TY  - JOUR
AU  - Popović, Aleksandra S.
AU  - Jugović, Dragana
AU  - Grgur, Branimir N.
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6436
AB  - Primary seawater magnesium-based cell with AgCl or PbCl2 cathodes is widely used as power sources. In this paper, we consider the cyclic galvanostatic formation of silver and lead chlorides and their electrochemical behavior for potential applications in the new concept of the seawater quasi-rechargeable magnesium cell. For potential cells, the voltage for Mg alloy AZ63 and AgCl is ~ 1.5 V, and for the PbCl2, ~ 1 V. High discharge specific capacity, energy, and power are obtained under the very high discharge rate. It is also presented that systems could be potentially used in emergency situations for a few days up to a few weeks as a power source in the life-saving boat for sporadic emitting GPS-SOS tacking signals and night signal lights.
PB  - Springer
T2  - Journal of Materials Science: Materials in Electronics
T1  - Electrochemical formation and behavior of silver and lead chlorides as potential cathodes for quasi-rechargeable magnesium seawater cell
IS  - 14
SP  - 1155
VL  - 34
DO  - 10.1007/s10854-023-10558-9
ER  - 

@article{
author = "Popović, Aleksandra S. and Jugović, Dragana and Grgur, Branimir N.",
year = "2023",
abstract = "Primary seawater magnesium-based cell with AgCl or PbCl2 cathodes is widely used as power sources. In this paper, we consider the cyclic galvanostatic formation of silver and lead chlorides and their electrochemical behavior for potential applications in the new concept of the seawater quasi-rechargeable magnesium cell. For potential cells, the voltage for Mg alloy AZ63 and AgCl is ~ 1.5 V, and for the PbCl2, ~ 1 V. High discharge specific capacity, energy, and power are obtained under the very high discharge rate. It is also presented that systems could be potentially used in emergency situations for a few days up to a few weeks as a power source in the life-saving boat for sporadic emitting GPS-SOS tacking signals and night signal lights.",
publisher = "Springer",
journal = "Journal of Materials Science: Materials in Electronics",
title = "Electrochemical formation and behavior of silver and lead chlorides as potential cathodes for quasi-rechargeable magnesium seawater cell",
number = "14",
pages = "1155",
volume = "34",
doi = "10.1007/s10854-023-10558-9"
}

Popović, A. S., Jugović, D.,& Grgur, B. N.. (2023). Electrochemical formation and behavior of silver and lead chlorides as potential cathodes for quasi-rechargeable magnesium seawater cell. in Journal of Materials Science: Materials in Electronics
Springer., 34(14), 1155.
https://doi.org/10.1007/s10854-023-10558-9

Popović AS, Jugović D, Grgur BN. Electrochemical formation and behavior of silver and lead chlorides as potential cathodes for quasi-rechargeable magnesium seawater cell. in Journal of Materials Science: Materials in Electronics. 2023;34(14):1155.
doi:10.1007/s10854-023-10558-9 .

Popović, Aleksandra S., Jugović, Dragana, Grgur, Branimir N., "Electrochemical formation and behavior of silver and lead chlorides as potential cathodes for quasi-rechargeable magnesium seawater cell" in Journal of Materials Science: Materials in Electronics, 34, no. 14 (2023):1155,
https://doi.org/10.1007/s10854-023-10558-9 . .

TY  - JOUR
AU  - Georgijević, Radovan
AU  - Vujković, Milica
AU  - Gutić, Sanjin J.
AU  - Aliefendić, Meho
AU  - Jugović, Dragana
AU  - Mitrić, Miodrag
AU  - Đokić, Veljko
AU  - Mentus, Slavko
PY  - 2019
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4329
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).
PB  - Elsevier Science Sa, Lausanne
T2  - Journal of Alloys and Compounds
T1  - The influence of synthesis conditions on the redox behaviour of LiFePO4 in aqueous solution
EP  - 485
SP  - 475
VL  - 776
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 and Mentus, Slavko",
year = "2019",
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).",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Journal of Alloys and Compounds",
title = "The influence of synthesis conditions on the redox behaviour of LiFePO4 in aqueous solution",
pages = "485-475",
volume = "776",
doi = "10.1016/j.jallcom.2018.10.246"
}

Georgijević, R., Vujković, M., Gutić, S. J., Aliefendić, M., Jugović, D., Mitrić, M., Đokić, V.,& Mentus, S.. (2019). The influence of synthesis conditions on the redox behaviour of LiFePO4 in aqueous solution. in Journal of Alloys and Compounds
Elsevier Science Sa, Lausanne., 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 V, Mentus S. The influence of synthesis conditions on the redox behaviour of LiFePO4 in aqueous solution. in Journal of Alloys and Compounds. 2019;776:475-485.
doi:10.1016/j.jallcom.2018.10.246 .

Georgijević, Radovan, Vujković, Milica, Gutić, Sanjin J., Aliefendić, Meho, Jugović, Dragana, Mitrić, Miodrag, Đokić, Veljko, Mentus, Slavko, "The influence of synthesis conditions on the redox behaviour of LiFePO4 in aqueous solution" in Journal of Alloys and Compounds, 776 (2019):475-485,
https://doi.org/10.1016/j.jallcom.2018.10.246 . .

TY  - JOUR
AU  - Jugović, Dragana
AU  - Mitrić, Miodrag
AU  - Milović, Miloš
AU  - Cvjetićanin, Nikola
AU  - Jokić, Bojan
AU  - Umićević, Ana
AU  - Uskoković, Dragan
PY  - 2017
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5856
AB  - Low intrinsic electronic conductivity is the main disadvantage of LiFePO4 when used as a cathode material in lithium ion batteries. The paper offers experimental proofs of the theoretical prediction that fluorine doping of LiFePO4 can enhance its electrical conductivity. The LiFePO4 and fluorine-doped LiFePO4 olivine type, carbon-free powders are synthesized and examined. The crystal structure refinements in the Pnma space group reveal that doping with fluorine ions preserves the olivine structure, while reducing both the lattice parameters and the antisite defect, and increasing the crystallite size. A small amount of incorporated fluorine enhances the electrical conductivity from 4.6×10−7 S cm−1 to 2.3×10−6 S cm−1 and has a positive impact on the electrochemical performance. Several spectroscopy techniques (Mössbauer, FTIR, and Raman) reveal differences between the two powders and additionally support the findings of both the Rietveld refinement and the conductivity measurements.
PB  - Elsevier
T2  - Ceramics International
T1  - The influence of fluorine doping on the structural and electrical properties of the LiFePO4 powder
EP  - 3230
IS  - 3
SP  - 3224
VL  - 43
DO  - 10.1016/j.ceramint.2016.11.149
UR  - https://hdl.handle.net/21.15107/rcub_dais_2352
ER  - 

@article{
author = "Jugović, Dragana and Mitrić, Miodrag and Milović, Miloš and Cvjetićanin, Nikola and Jokić, Bojan and Umićević, Ana and Uskoković, Dragan",
year = "2017",
abstract = "Low intrinsic electronic conductivity is the main disadvantage of LiFePO4 when used as a cathode material in lithium ion batteries. The paper offers experimental proofs of the theoretical prediction that fluorine doping of LiFePO4 can enhance its electrical conductivity. The LiFePO4 and fluorine-doped LiFePO4 olivine type, carbon-free powders are synthesized and examined. The crystal structure refinements in the Pnma space group reveal that doping with fluorine ions preserves the olivine structure, while reducing both the lattice parameters and the antisite defect, and increasing the crystallite size. A small amount of incorporated fluorine enhances the electrical conductivity from 4.6×10−7 S cm−1 to 2.3×10−6 S cm−1 and has a positive impact on the electrochemical performance. Several spectroscopy techniques (Mössbauer, FTIR, and Raman) reveal differences between the two powders and additionally support the findings of both the Rietveld refinement and the conductivity measurements.",
publisher = "Elsevier",
journal = "Ceramics International",
title = "The influence of fluorine doping on the structural and electrical properties of the LiFePO4 powder",
pages = "3230-3224",
number = "3",
volume = "43",
doi = "10.1016/j.ceramint.2016.11.149",
url = "https://hdl.handle.net/21.15107/rcub_dais_2352"
}

Jugović, D., Mitrić, M., Milović, M., Cvjetićanin, N., Jokić, B., Umićević, A.,& Uskoković, D.. (2017). The influence of fluorine doping on the structural and electrical properties of the LiFePO4 powder. in Ceramics International
Elsevier., 43(3), 3224-3230.
https://doi.org/10.1016/j.ceramint.2016.11.149
https://hdl.handle.net/21.15107/rcub_dais_2352

Jugović D, Mitrić M, Milović M, Cvjetićanin N, Jokić B, Umićević A, Uskoković D. The influence of fluorine doping on the structural and electrical properties of the LiFePO4 powder. in Ceramics International. 2017;43(3):3224-3230.
doi:10.1016/j.ceramint.2016.11.149
https://hdl.handle.net/21.15107/rcub_dais_2352 .

Jugović, Dragana, Mitrić, Miodrag, Milović, Miloš, Cvjetićanin, Nikola, Jokić, Bojan, Umićević, Ana, Uskoković, Dragan, "The influence of fluorine doping on the structural and electrical properties of the LiFePO4 powder" in Ceramics International, 43, no. 3 (2017):3224-3230,
https://doi.org/10.1016/j.ceramint.2016.11.149 .,
https://hdl.handle.net/21.15107/rcub_dais_2352 .

TY  - JOUR
AU  - Kuzmanović, Maja
AU  - Jugović, Dragana
AU  - Mitrić, Miodrag
AU  - Jokić, Bojan
AU  - Cvjetićanin, Nikola
AU  - Uskoković, Dragan
PY  - 2015
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5807
AB  - Olivine-type LiFePO4 composite powders with carbon were synthesized by freeze drying and subsequent thermal annealing. The main purpose of the research is to explore how various dicarboxylic acids as carbon sources influence the electrochemical properties of the resulting composites. Three dicarboxylic acids (oxalic, malonic, and adipic) were used as a carbon source. The synthesis was followed by X-ray powder diffraction, scanning electron microscopy, particle-size analysis, and electrochemical experiments. It is shown that the amount of the in situ formed carbon depends on the thermal behaviour of the acids in inert atmosphere rather than on their carbon content. Cyclic voltammetry experiments and galvanostatic cycling illustrate the behaviour of different powders: the powder obtained with oxalic acid yields the highest discharge capacity at small currents, while the one obtained with adipic acid shows better high-current response. Malonic acid has turned out to be a poor carbon source and it consequently yields powder with poor electrochemical performance. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
PB  - Elsevier Ltd.
T2  - Ceramics International
T1  - The use of various dicarboxylic acids as a carbon source for the preparation of LiFePO4/C composite
EP  - 6758
IS  - 5
SP  - 6753
VL  - 41
DO  - 10.1016/j.ceramint.2015.01.121
UR  - https://hdl.handle.net/21.15107/rcub_dais_2590
ER  - 

@article{
author = "Kuzmanović, Maja and Jugović, Dragana and Mitrić, Miodrag and Jokić, Bojan and Cvjetićanin, Nikola and Uskoković, Dragan",
year = "2015",
abstract = "Olivine-type LiFePO4 composite powders with carbon were synthesized by freeze drying and subsequent thermal annealing. The main purpose of the research is to explore how various dicarboxylic acids as carbon sources influence the electrochemical properties of the resulting composites. Three dicarboxylic acids (oxalic, malonic, and adipic) were used as a carbon source. The synthesis was followed by X-ray powder diffraction, scanning electron microscopy, particle-size analysis, and electrochemical experiments. It is shown that the amount of the in situ formed carbon depends on the thermal behaviour of the acids in inert atmosphere rather than on their carbon content. Cyclic voltammetry experiments and galvanostatic cycling illustrate the behaviour of different powders: the powder obtained with oxalic acid yields the highest discharge capacity at small currents, while the one obtained with adipic acid shows better high-current response. Malonic acid has turned out to be a poor carbon source and it consequently yields powder with poor electrochemical performance. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.",
publisher = "Elsevier Ltd.",
journal = "Ceramics International",
title = "The use of various dicarboxylic acids as a carbon source for the preparation of LiFePO4/C composite",
pages = "6758-6753",
number = "5",
volume = "41",
doi = "10.1016/j.ceramint.2015.01.121",
url = "https://hdl.handle.net/21.15107/rcub_dais_2590"
}

Kuzmanović, M., Jugović, D., Mitrić, M., Jokić, B., Cvjetićanin, N.,& Uskoković, D.. (2015). The use of various dicarboxylic acids as a carbon source for the preparation of LiFePO4/C composite. in Ceramics International
Elsevier Ltd.., 41(5), 6753-6758.
https://doi.org/10.1016/j.ceramint.2015.01.121
https://hdl.handle.net/21.15107/rcub_dais_2590

Kuzmanović M, Jugović D, Mitrić M, Jokić B, Cvjetićanin N, Uskoković D. The use of various dicarboxylic acids as a carbon source for the preparation of LiFePO4/C composite. in Ceramics International. 2015;41(5):6753-6758.
doi:10.1016/j.ceramint.2015.01.121
https://hdl.handle.net/21.15107/rcub_dais_2590 .

Kuzmanović, Maja, Jugović, Dragana, Mitrić, Miodrag, Jokić, Bojan, Cvjetićanin, Nikola, Uskoković, Dragan, "The use of various dicarboxylic acids as a carbon source for the preparation of LiFePO4/C composite" in Ceramics International, 41, no. 5 (2015):6753-6758,
https://doi.org/10.1016/j.ceramint.2015.01.121 .,
https://hdl.handle.net/21.15107/rcub_dais_2590 .

TY  - JOUR
AU  - Jugović, Dragana
AU  - Milović, Miloš
AU  - Ivanovski, Valentin N.
AU  - Avdeev, Maxim
AU  - Dominko, Robert
AU  - Jokić, Bojan
AU  - Uskoković, Dragan
PY  - 2014
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5786
AB  - A composite powder Li2FeSiO4/C is synthesized through a solid state reaction at 750 °C. The Rietveld crystal structure refinement is done in the monoclinic P21/n space group. It is found that the crystal structure is prone to “antisite” defect where small part of iron ion occupies exclusively Li(2) crystallographic position, of two different lithium tetrahedral positions (Li(1) and Li(2)). This finding is also confirmed by Mössbauer spectroscopy study: the sextet evidenced in the Mössbauer spectrum is assigned to the iron ions positioned at the Li(2) sites. A bond-valence energy landscape calculation is used to predict the conduction pathways of lithium ions. The calculations suggest that Li conductivity is two-dimensional in the (101) plane. Upon galvanostatic cyclings the structure starts to rearrange to inverse βII polymorph.
PB  - Elsevier B.V.
T2  - Journal of Power Sources
T1  - Structural study of monoclinic Li2FeSiO4 by X-ray diffraction and Mössbauer spectroscopy
EP  - 80
SP  - 75
VL  - 265
DO  - 10.1016/j.jpowsour.2014.04.121
UR  - https://hdl.handle.net/21.15107/rcub_dais_755
ER  - 

@article{
author = "Jugović, Dragana and Milović, Miloš and Ivanovski, Valentin N. and Avdeev, Maxim and Dominko, Robert and Jokić, Bojan and Uskoković, Dragan",
year = "2014",
abstract = "A composite powder Li2FeSiO4/C is synthesized through a solid state reaction at 750 °C. The Rietveld crystal structure refinement is done in the monoclinic P21/n space group. It is found that the crystal structure is prone to “antisite” defect where small part of iron ion occupies exclusively Li(2) crystallographic position, of two different lithium tetrahedral positions (Li(1) and Li(2)). This finding is also confirmed by Mössbauer spectroscopy study: the sextet evidenced in the Mössbauer spectrum is assigned to the iron ions positioned at the Li(2) sites. A bond-valence energy landscape calculation is used to predict the conduction pathways of lithium ions. The calculations suggest that Li conductivity is two-dimensional in the (101) plane. Upon galvanostatic cyclings the structure starts to rearrange to inverse βII polymorph.",
publisher = "Elsevier B.V.",
journal = "Journal of Power Sources",
title = "Structural study of monoclinic Li2FeSiO4 by X-ray diffraction and Mössbauer spectroscopy",
pages = "80-75",
volume = "265",
doi = "10.1016/j.jpowsour.2014.04.121",
url = "https://hdl.handle.net/21.15107/rcub_dais_755"
}

Jugović, D., Milović, M., Ivanovski, V. N., Avdeev, M., Dominko, R., Jokić, B.,& Uskoković, D.. (2014). Structural study of monoclinic Li2FeSiO4 by X-ray diffraction and Mössbauer spectroscopy. in Journal of Power Sources
Elsevier B.V.., 265, 75-80.
https://doi.org/10.1016/j.jpowsour.2014.04.121
https://hdl.handle.net/21.15107/rcub_dais_755

Jugović D, Milović M, Ivanovski VN, Avdeev M, Dominko R, Jokić B, Uskoković D. Structural study of monoclinic Li2FeSiO4 by X-ray diffraction and Mössbauer spectroscopy. in Journal of Power Sources. 2014;265:75-80.
doi:10.1016/j.jpowsour.2014.04.121
https://hdl.handle.net/21.15107/rcub_dais_755 .

Jugović, Dragana, Milović, Miloš, Ivanovski, Valentin N., Avdeev, Maxim, Dominko, Robert, Jokić, Bojan, Uskoković, Dragan, "Structural study of monoclinic Li2FeSiO4 by X-ray diffraction and Mössbauer spectroscopy" in Journal of Power Sources, 265 (2014):75-80,
https://doi.org/10.1016/j.jpowsour.2014.04.121 .,
https://hdl.handle.net/21.15107/rcub_dais_755 .

TY  - JOUR
AU  - Jugović, Dragana
AU  - Milović, Miloš
AU  - Ivanovski, Valentin N.
AU  - Avdeev, Maxim
AU  - Dominko, Robert
AU  - Jokić, Bojan
AU  - Uskoković, Dragan
PY  - 2014
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5787
AB  - A composite powder Li2FeSiO4/C is synthesized through a solid state reaction at 750 °C. The Rietveld crystal structure refinement is done in the monoclinic P21/n space group. It is found that the crystal structure is prone to “antisite” defect where small part of iron ion occupies exclusively Li(2) crystallographic position, of two different lithium tetrahedral positions (Li(1) and Li(2)). This finding is also confirmed by Mössbauer spectroscopy study: the sextet evidenced in the Mössbauer spectrum is assigned to the iron ions positioned at the Li(2) sites. A bond-valence energy landscape calculation is used to predict the conduction pathways of lithium ions. The calculations suggest that Li conductivity is two-dimensional in the (101) plane. Upon galvanostatic cyclings the structure starts to rearrange to inverse βII polymorph.
PB  - Elsevier B.V.
T2  - Journal of Power Sources
T1  - Structural study of monoclinic Li2FeSiO4 by X-ray diffraction and Mössbauer spectroscopy
EP  - 80
SP  - 75
VL  - 265
DO  - 10.1016/j.jpowsour.2014.04.121
UR  - https://hdl.handle.net/21.15107/rcub_dais_542
ER  - 

@article{
author = "Jugović, Dragana and Milović, Miloš and Ivanovski, Valentin N. and Avdeev, Maxim and Dominko, Robert and Jokić, Bojan and Uskoković, Dragan",
year = "2014",
abstract = "A composite powder Li2FeSiO4/C is synthesized through a solid state reaction at 750 °C. The Rietveld crystal structure refinement is done in the monoclinic P21/n space group. It is found that the crystal structure is prone to “antisite” defect where small part of iron ion occupies exclusively Li(2) crystallographic position, of two different lithium tetrahedral positions (Li(1) and Li(2)). This finding is also confirmed by Mössbauer spectroscopy study: the sextet evidenced in the Mössbauer spectrum is assigned to the iron ions positioned at the Li(2) sites. A bond-valence energy landscape calculation is used to predict the conduction pathways of lithium ions. The calculations suggest that Li conductivity is two-dimensional in the (101) plane. Upon galvanostatic cyclings the structure starts to rearrange to inverse βII polymorph.",
publisher = "Elsevier B.V.",
journal = "Journal of Power Sources",
title = "Structural study of monoclinic Li2FeSiO4 by X-ray diffraction and Mössbauer spectroscopy",
pages = "80-75",
volume = "265",
doi = "10.1016/j.jpowsour.2014.04.121",
url = "https://hdl.handle.net/21.15107/rcub_dais_542"
}

Jugović, D., Milović, M., Ivanovski, V. N., Avdeev, M., Dominko, R., Jokić, B.,& Uskoković, D.. (2014). Structural study of monoclinic Li2FeSiO4 by X-ray diffraction and Mössbauer spectroscopy. in Journal of Power Sources
Elsevier B.V.., 265, 75-80.
https://doi.org/10.1016/j.jpowsour.2014.04.121
https://hdl.handle.net/21.15107/rcub_dais_542

Jugović D, Milović M, Ivanovski VN, Avdeev M, Dominko R, Jokić B, Uskoković D. Structural study of monoclinic Li2FeSiO4 by X-ray diffraction and Mössbauer spectroscopy. in Journal of Power Sources. 2014;265:75-80.
doi:10.1016/j.jpowsour.2014.04.121
https://hdl.handle.net/21.15107/rcub_dais_542 .

Jugović, Dragana, Milović, Miloš, Ivanovski, Valentin N., Avdeev, Maxim, Dominko, Robert, Jokić, Bojan, Uskoković, Dragan, "Structural study of monoclinic Li2FeSiO4 by X-ray diffraction and Mössbauer spectroscopy" in Journal of Power Sources, 265 (2014):75-80,
https://doi.org/10.1016/j.jpowsour.2014.04.121 .,
https://hdl.handle.net/21.15107/rcub_dais_542 .

TY  - JOUR
AU  - Jugović, Dragana
AU  - Mitrić, Miodrag
AU  - Milović, Miloš
AU  - Jokić, Bojan M.
AU  - Vukomanovic, Marija
AU  - Suvorov, Danilo
AU  - Uskoković, Dragan
PY  - 2013
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5712
AB  - In this study, nanocrystalline LiFePO4/C composite powder has been synthesized via a cellulose matrix-assisted method. In an experiment conducted under extreme conditions involving rapid heating, short high-temperature delay, and subsequent quenching, well-ordered 35-nm crystallites have been obtained within 5 min. A quantitative filter paper has served both as a template and carbon source. It degrades pyrolytically through fragmentation reactions and formation of volatiles when exposed to rapid heating, which further has an impact on powder morphology, as revealed by electron microscopy studies. The electrochemical measurements in terms of galvanostatic cycling have shown that the approach presented in this study may enable to reach good rate capability and excellent cycling stability. (C) 2013 Elsevier B.V. All rights reserved.
T2  - Powder Technology
T1  - Properties of quenched LiFePO4/C powder obtained via cellulose matrix-assisted method
EP  - 544
SP  - 539
VL  - 246
DO  - 10.1016/j.powtec.2013.06.021
ER  - 

@article{
author = "Jugović, Dragana and Mitrić, Miodrag and Milović, Miloš and Jokić, Bojan M. and Vukomanovic, Marija and Suvorov, Danilo and Uskoković, Dragan",
year = "2013",
abstract = "In this study, nanocrystalline LiFePO4/C composite powder has been synthesized via a cellulose matrix-assisted method. In an experiment conducted under extreme conditions involving rapid heating, short high-temperature delay, and subsequent quenching, well-ordered 35-nm crystallites have been obtained within 5 min. A quantitative filter paper has served both as a template and carbon source. It degrades pyrolytically through fragmentation reactions and formation of volatiles when exposed to rapid heating, which further has an impact on powder morphology, as revealed by electron microscopy studies. The electrochemical measurements in terms of galvanostatic cycling have shown that the approach presented in this study may enable to reach good rate capability and excellent cycling stability. (C) 2013 Elsevier B.V. All rights reserved.",
journal = "Powder Technology",
title = "Properties of quenched LiFePO4/C powder obtained via cellulose matrix-assisted method",
pages = "544-539",
volume = "246",
doi = "10.1016/j.powtec.2013.06.021"
}

Jugović, D., Mitrić, M., Milović, M., Jokić, B. M., Vukomanovic, M., Suvorov, D.,& Uskoković, D.. (2013). Properties of quenched LiFePO4/C powder obtained via cellulose matrix-assisted method. in Powder Technology, 246, 539-544.
https://doi.org/10.1016/j.powtec.2013.06.021

Jugović D, Mitrić M, Milović M, Jokić BM, Vukomanovic M, Suvorov D, Uskoković D. Properties of quenched LiFePO4/C powder obtained via cellulose matrix-assisted method. in Powder Technology. 2013;246:539-544.
doi:10.1016/j.powtec.2013.06.021 .

Jugović, Dragana, Mitrić, Miodrag, Milović, Miloš, Jokić, Bojan M., Vukomanovic, Marija, Suvorov, Danilo, Uskoković, Dragan, "Properties of quenched LiFePO4/C powder obtained via cellulose matrix-assisted method" in Powder Technology, 246 (2013):539-544,
https://doi.org/10.1016/j.powtec.2013.06.021 . .