TY  - JOUR
AU  - Nikolić, Maria Vesna
AU  - Krstić, Jugoslav
AU  - Labus, Nebojša
AU  - Luković, Miloljub
AU  - Dojčinović, Milena P.
AU  - Radovanović, Milan
AU  - Tadić, Nenad
PY  - 2020
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3573
AB  - Iron manganite (FeMnO3) powder with a cubic (bixbyite,
−
Ia3) crystal structure was obtained by a solid state
reaction. Thick film paste (powder+organic vehicles) was screen printed on alumina substrate with test interdigitated
PdAg electrodes. Significant porosity (60.6%) composed of macropores (larger than 100 nm) was
determined by Hg porosimetry, changing only slightly from the first extrusion run indicating a stable pore
system. Hg porosimetry evaluation of thick film samples enabled estimation of true textural parameters of the
thick film compared to powder. Impedance response of the thick film sensor was monitored in a humidity
chamber in the relative humidity (RH) range 30–90%, at room temperature (25 °C) and frequency range from
42 Hz to 1 MHz. At 100 Hz the impedance reduced from 10.41 MΩ for RH 30% to 0.68 MΩ for RH 90%. Analysis
of complex impedance using an equivalent circuit showed the dominant influence of grain boundaries. The
sensor response and recovery was fast (several seconds) and a relatively low hysteresis value of 2.8% was
obtained.
PB  - Elsevier
T2  - Materials Science and Engineering B: Solid-State Materials for Advanced Technology
T1  - Structural, morphological and textural properties of iron manganite (FeMnO3) thick films applied for humidity sensing
VL  - 257
SP  - 114547
DO  - 10.1016/j.mseb.2020.114547
ER  - 

@article{
author = "Nikolić, Maria Vesna and Krstić, Jugoslav and Labus, Nebojša and Luković, Miloljub and Dojčinović, Milena P. and Radovanović, Milan and Tadić, Nenad",
year = "2020",
abstract = "Iron manganite (FeMnO3) powder with a cubic (bixbyite,
−
Ia3) crystal structure was obtained by a solid state
reaction. Thick film paste (powder+organic vehicles) was screen printed on alumina substrate with test interdigitated
PdAg electrodes. Significant porosity (60.6%) composed of macropores (larger than 100 nm) was
determined by Hg porosimetry, changing only slightly from the first extrusion run indicating a stable pore
system. Hg porosimetry evaluation of thick film samples enabled estimation of true textural parameters of the
thick film compared to powder. Impedance response of the thick film sensor was monitored in a humidity
chamber in the relative humidity (RH) range 30–90%, at room temperature (25 °C) and frequency range from
42 Hz to 1 MHz. At 100 Hz the impedance reduced from 10.41 MΩ for RH 30% to 0.68 MΩ for RH 90%. Analysis
of complex impedance using an equivalent circuit showed the dominant influence of grain boundaries. The
sensor response and recovery was fast (several seconds) and a relatively low hysteresis value of 2.8% was
obtained.",
publisher = "Elsevier",
journal = "Materials Science and Engineering B: Solid-State Materials for Advanced Technology",
title = "Structural, morphological and textural properties of iron manganite (FeMnO3) thick films applied for humidity sensing",
volume = "257",
pages = "114547",
doi = "10.1016/j.mseb.2020.114547"
}

Nikolić, M. V., Krstić, J., Labus, N., Luković, M., Dojčinović, M. P., Radovanović, M.,& Tadić, N.. (2020). Structural, morphological and textural properties of iron manganite (FeMnO3) thick films applied for humidity sensing. in Materials Science and Engineering B: Solid-State Materials for Advanced Technology
Elsevier., 257, 114547.
https://doi.org/10.1016/j.mseb.2020.114547

Nikolić MV, Krstić J, Labus N, Luković M, Dojčinović MP, Radovanović M, Tadić N. Structural, morphological and textural properties of iron manganite (FeMnO3) thick films applied for humidity sensing. in Materials Science and Engineering B: Solid-State Materials for Advanced Technology. 2020;257:114547.
doi:10.1016/j.mseb.2020.114547 .

Nikolić, Maria Vesna, Krstić, Jugoslav, Labus, Nebojša, Luković, Miloljub, Dojčinović, Milena P., Radovanović, Milan, Tadić, Nenad, "Structural, morphological and textural properties of iron manganite (FeMnO3) thick films applied for humidity sensing" in Materials Science and Engineering B: Solid-State Materials for Advanced Technology, 257 (2020):114547,
https://doi.org/10.1016/j.mseb.2020.114547 . .

TY  - JOUR
AU  - Nikolić, Maria Vesna
AU  - Krstić, Jugoslav
AU  - Labus, Nebojša
AU  - Luković, Miloljub
AU  - Dojčinović, Milena P.
AU  - Radovanović, Milan
AU  - Tadić, Nenad
PY  - 2020
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4278
AB  - Iron manganite (FeMnO3) powder with a cubic (bixbyite,−Ia3) crystal structure was obtained by a solid statereaction. Thick film paste (powder+organic vehicles) was screen printed on alumina substrate with test interdigitatedPdAg electrodes. Significant porosity (60.6%) composed of macropores (larger than 100 nm) wasdetermined by Hg porosimetry, changing only slightly from the first extrusion run indicating a stable poresystem. Hg porosimetry evaluation of thick film samples enabled estimation of true textural parameters of thethick film compared to powder. Impedance response of the thick film sensor was monitored in a humiditychamber in the relative humidity (RH) range 30–90%, at room temperature (25 °C) and frequency range from42 Hz to 1 MHz. At 100 Hz the impedance reduced from 10.41 MΩ for RH 30% to 0.68 MΩ for RH 90%. Analysisof complex impedance using an equivalent circuit showed the dominant influence of grain boundaries. Thesensor response and recovery was fast (several seconds) and a relatively low hysteresis value of 2.8% wasobtained.
PB  - Elsevier
T2  - Materials Science and Engineering B: Solid-State Materials for Advanced Technology
T1  - Structural, morphological and textural properties of iron manganite (FeMnO3) thick films applied for humidity sensing
VL  - 257
SP  - 114547
DO  - 10.1016/j.mseb.2020.114547
ER  - 

@article{
author = "Nikolić, Maria Vesna and Krstić, Jugoslav and Labus, Nebojša and Luković, Miloljub and Dojčinović, Milena P. and Radovanović, Milan and Tadić, Nenad",
year = "2020",
abstract = "Iron manganite (FeMnO3) powder with a cubic (bixbyite,−Ia3) crystal structure was obtained by a solid statereaction. Thick film paste (powder+organic vehicles) was screen printed on alumina substrate with test interdigitatedPdAg electrodes. Significant porosity (60.6%) composed of macropores (larger than 100 nm) wasdetermined by Hg porosimetry, changing only slightly from the first extrusion run indicating a stable poresystem. Hg porosimetry evaluation of thick film samples enabled estimation of true textural parameters of thethick film compared to powder. Impedance response of the thick film sensor was monitored in a humiditychamber in the relative humidity (RH) range 30–90%, at room temperature (25 °C) and frequency range from42 Hz to 1 MHz. At 100 Hz the impedance reduced from 10.41 MΩ for RH 30% to 0.68 MΩ for RH 90%. Analysisof complex impedance using an equivalent circuit showed the dominant influence of grain boundaries. Thesensor response and recovery was fast (several seconds) and a relatively low hysteresis value of 2.8% wasobtained.",
publisher = "Elsevier",
journal = "Materials Science and Engineering B: Solid-State Materials for Advanced Technology",
title = "Structural, morphological and textural properties of iron manganite (FeMnO3) thick films applied for humidity sensing",
volume = "257",
pages = "114547",
doi = "10.1016/j.mseb.2020.114547"
}

Nikolić, M. V., Krstić, J., Labus, N., Luković, M., Dojčinović, M. P., Radovanović, M.,& Tadić, N.. (2020). Structural, morphological and textural properties of iron manganite (FeMnO3) thick films applied for humidity sensing. in Materials Science and Engineering B: Solid-State Materials for Advanced Technology
Elsevier., 257, 114547.
https://doi.org/10.1016/j.mseb.2020.114547

Nikolić MV, Krstić J, Labus N, Luković M, Dojčinović MP, Radovanović M, Tadić N. Structural, morphological and textural properties of iron manganite (FeMnO3) thick films applied for humidity sensing. in Materials Science and Engineering B: Solid-State Materials for Advanced Technology. 2020;257:114547.
doi:10.1016/j.mseb.2020.114547 .

Nikolić, Maria Vesna, Krstić, Jugoslav, Labus, Nebojša, Luković, Miloljub, Dojčinović, Milena P., Radovanović, Milan, Tadić, Nenad, "Structural, morphological and textural properties of iron manganite (FeMnO3) thick films applied for humidity sensing" in Materials Science and Engineering B: Solid-State Materials for Advanced Technology, 257 (2020):114547,
https://doi.org/10.1016/j.mseb.2020.114547 . .

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  - Nikolić, Maria Vesna
AU  - Vasiljević, Zorka
AU  - Luković, Miloljub
AU  - Pavlović, Vera P.
AU  - Krstić, Jugoslav
AU  - Vujančević, Jelena
AU  - Tadić, Nenad
AU  - Vlahović, Branislav
AU  - Pavlović, Vladimir B.
PY  - 2019
UR  - https://ceramics.onlinelibrary.wiley.com/doi/abs/10.1111/ijac.13190
UR  - http://dais.sanu.ac.rs/123456789/4848
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2603
AB  - Zinc ferrite nanocrystalline powder was obtained by solid state synthesis of starting zinc oxide and hematite nanopowders. Field emission scanning electron microscopy (FESEM and transmission electron microscopy (TEM), X‐ray diffraction (XRD), X‐ray photoelectron spectroscopy (XPS) and Raman spectroscopy confirmed the formation of nanocrystalline zinc‐ferrite powder with a mixed spinel structure with small amounts of remaining zinc oxide and hematite as impurities. Thick film paste was formed and screen printed on test interdigitated PdAg electrodes on alumina substrate. Formation of a porous nanocrystalline structure was confirmed by scanning electron microscopy (SEM) and Hg porosimetry. Humidity sensing properties of zinc ferrite thick films were investigated by monitoring the change in impedance in the relative humidity interval 30‐90% in the frequency range 42 Hz – 1 MHz at room temperature (25 °C) and 50 °C. At 42 Hz at both analyzed temperatures the impedance reduced ~ 46 times in the humidity range 30‐90%. The dominant influence of grain boundaries was confirmed by analysis of complex impedance with an equivalent circuit.
PB  - John Wiley & Sons, Inc.
T2  - International Journal of Applied Ceramic Technology
T1  - Investigation of ZnFe2O4 spinel ferrite nanocrystalline screen‐printed thick films for application in humidity sensing
DO  - 10.1111/ijac.13190
ER  - 

@article{
author = "Nikolić, Maria Vesna and Vasiljević, Zorka and Luković, Miloljub and Pavlović, Vera P. and Krstić, Jugoslav and Vujančević, Jelena and Tadić, Nenad and Vlahović, Branislav and Pavlović, Vladimir B.",
year = "2019",
abstract = "Zinc ferrite nanocrystalline powder was obtained by solid state synthesis of starting zinc oxide and hematite nanopowders. Field emission scanning electron microscopy (FESEM and transmission electron microscopy (TEM), X‐ray diffraction (XRD), X‐ray photoelectron spectroscopy (XPS) and Raman spectroscopy confirmed the formation of nanocrystalline zinc‐ferrite powder with a mixed spinel structure with small amounts of remaining zinc oxide and hematite as impurities. Thick film paste was formed and screen printed on test interdigitated PdAg electrodes on alumina substrate. Formation of a porous nanocrystalline structure was confirmed by scanning electron microscopy (SEM) and Hg porosimetry. Humidity sensing properties of zinc ferrite thick films were investigated by monitoring the change in impedance in the relative humidity interval 30‐90% in the frequency range 42 Hz – 1 MHz at room temperature (25 °C) and 50 °C. At 42 Hz at both analyzed temperatures the impedance reduced ~ 46 times in the humidity range 30‐90%. The dominant influence of grain boundaries was confirmed by analysis of complex impedance with an equivalent circuit.",
publisher = "John Wiley & Sons, Inc.",
journal = "International Journal of Applied Ceramic Technology",
title = "Investigation of ZnFe2O4 spinel ferrite nanocrystalline screen‐printed thick films for application in humidity sensing",
doi = "10.1111/ijac.13190"
}

Nikolić, M. V., Vasiljević, Z., Luković, M., Pavlović, V. P., Krstić, J., Vujančević, J., Tadić, N., Vlahović, B.,& Pavlović, V. B.. (2019). Investigation of ZnFe2O4 spinel ferrite nanocrystalline screen‐printed thick films for application in humidity sensing. in International Journal of Applied Ceramic Technology
John Wiley & Sons, Inc...
https://doi.org/10.1111/ijac.13190

Nikolić MV, Vasiljević Z, Luković M, Pavlović VP, Krstić J, Vujančević J, Tadić N, Vlahović B, Pavlović VB. Investigation of ZnFe2O4 spinel ferrite nanocrystalline screen‐printed thick films for application in humidity sensing. in International Journal of Applied Ceramic Technology. 2019;.
doi:10.1111/ijac.13190 .

Nikolić, Maria Vesna, Vasiljević, Zorka, Luković, Miloljub, Pavlović, Vera P., Krstić, Jugoslav, Vujančević, Jelena, Tadić, Nenad, Vlahović, Branislav, Pavlović, Vladimir B., "Investigation of ZnFe2O4 spinel ferrite nanocrystalline screen‐printed thick films for application in humidity sensing" in International Journal of Applied Ceramic Technology (2019),
https://doi.org/10.1111/ijac.13190 . .

TY  - JOUR
AU  - Nikolić, Maria Vesna
AU  - Vasiljević, Zorka
AU  - Luković, Miloljub
AU  - Pavlović, Vera P.
AU  - Krstić, Jugoslav
AU  - Vujančević, Jelena
AU  - Tadić, Nenad
AU  - Vlahović, Branislav
AU  - Pavlović, Vladimir B.
PY  - 2019
UR  - https://ceramics.onlinelibrary.wiley.com/doi/abs/10.1111/ijac.13190
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2851
AB  - Zinc ferrite nanocrystalline powder was obtained by solid state synthesis of starting zinc oxide and hematite nanopowders. Field emission scanning electron microscopy (FESEM and transmission electron microscopy (TEM), X‐ray diffraction (XRD), X‐ray photoelectron spectroscopy (XPS) and Raman spectroscopy confirmed the formation of nanocrystalline zinc‐ferrite powder with a mixed spinel structure with small amounts of remaining zinc oxide and hematite as impurities. Thick film paste was formed and screen printed on test interdigitated PdAg electrodes on alumina substrate. Formation of a porous nanocrystalline structure was confirmed by scanning electron microscopy (SEM) and Hg porosimetry. Humidity sensing properties of zinc ferrite thick films were investigated by monitoring the change in impedance in the relative humidity interval 30‐90% in the frequency range 42 Hz – 1 MHz at room temperature (25 °C) and 50 °C. At 42 Hz at both analyzed temperatures the impedance reduced ~ 46 times in the humidity range 30‐90%. The dominant influence of grain boundaries was confirmed by analysis of complex impedance with an equivalent circuit.
PB  - John Wiley & Sons, Inc.
T2  - International Journal of Applied Ceramic Technology
T1  - Investigation of ZnFe2O4 spinel ferrite nanocrystalline screen‐printed thick films for application in humidity sensing
VL  - 16
IS  - 3
SP  - 981
EP  - 993
DO  - 10.1111/ijac.13190
ER  - 

@article{
author = "Nikolić, Maria Vesna and Vasiljević, Zorka and Luković, Miloljub and Pavlović, Vera P. and Krstić, Jugoslav and Vujančević, Jelena and Tadić, Nenad and Vlahović, Branislav and Pavlović, Vladimir B.",
year = "2019",
abstract = "Zinc ferrite nanocrystalline powder was obtained by solid state synthesis of starting zinc oxide and hematite nanopowders. Field emission scanning electron microscopy (FESEM and transmission electron microscopy (TEM), X‐ray diffraction (XRD), X‐ray photoelectron spectroscopy (XPS) and Raman spectroscopy confirmed the formation of nanocrystalline zinc‐ferrite powder with a mixed spinel structure with small amounts of remaining zinc oxide and hematite as impurities. Thick film paste was formed and screen printed on test interdigitated PdAg electrodes on alumina substrate. Formation of a porous nanocrystalline structure was confirmed by scanning electron microscopy (SEM) and Hg porosimetry. Humidity sensing properties of zinc ferrite thick films were investigated by monitoring the change in impedance in the relative humidity interval 30‐90% in the frequency range 42 Hz – 1 MHz at room temperature (25 °C) and 50 °C. At 42 Hz at both analyzed temperatures the impedance reduced ~ 46 times in the humidity range 30‐90%. The dominant influence of grain boundaries was confirmed by analysis of complex impedance with an equivalent circuit.",
publisher = "John Wiley & Sons, Inc.",
journal = "International Journal of Applied Ceramic Technology",
title = "Investigation of ZnFe2O4 spinel ferrite nanocrystalline screen‐printed thick films for application in humidity sensing",
volume = "16",
number = "3",
pages = "981-993",
doi = "10.1111/ijac.13190"
}

Nikolić, M. V., Vasiljević, Z., Luković, M., Pavlović, V. P., Krstić, J., Vujančević, J., Tadić, N., Vlahović, B.,& Pavlović, V. B.. (2019). Investigation of ZnFe2O4 spinel ferrite nanocrystalline screen‐printed thick films for application in humidity sensing. in International Journal of Applied Ceramic Technology
John Wiley & Sons, Inc.., 16(3), 981-993.
https://doi.org/10.1111/ijac.13190

Nikolić MV, Vasiljević Z, Luković M, Pavlović VP, Krstić J, Vujančević J, Tadić N, Vlahović B, Pavlović VB. Investigation of ZnFe2O4 spinel ferrite nanocrystalline screen‐printed thick films for application in humidity sensing. in International Journal of Applied Ceramic Technology. 2019;16(3):981-993.
doi:10.1111/ijac.13190 .

Nikolić, Maria Vesna, Vasiljević, Zorka, Luković, Miloljub, Pavlović, Vera P., Krstić, Jugoslav, Vujančević, Jelena, Tadić, Nenad, Vlahović, Branislav, Pavlović, Vladimir B., "Investigation of ZnFe2O4 spinel ferrite nanocrystalline screen‐printed thick films for application in humidity sensing" in International Journal of Applied Ceramic Technology, 16, no. 3 (2019):981-993,
https://doi.org/10.1111/ijac.13190 . .

TY  - JOUR
AU  - Pagnacco, Maja
AU  - Maksimović, Jelena
AU  - Mudrinić, Tihana
AU  - Mojović, Zorica
AU  - Nedić, Zoran P.
PY  - 2019
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3058
AB  - Briggs-Rauscher (BR) oscillatory reaction is a chemical system very sensitive to different analyte addition. Changes in oscillatory dynamics, by analyte addition, could be successfully used for the determination of analyte concentration, as well as for its antioxidative/antiradical activity assessment. In this work, the BR reaction is used as a system detector for distinguishing solid unsolvable materials, such as phosphate tungsten bronze (PWB) and phosphate molybdenum bronze (PMoB), obtained by thermal treatment. The addition of different masses of PWB in BR reaction decreases its oscillation time, while the addition of different masses of PMoB had no effects on the BR oscillation time. Additionally, the BR oscillation time is the linear function of added PWB mass. The mechanism of bronzes action is investigated by using pH and electric conductivity measurements, as well as inductively coupled plasma and the cyclic voltammetry measurements, and it can be ascribed to PWB better catalytic activity then PMoB, under BR reaction condition. This work extends the practical aspect of the BR reaction for testing solid (insoluble) materials, and opening the possibility of using oscillatory reactions in material science and catalysis, in general.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Briggs-Rauscher reaction as a novel electrochemical detector for phosphate tungsten and phosphate molybdenum bronzes
VL  - 849
SP  - 113369
DO  - 10.1016/j.jelechem.2019.113369
ER  - 

@article{
author = "Pagnacco, Maja and Maksimović, Jelena and Mudrinić, Tihana and Mojović, Zorica and Nedić, Zoran P.",
year = "2019",
abstract = "Briggs-Rauscher (BR) oscillatory reaction is a chemical system very sensitive to different analyte addition. Changes in oscillatory dynamics, by analyte addition, could be successfully used for the determination of analyte concentration, as well as for its antioxidative/antiradical activity assessment. In this work, the BR reaction is used as a system detector for distinguishing solid unsolvable materials, such as phosphate tungsten bronze (PWB) and phosphate molybdenum bronze (PMoB), obtained by thermal treatment. The addition of different masses of PWB in BR reaction decreases its oscillation time, while the addition of different masses of PMoB had no effects on the BR oscillation time. Additionally, the BR oscillation time is the linear function of added PWB mass. The mechanism of bronzes action is investigated by using pH and electric conductivity measurements, as well as inductively coupled plasma and the cyclic voltammetry measurements, and it can be ascribed to PWB better catalytic activity then PMoB, under BR reaction condition. This work extends the practical aspect of the BR reaction for testing solid (insoluble) materials, and opening the possibility of using oscillatory reactions in material science and catalysis, in general.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Briggs-Rauscher reaction as a novel electrochemical detector for phosphate tungsten and phosphate molybdenum bronzes",
volume = "849",
pages = "113369",
doi = "10.1016/j.jelechem.2019.113369"
}

Pagnacco, M., Maksimović, J., Mudrinić, T., Mojović, Z.,& Nedić, Z. P.. (2019). Briggs-Rauscher reaction as a novel electrochemical detector for phosphate tungsten and phosphate molybdenum bronzes. in Journal of Electroanalytical Chemistry
Elsevier., 849, 113369.
https://doi.org/10.1016/j.jelechem.2019.113369

Pagnacco M, Maksimović J, Mudrinić T, Mojović Z, Nedić ZP. Briggs-Rauscher reaction as a novel electrochemical detector for phosphate tungsten and phosphate molybdenum bronzes. in Journal of Electroanalytical Chemistry. 2019;849:113369.
doi:10.1016/j.jelechem.2019.113369 .

Pagnacco, Maja, Maksimović, Jelena, Mudrinić, Tihana, Mojović, Zorica, Nedić, Zoran P., "Briggs-Rauscher reaction as a novel electrochemical detector for phosphate tungsten and phosphate molybdenum bronzes" in Journal of Electroanalytical Chemistry, 849 (2019):113369,
https://doi.org/10.1016/j.jelechem.2019.113369 . .

TY  - JOUR
AU  - Milikić, Jadranka
AU  - Oliveira, Raisa C. P.
AU  - Stoševski, Ivan
AU  - Krstić, Jugoslav
AU  - Hercigonja, Radmila
AU  - Miljanić, Šćepan
AU  - Santos, Diogo M. F.
AU  - Šljukić, Biljana
PY  - 2019
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3317
AB  - Three zeolites (A, X and Y) with Ag incorporated in their cages are tested as bifunctional electrocatalysts
for direct borohydride fuel cells (DBFCs). Ag zeolites are characterised by XRD, FTIR, nitrogen sorption
and SEM, as well as by electrochemical methods. Ag zeolite shows good activity for the anodic reaction,
i.e., borohydride oxidation reaction (BOR) in alkaline media, presenting low onset potential and high
current densities. BOR kinetic and faradaic parameters at AgY are calculated, with the number of
exchanged electrons being 4.3. The BOR at AgY was found to be of 0.6 order with respect to BH4
 
concentration with an activation energy of 13 kJ mol 1. Regarding ORR, AgX shows the best
performance with the highest current densities and good stability over time. A two-electron pathway is
observed for ORR at AgX and specific capacitance was calculated to be 5.61 F g 1. The DBFC
performance is investigated based on half-cell measurements of the AgY anode and Pt/C cathode
PB  - Royal Society of Chemistry
T2  - New Journal of Chemistry
T1  - Evaluation of silver-incorporating zeolites as bifunctional electrocatalysts for direct borohydride fuel cells
VL  - 43
IS  - 36
SP  - 14270
EP  - 14280
DO  - 10.1039/c9nj02148e
ER  - 

@article{
author = "Milikić, Jadranka and Oliveira, Raisa C. P. and Stoševski, Ivan and Krstić, Jugoslav and Hercigonja, Radmila and Miljanić, Šćepan and Santos, Diogo M. F. and Šljukić, Biljana",
year = "2019",
abstract = "Three zeolites (A, X and Y) with Ag incorporated in their cages are tested as bifunctional electrocatalysts
for direct borohydride fuel cells (DBFCs). Ag zeolites are characterised by XRD, FTIR, nitrogen sorption
and SEM, as well as by electrochemical methods. Ag zeolite shows good activity for the anodic reaction,
i.e., borohydride oxidation reaction (BOR) in alkaline media, presenting low onset potential and high
current densities. BOR kinetic and faradaic parameters at AgY are calculated, with the number of
exchanged electrons being 4.3. The BOR at AgY was found to be of 0.6 order with respect to BH4
 
concentration with an activation energy of 13 kJ mol 1. Regarding ORR, AgX shows the best
performance with the highest current densities and good stability over time. A two-electron pathway is
observed for ORR at AgX and specific capacitance was calculated to be 5.61 F g 1. The DBFC
performance is investigated based on half-cell measurements of the AgY anode and Pt/C cathode",
publisher = "Royal Society of Chemistry",
journal = "New Journal of Chemistry",
title = "Evaluation of silver-incorporating zeolites as bifunctional electrocatalysts for direct borohydride fuel cells",
volume = "43",
number = "36",
pages = "14270-14280",
doi = "10.1039/c9nj02148e"
}

Milikić, J., Oliveira, R. C. P., Stoševski, I., Krstić, J., Hercigonja, R., Miljanić, Š., Santos, D. M. F.,& Šljukić, B.. (2019). Evaluation of silver-incorporating zeolites as bifunctional electrocatalysts for direct borohydride fuel cells. in New Journal of Chemistry
Royal Society of Chemistry., 43(36), 14270-14280.
https://doi.org/10.1039/c9nj02148e

Milikić J, Oliveira RCP, Stoševski I, Krstić J, Hercigonja R, Miljanić Š, Santos DMF, Šljukić B. Evaluation of silver-incorporating zeolites as bifunctional electrocatalysts for direct borohydride fuel cells. in New Journal of Chemistry. 2019;43(36):14270-14280.
doi:10.1039/c9nj02148e .

Milikić, Jadranka, Oliveira, Raisa C. P., Stoševski, Ivan, Krstić, Jugoslav, Hercigonja, Radmila, Miljanić, Šćepan, Santos, Diogo M. F., Šljukić, Biljana, "Evaluation of silver-incorporating zeolites as bifunctional electrocatalysts for direct borohydride fuel cells" in New Journal of Chemistry, 43, no. 36 (2019):14270-14280,
https://doi.org/10.1039/c9nj02148e . .

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  - Nikolić, Maria Vesna
AU  - Vasiljević, Zorka
AU  - Luković, Miloljub
AU  - Pavlović, Vera P.
AU  - Vujancevic, J.
AU  - Radovanović, M.
AU  - Krstić, Jugoslav
AU  - Vlahovic, B.
AU  - Pavlović, Vladimir B.
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4277
AB  - Pseudobrookite based nanopowder was obtained by solid state synthesis of starting hematite and anatase nanopowders in the weight ratio 55:45. Structural and morphological properties were analyzed using X-ray diffraction (XRD), BET, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, UV/Vis diffuse reflectance spectroscopy, Field emission scanning electron microscopy (FESEM) and Transmission electron microscopy (TEM) confirming the formation of nanocrystalline pseudobrookite. The obtained powder was mixed with a binder (ethyl cellulose), dispersant (α-terpinol) and adhesion agents (acetic acid and distilled water) to obtain a thick film paste. It was screen printed on alumina substrate with interdigitated PdAg electrodes and fired at 600 °C for 30 min. Formation of a porous nanocrystalline thick film structure was shown using Scanning electron microscopy (SEM), while Hall measurements enabled determination of carrier mobility. Change of impedance response in the frequency range 42 Hz–1 MHz with humidity was analyzed at room temperature (25 °C) and 50 °C in the relative humidity range 30–90% and 40–90%, respectively. At 42 Hz, and room temperature the impedance reduced ∼28 times, while at 50 °C it reduced ∼147 times in the relative humidity range 40–90%. The sensor showed rapid response (16 s) and relatively low hysteresis (8.39% at 25 °C and 2.64% at 50 °C) showing that this is a promising material for application in humidity sensing.
PB  - Elsevier
T2  - Sensors and Actuators, B: Chemical
T1  - Humidity sensing properties of nanocrystalline pseudobrookite (Fe2TiO5) based thick films
VL  - 277
SP  - 654
EP  - 664
DO  - 10.1016/j.snb.2018.09.063
ER  - 

@article{
author = "Nikolić, Maria Vesna and Vasiljević, Zorka and Luković, Miloljub and Pavlović, Vera P. and Vujancevic, J. and Radovanović, M. and Krstić, Jugoslav and Vlahovic, B. and Pavlović, Vladimir B.",
year = "2018",
abstract = "Pseudobrookite based nanopowder was obtained by solid state synthesis of starting hematite and anatase nanopowders in the weight ratio 55:45. Structural and morphological properties were analyzed using X-ray diffraction (XRD), BET, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, UV/Vis diffuse reflectance spectroscopy, Field emission scanning electron microscopy (FESEM) and Transmission electron microscopy (TEM) confirming the formation of nanocrystalline pseudobrookite. The obtained powder was mixed with a binder (ethyl cellulose), dispersant (α-terpinol) and adhesion agents (acetic acid and distilled water) to obtain a thick film paste. It was screen printed on alumina substrate with interdigitated PdAg electrodes and fired at 600 °C for 30 min. Formation of a porous nanocrystalline thick film structure was shown using Scanning electron microscopy (SEM), while Hall measurements enabled determination of carrier mobility. Change of impedance response in the frequency range 42 Hz–1 MHz with humidity was analyzed at room temperature (25 °C) and 50 °C in the relative humidity range 30–90% and 40–90%, respectively. At 42 Hz, and room temperature the impedance reduced ∼28 times, while at 50 °C it reduced ∼147 times in the relative humidity range 40–90%. The sensor showed rapid response (16 s) and relatively low hysteresis (8.39% at 25 °C and 2.64% at 50 °C) showing that this is a promising material for application in humidity sensing.",
publisher = "Elsevier",
journal = "Sensors and Actuators, B: Chemical",
title = "Humidity sensing properties of nanocrystalline pseudobrookite (Fe2TiO5) based thick films",
volume = "277",
pages = "654-664",
doi = "10.1016/j.snb.2018.09.063"
}

Nikolić, M. V., Vasiljević, Z., Luković, M., Pavlović, V. P., Vujancevic, J., Radovanović, M., Krstić, J., Vlahovic, B.,& Pavlović, V. B.. (2018). Humidity sensing properties of nanocrystalline pseudobrookite (Fe2TiO5) based thick films. in Sensors and Actuators, B: Chemical
Elsevier., 277, 654-664.
https://doi.org/10.1016/j.snb.2018.09.063

Nikolić MV, Vasiljević Z, Luković M, Pavlović VP, Vujancevic J, Radovanović M, Krstić J, Vlahovic B, Pavlović VB. Humidity sensing properties of nanocrystalline pseudobrookite (Fe2TiO5) based thick films. in Sensors and Actuators, B: Chemical. 2018;277:654-664.
doi:10.1016/j.snb.2018.09.063 .

Nikolić, Maria Vesna, Vasiljević, Zorka, Luković, Miloljub, Pavlović, Vera P., Vujancevic, J., Radovanović, M., Krstić, Jugoslav, Vlahovic, B., Pavlović, Vladimir B., "Humidity sensing properties of nanocrystalline pseudobrookite (Fe2TiO5) based thick films" in Sensors and Actuators, B: Chemical, 277 (2018):654-664,
https://doi.org/10.1016/j.snb.2018.09.063 . .

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  - Jović, Aleksandar
AU  - Milikić, Jadranka
AU  - Bajuk-Bogdanovic, Danica
AU  - Milojević-Rakić, Maja
AU  - Nedić-Vasiljević, Bojana
AU  - Krstić, Jugoslav
AU  - Cvjetićanin, Nikola
AU  - Šljukić, Biljana
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2351
AB  - Heteropoly acid (HPA) was supported on BEA zeolite by optimized synthesis method yielding samples containing different amounts (20 to 50 wt%) of 12-phosphotungstic acid (HPW). The prepared supported HPW samples were subjected to different post-synthesis procedures including calcination and ultrasonication resulting in BEA-HPW (BPW) hybrid materials. These BPW samples were characterized using SEM, N-2-sorption and electrical conductivity measurements. They were subsequently used for the preparation of composites with carbonized polyaniline synthesized in the presence of 5-sulfosalicylic acid, and studied as electrode materials for phenols sensing in acidic, neutral and alkaline media. Linear dependence of current on p-nitrophenol concentration in acidic media was obtained enabling evaluation of limit of detection. Composite electrode gave response to p-nitrophenol presence in alkaline media as well, while no response was recorded in neutral media. The work demonstrates benefits of using novel composite based on BPW hybrid materials and carbonized polyaniline for sensing of phenols in aqueous environmental samples.
PB  - Electrochemical Soc Inc, Pennington
T2  - Journal of the Electrochemical Society
T1  - 12-phosphotungstic Acid Supported on BEA Zeolite Composite with Carbonized Polyaniline for Electroanalytical Sensing of Phenols in Environmental Samples
VL  - 165
IS  - 16
DO  - 10.1149/2.0021816jes
ER  - 

@article{
author = "Jović, Aleksandar and Milikić, Jadranka and Bajuk-Bogdanovic, Danica and Milojević-Rakić, Maja and Nedić-Vasiljević, Bojana and Krstić, Jugoslav and Cvjetićanin, Nikola and Šljukić, Biljana",
year = "2018",
abstract = "Heteropoly acid (HPA) was supported on BEA zeolite by optimized synthesis method yielding samples containing different amounts (20 to 50 wt%) of 12-phosphotungstic acid (HPW). The prepared supported HPW samples were subjected to different post-synthesis procedures including calcination and ultrasonication resulting in BEA-HPW (BPW) hybrid materials. These BPW samples were characterized using SEM, N-2-sorption and electrical conductivity measurements. They were subsequently used for the preparation of composites with carbonized polyaniline synthesized in the presence of 5-sulfosalicylic acid, and studied as electrode materials for phenols sensing in acidic, neutral and alkaline media. Linear dependence of current on p-nitrophenol concentration in acidic media was obtained enabling evaluation of limit of detection. Composite electrode gave response to p-nitrophenol presence in alkaline media as well, while no response was recorded in neutral media. The work demonstrates benefits of using novel composite based on BPW hybrid materials and carbonized polyaniline for sensing of phenols in aqueous environmental samples.",
publisher = "Electrochemical Soc Inc, Pennington",
journal = "Journal of the Electrochemical Society",
title = "12-phosphotungstic Acid Supported on BEA Zeolite Composite with Carbonized Polyaniline for Electroanalytical Sensing of Phenols in Environmental Samples",
volume = "165",
number = "16",
doi = "10.1149/2.0021816jes"
}

Jović, A., Milikić, J., Bajuk-Bogdanovic, D., Milojević-Rakić, M., Nedić-Vasiljević, B., Krstić, J., Cvjetićanin, N.,& Šljukić, B.. (2018). 12-phosphotungstic Acid Supported on BEA Zeolite Composite with Carbonized Polyaniline for Electroanalytical Sensing of Phenols in Environmental Samples. in Journal of the Electrochemical Society
Electrochemical Soc Inc, Pennington., 165(16).
https://doi.org/10.1149/2.0021816jes

Jović A, Milikić J, Bajuk-Bogdanovic D, Milojević-Rakić M, Nedić-Vasiljević B, Krstić J, Cvjetićanin N, Šljukić B. 12-phosphotungstic Acid Supported on BEA Zeolite Composite with Carbonized Polyaniline for Electroanalytical Sensing of Phenols in Environmental Samples. in Journal of the Electrochemical Society. 2018;165(16).
doi:10.1149/2.0021816jes .

Jović, Aleksandar, Milikić, Jadranka, Bajuk-Bogdanovic, Danica, Milojević-Rakić, Maja, Nedić-Vasiljević, Bojana, Krstić, Jugoslav, Cvjetićanin, Nikola, Šljukić, Biljana, "12-phosphotungstic Acid Supported on BEA Zeolite Composite with Carbonized Polyaniline for Electroanalytical Sensing of Phenols in Environmental Samples" in Journal of the Electrochemical Society, 165, no. 16 (2018),
https://doi.org/10.1149/2.0021816jes . .

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  - CONF
AU  - Maksimović, Tijana
AU  - Maksimović, Jelena
AU  - Stojadinović, Stevan
AU  - Tančić, Pavle
AU  - Nedić, Zoran
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5977
AB  - A study is presented of phase transitions of acid CaHPW12O40∙6H2O salt of 12-tungstophosphoric acid and characterized in the temperature range from room temperature to 1093 K. The structure and its phase transformations were characterized by thermal analysis (TGA and DSC), X-ray powder diffraction (XRPD) and Fourier-transform infrared spectra (FTIR). 
Dehydration processes are finished at about 770 K. Keggin’s anions are transformed by solid-solid recrystallization at about 873 K in calcium doped phosphate tungsten bronze.
PB  - Society of Physical Chemists of Serbia
C3  - Proceedings - 14th International Conference on Fundamental and Applied aspects of Physical Chemistry - Physical Chemistry 2018, September 24-28, 2018 Belgrade, Serbia
T1  - Synthesis of calcium doped phosphate tungsten bronze
VL  - 2
SP  - 673
EP  - 676
UR  - https://hdl.handle.net/21.15107/rcub_cer_5977
ER  - 

@conference{
author = "Maksimović, Tijana and Maksimović, Jelena and Stojadinović, Stevan and Tančić, Pavle and Nedić, Zoran",
year = "2018",
abstract = "A study is presented of phase transitions of acid CaHPW12O40∙6H2O salt of 12-tungstophosphoric acid and characterized in the temperature range from room temperature to 1093 K. The structure and its phase transformations were characterized by thermal analysis (TGA and DSC), X-ray powder diffraction (XRPD) and Fourier-transform infrared spectra (FTIR). 
Dehydration processes are finished at about 770 K. Keggin’s anions are transformed by solid-solid recrystallization at about 873 K in calcium doped phosphate tungsten bronze.",
publisher = "Society of Physical Chemists of Serbia",
journal = "Proceedings - 14th International Conference on Fundamental and Applied aspects of Physical Chemistry - Physical Chemistry 2018, September 24-28, 2018 Belgrade, Serbia",
title = "Synthesis of calcium doped phosphate tungsten bronze",
volume = "2",
pages = "673-676",
url = "https://hdl.handle.net/21.15107/rcub_cer_5977"
}

Maksimović, T., Maksimović, J., Stojadinović, S., Tančić, P.,& Nedić, Z.. (2018). Synthesis of calcium doped phosphate tungsten bronze. in Proceedings - 14th International Conference on Fundamental and Applied aspects of Physical Chemistry - Physical Chemistry 2018, September 24-28, 2018 Belgrade, Serbia
Society of Physical Chemists of Serbia., 2, 673-676.
https://hdl.handle.net/21.15107/rcub_cer_5977

Maksimović T, Maksimović J, Stojadinović S, Tančić P, Nedić Z. Synthesis of calcium doped phosphate tungsten bronze. in Proceedings - 14th International Conference on Fundamental and Applied aspects of Physical Chemistry - Physical Chemistry 2018, September 24-28, 2018 Belgrade, Serbia. 2018;2:673-676.
https://hdl.handle.net/21.15107/rcub_cer_5977 .

Maksimović, Tijana, Maksimović, Jelena, Stojadinović, Stevan, Tančić, Pavle, Nedić, Zoran, "Synthesis of calcium doped phosphate tungsten bronze" in Proceedings - 14th International Conference on Fundamental and Applied aspects of Physical Chemistry - Physical Chemistry 2018, September 24-28, 2018 Belgrade, Serbia, 2 (2018):673-676,
https://hdl.handle.net/21.15107/rcub_cer_5977 .

TY  - JOUR
AU  - Nikolić, Maria Vesna
AU  - Vasiljević, Zorka
AU  - Luković, Miloljub
AU  - Pavlović, Vera P.
AU  - Vujancevic, J.
AU  - Radovanović, M.
AU  - Krstić, Jugoslav
AU  - Vlahovic, B.
AU  - Pavlović, Vladimir B.
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2414
AB  - Pseudobrookite based nanopowder was obtained by solid state synthesis of starting hematite and anatase nanopowders in the weight ratio 55:45. Structural and morphological properties were analyzed using X-ray diffraction (XRD), BET, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, UV/Vis diffuse reflectance spectroscopy, Field emission scanning electron microscopy (FESEM) and Transmission electron microscopy (TEM) confirming the formation of nanocrystalline pseudobrookite. The obtained powder was mixed with a binder (ethyl cellulose), dispersant (α-terpinol) and adhesion agents (acetic acid and distilled water) to obtain a thick film paste. It was screen printed on alumina substrate with interdigitated PdAg electrodes and fired at 600 °C for 30 min. Formation of a porous nanocrystalline thick film structure was shown using Scanning electron microscopy (SEM), while Hall measurements enabled determination of carrier mobility. Change of impedance response in the frequency range 42 Hz–1 MHz with humidity was analyzed at room temperature (25 °C) and 50 °C in the relative humidity range 30–90% and 40–90%, respectively. At 42 Hz, and room temperature the impedance reduced ∼28 times, while at 50 °C it reduced ∼147 times in the relative humidity range 40–90%. The sensor showed rapid response (16 s) and relatively low hysteresis (8.39% at 25 °C and 2.64% at 50 °C) showing that this is a promising material for application in humidity sensing.
PB  - Elsevier
T2  - Sensors and Actuators, B: Chemical
T1  - Humidity sensing properties of nanocrystalline pseudobrookite (Fe2TiO5) based thick films
VL  - 277
SP  - 654
EP  - 664
DO  - 10.1016/j.snb.2018.09.063
ER  - 

@article{
author = "Nikolić, Maria Vesna and Vasiljević, Zorka and Luković, Miloljub and Pavlović, Vera P. and Vujancevic, J. and Radovanović, M. and Krstić, Jugoslav and Vlahovic, B. and Pavlović, Vladimir B.",
year = "2018",
abstract = "Pseudobrookite based nanopowder was obtained by solid state synthesis of starting hematite and anatase nanopowders in the weight ratio 55:45. Structural and morphological properties were analyzed using X-ray diffraction (XRD), BET, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, UV/Vis diffuse reflectance spectroscopy, Field emission scanning electron microscopy (FESEM) and Transmission electron microscopy (TEM) confirming the formation of nanocrystalline pseudobrookite. The obtained powder was mixed with a binder (ethyl cellulose), dispersant (α-terpinol) and adhesion agents (acetic acid and distilled water) to obtain a thick film paste. It was screen printed on alumina substrate with interdigitated PdAg electrodes and fired at 600 °C for 30 min. Formation of a porous nanocrystalline thick film structure was shown using Scanning electron microscopy (SEM), while Hall measurements enabled determination of carrier mobility. Change of impedance response in the frequency range 42 Hz–1 MHz with humidity was analyzed at room temperature (25 °C) and 50 °C in the relative humidity range 30–90% and 40–90%, respectively. At 42 Hz, and room temperature the impedance reduced ∼28 times, while at 50 °C it reduced ∼147 times in the relative humidity range 40–90%. The sensor showed rapid response (16 s) and relatively low hysteresis (8.39% at 25 °C and 2.64% at 50 °C) showing that this is a promising material for application in humidity sensing.",
publisher = "Elsevier",
journal = "Sensors and Actuators, B: Chemical",
title = "Humidity sensing properties of nanocrystalline pseudobrookite (Fe2TiO5) based thick films",
volume = "277",
pages = "654-664",
doi = "10.1016/j.snb.2018.09.063"
}

Nikolić, M. V., Vasiljević, Z., Luković, M., Pavlović, V. P., Vujancevic, J., Radovanović, M., Krstić, J., Vlahovic, B.,& Pavlović, V. B.. (2018). Humidity sensing properties of nanocrystalline pseudobrookite (Fe2TiO5) based thick films. in Sensors and Actuators, B: Chemical
Elsevier., 277, 654-664.
https://doi.org/10.1016/j.snb.2018.09.063

Nikolić MV, Vasiljević Z, Luković M, Pavlović VP, Vujancevic J, Radovanović M, Krstić J, Vlahovic B, Pavlović VB. Humidity sensing properties of nanocrystalline pseudobrookite (Fe2TiO5) based thick films. in Sensors and Actuators, B: Chemical. 2018;277:654-664.
doi:10.1016/j.snb.2018.09.063 .

Nikolić, Maria Vesna, Vasiljević, Zorka, Luković, Miloljub, Pavlović, Vera P., Vujancevic, J., Radovanović, M., Krstić, Jugoslav, Vlahovic, B., Pavlović, Vladimir B., "Humidity sensing properties of nanocrystalline pseudobrookite (Fe2TiO5) based thick films" in Sensors and Actuators, B: Chemical, 277 (2018):654-664,
https://doi.org/10.1016/j.snb.2018.09.063 . .

TY  - JOUR
AU  - Vujković, Milica
AU  - Matovic, Ljiljana
AU  - Krstić, Jugoslav
AU  - Stojmenović, Marija
AU  - Dukić, Andelka
AU  - Babić, Biljana M.
AU  - Mentus, Slavko
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2135
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, Boehm's 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.
PB  - Oxford : Pergamon-Elsevier Science Ltd
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 Matovic, Ljiljana and Krstić, Jugoslav and Stojmenović, Marija and Dukić, Andelka and Babić, Biljana M. and Mentus, Slavko",
year = "2017",
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, Boehm's 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.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
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., Matovic, L., Krstić, J., Stojmenović, M., Dukić, A., Babić, B. M.,& Mentus, S.. (2017). Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions. in Electrochimica Acta
Oxford : Pergamon-Elsevier Science Ltd., 245, 796-806.
https://doi.org/10.1016/j.electacta.2017.06.018

Vujković M, Matovic L, Krstić J, Stojmenović M, Dukić A, Babić BM, Mentus S. Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions. in Electrochimica Acta. 2017;245:796-806.
doi:10.1016/j.electacta.2017.06.018 .

Vujković, Milica, Matovic, Ljiljana, Krstić, Jugoslav, Stojmenović, Marija, Dukić, Andelka, Babić, Biljana M., Mentus, Slavko, "Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions" in Electrochimica Acta, 245 (2017):796-806,
https://doi.org/10.1016/j.electacta.2017.06.018 . .

TY  - JOUR
AU  - Vujković, Milica
AU  - Matovic, Ljiljana
AU  - Krstić, Jugoslav
AU  - Stojmenović, Marija
AU  - Dukić, Andelka
AU  - Babić, Biljana M.
AU  - Mentus, Slavko
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3011
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, Boehm's 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.
PB  - Oxford : Pergamon-Elsevier Science Ltd
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 Matovic, Ljiljana and Krstić, Jugoslav and Stojmenović, Marija and Dukić, Andelka and Babić, Biljana M. and Mentus, Slavko",
year = "2017",
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, Boehm's 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.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
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., Matovic, L., Krstić, J., Stojmenović, M., Dukić, A., Babić, B. M.,& Mentus, S.. (2017). Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions. in Electrochimica Acta
Oxford : Pergamon-Elsevier Science Ltd., 245, 796-806.
https://doi.org/10.1016/j.electacta.2017.06.018

Vujković M, Matovic L, Krstić J, Stojmenović M, Dukić A, Babić BM, Mentus S. Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions. in Electrochimica Acta. 2017;245:796-806.
doi:10.1016/j.electacta.2017.06.018 .

Vujković, Milica, Matovic, Ljiljana, Krstić, Jugoslav, Stojmenović, Marija, Dukić, Andelka, Babić, Biljana M., Mentus, Slavko, "Mechanically activated carbonized rayon fibers as an electrochemical supercapacitor in aqueous solutions" in Electrochimica Acta, 245 (2017):796-806,
https://doi.org/10.1016/j.electacta.2017.06.018 . .

TY  - JOUR
AU  - Dodevski, Vladimir
AU  - Stojmenović, Marija
AU  - Vujković, Milica
AU  - Krstić, Jugoslav
AU  - Krstić, Jugoslav
AU  - Bajuk-Bogdanovic, Danica
AU  - Kuzmanovic, Bojana
AU  - Kaluderovic, Branka
AU  - Mentus, Slavko
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1912
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.
PB  - Oxford : Pergamon-Elsevier Science Ltd
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 and Krstić, Jugoslav and Bajuk-Bogdanovic, Danica and Kuzmanovic, Bojana and Kaluderovic, Branka and Mentus, Slavko",
year = "2016",
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.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
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., Krstić, J., Bajuk-Bogdanovic, D., Kuzmanovic, B., Kaluderovic, B.,& Mentus, S.. (2016). Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed. in Electrochimica Acta
Oxford : Pergamon-Elsevier Science Ltd., 222, 156-171.
https://doi.org/10.1016/j.electacta.2016.10.182

Dodevski V, Stojmenović M, Vujković M, Krstić J, Krstić J, Bajuk-Bogdanovic D, Kuzmanovic B, Kaluderovic B, Mentus S. Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed. in Electrochimica Acta. 2016;222:156-171.
doi:10.1016/j.electacta.2016.10.182 .

Dodevski, Vladimir, Stojmenović, Marija, Vujković, Milica, Krstić, Jugoslav, Krstić, Jugoslav, Bajuk-Bogdanovic, Danica, Kuzmanovic, Bojana, Kaluderovic, Branka, Mentus, Slavko, "Complex insight into the charge storage behavior of active carbons obtained by carbonization of the plane tree seed" in Electrochimica Acta, 222 (2016):156-171,
https://doi.org/10.1016/j.electacta.2016.10.182 . .

TY  - JOUR
AU  - Vujković, Milica
AU  - Nedić, Zoran
AU  - Tančić, Pavle
AU  - Aleksić, Obrad
AU  - Nikolić, Maria Vesna
AU  - Mioč, Ubavka
AU  - Mentus, Slavko
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5899
AB  - Monophosphate bronze (PW8O26, WPB) was synthesized by low-temperature (650 °C) heating of 12-tungstophosphoric acid (WPA). Its lithiated derivative with a low lithium content (Li3-WPB) was synthesized by heating lithium salt of WPA at 650 °C. Its lithiated derivative with a high lithium content was synthesized by mechanochemical lithiation of Li3WPB (Li n -WPB) (n > 3), followed by heat treatment at 650 °C. X-ray powder diffraction analysis confirmed that the bronze structure changed with the increase of the incorporated lithium content. These bronzes were investigated from the aspect of lithiation/delithiation kinetics in an aqueous saturated LiNO3 electrolyte solution. By cyclic voltammetry, both the kinetics of intercalation/deintercalation and the coulombic capacity were found to decrease with the increase of initial lithium content, in agreement with literature data for electrochemically lithiated tungstophosphate bronzes. Monoclinic lithium-free bronze PW8O26, as the most promising material, was subjected to a further detailed galvanostatic investigation coupled with the LiFe0.95V0.05PO4/C composite as a cathode material in an aqueous battery. In comparison to its behavior in an organic electrolyte, a considerably lower initial capacity of the bronze electrode was measured. However, its cyclic stability was much better in an aqueous than in an organic electrolyte.
PB  - Springer
T2  - Journal of Materials Science
T1  - Electrochemical lithiation/delithiation kinetics and capacity of phosphate tungsten bronze and its chemically pre-lithiated derivatives in aqueous solutions
VL  - 51
IS  - 5
SP  - 2481
EP  - 2489
DO  - 10.1007/s10853-015-9560-5
ER  - 

@article{
author = "Vujković, Milica and Nedić, Zoran and Tančić, Pavle and Aleksić, Obrad and Nikolić, Maria Vesna and Mioč, Ubavka and Mentus, Slavko",
year = "2016",
abstract = "Monophosphate bronze (PW8O26, WPB) was synthesized by low-temperature (650 °C) heating of 12-tungstophosphoric acid (WPA). Its lithiated derivative with a low lithium content (Li3-WPB) was synthesized by heating lithium salt of WPA at 650 °C. Its lithiated derivative with a high lithium content was synthesized by mechanochemical lithiation of Li3WPB (Li n -WPB) (n > 3), followed by heat treatment at 650 °C. X-ray powder diffraction analysis confirmed that the bronze structure changed with the increase of the incorporated lithium content. These bronzes were investigated from the aspect of lithiation/delithiation kinetics in an aqueous saturated LiNO3 electrolyte solution. By cyclic voltammetry, both the kinetics of intercalation/deintercalation and the coulombic capacity were found to decrease with the increase of initial lithium content, in agreement with literature data for electrochemically lithiated tungstophosphate bronzes. Monoclinic lithium-free bronze PW8O26, as the most promising material, was subjected to a further detailed galvanostatic investigation coupled with the LiFe0.95V0.05PO4/C composite as a cathode material in an aqueous battery. In comparison to its behavior in an organic electrolyte, a considerably lower initial capacity of the bronze electrode was measured. However, its cyclic stability was much better in an aqueous than in an organic electrolyte.",
publisher = "Springer",
journal = "Journal of Materials Science",
title = "Electrochemical lithiation/delithiation kinetics and capacity of phosphate tungsten bronze and its chemically pre-lithiated derivatives in aqueous solutions",
volume = "51",
number = "5",
pages = "2481-2489",
doi = "10.1007/s10853-015-9560-5"
}

Vujković, M., Nedić, Z., Tančić, P., Aleksić, O., Nikolić, M. V., Mioč, U.,& Mentus, S.. (2016). Electrochemical lithiation/delithiation kinetics and capacity of phosphate tungsten bronze and its chemically pre-lithiated derivatives in aqueous solutions. in Journal of Materials Science
Springer., 51(5), 2481-2489.
https://doi.org/10.1007/s10853-015-9560-5

Vujković M, Nedić Z, Tančić P, Aleksić O, Nikolić MV, Mioč U, Mentus S. Electrochemical lithiation/delithiation kinetics and capacity of phosphate tungsten bronze and its chemically pre-lithiated derivatives in aqueous solutions. in Journal of Materials Science. 2016;51(5):2481-2489.
doi:10.1007/s10853-015-9560-5 .

Vujković, Milica, Nedić, Zoran, Tančić, Pavle, Aleksić, Obrad, Nikolić, Maria Vesna, Mioč, Ubavka, Mentus, Slavko, "Electrochemical lithiation/delithiation kinetics and capacity of phosphate tungsten bronze and its chemically pre-lithiated derivatives in aqueous solutions" in Journal of Materials Science, 51, no. 5 (2016):2481-2489,
https://doi.org/10.1007/s10853-015-9560-5 . .

TY  - JOUR
AU  - Stojmenović, Marija
AU  - Vujković, Milica
AU  - Matovic, Ljiljana
AU  - Krstić, Jugoslav
AU  - Dukić, Andelka
AU  - Dodevski, Vladimir
AU  - Zivkovic, Sanja M
AU  - Mentus, Slavko
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4318
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)
PB  - Elsevier
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 Matovic, Ljiljana and Krstić, Jugoslav and Dukić, Andelka and Dodevski, Vladimir and Zivkovic, Sanja M and Mentus, Slavko",
year = "2016",
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)",
publisher = "Elsevier",
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., Matovic, L., Krstić, J., Dukić, A., Dodevski, V., Zivkovic, S. M.,& Mentus, S.. (2016). Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template. in Microporous and Mesoporous Materials
Elsevier., 228, 94-106.
https://doi.org/10.1016/j.micromeso.2016.03.029

Stojmenović M, Vujković M, Matovic L, Krstić J, Dukić A, Dodevski V, Zivkovic SM, Mentus S. Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template. in Microporous and Mesoporous Materials. 2016;228:94-106.
doi:10.1016/j.micromeso.2016.03.029 .

Stojmenović, Marija, Vujković, Milica, Matovic, Ljiljana, Krstić, Jugoslav, Dukić, Andelka, Dodevski, Vladimir, Zivkovic, Sanja M, Mentus, Slavko, "Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template" in Microporous and Mesoporous Materials, 228 (2016):94-106,
https://doi.org/10.1016/j.micromeso.2016.03.029 . .

TY  - JOUR
AU  - Stojmenović, Marija
AU  - Vujković, Milica
AU  - Matovic, Ljiljana
AU  - Krstić, Jugoslav
AU  - Dukić, Andelka
AU  - Dodevski, Vladimir
AU  - Zivkovic, Sanja M
AU  - Mentus, Slavko
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1954
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)
PB  - Elsevier
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 Matovic, Ljiljana and Krstić, Jugoslav and Dukić, Andelka and Dodevski, Vladimir and Zivkovic, Sanja M and Mentus, Slavko",
year = "2016",
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)",
publisher = "Elsevier",
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., Matovic, L., Krstić, J., Dukić, A., Dodevski, V., Zivkovic, S. M.,& Mentus, S.. (2016). Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template. in Microporous and Mesoporous Materials
Elsevier., 228, 94-106.
https://doi.org/10.1016/j.micromeso.2016.03.029

Stojmenović M, Vujković M, Matovic L, Krstić J, Dukić A, Dodevski V, Zivkovic SM, Mentus S. Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template. in Microporous and Mesoporous Materials. 2016;228:94-106.
doi:10.1016/j.micromeso.2016.03.029 .

Stojmenović, Marija, Vujković, Milica, Matovic, Ljiljana, Krstić, Jugoslav, Dukić, Andelka, Dodevski, Vladimir, Zivkovic, Sanja M, Mentus, Slavko, "Complex investigation of charge storage behavior of microporous carbon synthesized by zeolite template" in Microporous and Mesoporous Materials, 228 (2016):94-106,
https://doi.org/10.1016/j.micromeso.2016.03.029 . .

TY  - JOUR
AU  - Ciric-Marjanovic, Gordana
AU  - Mentus, Slavko
AU  - Pasti, Igor
AU  - Gavrilov, Nemanja
AU  - Krstić, Jugoslav
AU  - Travas-Sejdic, Jadranka
AU  - Strover, Lisa T.
AU  - Kopecka, Jitka
AU  - Moravkova, Zuzana
AU  - Trchova, Miroslava
AU  - Stejskal, Jaroslav
PY  - 2014
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1594
AB  - Polypyrrole nanotubes (PPy-NTs) were prepared by the oxidation of pyrrole with iron(III) chloride in the presence of a structure-guiding agent, methyl orange. Upon carbonization of the salt form of PPy-NTs, the conducting nitrogen-containing nanotubular carbonaceous material (C-PPy-NT) was obtained. The morphology, structure, and physicochemical properties of PPy-NTs in salt and base form as well as C-PPy-NTs were investigated by transmission electron microscopy, Fourier transform infrared and Raman spectroscopies, conductivity measurements, elemental microanalysis, inductively coupled plasma optical emission spectroscopy, X-ray photoelectron spectroscopy, and nitrogen physisorption. Results of the material characterization were linked to their electrochemical behavior. Specific capacitance of around 120 F g(-1) at low potential sweep rate of 5 mV s(-1) was observed for original PPy-NTs. However, when the potential sweep rate was increased to 100 mV s(-1), PPy-NT salt retained the value of specific capacitance, while the capacitance of PPy-NT base decreased by 70%. Upon carbonization of PPy-NT salt, the specific capacitance was doubled and capacitance fade measured in the interval 5-100 mV s(-1) was determined to be around 45%. It is proposed that the absolute value of specific capacitance is determined by specific surface area and surface functional groups, while the capacitance fade is determined by the conductivity of the electrode material. In this manner, a linear relationship between the percent of capacitance fade and the logarithm of the conductivity was revealed. C-PPy-NTs were also tested as an electrocatalyst for the oxygen reduction reaction (ORR) in alkaline media. High ORR activity was observed, characterized by the onset potential of -0.1 V versus saturated calomel electrode and the apparent number of electrons consumed per oxygen molecule higher than 3. Appreciable ORR activity can be linked with a high fraction of mesopores and the presence of surface functional groups, especially pyridinic and pyrrolic nitrogens, and also with a high degree of structural disorder.
PB  - American Chemical Society (ACS)
T2  - Journal of Physical Chemistry C
T1  - Synthesis, Characterization, and Electrochemistry of Nanotubular Polypyrrole and Polypyrrole-Derived Carbon Nanotubes
VL  - 118
IS  - 27
SP  - 14770
EP  - 14784
DO  - 10.1021/jp502862d
ER  - 

@article{
author = "Ciric-Marjanovic, Gordana and Mentus, Slavko and Pasti, Igor and Gavrilov, Nemanja and Krstić, Jugoslav and Travas-Sejdic, Jadranka and Strover, Lisa T. and Kopecka, Jitka and Moravkova, Zuzana and Trchova, Miroslava and Stejskal, Jaroslav",
year = "2014",
abstract = "Polypyrrole nanotubes (PPy-NTs) were prepared by the oxidation of pyrrole with iron(III) chloride in the presence of a structure-guiding agent, methyl orange. Upon carbonization of the salt form of PPy-NTs, the conducting nitrogen-containing nanotubular carbonaceous material (C-PPy-NT) was obtained. The morphology, structure, and physicochemical properties of PPy-NTs in salt and base form as well as C-PPy-NTs were investigated by transmission electron microscopy, Fourier transform infrared and Raman spectroscopies, conductivity measurements, elemental microanalysis, inductively coupled plasma optical emission spectroscopy, X-ray photoelectron spectroscopy, and nitrogen physisorption. Results of the material characterization were linked to their electrochemical behavior. Specific capacitance of around 120 F g(-1) at low potential sweep rate of 5 mV s(-1) was observed for original PPy-NTs. However, when the potential sweep rate was increased to 100 mV s(-1), PPy-NT salt retained the value of specific capacitance, while the capacitance of PPy-NT base decreased by 70%. Upon carbonization of PPy-NT salt, the specific capacitance was doubled and capacitance fade measured in the interval 5-100 mV s(-1) was determined to be around 45%. It is proposed that the absolute value of specific capacitance is determined by specific surface area and surface functional groups, while the capacitance fade is determined by the conductivity of the electrode material. In this manner, a linear relationship between the percent of capacitance fade and the logarithm of the conductivity was revealed. C-PPy-NTs were also tested as an electrocatalyst for the oxygen reduction reaction (ORR) in alkaline media. High ORR activity was observed, characterized by the onset potential of -0.1 V versus saturated calomel electrode and the apparent number of electrons consumed per oxygen molecule higher than 3. Appreciable ORR activity can be linked with a high fraction of mesopores and the presence of surface functional groups, especially pyridinic and pyrrolic nitrogens, and also with a high degree of structural disorder.",
publisher = "American Chemical Society (ACS)",
journal = "Journal of Physical Chemistry C",
title = "Synthesis, Characterization, and Electrochemistry of Nanotubular Polypyrrole and Polypyrrole-Derived Carbon Nanotubes",
volume = "118",
number = "27",
pages = "14770-14784",
doi = "10.1021/jp502862d"
}

Ciric-Marjanovic, G., Mentus, S., Pasti, I., Gavrilov, N., Krstić, J., Travas-Sejdic, J., Strover, L. T., Kopecka, J., Moravkova, Z., Trchova, M.,& Stejskal, J.. (2014). Synthesis, Characterization, and Electrochemistry of Nanotubular Polypyrrole and Polypyrrole-Derived Carbon Nanotubes. in Journal of Physical Chemistry C
American Chemical Society (ACS)., 118(27), 14770-14784.
https://doi.org/10.1021/jp502862d

Ciric-Marjanovic G, Mentus S, Pasti I, Gavrilov N, Krstić J, Travas-Sejdic J, Strover LT, Kopecka J, Moravkova Z, Trchova M, Stejskal J. Synthesis, Characterization, and Electrochemistry of Nanotubular Polypyrrole and Polypyrrole-Derived Carbon Nanotubes. in Journal of Physical Chemistry C. 2014;118(27):14770-14784.
doi:10.1021/jp502862d .

Ciric-Marjanovic, Gordana, Mentus, Slavko, Pasti, Igor, Gavrilov, Nemanja, Krstić, Jugoslav, Travas-Sejdic, Jadranka, Strover, Lisa T., Kopecka, Jitka, Moravkova, Zuzana, Trchova, Miroslava, Stejskal, Jaroslav, "Synthesis, Characterization, and Electrochemistry of Nanotubular Polypyrrole and Polypyrrole-Derived Carbon Nanotubes" in Journal of Physical Chemistry C, 118, no. 27 (2014):14770-14784,
https://doi.org/10.1021/jp502862d . .

TY  - JOUR
AU  - Vujković, Milica
AU  - Gavrilov, Nemanja
AU  - Pasti, Igor
AU  - Krstić, Jugoslav
AU  - Travas-Sejdic, Jadranka
AU  - Ciric-Marjanovic, Gordana
AU  - Mentus, Slavko
PY  - 2013
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1162
AB  - Carbonized nanostructured polyaniline (C.PANI) was hydrothermally treated in 1 mol dm(-3) KOH at 200 degrees C. The treatment caused significant reduction of micropore volume but negligible changes in mesoporous domain, as evidenced by nitrogen adsorption measurements, as well as significant increase of surface N/C and O/C ratios, as evidenced by XPS method. In comparison to the C.PANI precursor, the new material, denoted as C.PANI.HAT200, delivered twice as high gravimetric capacitances, amounting to 363, 220 and 432 F g(-1), in 6 mol dm(-3) KOH, 2 mol dm(-3) KNO3 and 1 mol dm(-3) H2SO4, respectively, when measured potentiodynamically at a scan rate of 5 mV s(-1). Moreover, its exceptionally high electrocatalytic activity towards the oxygen reduction reaction (ORR), almost one order of magnitude higher than that of C.PANI was evidenced in alkaline media, approaching closely a four-electron pathway. The onset potential for ORR matched the one of platinum-based electrocatalyst. Significant improvements of both capacitive and electrocatalytic properties of C.PANI.HAT200 were discussed in correlation to the modification of surface functional groups. These findings affirm the low temperature hydrothermal post-synthetic modification of N-doped nanocarbons as a route of production of advanced multifunctional carbon materials with exceptional characteristics.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Carbon
T1  - Superior capacitive and electrocatalytic properties of carbonized nanostructured polyaniline upon a low-temperature hydrothermal treatment
VL  - 64
SP  - 472
EP  - 486
DO  - 10.1016/j.carbon.2013.07.100
ER  - 

@article{
author = "Vujković, Milica and Gavrilov, Nemanja and Pasti, Igor and Krstić, Jugoslav and Travas-Sejdic, Jadranka and Ciric-Marjanovic, Gordana and Mentus, Slavko",
year = "2013",
abstract = "Carbonized nanostructured polyaniline (C.PANI) was hydrothermally treated in 1 mol dm(-3) KOH at 200 degrees C. The treatment caused significant reduction of micropore volume but negligible changes in mesoporous domain, as evidenced by nitrogen adsorption measurements, as well as significant increase of surface N/C and O/C ratios, as evidenced by XPS method. In comparison to the C.PANI precursor, the new material, denoted as C.PANI.HAT200, delivered twice as high gravimetric capacitances, amounting to 363, 220 and 432 F g(-1), in 6 mol dm(-3) KOH, 2 mol dm(-3) KNO3 and 1 mol dm(-3) H2SO4, respectively, when measured potentiodynamically at a scan rate of 5 mV s(-1). Moreover, its exceptionally high electrocatalytic activity towards the oxygen reduction reaction (ORR), almost one order of magnitude higher than that of C.PANI was evidenced in alkaline media, approaching closely a four-electron pathway. The onset potential for ORR matched the one of platinum-based electrocatalyst. Significant improvements of both capacitive and electrocatalytic properties of C.PANI.HAT200 were discussed in correlation to the modification of surface functional groups. These findings affirm the low temperature hydrothermal post-synthetic modification of N-doped nanocarbons as a route of production of advanced multifunctional carbon materials with exceptional characteristics.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Carbon",
title = "Superior capacitive and electrocatalytic properties of carbonized nanostructured polyaniline upon a low-temperature hydrothermal treatment",
volume = "64",
pages = "472-486",
doi = "10.1016/j.carbon.2013.07.100"
}

Vujković, M., Gavrilov, N., Pasti, I., Krstić, J., Travas-Sejdic, J., Ciric-Marjanovic, G.,& Mentus, S.. (2013). Superior capacitive and electrocatalytic properties of carbonized nanostructured polyaniline upon a low-temperature hydrothermal treatment. in Carbon
Oxford : Pergamon-Elsevier Science Ltd., 64, 472-486.
https://doi.org/10.1016/j.carbon.2013.07.100

Vujković M, Gavrilov N, Pasti I, Krstić J, Travas-Sejdic J, Ciric-Marjanovic G, Mentus S. Superior capacitive and electrocatalytic properties of carbonized nanostructured polyaniline upon a low-temperature hydrothermal treatment. in Carbon. 2013;64:472-486.
doi:10.1016/j.carbon.2013.07.100 .

Vujković, Milica, Gavrilov, Nemanja, Pasti, Igor, Krstić, Jugoslav, Travas-Sejdic, Jadranka, Ciric-Marjanovic, Gordana, Mentus, Slavko, "Superior capacitive and electrocatalytic properties of carbonized nanostructured polyaniline upon a low-temperature hydrothermal treatment" in Carbon, 64 (2013):472-486,
https://doi.org/10.1016/j.carbon.2013.07.100 . .

TY  - JOUR
AU  - Gavrilov, Nemanja
AU  - Pasti, Igor
AU  - Krstić, Jugoslav
AU  - Mitrić, Miodrag
AU  - Ciric-Marjanovic, Gordana
AU  - Mentus, Slavko
PY  - 2013
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1261
AB  - Single phase tungsten carbide nanoparticles (WC-NPs), (mean particle diameter 5.4 nm), distributed over carbonized polyaniline (C-PANT) nanotubes/nanosheets were synthesized by a solid state reaction between WO3 and nitrogen-rich carbonized polyaniline at 1000 degrees C in a reducing atmosphere. The resulting composite was characterized by X-ray diffractometry, electron microscopy, thermogravimetry in oxidizing and reduction atmospheres and elemental analysis. We suggested that the synthesis of WC as a single phase was facilitated by reactive C atoms with dangling bonds, formed upon nitrogen removal.
PB  - Elsevier Sci Ltd, Oxford
T2  - Ceramics International
T1  - The synthesis of single phase WC nanoparticles/C composite by solid state reaction involving nitrogen-rich carbonized polyaniline
VL  - 39
IS  - 8
SP  - 8761
EP  - 8765
DO  - 10.1016/j.ceramint.2013.04.062
ER  - 

@article{
author = "Gavrilov, Nemanja and Pasti, Igor and Krstić, Jugoslav and Mitrić, Miodrag and Ciric-Marjanovic, Gordana and Mentus, Slavko",
year = "2013",
abstract = "Single phase tungsten carbide nanoparticles (WC-NPs), (mean particle diameter 5.4 nm), distributed over carbonized polyaniline (C-PANT) nanotubes/nanosheets were synthesized by a solid state reaction between WO3 and nitrogen-rich carbonized polyaniline at 1000 degrees C in a reducing atmosphere. The resulting composite was characterized by X-ray diffractometry, electron microscopy, thermogravimetry in oxidizing and reduction atmospheres and elemental analysis. We suggested that the synthesis of WC as a single phase was facilitated by reactive C atoms with dangling bonds, formed upon nitrogen removal.",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "Ceramics International",
title = "The synthesis of single phase WC nanoparticles/C composite by solid state reaction involving nitrogen-rich carbonized polyaniline",
volume = "39",
number = "8",
pages = "8761-8765",
doi = "10.1016/j.ceramint.2013.04.062"
}

Gavrilov, N., Pasti, I., Krstić, J., Mitrić, M., Ciric-Marjanovic, G.,& Mentus, S.. (2013). The synthesis of single phase WC nanoparticles/C composite by solid state reaction involving nitrogen-rich carbonized polyaniline. in Ceramics International
Elsevier Sci Ltd, Oxford., 39(8), 8761-8765.
https://doi.org/10.1016/j.ceramint.2013.04.062

Gavrilov N, Pasti I, Krstić J, Mitrić M, Ciric-Marjanovic G, Mentus S. The synthesis of single phase WC nanoparticles/C composite by solid state reaction involving nitrogen-rich carbonized polyaniline. in Ceramics International. 2013;39(8):8761-8765.
doi:10.1016/j.ceramint.2013.04.062 .

Gavrilov, Nemanja, Pasti, Igor, Krstić, Jugoslav, Mitrić, Miodrag, Ciric-Marjanovic, Gordana, Mentus, Slavko, "The synthesis of single phase WC nanoparticles/C composite by solid state reaction involving nitrogen-rich carbonized polyaniline" in Ceramics International, 39, no. 8 (2013):8761-8765,
https://doi.org/10.1016/j.ceramint.2013.04.062 . .

TY  - JOUR
AU  - Nikolic, P. M.
AU  - Paraskevopoulos, Konstantinos M.
AU  - Aleksić, Obrad S.
AU  - Vujatovic, S. S.
AU  - Vasiljević-Radović, Dana
AU  - Zorba, T. T.
AU  - Blagojevic, V.
AU  - Nikolic, N.
AU  - Radovanović, M.
AU  - Nikolić, Maria Vesna
PY  - 2012
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/942
AB  - Single crystal samples of PbTe doped with PbI2 were made using the Bridgman technique. Far infrared reflectivity diagrams of PbTe doped with 0.4 at% and 0.6 at% Iodine were measured and numerically analyzed. A plasma resonance at about 650 cm(-1) with the reflectivity minima very close to zero was observed for both samples. Thermal diffusivity was determined for the same samples using the photoacoustic method with a transmission detection configuration and the values of the minority free carrier (holes) mobility were calculated.
PB  - National Institute of Optoelectronics
T2  - Optoelectronics and Advanced Materials, Rapid Communications
T1  - Far infrared and photoacoustic characterization of iodine doped PbTe
VL  - 6
IS  - 3-4
SP  - 352
EP  - 356
UR  - https://hdl.handle.net/21.15107/rcub_cer_942
ER  - 

@article{
author = "Nikolic, P. M. and Paraskevopoulos, Konstantinos M. and Aleksić, Obrad S. and Vujatovic, S. S. and Vasiljević-Radović, Dana and Zorba, T. T. and Blagojevic, V. and Nikolic, N. and Radovanović, M. and Nikolić, Maria Vesna",
year = "2012",
abstract = "Single crystal samples of PbTe doped with PbI2 were made using the Bridgman technique. Far infrared reflectivity diagrams of PbTe doped with 0.4 at% and 0.6 at% Iodine were measured and numerically analyzed. A plasma resonance at about 650 cm(-1) with the reflectivity minima very close to zero was observed for both samples. Thermal diffusivity was determined for the same samples using the photoacoustic method with a transmission detection configuration and the values of the minority free carrier (holes) mobility were calculated.",
publisher = "National Institute of Optoelectronics",
journal = "Optoelectronics and Advanced Materials, Rapid Communications",
title = "Far infrared and photoacoustic characterization of iodine doped PbTe",
volume = "6",
number = "3-4",
pages = "352-356",
url = "https://hdl.handle.net/21.15107/rcub_cer_942"
}

Nikolic, P. M., Paraskevopoulos, K. M., Aleksić, O. S., Vujatovic, S. S., Vasiljević-Radović, D., Zorba, T. T., Blagojevic, V., Nikolic, N., Radovanović, M.,& Nikolić, M. V.. (2012). Far infrared and photoacoustic characterization of iodine doped PbTe. in Optoelectronics and Advanced Materials, Rapid Communications
National Institute of Optoelectronics., 6(3-4), 352-356.
https://hdl.handle.net/21.15107/rcub_cer_942

Nikolic PM, Paraskevopoulos KM, Aleksić OS, Vujatovic SS, Vasiljević-Radović D, Zorba TT, Blagojevic V, Nikolic N, Radovanović M, Nikolić MV. Far infrared and photoacoustic characterization of iodine doped PbTe. in Optoelectronics and Advanced Materials, Rapid Communications. 2012;6(3-4):352-356.
https://hdl.handle.net/21.15107/rcub_cer_942 .

Nikolic, P. M., Paraskevopoulos, Konstantinos M., Aleksić, Obrad S., Vujatovic, S. S., Vasiljević-Radović, Dana, Zorba, T. T., Blagojevic, V., Nikolic, N., Radovanović, M., Nikolić, Maria Vesna, "Far infrared and photoacoustic characterization of iodine doped PbTe" in Optoelectronics and Advanced Materials, Rapid Communications, 6, no. 3-4 (2012):352-356,
https://hdl.handle.net/21.15107/rcub_cer_942 .

TY  - JOUR
AU  - Nikolic, P. M.
AU  - Paraskevopoulos, Konstantinos M.
AU  - Zachariadis, G.
AU  - Valasiadis, O.
AU  - Zorba, T. T.
AU  - Vujatovic, S. S.
AU  - Nikolic, N.
AU  - Aleksić, Obrad S.
AU  - Ivetic, T.
AU  - Cvetković, Olga
AU  - Blagojevic, V.
AU  - Nikolić, Maria Vesna
PY  - 2012
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1007
AB  - PbTe single crystals, doped with B, were grown using the Bridgman method. Far infrared spectra were measured in the temperature range between 10 K and room temperature. The experimental spectra were numerically analyzed, and optical parameters were calculated. Local impurity modes of boron were observed at about 150 and 240 cm(-1). For all samples, after FIR measurements, the content of boron was measured using inductively coupled plasma atomic emission spectrometry. Optical mobility of free carriers was calculated and it was the highest for the sample with only 0.014 at.% of boron in PbTe. A negative photoconductivity effect at 130 K for PbTe + B was also observed.
PB  - Springer, New York
T2  - Journal of Materials Science
T1  - Far infrared study of local impurity modes of Boron-doped PbTe
VL  - 47
IS  - 5
SP  - 2384
EP  - 2389
DO  - 10.1007/s10853-011-6057-8
ER  - 

@article{
author = "Nikolic, P. M. and Paraskevopoulos, Konstantinos M. and Zachariadis, G. and Valasiadis, O. and Zorba, T. T. and Vujatovic, S. S. and Nikolic, N. and Aleksić, Obrad S. and Ivetic, T. and Cvetković, Olga and Blagojevic, V. and Nikolić, Maria Vesna",
year = "2012",
abstract = "PbTe single crystals, doped with B, were grown using the Bridgman method. Far infrared spectra were measured in the temperature range between 10 K and room temperature. The experimental spectra were numerically analyzed, and optical parameters were calculated. Local impurity modes of boron were observed at about 150 and 240 cm(-1). For all samples, after FIR measurements, the content of boron was measured using inductively coupled plasma atomic emission spectrometry. Optical mobility of free carriers was calculated and it was the highest for the sample with only 0.014 at.% of boron in PbTe. A negative photoconductivity effect at 130 K for PbTe + B was also observed.",
publisher = "Springer, New York",
journal = "Journal of Materials Science",
title = "Far infrared study of local impurity modes of Boron-doped PbTe",
volume = "47",
number = "5",
pages = "2384-2389",
doi = "10.1007/s10853-011-6057-8"
}

Nikolic, P. M., Paraskevopoulos, K. M., Zachariadis, G., Valasiadis, O., Zorba, T. T., Vujatovic, S. S., Nikolic, N., Aleksić, O. S., Ivetic, T., Cvetković, O., Blagojevic, V.,& Nikolić, M. V.. (2012). Far infrared study of local impurity modes of Boron-doped PbTe. in Journal of Materials Science
Springer, New York., 47(5), 2384-2389.
https://doi.org/10.1007/s10853-011-6057-8

Nikolic PM, Paraskevopoulos KM, Zachariadis G, Valasiadis O, Zorba TT, Vujatovic SS, Nikolic N, Aleksić OS, Ivetic T, Cvetković O, Blagojevic V, Nikolić MV. Far infrared study of local impurity modes of Boron-doped PbTe. in Journal of Materials Science. 2012;47(5):2384-2389.
doi:10.1007/s10853-011-6057-8 .

Nikolic, P. M., Paraskevopoulos, Konstantinos M., Zachariadis, G., Valasiadis, O., Zorba, T. T., Vujatovic, S. S., Nikolic, N., Aleksić, Obrad S., Ivetic, T., Cvetković, Olga, Blagojevic, V., Nikolić, Maria Vesna, "Far infrared study of local impurity modes of Boron-doped PbTe" in Journal of Materials Science, 47, no. 5 (2012):2384-2389,
https://doi.org/10.1007/s10853-011-6057-8 . .