Gutić, Sanjin J.

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orcid::0000-0002-5780-8022
  • Gutić, Sanjin J. (5)
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Author's Bibliography

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 .
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Electrochemical tuning of capacitive response of graphene oxide

Gutić, Sanjin J.; Kozlica, Dževad K.; Korać, Fehim; Bajuk-Bogdanović, Danica V.; Mitrić, Miodrag; Mirsky, Vladimir M.; Mentus, Slavko V.; Pašti, Igor A.

(2018)

TY  - JOUR
AU  - Gutić, Sanjin J.
AU  - Kozlica, Dževad K.
AU  - Korać, Fehim
AU  - Bajuk-Bogdanović, Danica V.
AU  - Mitrić, Miodrag
AU  - Mirsky, Vladimir M.
AU  - Mentus, Slavko V.
AU  - Pašti, Igor A.
PY  - 2018
UR  - http://xlink.rsc.org/?DOI=C8CP03631D
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7877
AB  - The increasing energy demands of modern society require a deep understanding of the properties of energy storage materials, as well as the tuning of their performance. We show that the capacitance of graphene oxide (GO) can be precisely tuned using a simple electrochemical reduction route. In situ resistance measurements, in combination with cyclic voltammetry measurements and Raman spectroscopy, have shown that upon reduction GO is irreversibly deoxygenated, which is further accompanied by structural ordering and an increase in electrical conductivity. The capacitance is maximized when the concentration of oxygen functional groups is properly balanced with the conductivity. Any further reduction and deoxygenation leads to a gradual loss of capacitance. The observed trend is independent of the preparation route and the exact chemical and structural properties of GO. It is proposed that an improvement in the capacitive properties of any GO can be achieved by optimization of its reduction conditions.
T2  - Physical Chemistry Chemical Physics
T1  - Electrochemical tuning of capacitive response of graphene oxide
VL  - 20
IS  - 35
SP  - 22698
EP  - 22709
DO  - 10.1039/C8CP03631D
ER  - 
@article{
author = "Gutić, Sanjin J. and Kozlica, Dževad K. and Korać, Fehim and Bajuk-Bogdanović, Danica V. and Mitrić, Miodrag and Mirsky, Vladimir M. and Mentus, Slavko V. and Pašti, Igor A.",
year = "2018",
url = "http://xlink.rsc.org/?DOI=C8CP03631D, http://vinar.vin.bg.ac.rs/handle/123456789/7877",
abstract = "The increasing energy demands of modern society require a deep understanding of the properties of energy storage materials, as well as the tuning of their performance. We show that the capacitance of graphene oxide (GO) can be precisely tuned using a simple electrochemical reduction route. In situ resistance measurements, in combination with cyclic voltammetry measurements and Raman spectroscopy, have shown that upon reduction GO is irreversibly deoxygenated, which is further accompanied by structural ordering and an increase in electrical conductivity. The capacitance is maximized when the concentration of oxygen functional groups is properly balanced with the conductivity. Any further reduction and deoxygenation leads to a gradual loss of capacitance. The observed trend is independent of the preparation route and the exact chemical and structural properties of GO. It is proposed that an improvement in the capacitive properties of any GO can be achieved by optimization of its reduction conditions.",
journal = "Physical Chemistry Chemical Physics",
title = "Electrochemical tuning of capacitive response of graphene oxide",
volume = "20",
number = "35",
pages = "22698-22709",
doi = "10.1039/C8CP03631D"
}
Gutić, S. J., Kozlica, D. K., Korać, F., Bajuk-Bogdanović, D. V., Mitrić, M., Mirsky, V. M., Mentus, S. V.,& Pašti, I. A. (2018). Electrochemical tuning of capacitive response of graphene oxide.
Physical Chemistry Chemical Physics, 20(35), 22698-22709.
https://doi.org/10.1039/C8CP03631D
Gutić SJ, Kozlica DK, Korać F, Bajuk-Bogdanović DV, Mitrić M, Mirsky VM, Mentus SV, Pašti IA. Electrochemical tuning of capacitive response of graphene oxide. Physical Chemistry Chemical Physics. 2018;20(35):22698-22709
Gutić Sanjin J., Kozlica Dževad K., Korać Fehim, Bajuk-Bogdanović Danica V., Mitrić Miodrag, Mirsky Vladimir M., Mentus Slavko V., Pašti Igor A., "Electrochemical tuning of capacitive response of graphene oxide" Physical Chemistry Chemical Physics, 20, no. 35 (2018):22698-22709,
https://doi.org/10.1039/C8CP03631D .
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Electrochemical tuning of capacitive response of graphene oxide

Gutić, Sanjin J.; Kozlica, Dževad K.; Korać, Fehim; Bajuk-Bogdanović, Danica V.; Mitrić, Miodrag; Mirsky, Vladimir M.; Mentus, Slavko V.; Pašti, Igor A.

(2018)

TY  - JOUR
AU  - Gutić, Sanjin J.
AU  - Kozlica, Dževad K.
AU  - Korać, Fehim
AU  - Bajuk-Bogdanović, Danica V.
AU  - Mitrić, Miodrag
AU  - Mirsky, Vladimir M.
AU  - Mentus, Slavko V.
AU  - Pašti, Igor A.
PY  - 2018
UR  - http://xlink.rsc.org/?DOI=C8CP03631D
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7887
AB  - The increasing energy demands of modern society require a deep understanding of the properties of energy storage materials, as well as the tuning of their performance. We show that the capacitance of graphene oxide (GO) can be precisely tuned using a simple electrochemical reduction route. In situ resistance measurements, in combination with cyclic voltammetry measurements and Raman spectroscopy, have shown that upon reduction GO is irreversibly deoxygenated, which is further accompanied by structural ordering and an increase in electrical conductivity. The capacitance is maximized when the concentration of oxygen functional groups is properly balanced with the conductivity. Any further reduction and deoxygenation leads to a gradual loss of capacitance. The observed trend is independent of the preparation route and the exact chemical and structural properties of GO. It is proposed that an improvement in the capacitive properties of any GO can be achieved by optimization of its reduction conditions.
T2  - Physical Chemistry Chemical Physics
T1  - Electrochemical tuning of capacitive response of graphene oxide
VL  - 20
IS  - 35
SP  - 22698
EP  - 22709
DO  - 10.1039/C8CP03631D
ER  - 
@article{
author = "Gutić, Sanjin J. and Kozlica, Dževad K. and Korać, Fehim and Bajuk-Bogdanović, Danica V. and Mitrić, Miodrag and Mirsky, Vladimir M. and Mentus, Slavko V. and Pašti, Igor A.",
year = "2018",
url = "http://xlink.rsc.org/?DOI=C8CP03631D, http://vinar.vin.bg.ac.rs/handle/123456789/7887",
abstract = "The increasing energy demands of modern society require a deep understanding of the properties of energy storage materials, as well as the tuning of their performance. We show that the capacitance of graphene oxide (GO) can be precisely tuned using a simple electrochemical reduction route. In situ resistance measurements, in combination with cyclic voltammetry measurements and Raman spectroscopy, have shown that upon reduction GO is irreversibly deoxygenated, which is further accompanied by structural ordering and an increase in electrical conductivity. The capacitance is maximized when the concentration of oxygen functional groups is properly balanced with the conductivity. Any further reduction and deoxygenation leads to a gradual loss of capacitance. The observed trend is independent of the preparation route and the exact chemical and structural properties of GO. It is proposed that an improvement in the capacitive properties of any GO can be achieved by optimization of its reduction conditions.",
journal = "Physical Chemistry Chemical Physics",
title = "Electrochemical tuning of capacitive response of graphene oxide",
volume = "20",
number = "35",
pages = "22698-22709",
doi = "10.1039/C8CP03631D"
}
Gutić, S. J., Kozlica, D. K., Korać, F., Bajuk-Bogdanović, D. V., Mitrić, M., Mirsky, V. M., Mentus, S. V.,& Pašti, I. A. (2018). Electrochemical tuning of capacitive response of graphene oxide.
Physical Chemistry Chemical Physics, 20(35), 22698-22709.
https://doi.org/10.1039/C8CP03631D
Gutić SJ, Kozlica DK, Korać F, Bajuk-Bogdanović DV, Mitrić M, Mirsky VM, Mentus SV, Pašti IA. Electrochemical tuning of capacitive response of graphene oxide. Physical Chemistry Chemical Physics. 2018;20(35):22698-22709
Gutić Sanjin J., Kozlica Dževad K., Korać Fehim, Bajuk-Bogdanović Danica V., Mitrić Miodrag, Mirsky Vladimir M., Mentus Slavko V., Pašti Igor A., "Electrochemical tuning of capacitive response of graphene oxide" Physical Chemistry Chemical Physics, 20, no. 35 (2018):22698-22709,
https://doi.org/10.1039/C8CP03631D .
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The impact of the structure of graphene-based materials on the removal of organophosphorus pesticides from water

Lazarević-Pašti, Tamara; Anićijević, Vladan J.; Baljozović, Miloš; Vasić Anićijević, Dragana D.; Gutić, Sanjin J.; Vasić, Vesna M.; Skorodumova, Natalia V.; Pašti, Igor A.

(2018)

TY  - JOUR
AU  - Lazarević-Pašti, Tamara
AU  - Anićijević, Vladan J.
AU  - Baljozović, Miloš
AU  - Vasić Anićijević, Dragana D.
AU  - Gutić, Sanjin J.
AU  - Vasić, Vesna M.
AU  - Skorodumova, Natalia V.
AU  - Pašti, Igor A.
PY  - 2018
UR  - http://xlink.rsc.org/?DOI=C8EN00171E
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/7730
AB  - The wide use of pesticides in modern agriculture and other areas results in an urgent need for their efficient removal from the environment. Adsorption of pesticides is one of the most commonly used strategies for this task. Here we analyze the adsorption of two organophosphorus pesticides, dimethoate (DMT) and chlorpyrifos (CPF), on graphene-based materials. The adsorption was found to be very sensitive to the structure of the adsorbents used. In particular, aliphatic DMT was found to prefer hydrophilic oxidized graphene surfaces. The CPF molecule, which contains an aromatic moiety, prefers adsorption on the surface of a graphene basal plane with high structural order and preserved π electron system. The toxicity of pesticide solutions is reduced after adsorption, suggesting that there is no oxidation of DMT and CPF to more toxic oxo forms. We emphasize that the combination of structural properties of adsorbents and adsorbates defines the adsorption of organophosphorus pesticides on graphene-based materials, while the specific surface area of adsorbents is not the major factor.
T2  - Environmental Science: Nano
T1  - The impact of the structure of graphene-based materials on the removal of organophosphorus pesticides from water
VL  - 5
IS  - 6
SP  - 1482
EP  - 1494
DO  - 10.1039/C8EN00171E
ER  - 
@article{
author = "Lazarević-Pašti, Tamara and Anićijević, Vladan J. and Baljozović, Miloš and Vasić Anićijević, Dragana D. and Gutić, Sanjin J. and Vasić, Vesna M. and Skorodumova, Natalia V. and Pašti, Igor A.",
year = "2018",
url = "http://xlink.rsc.org/?DOI=C8EN00171E, http://vinar.vin.bg.ac.rs/handle/123456789/7730",
abstract = "The wide use of pesticides in modern agriculture and other areas results in an urgent need for their efficient removal from the environment. Adsorption of pesticides is one of the most commonly used strategies for this task. Here we analyze the adsorption of two organophosphorus pesticides, dimethoate (DMT) and chlorpyrifos (CPF), on graphene-based materials. The adsorption was found to be very sensitive to the structure of the adsorbents used. In particular, aliphatic DMT was found to prefer hydrophilic oxidized graphene surfaces. The CPF molecule, which contains an aromatic moiety, prefers adsorption on the surface of a graphene basal plane with high structural order and preserved π electron system. The toxicity of pesticide solutions is reduced after adsorption, suggesting that there is no oxidation of DMT and CPF to more toxic oxo forms. We emphasize that the combination of structural properties of adsorbents and adsorbates defines the adsorption of organophosphorus pesticides on graphene-based materials, while the specific surface area of adsorbents is not the major factor.",
journal = "Environmental Science: Nano",
title = "The impact of the structure of graphene-based materials on the removal of organophosphorus pesticides from water",
volume = "5",
number = "6",
pages = "1482-1494",
doi = "10.1039/C8EN00171E"
}
Lazarević-Pašti, T., Anićijević, V. J., Baljozović, M., Vasić Anićijević, D. D., Gutić, S. J., Vasić, V. M., Skorodumova, N. V.,& Pašti, I. A. (2018). The impact of the structure of graphene-based materials on the removal of organophosphorus pesticides from water.
Environmental Science: Nano, 5(6), 1482-1494.
https://doi.org/10.1039/C8EN00171E
Lazarević-Pašti T, Anićijević VJ, Baljozović M, Vasić Anićijević DD, Gutić SJ, Vasić VM, Skorodumova NV, Pašti IA. The impact of the structure of graphene-based materials on the removal of organophosphorus pesticides from water. Environmental Science: Nano. 2018;5(6):1482-1494
Lazarević-Pašti Tamara, Anićijević Vladan J., Baljozović Miloš, Vasić Anićijević Dragana D., Gutić Sanjin J., Vasić Vesna M., Skorodumova Natalia V., Pašti Igor A., "The impact of the structure of graphene-based materials on the removal of organophosphorus pesticides from water" Environmental Science: Nano, 5, no. 6 (2018):1482-1494,
https://doi.org/10.1039/C8EN00171E .
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Stabilization of alkali metal ions interaction with OH-functionalized graphene via clustering of OH groups - implications in charge storage applications

Dobrota, Ana S.; Gutić, Sanjin J.; Kalijadis, Ana; Baljozović, Miloš; Mentus, Slavko V.; Skorodumova, Natalia V.; Pašti, Igor A.

(2016)

TY  - JOUR
AU  - Dobrota, Ana S.
AU  - Gutić, Sanjin J.
AU  - Kalijadis, Ana
AU  - Baljozović, Miloš
AU  - Mentus, Slavko V.
AU  - Skorodumova, Natalia V.
AU  - Pašti, Igor A.
PY  - 2016
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/1155
AB  - Graphene synthesized by reduction of graphene oxide, depending on the degree of reduction, retains a certain amount of surface OH groups. Considering the surface OH groups/graphene layer system by means of density functional theory calculations, we evidenced the tendency of OH groups to cluster, resulting in enhanced system stability and no band gap opening. In the oxygen concentration range between 1.8 and 8.47 at%, with the addition of each new OH group, integral binding energy decreases, while differential binding energy shows the boost at even numbers of OH groups. Furthermore, we found that the clustering of OH groups over graphene basal plane plays a crucial role in enhancing the interactions with alkali metals. Namely, if alkali metal atoms interact with individual OH groups only, the interaction leads to an irreversible formation of MOH phase. When alkali atoms interact with clusters containing odd number of OH groups, a reversible transfer of an electron charge from the metal atom to the substrate takes place without OH removal. The strength of the interaction in general increases from Li to K. In an experimental investigation of a graphene sample which dominantly contains OH groups, we have shown that the trend in the specific interaction strength reflects to gravimetric capacitances measured in alkali metal chloride solutions. We propose that the charge stored in OH groups which interact with alkali metal cation and the pi electronic system of the graphene basal plane presents the main part of its pseudocapacitance.
T2  - RSC Advances
T1  - Stabilization of alkali metal ions interaction with OH-functionalized graphene via clustering of OH groups - implications in charge storage applications
VL  - 6
IS  - 63
SP  - 57910
EP  - 57919
DO  - 10.1039/c6ra13509a
ER  - 
@article{
author = "Dobrota, Ana S. and Gutić, Sanjin J. and Kalijadis, Ana and Baljozović, Miloš and Mentus, Slavko V. and Skorodumova, Natalia V. and Pašti, Igor A.",
year = "2016",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/1155",
abstract = "Graphene synthesized by reduction of graphene oxide, depending on the degree of reduction, retains a certain amount of surface OH groups. Considering the surface OH groups/graphene layer system by means of density functional theory calculations, we evidenced the tendency of OH groups to cluster, resulting in enhanced system stability and no band gap opening. In the oxygen concentration range between 1.8 and 8.47 at%, with the addition of each new OH group, integral binding energy decreases, while differential binding energy shows the boost at even numbers of OH groups. Furthermore, we found that the clustering of OH groups over graphene basal plane plays a crucial role in enhancing the interactions with alkali metals. Namely, if alkali metal atoms interact with individual OH groups only, the interaction leads to an irreversible formation of MOH phase. When alkali atoms interact with clusters containing odd number of OH groups, a reversible transfer of an electron charge from the metal atom to the substrate takes place without OH removal. The strength of the interaction in general increases from Li to K. In an experimental investigation of a graphene sample which dominantly contains OH groups, we have shown that the trend in the specific interaction strength reflects to gravimetric capacitances measured in alkali metal chloride solutions. We propose that the charge stored in OH groups which interact with alkali metal cation and the pi electronic system of the graphene basal plane presents the main part of its pseudocapacitance.",
journal = "RSC Advances",
title = "Stabilization of alkali metal ions interaction with OH-functionalized graphene via clustering of OH groups - implications in charge storage applications",
volume = "6",
number = "63",
pages = "57910-57919",
doi = "10.1039/c6ra13509a"
}
Dobrota, A. S., Gutić, S. J., Kalijadis, A., Baljozović, M., Mentus, S. V., Skorodumova, N. V.,& Pašti, I. A. (2016). Stabilization of alkali metal ions interaction with OH-functionalized graphene via clustering of OH groups - implications in charge storage applications.
RSC Advances, 6(63), 57910-57919.
https://doi.org/10.1039/c6ra13509a
Dobrota AS, Gutić SJ, Kalijadis A, Baljozović M, Mentus SV, Skorodumova NV, Pašti IA. Stabilization of alkali metal ions interaction with OH-functionalized graphene via clustering of OH groups - implications in charge storage applications. RSC Advances. 2016;6(63):57910-57919
Dobrota Ana S., Gutić Sanjin J., Kalijadis Ana, Baljozović Miloš, Mentus Slavko V., Skorodumova Natalia V., Pašti Igor A., "Stabilization of alkali metal ions interaction with OH-functionalized graphene via clustering of OH groups - implications in charge storage applications" RSC Advances, 6, no. 63 (2016):57910-57919,
https://doi.org/10.1039/c6ra13509a .
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