TY  - JOUR
AU  - Bajuk-Bogdanović, Danica
AU  - Holclajtner-Antunović, Ivanka
AU  - Jovanović, Zoran
AU  - Mravik, Željko
AU  - Krstić, Jugoslav
AU  - Uskoković-Marković, Snežana
AU  - Vujković, Milica
PY  - 2019
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3368
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.
PB  - Springer Science and Business Media LLC
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 and Holclajtner-Antunović, Ivanka and Jovanović, Zoran and Mravik, Željko and Krstić, Jugoslav and Uskoković-Marković, Snežana and Vujković, Milica",
year = "2019",
abstract = "The synergistic effects between two Keggin-type heteropoly acids (HPAs) and carbon surface were examined and elucidated. An improved high rate capability (and potential high capacitor electrode for supercapacitors) of the hybrid materials, obtained by anchoring of α-dodecamolybdophosphoric (MoPA), α-dodecatungstophosphoric (WPA), and their mixture to activated carbon (AC), was achieved through the different mechanism of interaction. In order to elaborate this, a detailed analysis of AC-HPA composites has been performed by scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) analysis, temperature-programmed desorption (TPD), Fourier-transform infrared spectroscopy (FTIR), micro Raman spectroscopy, and zeta potential measurements. The zeta potential measurements revealed positive charge of carbon surface thus indicating attractive interactions with negatively charged Keggin anion. The surface analysis has shown that WPA spontaneously reduces the carbon surface, while interaction with MoPA leads to its oxidation. As the consequence of the tailoring of the functional groups at carbon surface through HPAs’ action, the distortion of cyclic voltammograms (CVs) decreased in the following order: AC-MoPA, AC-MoPA-WPA, and AC-WPA. A prominent rectangular shape of AC-WPA, even at an extremely high scan rate of 400 mVs−1, was measured, which is rarely demonstrated for carbon-based composites. By applying the theory of electrode potentials, the HPA-AC synergistic effect was explained and discussed in terms of charge storage improvement of HPA-modified carbon.",
publisher = "Springer Science and Business Media LLC",
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., Holclajtner-Antunović, I., Jovanović, Z., Mravik, Ž., Krstić, J., Uskoković-Marković, S.,& Vujković, M.. (2019). Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?. in Journal of Solid State Electrochemistry
Springer Science and Business Media LLC., 23(9), 2747-2758.
https://doi.org/10.1007/s10008-019-04369-4

Bajuk-Bogdanović D, Holclajtner-Antunović I, Jovanović Z, Mravik Ž, Krstić J, Uskoković-Marković S, Vujković M. Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?. in Journal of Solid State Electrochemistry. 2019;23(9):2747-2758.
doi:10.1007/s10008-019-04369-4 .

Bajuk-Bogdanović, Danica, Holclajtner-Antunović, Ivanka, Jovanović, Zoran, Mravik, Željko, Krstić, Jugoslav, Uskoković-Marković, Snežana, Vujković, Milica, "Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?" in Journal of Solid State Electrochemistry, 23, no. 9 (2019):2747-2758,
https://doi.org/10.1007/s10008-019-04369-4 . .

TY  - JOUR
AU  - Zdolšek, N.
AU  - Rocha, R.P.
AU  - Krstić, Jugoslav
AU  - Trtić-Petrović, Tatjana
AU  - Šljukić, Biljana
AU  - Figueiredo, J.L.
AU  - Vujković, Milica
PY  - 2019
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2488
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.
PB  - Elsevier
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, N. and Rocha, R.P. and Krstić, Jugoslav and Trtić-Petrović, Tatjana and Šljukić, Biljana and Figueiredo, J.L. and Vujković, Milica",
year = "2019",
abstract = "This work shows the potential application of carbon materials prepared by three different ionic liquid-based methods, using 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3], for electrochemical supercapacitors. The effects of [bmim][MeSO3] on morphology, texture and surface chemistry of prepared materials has been explored by SEM/TEM, N2/CO2 adsorption measurements and XPS. The results indicate the possibility of synthesis of carbon materials with tunable physicochemical properties using ionic liquid based methods. The charge storage behavior of all materials was studied in three different pH aqueous electrolytes. The pseudocapacitive and double layer contributions were estimated and discussed from the aspect of the textural changes and the changes of the chemical composition of surface functional groups containing heteroatoms. C[dbnd]O type functional groups, with the contribution of COOH groups, were found to be responsible for a different amount of charge, which could be stored in alkaline and acidic electrolytic solution. The material prepared by direct carbonization of [bmim][MeSO3], showed the best electrochemical performance in alkaline electrolyte with a capacitance of 187 F g−1 at 5 mV s−1 (or 148 F g−1 at 1 A g−1), due to the contribution of both electric-double layer capacitance and pseudocapacitance which arises from oxygen, nitrogen and sulfur functional groups.",
publisher = "Elsevier",
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., Trtić-Petrović, T., Šljukić, B., Figueiredo, J.L.,& Vujković, M.. (2019). Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer. in Electrochimica Acta
Elsevier., 298, 541-551.
https://doi.org/10.1016/j.electacta.2018.12.129

Zdolšek N, Rocha R, Krstić J, Trtić-Petrović T, Šljukić B, Figueiredo J, Vujković M. Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer. in Electrochimica Acta. 2019;298:541-551.
doi:10.1016/j.electacta.2018.12.129 .

Zdolšek, N., Rocha, R.P., Krstić, Jugoslav, Trtić-Petrović, Tatjana, Šljukić, Biljana, Figueiredo, J.L., Vujković, Milica, "Electrochemical investigation of ionic liquid-derived porous carbon materials for supercapacitors: pseudocapacitance versus electrical double layer" in Electrochimica Acta, 298 (2019):541-551,
https://doi.org/10.1016/j.electacta.2018.12.129 . .

TY  - JOUR
AU  - Zdolsek, Nikola
AU  - Dimitrijević, Aleksandra
AU  - Bendova, Magdalena
AU  - Krstić, Jugoslav
AU  - Rocha, Raquel P.
AU  - Figueiredo, Jose L.
AU  - Bajuk-Bogdanovic, Danica
AU  - Trtic-Petrovic, Tatjana
AU  - Šljukić, Biljana
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2337
AB  - Carbon materials, prepared by using different methods with ionic liquids, are compared as electrocatalysts for the oxygen reduction reaction (ORR). Materials were synthesized through the hydrothermal carbonization of glucose and by using the same method in the presence of 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3] as an additive. Another two carbon-based materials were prepared by using ionic-liquid-based methods: ionothermal carbonization of glucose using [bmim][MeSO3] as a recyclable medium for the carbonization reaction and by direct carbonization of the ionic liquid in a one-step method using [bmim][MeSO3] as the precursor for N- and S-doped porous carbon (Carb-IL). Characterization results showed the possibility of morphology and porosity control by using [bmim][MeSO3]. All materials were subsequently tested for the ORR in alkaline media. Carb-IL showed enhanced and stable electrocatalytic ORR activity, even in the presence of methanol, ethanol, and borohydride, opening the possibility for its application in fuel cells.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - Chemelectrochem
T1  - Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction
VL  - 5
IS  - 7
SP  - 1037
EP  - 1046
DO  - 10.1002/celc.201701369
ER  - 

@article{
author = "Zdolsek, Nikola and Dimitrijević, Aleksandra and Bendova, Magdalena and Krstić, Jugoslav and Rocha, Raquel P. and Figueiredo, Jose L. and Bajuk-Bogdanovic, Danica and Trtic-Petrovic, Tatjana and Šljukić, Biljana",
year = "2018",
abstract = "Carbon materials, prepared by using different methods with ionic liquids, are compared as electrocatalysts for the oxygen reduction reaction (ORR). Materials were synthesized through the hydrothermal carbonization of glucose and by using the same method in the presence of 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3] as an additive. Another two carbon-based materials were prepared by using ionic-liquid-based methods: ionothermal carbonization of glucose using [bmim][MeSO3] as a recyclable medium for the carbonization reaction and by direct carbonization of the ionic liquid in a one-step method using [bmim][MeSO3] as the precursor for N- and S-doped porous carbon (Carb-IL). Characterization results showed the possibility of morphology and porosity control by using [bmim][MeSO3]. All materials were subsequently tested for the ORR in alkaline media. Carb-IL showed enhanced and stable electrocatalytic ORR activity, even in the presence of methanol, ethanol, and borohydride, opening the possibility for its application in fuel cells.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "Chemelectrochem",
title = "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction",
volume = "5",
number = "7",
pages = "1037-1046",
doi = "10.1002/celc.201701369"
}

Zdolsek, N., Dimitrijević, A., Bendova, M., Krstić, J., Rocha, R. P., Figueiredo, J. L., Bajuk-Bogdanovic, D., Trtic-Petrovic, T.,& Šljukić, B.. (2018). Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in Chemelectrochem
Wiley-V C H Verlag Gmbh, Weinheim., 5(7), 1037-1046.
https://doi.org/10.1002/celc.201701369

Zdolsek N, Dimitrijević A, Bendova M, Krstić J, Rocha RP, Figueiredo JL, Bajuk-Bogdanovic D, Trtic-Petrovic T, Šljukić B. Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in Chemelectrochem. 2018;5(7):1037-1046.
doi:10.1002/celc.201701369 .

Zdolsek, Nikola, Dimitrijević, Aleksandra, Bendova, Magdalena, Krstić, Jugoslav, Rocha, Raquel P., Figueiredo, Jose L., Bajuk-Bogdanovic, Danica, Trtic-Petrovic, Tatjana, Šljukić, Biljana, "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction" in Chemelectrochem, 5, no. 7 (2018):1037-1046,
https://doi.org/10.1002/celc.201701369 . .

TY  - JOUR
AU  - Zdolsek, Nikola
AU  - Dimitrijević, Aleksandra
AU  - Bendova, Magdalena
AU  - Krstić, Jugoslav
AU  - Rocha, Raquel P.
AU  - Figueiredo, Jose L.
AU  - Bajuk-Bogdanovic, Danica
AU  - Trtic-Petrovic, Tatjana
AU  - Šljukić, Biljana
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3138
AB  - Carbon materials, prepared by using different methods with ionic liquids, are compared as electrocatalysts for the oxygen reduction reaction (ORR). Materials were synthesized through the hydrothermal carbonization of glucose and by using the same method in the presence of 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3] as an additive. Another two carbon-based materials were prepared by using ionic-liquid-based methods: ionothermal carbonization of glucose using [bmim][MeSO3] as a recyclable medium for the carbonization reaction and by direct carbonization of the ionic liquid in a one-step method using [bmim][MeSO3] as the precursor for N- and S-doped porous carbon (Carb-IL). Characterization results showed the possibility of morphology and porosity control by using [bmim][MeSO3]. All materials were subsequently tested for the ORR in alkaline media. Carb-IL showed enhanced and stable electrocatalytic ORR activity, even in the presence of methanol, ethanol, and borohydride, opening the possibility for its application in fuel cells.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - Chemelectrochem
T1  - Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction
VL  - 5
IS  - 7
SP  - 1037
EP  - 1046
DO  - 10.1002/celc.201701369
ER  - 

@article{
author = "Zdolsek, Nikola and Dimitrijević, Aleksandra and Bendova, Magdalena and Krstić, Jugoslav and Rocha, Raquel P. and Figueiredo, Jose L. and Bajuk-Bogdanovic, Danica and Trtic-Petrovic, Tatjana and Šljukić, Biljana",
year = "2018",
abstract = "Carbon materials, prepared by using different methods with ionic liquids, are compared as electrocatalysts for the oxygen reduction reaction (ORR). Materials were synthesized through the hydrothermal carbonization of glucose and by using the same method in the presence of 1-butyl-3-methylimidazolium methanesulfonate [bmim][MeSO3] as an additive. Another two carbon-based materials were prepared by using ionic-liquid-based methods: ionothermal carbonization of glucose using [bmim][MeSO3] as a recyclable medium for the carbonization reaction and by direct carbonization of the ionic liquid in a one-step method using [bmim][MeSO3] as the precursor for N- and S-doped porous carbon (Carb-IL). Characterization results showed the possibility of morphology and porosity control by using [bmim][MeSO3]. All materials were subsequently tested for the ORR in alkaline media. Carb-IL showed enhanced and stable electrocatalytic ORR activity, even in the presence of methanol, ethanol, and borohydride, opening the possibility for its application in fuel cells.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "Chemelectrochem",
title = "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction",
volume = "5",
number = "7",
pages = "1037-1046",
doi = "10.1002/celc.201701369"
}

Zdolsek, N., Dimitrijević, A., Bendova, M., Krstić, J., Rocha, R. P., Figueiredo, J. L., Bajuk-Bogdanovic, D., Trtic-Petrovic, T.,& Šljukić, B.. (2018). Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in Chemelectrochem
Wiley-V C H Verlag Gmbh, Weinheim., 5(7), 1037-1046.
https://doi.org/10.1002/celc.201701369

Zdolsek N, Dimitrijević A, Bendova M, Krstić J, Rocha RP, Figueiredo JL, Bajuk-Bogdanovic D, Trtic-Petrovic T, Šljukić B. Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction. in Chemelectrochem. 2018;5(7):1037-1046.
doi:10.1002/celc.201701369 .

Zdolsek, Nikola, Dimitrijević, Aleksandra, Bendova, Magdalena, Krstić, Jugoslav, Rocha, Raquel P., Figueiredo, Jose L., Bajuk-Bogdanovic, Danica, Trtic-Petrovic, Tatjana, Šljukić, Biljana, "Electrocatalytic Activity of Ionic-Liquid-Derived Porous Carbon Materials for the Oxygen Reduction Reaction" in Chemelectrochem, 5, no. 7 (2018):1037-1046,
https://doi.org/10.1002/celc.201701369 . .

TY  - JOUR
AU  - Laušević, Zoran
AU  - Apel, Pavel Yu
AU  - Krstić, Jugoslav
AU  - Blonskaya, Irina V.
PY  - 2013
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1299
AB  - Activation effects on carbon films, derived from commercial aromatic polyimide films (Kapton, DuPont), in CO2 atmosphere at 1203 K on capacitance properties were studied. Two thicknesses of polyimide films were used: 7 and 25 gm. Pore formation during the activation process progresses in two steps due to the existence of a denser surface layer and a more porous core material. In the first step micropores are opening in the dense surface region of the material with average pore diameter smaller than 1 nm. During the second step, mesopores start opening, while micropore volume remains constant with the average micropore diameter of over 1 nm, producing bimodal texture. The first step finishes after 30 min for the thinner samples while for the thicker samples it finishes after 60 mm of activation. As a consequence of such textural changes during activation, the thicker sample has a maximum areal capacitance of 0.35 F/cm(2). The thinner sample activated for 30 min has a maximum volumetric capacitance of 220 F/cm(3) and achieves a maximum gravimetric capacitance of 240 F/g when the texture becomes bimodal after 240 min of activation. These results confirm that activation of carbonized Kapton films gives promising electrode materials for supercapacitors.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Carbon
T1  - Porous carbon thin films for electrochemical capacitors
VL  - 64
SP  - 456
EP  - 463
DO  - 10.1016/j.carbon.2013.07.098
ER  - 

@article{
author = "Laušević, Zoran and Apel, Pavel Yu and Krstić, Jugoslav and Blonskaya, Irina V.",
year = "2013",
abstract = "Activation effects on carbon films, derived from commercial aromatic polyimide films (Kapton, DuPont), in CO2 atmosphere at 1203 K on capacitance properties were studied. Two thicknesses of polyimide films were used: 7 and 25 gm. Pore formation during the activation process progresses in two steps due to the existence of a denser surface layer and a more porous core material. In the first step micropores are opening in the dense surface region of the material with average pore diameter smaller than 1 nm. During the second step, mesopores start opening, while micropore volume remains constant with the average micropore diameter of over 1 nm, producing bimodal texture. The first step finishes after 30 min for the thinner samples while for the thicker samples it finishes after 60 mm of activation. As a consequence of such textural changes during activation, the thicker sample has a maximum areal capacitance of 0.35 F/cm(2). The thinner sample activated for 30 min has a maximum volumetric capacitance of 220 F/cm(3) and achieves a maximum gravimetric capacitance of 240 F/g when the texture becomes bimodal after 240 min of activation. These results confirm that activation of carbonized Kapton films gives promising electrode materials for supercapacitors.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Carbon",
title = "Porous carbon thin films for electrochemical capacitors",
volume = "64",
pages = "456-463",
doi = "10.1016/j.carbon.2013.07.098"
}

Laušević, Z., Apel, P. Y., Krstić, J.,& Blonskaya, I. V.. (2013). Porous carbon thin films for electrochemical capacitors. in Carbon
Oxford : Pergamon-Elsevier Science Ltd., 64, 456-463.
https://doi.org/10.1016/j.carbon.2013.07.098

Laušević Z, Apel PY, Krstić J, Blonskaya IV. Porous carbon thin films for electrochemical capacitors. in Carbon. 2013;64:456-463.
doi:10.1016/j.carbon.2013.07.098 .

Laušević, Zoran, Apel, Pavel Yu, Krstić, Jugoslav, Blonskaya, Irina V., "Porous carbon thin films for electrochemical capacitors" in Carbon, 64 (2013):456-463,
https://doi.org/10.1016/j.carbon.2013.07.098 . .

TY  - JOUR
AU  - Jovanovic, Zoran
AU  - Kalijadis, Ana
AU  - Vasiljević-Radović, Dana
AU  - Eric, Marko
AU  - Lausevic, Mila
AU  - Mentus, Slavko
AU  - Laušević, Zoran
PY  - 2011
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/796
AB  - Glassy carbon plates were irradiated with 15 key H(+) ion-beam in the fluence range of 1 x 10(16)-3 x 10(18) ion cm(-2). The influence of ion irradiation on surface morphology and topology was examined by scanning electron and atomic force microscopy. Structural changes were monitored by Raman spectrometry, while changes of wettability and the content of surface oxygen complexes were examined by contact angle measurements and temperature programmed desorption. Elastic recoil detection analysis was applied for determination of hydrogen concentration profiles in irradiated samples. Cyclic voltammetry was used for the assessment of the electrochemical properties of modified glassy carbon electrodes. It was concluded that there is critical fluence range (2 x 10(17)-5 x 10(17) ion cm(-2)) inside of which significant changes of glassy carbon properties occur.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Carbon
T1  - Modification of glassy carbon properties under low energy proton irradiation
VL  - 49
IS  - 12
SP  - 3737
EP  - 3746
DO  - 10.1016/j.carbon.2011.05.006
ER  - 

@article{
author = "Jovanovic, Zoran and Kalijadis, Ana and Vasiljević-Radović, Dana and Eric, Marko and Lausevic, Mila and Mentus, Slavko and Laušević, Zoran",
year = "2011",
abstract = "Glassy carbon plates were irradiated with 15 key H(+) ion-beam in the fluence range of 1 x 10(16)-3 x 10(18) ion cm(-2). The influence of ion irradiation on surface morphology and topology was examined by scanning electron and atomic force microscopy. Structural changes were monitored by Raman spectrometry, while changes of wettability and the content of surface oxygen complexes were examined by contact angle measurements and temperature programmed desorption. Elastic recoil detection analysis was applied for determination of hydrogen concentration profiles in irradiated samples. Cyclic voltammetry was used for the assessment of the electrochemical properties of modified glassy carbon electrodes. It was concluded that there is critical fluence range (2 x 10(17)-5 x 10(17) ion cm(-2)) inside of which significant changes of glassy carbon properties occur.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Carbon",
title = "Modification of glassy carbon properties under low energy proton irradiation",
volume = "49",
number = "12",
pages = "3737-3746",
doi = "10.1016/j.carbon.2011.05.006"
}

Jovanovic, Z., Kalijadis, A., Vasiljević-Radović, D., Eric, M., Lausevic, M., Mentus, S.,& Laušević, Z.. (2011). Modification of glassy carbon properties under low energy proton irradiation. in Carbon
Oxford : Pergamon-Elsevier Science Ltd., 49(12), 3737-3746.
https://doi.org/10.1016/j.carbon.2011.05.006

Jovanovic Z, Kalijadis A, Vasiljević-Radović D, Eric M, Lausevic M, Mentus S, Laušević Z. Modification of glassy carbon properties under low energy proton irradiation. in Carbon. 2011;49(12):3737-3746.
doi:10.1016/j.carbon.2011.05.006 .

Jovanovic, Zoran, Kalijadis, Ana, Vasiljević-Radović, Dana, Eric, Marko, Lausevic, Mila, Mentus, Slavko, Laušević, Zoran, "Modification of glassy carbon properties under low energy proton irradiation" in Carbon, 49, no. 12 (2011):3737-3746,
https://doi.org/10.1016/j.carbon.2011.05.006 . .