan rate as high as 10 mV s(-1), while, by galvanostatic cycling, the coulombic capacity of 150 mAh g(-1) was evidenced at a discharging rate of 10 C. (c) 2012 Elsevier Ltd. All rights reserved.
T2  - Materials Research Bulletin
T1  - Hydrothermal synthesis of Li4Ti5O12/C nanostructured composites: Morphology and electrochemical performance
VL  - 48
IS  - 2
SP  - 218
EP  - 223
DO  - 10.1016/j.materresbull.2012.09.071
ER  - 
@article{
author = "Vujković, Milica and Stojković, Ivana and Mitrić, Miodrag and Mentus, Slavko V. and Cvjeticanin, Nikola",
year = "2013",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/5356",
abstract = "Li4Ti5O12/C composites with low (3 wt.%) and high (33 wt.%) carbon black content as well as carbon-free Li4Ti5O12 were prepared in two steps under identical conditions: hydrothermal reaction at 130 degrees C and post-calcination at 400 degrees C. The X-ray diffraction experiments confirmed the spinet structure of Li4Ti5O12 in all samples. The carbon content altered significantly the morphology of obtained micro/nanoparticles. The Li4Ti5O12/C composite with the high carbon content showed the highest electrical conductivity (2.0 S cm(-1)), and displayed also extraordinary electrochemical performance: the cyclovoltammograms consisted of well defined reversible redox peaks at a scan rate as high as 10 mV s(-1), while, by galvanostatic cycling, the coulombic capacity of 150 mAh g(-1) was evidenced at a discharging rate of 10 C. (c) 2012 Elsevier Ltd. All rights reserved.",
journal = "Materials Research Bulletin",
title = "Hydrothermal synthesis of Li4Ti5O12/C nanostructured composites: Morphology and electrochemical performance",
volume = "48",
number = "2",
pages = "218-223",
doi = "10.1016/j.materresbull.2012.09.071"
}
Vujković, M., Stojković, I., Mitrić, M., Mentus, S. V.,& Cvjeticanin, N. (2013). Hydrothermal synthesis of Li4Ti5O12/C nanostructured composites: Morphology and electrochemical performance.
Materials Research Bulletin, 48(2), 218-223.
https://doi.org/10.1016/j.materresbull.2012.09.071
Vujković M, Stojković I, Mitrić M, Mentus SV, Cvjeticanin N. Hydrothermal synthesis of Li4Ti5O12/C nanostructured composites: Morphology and electrochemical performance. Materials Research Bulletin. 2013;48(2):218-223
Vujković Milica, Stojković Ivana, Mitrić Miodrag, Mentus Slavko V., Cvjeticanin Nikola, "Hydrothermal synthesis of Li4Ti5O12/C nanostructured composites: Morphology and electrochemical performance" Materials Research Bulletin, 48, no. 2 (2013):218-223,
https://doi.org/10.1016/j.materresbull.2012.09.071 .
22
22
24

The LiFe(1-x)VxPO4/C composite synthesized by gel-combustion method, with improved rate capability and cycle life in aerated aqueous solutions

Vujković, Milica; Jugović, Dragana; Mitrić, Miodrag; Stojković, Ivana; Cvjeticanin, Nikola; Mentus, Slavko V.

(2013)

TY  - JOUR
AU  - Vujković, Milica
AU  - Jugović, Dragana
AU  - Mitrić, Miodrag
AU  - Stojković, Ivana
AU  - Cvjeticanin, Nikola
AU  - Mentus, Slavko V.
PY  - 2013
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/5784
AB  - The nitrate-(glycine + malonic acid)-assisted gel-combustion process, followed by a heat treatment at 750 degrees C under reductive atmosphere, was used as a fast and effective way to synthesize vanadium doped olivine incorporated in carbon matrix, of general formula LiFe(1-x)VxPO4/C. The two-phased Rietveld refinement confirmed that vanadium incorporation into olivine structure was complete. The heating under reduction atmosphere caused the formation of iron phosphide to some extent, the concentration was determined by Rietveld analysis. The capacity and rate capability of these composites were tested by both cyclic voltammetry and galvanostatic cycling. Specifically, the average discharging capacities of the composite with x=0.055, determined in an saturated aqueous LiNO3 solution equilibrated with air, at the rates of 1, 10 and 100 C, amounted to 91, 73 and 35 mAh g(-1), respectively, with no perceivable capacity fade. (C) 2013 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - The LiFe(1-x)VxPO4/C composite synthesized by gel-combustion method, with improved rate capability and cycle life in aerated aqueous solutions
VL  - 109
SP  - 835
EP  - 842
DO  - 10.1016/j.electacta.2013.07.219
ER  - 
@article{
author = "Vujković, Milica and Jugović, Dragana and Mitrić, Miodrag and Stojković, Ivana and Cvjeticanin, Nikola and Mentus, Slavko V.",
year = "2013",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/5784",
abstract = "The nitrate-(glycine + malonic acid)-assisted gel-combustion process, followed by a heat treatment at 750 degrees C under reductive atmosphere, was used as a fast and effective way to synthesize vanadium doped olivine incorporated in carbon matrix, of general formula LiFe(1-x)VxPO4/C. The two-phased Rietveld refinement confirmed that vanadium incorporation into olivine structure was complete. The heating under reduction atmosphere caused the formation of iron phosphide to some extent, the concentration was determined by Rietveld analysis. The capacity and rate capability of these composites were tested by both cyclic voltammetry and galvanostatic cycling. Specifically, the average discharging capacities of the composite with x=0.055, determined in an saturated aqueous LiNO3 solution equilibrated with air, at the rates of 1, 10 and 100 C, amounted to 91, 73 and 35 mAh g(-1), respectively, with no perceivable capacity fade. (C) 2013 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "The LiFe(1-x)VxPO4/C composite synthesized by gel-combustion method, with improved rate capability and cycle life in aerated aqueous solutions",
volume = "109",
pages = "835-842",
doi = "10.1016/j.electacta.2013.07.219"
}
Vujković, M., Jugović, D., Mitrić, M., Stojković, I., Cvjeticanin, N.,& Mentus, S. V. (2013). The LiFe(1-x)VxPO4/C composite synthesized by gel-combustion method, with improved rate capability and cycle life in aerated aqueous solutions.
Electrochimica Acta, 109, 835-842.
https://doi.org/10.1016/j.electacta.2013.07.219
Vujković M, Jugović D, Mitrić M, Stojković I, Cvjeticanin N, Mentus SV. The LiFe(1-x)VxPO4/C composite synthesized by gel-combustion method, with improved rate capability and cycle life in aerated aqueous solutions. Electrochimica Acta. 2013;109:835-842
Vujković Milica, Jugović Dragana, Mitrić Miodrag, Stojković Ivana, Cvjeticanin Nikola, Mentus Slavko V., "The LiFe(1-x)VxPO4/C composite synthesized by gel-combustion method, with improved rate capability and cycle life in aerated aqueous solutions" Electrochimica Acta, 109 (2013):835-842,
https://doi.org/10.1016/j.electacta.2013.07.219 .
19
23
22

The incorporation of vanadium into olivine LiFePO4/C: improvement of lithium intercalation from both organic and aqueous electrolyte

Vujković, Milica; Jugović, Dragana; Mitrić, Miodrag; Stojković-Simatović, Ivana; Cvjetićanin, Nikola; Mentus, Slavko V.

(Belgrade : Materials Research Society of Serbia, 2013)

TY  - CONF
AU  - Vujković, Milica
AU  - Jugović, Dragana
AU  - Mitrić, Miodrag
AU  - Stojković-Simatović, Ivana
AU  - Cvjetićanin, Nikola
AU  - Mentus, Slavko V.
PY  - 2013
UR  - http://www.itn.sanu.ac.rs/opus4/frontdoor/index/index/docId/668
UR  - http://dais.sanu.ac.rs/123456789/407
UR  - http://www.itn.sanu.ac.rs/opus4/files/668/Vujkovic_YUCOMAT2013_101.pdf
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7423
AB  - The simple and fast (malonic acid+glycine)-assisted gel-combustion process, followed by a heat treatment at 750oC under reductive atmosphere, is found to be a very effective way for the synthesis of (V-doped LiFePO4)/C composites. The Rietveld refinement confirms that vanadium incorporation into olivine structure was accompanied by the formation of iron phosphide conducting phase. The coulombic capacity and rate capability of (V-doped LiFePO4)/C composite, in both organic and aqueous electrolyte solutions, were significantly improved relative to an undoped sample, as revealed by both galvanostatic cycling and cyclic voltammetry. The average discharging capacities of ~5mol.%V-doped LiFePO4/C composite in an aqueous LiNO3 solution were 91, 73 and 35 mAh g-1 at 1, 10 and 100 C, respectively, with no perceivable capacity fade upon 100 charging/discharging cycles.
PB  - Belgrade : Materials Research Society of Serbia
C3  - The Fifteenth Annual Conference YUCOMAT 2013: Programme and the Book of Abstracts
T1  - The incorporation of vanadium into olivine LiFePO4/C: improvement of lithium intercalation from both organic and aqueous electrolyte
SP  - 101
EP  - 101
ER  - 
@conference{
author = "Vujković, Milica and Jugović, Dragana and Mitrić, Miodrag and Stojković-Simatović, Ivana and Cvjetićanin, Nikola and Mentus, Slavko V.",
year = "2013",
url = "http://www.itn.sanu.ac.rs/opus4/frontdoor/index/index/docId/668, http://dais.sanu.ac.rs/123456789/407, http://www.itn.sanu.ac.rs/opus4/files/668/Vujkovic_YUCOMAT2013_101.pdf, http://vinar.vin.bg.ac.rs/handle/123456789/7423",
abstract = "The simple and fast (malonic acid+glycine)-assisted gel-combustion process, followed by a heat treatment at 750oC under reductive atmosphere, is found to be a very effective way for the synthesis of (V-doped LiFePO4)/C composites. The Rietveld refinement confirms that vanadium incorporation into olivine structure was accompanied by the formation of iron phosphide conducting phase. The coulombic capacity and rate capability of (V-doped LiFePO4)/C composite, in both organic and aqueous electrolyte solutions, were significantly improved relative to an undoped sample, as revealed by both galvanostatic cycling and cyclic voltammetry. The average discharging capacities of ~5mol.%V-doped LiFePO4/C composite in an aqueous LiNO3 solution were 91, 73 and 35 mAh g-1 at 1, 10 and 100 C, respectively, with no perceivable capacity fade upon 100 charging/discharging cycles.",
publisher = "Belgrade : Materials Research Society of Serbia",
journal = "The Fifteenth Annual Conference YUCOMAT 2013: Programme and the Book of Abstracts",
title = "The incorporation of vanadium into olivine LiFePO4/C: improvement of lithium intercalation from both organic and aqueous electrolyte",
pages = "101-101"
}
Vujković, M., Jugović, D., Mitrić, M., Stojković-Simatović, I., Cvjetićanin, N.,& Mentus, S. V. (2013). The incorporation of vanadium into olivine LiFePO4/C: improvement of lithium intercalation from both organic and aqueous electrolyte.
The Fifteenth Annual Conference YUCOMAT 2013: Programme and the Book of Abstracts
Belgrade : Materials Research Society of Serbia., 101-101.
Vujković M, Jugović D, Mitrić M, Stojković-Simatović I, Cvjetićanin N, Mentus SV. The incorporation of vanadium into olivine LiFePO4/C: improvement of lithium intercalation from both organic and aqueous electrolyte. The Fifteenth Annual Conference YUCOMAT 2013: Programme and the Book of Abstracts. 2013;:101-101
Vujković Milica, Jugović Dragana, Mitrić Miodrag, Stojković-Simatović Ivana, Cvjetićanin Nikola, Mentus Slavko V., "The incorporation of vanadium into olivine LiFePO4/C: improvement of lithium intercalation from both organic and aqueous electrolyte" The Fifteenth Annual Conference YUCOMAT 2013: Programme and the Book of Abstracts (2013):101-101