TY  - JOUR
AU  - Savić-Biserčić, Marjetka
AU  - Marjanović, Budimir
AU  - Zasonska, Beata A.
AU  - Stojadinović, Stevan
AU  - Ćirić-Marjanović, Gordana N.
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8847
AB  - Composites of metal organic framework MOF-5 and conjugated polymer polyaniline (PANI) were synthesized for the first time. Two procedures, which avoid humidity during the synthesis in order to preserve the structure of MOF-5, were applied. In the first one, dissolved part of nonconducting emeraldine base form of PANI (PANI-EB) in N,N΄-dimethylformamide was mixed with MOF-5 in different mass ratios. In the second one, the composites were prepared mechano-chemically, by using powdered conducting emeraldine salt form of PANI (PANI-ES) and solid MOF-5, mixed in chloroform in different mass ratios. The composites were characterized by various techniques: scanning electron microscopy (SEM), FTIR spectroscopy, nitrogen sorption and electrical conductivity measurements, XRD, and flame atomic absorption spectroscopy (FAAS). The procedure which used PANI-EB led to microporous PANI/MOF-5 composites with very high BET specific surface area, SBET (the highest value SBET of c.a. 2700 m2 g−1, even higher than SBET of starting pure MOF-5, showed the composite which contains 89 wt.% of MOF-5) and low conductivity (∼10-7 S cm−1). The second procedure which used PANI-ES gave microporous PANI/MOF-5 composites which showed moderate conductivities (the highest conductivity of 1.0 ⋅ 10−3 S cm-1 exhibited the composite which contains 25 wt.% of MOF-5) and also high SBET values, but lower than those measured for the composites with PANI-EB (the highest SBET of c.a. 850 m2 g-1 showed the composite of PANI doped with HCl which contains c.a. 77 wt.% of MOF-5). XRD measurements confirmed that predominately cubic crystalline structure of MOF-5 was present in almost all composites. © 2020 Elsevier B.V.
T2  - Synthetic Metals
T1  - Novel microporous composites of MOF-5 and polyaniline with high specific surface area
VL  - 262
SP  - 116348
DO  - 10.1016/j.synthmet.2020.116348
ER  - 

@article{
author = "Savić-Biserčić, Marjetka and Marjanović, Budimir and Zasonska, Beata A. and Stojadinović, Stevan and Ćirić-Marjanović, Gordana N.",
year = "2020",
abstract = "Composites of metal organic framework MOF-5 and conjugated polymer polyaniline (PANI) were synthesized for the first time. Two procedures, which avoid humidity during the synthesis in order to preserve the structure of MOF-5, were applied. In the first one, dissolved part of nonconducting emeraldine base form of PANI (PANI-EB) in N,N΄-dimethylformamide was mixed with MOF-5 in different mass ratios. In the second one, the composites were prepared mechano-chemically, by using powdered conducting emeraldine salt form of PANI (PANI-ES) and solid MOF-5, mixed in chloroform in different mass ratios. The composites were characterized by various techniques: scanning electron microscopy (SEM), FTIR spectroscopy, nitrogen sorption and electrical conductivity measurements, XRD, and flame atomic absorption spectroscopy (FAAS). The procedure which used PANI-EB led to microporous PANI/MOF-5 composites with very high BET specific surface area, SBET (the highest value SBET of c.a. 2700 m2 g−1, even higher than SBET of starting pure MOF-5, showed the composite which contains 89 wt.% of MOF-5) and low conductivity (∼10-7 S cm−1). The second procedure which used PANI-ES gave microporous PANI/MOF-5 composites which showed moderate conductivities (the highest conductivity of 1.0 ⋅ 10−3 S cm-1 exhibited the composite which contains 25 wt.% of MOF-5) and also high SBET values, but lower than those measured for the composites with PANI-EB (the highest SBET of c.a. 850 m2 g-1 showed the composite of PANI doped with HCl which contains c.a. 77 wt.% of MOF-5). XRD measurements confirmed that predominately cubic crystalline structure of MOF-5 was present in almost all composites. © 2020 Elsevier B.V.",
journal = "Synthetic Metals",
title = "Novel microporous composites of MOF-5 and polyaniline with high specific surface area",
volume = "262",
pages = "116348",
doi = "10.1016/j.synthmet.2020.116348"
}

Savić-Biserčić, M., Marjanović, B., Zasonska, B. A., Stojadinović, S.,& Ćirić-Marjanović, G. N.. (2020). Novel microporous composites of MOF-5 and polyaniline with high specific surface area. in Synthetic Metals, 262, 116348.
https://doi.org/10.1016/j.synthmet.2020.116348

Savić-Biserčić M, Marjanović B, Zasonska BA, Stojadinović S, Ćirić-Marjanović GN. Novel microporous composites of MOF-5 and polyaniline with high specific surface area. in Synthetic Metals. 2020;262:116348.
doi:10.1016/j.synthmet.2020.116348 .

Savić-Biserčić, Marjetka, Marjanović, Budimir, Zasonska, Beata A., Stojadinović, Stevan, Ćirić-Marjanović, Gordana N., "Novel microporous composites of MOF-5 and polyaniline with high specific surface area" in Synthetic Metals, 262 (2020):116348,
https://doi.org/10.1016/j.synthmet.2020.116348 . .

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

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

Jovanović, Z. M., Mravik, Ž., Bajuk-Bogdanović, D. V., Jovanović, S., Marković, S., Vujković, M., Kovač, J., Vengust, D., Uskoković-Marković, S.,& Holclajtner-Antunović, I. D.. (2020). Self-limiting interactions in 2D–0D systems: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite. in Carbon, 156, 166-178.
https://doi.org/10.1016/j.carbon.2019.09.072

Jovanović ZM, Mravik Ž, Bajuk-Bogdanović DV, Jovanović S, Marković S, Vujković M, Kovač J, Vengust D, Uskoković-Marković S, Holclajtner-Antunović ID. Self-limiting interactions in 2D–0D systems: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite. in Carbon. 2020;156:166-178.
doi:10.1016/j.carbon.2019.09.072 .

Jovanović, Zoran M., Mravik, Željko, Bajuk-Bogdanović, Danica V., Jovanović, Sonja, Marković, Smilja, Vujković, Milica, Kovač, Janez, Vengust, Damjan, Uskoković-Marković, Snežana, Holclajtner-Antunović, Ivanka D., "Self-limiting interactions in 2D–0D systems: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite" in Carbon, 156 (2020):166-178,
https://doi.org/10.1016/j.carbon.2019.09.072 . .

TY  - JOUR
AU  - Savić-Biserčić, Marjetka
AU  - Marjanović, Budimir
AU  - Vasiljević-Nedić, Bojana
AU  - Mentus, Slavko V.
AU  - Zasonska, Beata A.
AU  - Ćirić-Marjanović, Gordana N.
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S1387181118305766
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7969
AB  - Efficient and simple room temperature synthesis of pure phase metal-organic framework MOF-5 has been developed, based on the use of anhydrous zinc acetate, Zn(OAc)2, as a precursor, instead of zinc acetate dihydrate. Crucial influence of water on a reaction pathway was revealed. In order to obtain MOF-5, different amounts of water have been added into the solutions of Zn(OAc)2 in N,N-dimethylformamide (DMF) to prepare in situ zinc acetate hydrates with 0.25, 0.5, and 1.0 mol of water. Commercially available zinc acetate dihydrate was also used as a precursor for comparison. These solutions were mixed at room temperature with the solution of 1,4-benzenedicarboxylic acid in DMF in the absence of any base. Based on XRD, FTIR, and SEM measurements, it was shown that the optimal amount of water for the synthesis of completely pure, crystalline phase MOF-5 is 0.25–0.5 mol of water per one mole of Zn. The reaction systems with 1.0 and 2.0 mol of water per one mole of Zn also led to solids with MOF-5 as the dominant phase, but they also contain small amounts of another phase, formed due to the decomposition (hydrolysis) and/or distortion of the MOF-5 framework in the presence of excess amounts of water. The product synthesized in the system without any added water contains MOF-5 phase in a very small amount, while main phase is zinc 1,4-benzenedicarboxylate and/or zinc hydrogen 1,4-benzenedicarboxylate. Regular cubic submicro/microcrystal morphology exhibited the samples synthesized using 0.5 and 0.25 mol water per one mole of Zn (pure MOF-5), while for the samples synthesized at mole ratios H2O/Zn2+ = 1.0 and 2.0 other particle shapes are also seen. By nitrogen sorption measurements it was found that the highest values of BET specific surface area (1937 m2 g−1), micropore volume (0.83 cm3 g−1), and micropore area (1590 m2 g−1) showed MOF-5 prepared at mole ratio H2O/Zn2+ = 0.5, while the highest yield of MOF-5 is obtained with the theoretical mole ratio H2O/Zn2+ = 0.25. Thermal stability of synthesized materials was investigated by TGA. © 2018 Elsevier Inc.
T2  - Microporous and Mesoporous Materials
T1  - The quest for optimal water quantity in the synthesis of metal-organic framework MOF-5
VL  - 278
SP  - 23
EP  - 29
DO  - 10.1016/j.micromeso.2018.11.005
ER  - 

@article{
author = "Savić-Biserčić, Marjetka and Marjanović, Budimir and Vasiljević-Nedić, Bojana and Mentus, Slavko V. and Zasonska, Beata A. and Ćirić-Marjanović, Gordana N.",
year = "2019",
abstract = "Efficient and simple room temperature synthesis of pure phase metal-organic framework MOF-5 has been developed, based on the use of anhydrous zinc acetate, Zn(OAc)2, as a precursor, instead of zinc acetate dihydrate. Crucial influence of water on a reaction pathway was revealed. In order to obtain MOF-5, different amounts of water have been added into the solutions of Zn(OAc)2 in N,N-dimethylformamide (DMF) to prepare in situ zinc acetate hydrates with 0.25, 0.5, and 1.0 mol of water. Commercially available zinc acetate dihydrate was also used as a precursor for comparison. These solutions were mixed at room temperature with the solution of 1,4-benzenedicarboxylic acid in DMF in the absence of any base. Based on XRD, FTIR, and SEM measurements, it was shown that the optimal amount of water for the synthesis of completely pure, crystalline phase MOF-5 is 0.25–0.5 mol of water per one mole of Zn. The reaction systems with 1.0 and 2.0 mol of water per one mole of Zn also led to solids with MOF-5 as the dominant phase, but they also contain small amounts of another phase, formed due to the decomposition (hydrolysis) and/or distortion of the MOF-5 framework in the presence of excess amounts of water. The product synthesized in the system without any added water contains MOF-5 phase in a very small amount, while main phase is zinc 1,4-benzenedicarboxylate and/or zinc hydrogen 1,4-benzenedicarboxylate. Regular cubic submicro/microcrystal morphology exhibited the samples synthesized using 0.5 and 0.25 mol water per one mole of Zn (pure MOF-5), while for the samples synthesized at mole ratios H2O/Zn2+ = 1.0 and 2.0 other particle shapes are also seen. By nitrogen sorption measurements it was found that the highest values of BET specific surface area (1937 m2 g−1), micropore volume (0.83 cm3 g−1), and micropore area (1590 m2 g−1) showed MOF-5 prepared at mole ratio H2O/Zn2+ = 0.5, while the highest yield of MOF-5 is obtained with the theoretical mole ratio H2O/Zn2+ = 0.25. Thermal stability of synthesized materials was investigated by TGA. © 2018 Elsevier Inc.",
journal = "Microporous and Mesoporous Materials",
title = "The quest for optimal water quantity in the synthesis of metal-organic framework MOF-5",
volume = "278",
pages = "23-29",
doi = "10.1016/j.micromeso.2018.11.005"
}

Savić-Biserčić, M., Marjanović, B., Vasiljević-Nedić, B., Mentus, S. V., Zasonska, B. A.,& Ćirić-Marjanović, G. N.. (2019). The quest for optimal water quantity in the synthesis of metal-organic framework MOF-5. in Microporous and Mesoporous Materials, 278, 23-29.
https://doi.org/10.1016/j.micromeso.2018.11.005

Savić-Biserčić M, Marjanović B, Vasiljević-Nedić B, Mentus SV, Zasonska BA, Ćirić-Marjanović GN. The quest for optimal water quantity in the synthesis of metal-organic framework MOF-5. in Microporous and Mesoporous Materials. 2019;278:23-29.
doi:10.1016/j.micromeso.2018.11.005 .

Savić-Biserčić, Marjetka, Marjanović, Budimir, Vasiljević-Nedić, Bojana, Mentus, Slavko V., Zasonska, Beata A., Ćirić-Marjanović, Gordana N., "The quest for optimal water quantity in the synthesis of metal-organic framework MOF-5" in Microporous and Mesoporous Materials, 278 (2019):23-29,
https://doi.org/10.1016/j.micromeso.2018.11.005 . .

TY  - JOUR
AU  - Vasiljević-Nedić, Bojana
AU  - Obradović, Milena
AU  - Bajuk-Bogdanović, Danica V.
AU  - Milojević-Rakić, Maja
AU  - Jovanović, Zoran M.
AU  - Gavrilov, Nemanja M.
AU  - Holclajtner-Antunović, Ivanka D.
PY  - 2019
UR  - https://linkinghub.elsevier.com/retrieve/pii/S1001074218314682
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8217
AB  - Potassium tungstophosphate is supported on BEA zeolite by in situ synthesis for glyphosate removal. Spectroscopic measurements identified hydrogen bonding as a primal interaction of potassium salt and BEA zeolite. Composites are evaluated for glyphosate herbicide removal and adsorption process is analyzed using two isotherm models. Obtained adsorption capacities for all prepared composites lay between 45.2 and 92.2 mg of glyphosate per gram of investigated composite. Suspension acidity revealed that glyphosate is adsorbed mainly in the zwitter-ion form at the composite surface while the amount of potassium salt in the composites is crucial for the adsorption application. Exceptional adsorption behavior is postulated to come from a high degree of homogeneity among surface active sites which is confirmed by different experimental methods. Temperature programmed desorption of glyphosate coupled with mass spectrometer detected one broad, high-temperature peak which represents overlapped desorption processes from active sights of similar strength. Introduction of potassium tungstophosphate affects active sites present in BEA zeolite for glyphosate desorption and significantly increases the amount of adsorbed pesticide in comparison to BEA zeolite. Supporting of potassium tungstophosphate on BEA zeolite via in situ synthesis procedure enables the formation of highly efficient adsorbents and revealed their perspective environmental application. © 2019
T2  - Journal of Environmental Sciences
T1  - In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal
VL  - 81
SP  - 136
EP  - 147
DO  - 10.1016/j.jes.2019.01.018
ER  - 

@article{
author = "Vasiljević-Nedić, Bojana and Obradović, Milena and Bajuk-Bogdanović, Danica V. and Milojević-Rakić, Maja and Jovanović, Zoran M. and Gavrilov, Nemanja M. and Holclajtner-Antunović, Ivanka D.",
year = "2019",
abstract = "Potassium tungstophosphate is supported on BEA zeolite by in situ synthesis for glyphosate removal. Spectroscopic measurements identified hydrogen bonding as a primal interaction of potassium salt and BEA zeolite. Composites are evaluated for glyphosate herbicide removal and adsorption process is analyzed using two isotherm models. Obtained adsorption capacities for all prepared composites lay between 45.2 and 92.2 mg of glyphosate per gram of investigated composite. Suspension acidity revealed that glyphosate is adsorbed mainly in the zwitter-ion form at the composite surface while the amount of potassium salt in the composites is crucial for the adsorption application. Exceptional adsorption behavior is postulated to come from a high degree of homogeneity among surface active sites which is confirmed by different experimental methods. Temperature programmed desorption of glyphosate coupled with mass spectrometer detected one broad, high-temperature peak which represents overlapped desorption processes from active sights of similar strength. Introduction of potassium tungstophosphate affects active sites present in BEA zeolite for glyphosate desorption and significantly increases the amount of adsorbed pesticide in comparison to BEA zeolite. Supporting of potassium tungstophosphate on BEA zeolite via in situ synthesis procedure enables the formation of highly efficient adsorbents and revealed their perspective environmental application. © 2019",
journal = "Journal of Environmental Sciences",
title = "In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal",
volume = "81",
pages = "136-147",
doi = "10.1016/j.jes.2019.01.018"
}

Vasiljević-Nedić, B., Obradović, M., Bajuk-Bogdanović, D. V., Milojević-Rakić, M., Jovanović, Z. M., Gavrilov, N. M.,& Holclajtner-Antunović, I. D.. (2019). In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal. in Journal of Environmental Sciences, 81, 136-147.
https://doi.org/10.1016/j.jes.2019.01.018

Vasiljević-Nedić B, Obradović M, Bajuk-Bogdanović DV, Milojević-Rakić M, Jovanović ZM, Gavrilov NM, Holclajtner-Antunović ID. In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal. in Journal of Environmental Sciences. 2019;81:136-147.
doi:10.1016/j.jes.2019.01.018 .

Vasiljević-Nedić, Bojana, Obradović, Milena, Bajuk-Bogdanović, Danica V., Milojević-Rakić, Maja, Jovanović, Zoran M., Gavrilov, Nemanja M., Holclajtner-Antunović, Ivanka D., "In situ synthesis of potassium tungstophosphate supported on BEA zeolite and perspective application for pesticide removal" in Journal of Environmental Sciences, 81 (2019):136-147,
https://doi.org/10.1016/j.jes.2019.01.018 . .

TY  - JOUR
AU  - Bajuk-Bogdanović, Danica V.
AU  - Holclajtner-Antunović, Ivanka D.
AU  - Jovanović, Zoran M.
AU  - Mravik, Željko
AU  - Krstić, Jugoslav B.
AU  - Uskoković-Marković, Snežana
AU  - Vujković, Milica
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8500
AB  - The synergistic effects between two Keggin-type heteropoly acids (HPAs) and carbon surface were examined and elucidated. An improved high rate capability (and potential high capacitor electrode for supercapacitors) of the hybrid materials, obtained by anchoring of α-dodecamolybdophosphoric (MoPA), α-dodecatungstophosphoric (WPA), and their mixture to activated carbon (AC), was achieved through the different mechanism of interaction. In order to elaborate this, a detailed analysis of AC-HPA composites has been performed by scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) analysis, temperature-programmed desorption (TPD), Fourier-transform infrared spectroscopy (FTIR), micro Raman spectroscopy, and zeta potential measurements. The zeta potential measurements revealed positive charge of carbon surface thus indicating attractive interactions with negatively charged Keggin anion. The surface analysis has shown that WPA spontaneously reduces the carbon surface, while interaction with MoPA leads to its oxidation. As the consequence of the tailoring of the functional groups at carbon surface through HPAs’ action, the distortion of cyclic voltammograms (CVs) decreased in the following order: AC-MoPA, AC-MoPA-WPA, and AC-WPA. A prominent rectangular shape of AC-WPA, even at an extremely high scan rate of 400 mVs−1, was measured, which is rarely demonstrated for carbon-based composites. By applying the theory of electrode potentials, the HPA-AC synergistic effect was explained and discussed in terms of charge storage improvement of HPA-modified carbon. © 2019, Springer-Verlag GmbH Germany, part of Springer Nature.
T2  - Journal of Solid State Electrochemistry
T1  - Tailoring the electrochemical charge storage properties of carbonaceous support by redox properties of heteropoly acids: where does the synergy come from?
VL  - 23
IS  - 9
SP  - 2747
EP  - 2758
DO  - 10.1007/s10008-019-04369-4
ER  - 

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

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

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

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

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

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

Kuzmanović, B., Vujković, M., Tomić, N. M., Bajuk-Bogdanović, D. V., Lazović, V. M., Šljukić, B., Ivanović, N.,& Mentus, S. V.. (2019). The influence of oxygen vacancy concentration in nanodispersed non-stoichiometric CeO2-δ oxides on the physico-chemical properties of conducting polyaniline/CeO2 composites. in Electrochimica Acta, 306, 506-515.
https://doi.org/10.1016/j.electacta.2019.03.135

Kuzmanović B, Vujković M, Tomić NM, Bajuk-Bogdanović DV, Lazović VM, Šljukić B, Ivanović N, Mentus SV. The influence of oxygen vacancy concentration in nanodispersed non-stoichiometric CeO2-δ oxides on the physico-chemical properties of conducting polyaniline/CeO2 composites. in Electrochimica Acta. 2019;306:506-515.
doi:10.1016/j.electacta.2019.03.135 .

Kuzmanović, Bojana, Vujković, Milica, Tomić, Nataša M., Bajuk-Bogdanović, Danica V., Lazović, Vladimir M., Šljukić, Biljana, Ivanović, Nenad, Mentus, Slavko V., "The influence of oxygen vacancy concentration in nanodispersed non-stoichiometric CeO2-δ oxides on the physico-chemical properties of conducting polyaniline/CeO2 composites" in Electrochimica Acta, 306 (2019):506-515,
https://doi.org/10.1016/j.electacta.2019.03.135 . .

TY  - JOUR
AU  - Milikić, Jadranka
AU  - Stamenović, Una
AU  - Vodnik, Vesna
AU  - Ahrenkiel, Scott Phillip
AU  - Šljukić, Biljana
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8609
AB  - Two gold nanorod-polyaniline (Au-PANI) composites with different contents of Au were prepared by two methods. An ex situ method, in the presence of preformed gold nanorods (AuNRs) and in situ one, when an AuNRs and PANI matrix is produced simultaneously, were used. Both methods were performed in immiscible water/toluene biphasic system as a simple interfacial polymerization process. Optical, structural and morphological characteristics of the formed nanocomposites were identified. It was found that AuNRs are embedded in the conducting emeraldine salt form of PANI. Nanocomposites containing 2.0 and 28.9 wt% of Au were subsequently systematically studied for borohydride oxidation reaction (BOR) for potential application in direct borohydride-peroxide fuel cell (DBPFC). Reaction parameters: number of electrons exchanged, order of reaction and activation energy, were evaluated. Both Au-PANI nanocomposites showed activity for BOR. A laboratory DBPFC was tested reaching specific peak power density of 184 Wg(-1) at 65 degrees C with Au-PANI 1 nanocomposite (containing only 2.0 wt% of Au) as anode.
T2  - Electrochimica Acta
T1  - Gold nanorod-polyaniline composites: Synthesis and evaluation as anode electrocatalysts for direct borohydride fuel cells
VL  - 328
SP  - 135115
DO  - 10.1016/j.electacta.2019.135115
ER  - 

@article{
author = "Milikić, Jadranka and Stamenović, Una and Vodnik, Vesna and Ahrenkiel, Scott Phillip and Šljukić, Biljana",
year = "2019",
abstract = "Two gold nanorod-polyaniline (Au-PANI) composites with different contents of Au were prepared by two methods. An ex situ method, in the presence of preformed gold nanorods (AuNRs) and in situ one, when an AuNRs and PANI matrix is produced simultaneously, were used. Both methods were performed in immiscible water/toluene biphasic system as a simple interfacial polymerization process. Optical, structural and morphological characteristics of the formed nanocomposites were identified. It was found that AuNRs are embedded in the conducting emeraldine salt form of PANI. Nanocomposites containing 2.0 and 28.9 wt% of Au were subsequently systematically studied for borohydride oxidation reaction (BOR) for potential application in direct borohydride-peroxide fuel cell (DBPFC). Reaction parameters: number of electrons exchanged, order of reaction and activation energy, were evaluated. Both Au-PANI nanocomposites showed activity for BOR. A laboratory DBPFC was tested reaching specific peak power density of 184 Wg(-1) at 65 degrees C with Au-PANI 1 nanocomposite (containing only 2.0 wt% of Au) as anode.",
journal = "Electrochimica Acta",
title = "Gold nanorod-polyaniline composites: Synthesis and evaluation as anode electrocatalysts for direct borohydride fuel cells",
volume = "328",
pages = "135115",
doi = "10.1016/j.electacta.2019.135115"
}

Milikić, J., Stamenović, U., Vodnik, V., Ahrenkiel, S. P.,& Šljukić, B.. (2019). Gold nanorod-polyaniline composites: Synthesis and evaluation as anode electrocatalysts for direct borohydride fuel cells. in Electrochimica Acta, 328, 135115.
https://doi.org/10.1016/j.electacta.2019.135115

Milikić J, Stamenović U, Vodnik V, Ahrenkiel SP, Šljukić B. Gold nanorod-polyaniline composites: Synthesis and evaluation as anode electrocatalysts for direct borohydride fuel cells. in Electrochimica Acta. 2019;328:135115.
doi:10.1016/j.electacta.2019.135115 .

Milikić, Jadranka, Stamenović, Una, Vodnik, Vesna, Ahrenkiel, Scott Phillip, Šljukić, Biljana, "Gold nanorod-polyaniline composites: Synthesis and evaluation as anode electrocatalysts for direct borohydride fuel cells" in Electrochimica Acta, 328 (2019):135115,
https://doi.org/10.1016/j.electacta.2019.135115 . .

TY  - JOUR
AU  - Stamenović, Una
AU  - Gavrilov, Nemanja M.
AU  - Pašti, Igor A.
AU  - Otoničar, Mojca
AU  - Ćirić-Marjanović, Gordana N.
AU  - Škapin, Srečo Davor
AU  - Mitrić, Miodrag
AU  - Vodnik, Vesna
PY  - 2018
UR  - https://linkinghub.elsevier.com/retrieve/pii/S0013468618312799
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7717
AB  - A facile and fast aqueous phase-based strategy to synthesize silver-polyaniline-polyvinylpyrrolidone (Ag-PANI-PVP) nanocomposites, via chemical oxidative polymerization method is presented. In the presence of polyvinylpyrrolidone (PVP), which has an accelerating effect on the oxidation of aniline with silver nitrate, Ag nanoparticles (AgNPs) were in situ generated in aqueous solution during simultaneous formation of polyaniline (PANI), without any additional reducing agent or complicated treatment. We have demonstrated synthesis of three stabile Ag-PANI-PVP nanocomposites with different content, size, and morphology of Ag nanoparticles by varying the experimental parameters, such as pH and PVP concentration. As a result, this led to different Ag nanostructures (spherical and polyhedral NPs), and, consequently, different morphology of formed nanocomposites (granular and nanosheets). The physicochemical properties of nanocomposites were examined by using different analytical techniques (UV–Vis, TEM, FESEM, FT-IR, XRD, and Raman). It is found that optical properties, electrical conductivity and the content of Ag in the composites vary depending on the synthetic conditions. The electrocatalytic behavior of Ag-PANI-PVP nanocomposites was examined towards the oxygen reduction reaction in acidic and alkaline media. All tested nanocomposites showed high electrocatalytic activity, while the most active catalyst is the one with the highest electrical conductivity (≈0.6 S cm−1) and the lowest Ag content (3.4 wt%), synthesized in the solution without added acid. The simplicity of synthesis and good electrocatalytic efficiency of prepared nanocomposites combined with large-scale availability make them attractive as Pt-free electrocatalysts.
T2  - Electrochimica Acta
T1  - One-pot synthesis of novel silver-polyaniline-polyvinylpyrrolidone electrocatalysts for efficient oxygen reduction reaction
VL  - 281
SP  - 549
EP  - 561
DO  - 10.1016/j.electacta.2018.05.202
ER  - 

@article{
author = "Stamenović, Una and Gavrilov, Nemanja M. and Pašti, Igor A. and Otoničar, Mojca and Ćirić-Marjanović, Gordana N. and Škapin, Srečo Davor and Mitrić, Miodrag and Vodnik, Vesna",
year = "2018",
abstract = "A facile and fast aqueous phase-based strategy to synthesize silver-polyaniline-polyvinylpyrrolidone (Ag-PANI-PVP) nanocomposites, via chemical oxidative polymerization method is presented. In the presence of polyvinylpyrrolidone (PVP), which has an accelerating effect on the oxidation of aniline with silver nitrate, Ag nanoparticles (AgNPs) were in situ generated in aqueous solution during simultaneous formation of polyaniline (PANI), without any additional reducing agent or complicated treatment. We have demonstrated synthesis of three stabile Ag-PANI-PVP nanocomposites with different content, size, and morphology of Ag nanoparticles by varying the experimental parameters, such as pH and PVP concentration. As a result, this led to different Ag nanostructures (spherical and polyhedral NPs), and, consequently, different morphology of formed nanocomposites (granular and nanosheets). The physicochemical properties of nanocomposites were examined by using different analytical techniques (UV–Vis, TEM, FESEM, FT-IR, XRD, and Raman). It is found that optical properties, electrical conductivity and the content of Ag in the composites vary depending on the synthetic conditions. The electrocatalytic behavior of Ag-PANI-PVP nanocomposites was examined towards the oxygen reduction reaction in acidic and alkaline media. All tested nanocomposites showed high electrocatalytic activity, while the most active catalyst is the one with the highest electrical conductivity (≈0.6 S cm−1) and the lowest Ag content (3.4 wt%), synthesized in the solution without added acid. The simplicity of synthesis and good electrocatalytic efficiency of prepared nanocomposites combined with large-scale availability make them attractive as Pt-free electrocatalysts.",
journal = "Electrochimica Acta",
title = "One-pot synthesis of novel silver-polyaniline-polyvinylpyrrolidone electrocatalysts for efficient oxygen reduction reaction",
volume = "281",
pages = "549-561",
doi = "10.1016/j.electacta.2018.05.202"
}

Stamenović, U., Gavrilov, N. M., Pašti, I. A., Otoničar, M., Ćirić-Marjanović, G. N., Škapin, S. D., Mitrić, M.,& Vodnik, V.. (2018). One-pot synthesis of novel silver-polyaniline-polyvinylpyrrolidone electrocatalysts for efficient oxygen reduction reaction. in Electrochimica Acta, 281, 549-561.
https://doi.org/10.1016/j.electacta.2018.05.202

Stamenović U, Gavrilov NM, Pašti IA, Otoničar M, Ćirić-Marjanović GN, Škapin SD, Mitrić M, Vodnik V. One-pot synthesis of novel silver-polyaniline-polyvinylpyrrolidone electrocatalysts for efficient oxygen reduction reaction. in Electrochimica Acta. 2018;281:549-561.
doi:10.1016/j.electacta.2018.05.202 .

Stamenović, Una, Gavrilov, Nemanja M., Pašti, Igor A., Otoničar, Mojca, Ćirić-Marjanović, Gordana N., Škapin, Srečo Davor, Mitrić, Miodrag, Vodnik, Vesna, "One-pot synthesis of novel silver-polyaniline-polyvinylpyrrolidone electrocatalysts for efficient oxygen reduction reaction" in Electrochimica Acta, 281 (2018):549-561,
https://doi.org/10.1016/j.electacta.2018.05.202 . .

TY  - JOUR
AU  - Jovanović, Svetlana P.
AU  - Holclajtner-Antunović, Ivanka D.
AU  - Uskoković-Marković, Snežana
AU  - Bajuk-Bogdanović, Danica V.
AU  - Pavlović, Vladimir B.
AU  - Tošić, Dragana
AU  - Milenković, Marina
AU  - Todorović-Marković, Biljana
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7611
AB  - © 2018 Antibacterial properties of graphene oxide (GO) have been studied extensively in the last few years, while for polyoxometalates there are just a few researches. Herein, we prepared nanocomposites of GO and different amounts of 12-molybdophosphoric acid (MoPA) and analyzed their antibacterial activity and both structural and morphological properties. In nanocomposites with higher amounts of MoPA, graphene sheets were significantly changed with disrupted flat, graphene-like morphology of GO. In the nanocomposites with low MoPA content, flat GO morphology was preserved. Additionally, structural analyses showed some changes in symmetry of the Keggin anion as a consequence of interactions between GO and MoPA, the increase in structural disorder and the lowering of electron density in GO structure due to interaction with MoPA. We have studied antibacterial properties on the gram-positive: Staphylococcus aureus, Staphylococcus epidermidis, Bacillus subtilis; and the gram-negative bacteria: Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and Salmonella abony. Only a mild antibacterial effect of GO and nanocomposites with low amount of MoPA against Bacillus subtilis was observed, while the rest of analyzed materials did not show any antibacterial activity.
T2  - Materials Chemistry and Physics
T1  - Modification of graphene oxide surfaces with 12-molybdophosphoric acid: Structural and antibacterial study
VL  - 213
SP  - 157
EP  - 167
DO  - 10.1016/j.matchemphys.2018.04.011
ER  - 

@article{
author = "Jovanović, Svetlana P. and Holclajtner-Antunović, Ivanka D. and Uskoković-Marković, Snežana and Bajuk-Bogdanović, Danica V. and Pavlović, Vladimir B. and Tošić, Dragana and Milenković, Marina and Todorović-Marković, Biljana",
year = "2018",
abstract = "© 2018 Antibacterial properties of graphene oxide (GO) have been studied extensively in the last few years, while for polyoxometalates there are just a few researches. Herein, we prepared nanocomposites of GO and different amounts of 12-molybdophosphoric acid (MoPA) and analyzed their antibacterial activity and both structural and morphological properties. In nanocomposites with higher amounts of MoPA, graphene sheets were significantly changed with disrupted flat, graphene-like morphology of GO. In the nanocomposites with low MoPA content, flat GO morphology was preserved. Additionally, structural analyses showed some changes in symmetry of the Keggin anion as a consequence of interactions between GO and MoPA, the increase in structural disorder and the lowering of electron density in GO structure due to interaction with MoPA. We have studied antibacterial properties on the gram-positive: Staphylococcus aureus, Staphylococcus epidermidis, Bacillus subtilis; and the gram-negative bacteria: Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and Salmonella abony. Only a mild antibacterial effect of GO and nanocomposites with low amount of MoPA against Bacillus subtilis was observed, while the rest of analyzed materials did not show any antibacterial activity.",
journal = "Materials Chemistry and Physics",
title = "Modification of graphene oxide surfaces with 12-molybdophosphoric acid: Structural and antibacterial study",
volume = "213",
pages = "157-167",
doi = "10.1016/j.matchemphys.2018.04.011"
}

Jovanović, S. P., Holclajtner-Antunović, I. D., Uskoković-Marković, S., Bajuk-Bogdanović, D. V., Pavlović, V. B., Tošić, D., Milenković, M.,& Todorović-Marković, B.. (2018). Modification of graphene oxide surfaces with 12-molybdophosphoric acid: Structural and antibacterial study. in Materials Chemistry and Physics, 213, 157-167.
https://doi.org/10.1016/j.matchemphys.2018.04.011

Jovanović SP, Holclajtner-Antunović ID, Uskoković-Marković S, Bajuk-Bogdanović DV, Pavlović VB, Tošić D, Milenković M, Todorović-Marković B. Modification of graphene oxide surfaces with 12-molybdophosphoric acid: Structural and antibacterial study. in Materials Chemistry and Physics. 2018;213:157-167.
doi:10.1016/j.matchemphys.2018.04.011 .

Jovanović, Svetlana P., Holclajtner-Antunović, Ivanka D., Uskoković-Marković, Snežana, Bajuk-Bogdanović, Danica V., Pavlović, Vladimir B., Tošić, Dragana, Milenković, Marina, Todorović-Marković, Biljana, "Modification of graphene oxide surfaces with 12-molybdophosphoric acid: Structural and antibacterial study" in Materials Chemistry and Physics, 213 (2018):157-167,
https://doi.org/10.1016/j.matchemphys.2018.04.011 . .

TY  - JOUR
AU  - Gajić-Kvaščev, Maja
AU  - Bikić, Vesna
AU  - Wright, Victoria J.
AU  - Radosavjević Evans, Ivana
AU  - Damjanović-Vasilić, Ljiljana S.
PY  - 2018
UR  - https://linkinghub.elsevier.com/retrieve/pii/S1296207417304478
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7923
AB  - The chemical and mineralogical composition of ceramic bodies, glazes and pigments, as well as the firing temperatures of main groups of Austrian period painted pottery excavated at the Belgrade Fortress on the territory of Serbia, two groups of Malhornware and one group of Anabaptist faience, were determined by a combination of powder X-ray diffraction (PXRD), Fourier transform infrared (FTIR) spectroscopy, energy dispersive X-ray fluorescence (XRF) and micro-Raman spectroscopy. Investigated pottery was uncovered in the same archaeological context and dated the end of 17th/first decade of 18th century. The obtained mineralogical and chemical composition shows the similarities between the Malhornware groups that indicate a similar production technology. Use of calcareous clay fired at temperatures in the range 850-900 degrees C indicates a different production technology for the Anabaptists faience. The compositional data treatment by multivariate statistical analysis reveals heterogeneity in the Anabaptist faience group of samples, suggesting potential interactions between the local potters and the Anabaptist communities. (C) 2018 Elsevier Masson SAS. All rights reserved.
T2  - Journal of Cultural Heritage
T1  - Archaeometric study of 17th/18th century painted pottery from the Belgrade Fortress
VL  - 32
SP  - 9
EP  - 21
DO  - 10.1016/j.culher.2018.01.018
ER  - 

@article{
author = "Gajić-Kvaščev, Maja and Bikić, Vesna and Wright, Victoria J. and Radosavjević Evans, Ivana and Damjanović-Vasilić, Ljiljana S.",
year = "2018",
abstract = "The chemical and mineralogical composition of ceramic bodies, glazes and pigments, as well as the firing temperatures of main groups of Austrian period painted pottery excavated at the Belgrade Fortress on the territory of Serbia, two groups of Malhornware and one group of Anabaptist faience, were determined by a combination of powder X-ray diffraction (PXRD), Fourier transform infrared (FTIR) spectroscopy, energy dispersive X-ray fluorescence (XRF) and micro-Raman spectroscopy. Investigated pottery was uncovered in the same archaeological context and dated the end of 17th/first decade of 18th century. The obtained mineralogical and chemical composition shows the similarities between the Malhornware groups that indicate a similar production technology. Use of calcareous clay fired at temperatures in the range 850-900 degrees C indicates a different production technology for the Anabaptists faience. The compositional data treatment by multivariate statistical analysis reveals heterogeneity in the Anabaptist faience group of samples, suggesting potential interactions between the local potters and the Anabaptist communities. (C) 2018 Elsevier Masson SAS. All rights reserved.",
journal = "Journal of Cultural Heritage",
title = "Archaeometric study of 17th/18th century painted pottery from the Belgrade Fortress",
volume = "32",
pages = "9-21",
doi = "10.1016/j.culher.2018.01.018"
}

Gajić-Kvaščev, M., Bikić, V., Wright, V. J., Radosavjević Evans, I.,& Damjanović-Vasilić, L. S.. (2018). Archaeometric study of 17th/18th century painted pottery from the Belgrade Fortress. in Journal of Cultural Heritage, 32, 9-21.
https://doi.org/10.1016/j.culher.2018.01.018

Gajić-Kvaščev M, Bikić V, Wright VJ, Radosavjević Evans I, Damjanović-Vasilić LS. Archaeometric study of 17th/18th century painted pottery from the Belgrade Fortress. in Journal of Cultural Heritage. 2018;32:9-21.
doi:10.1016/j.culher.2018.01.018 .

Gajić-Kvaščev, Maja, Bikić, Vesna, Wright, Victoria J., Radosavjević Evans, Ivana, Damjanović-Vasilić, Ljiljana S., "Archaeometric study of 17th/18th century painted pottery from the Belgrade Fortress" in Journal of Cultural Heritage, 32 (2018):9-21,
https://doi.org/10.1016/j.culher.2018.01.018 . .

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

@article{
author = "Vujković, Milica and Bajuk-Bogdanović, Danica V. and Matović, Ljiljana and Stojmenović, Marija and Mentus, Slavko V.",
year = "2018",
abstract = "Coulombic capacity of zeolite-templated carbon (ZTC) measured in alkaline solution was roughly doubled by a previous potentiodynamic treatment in sulfuric acidic solution. In order to explain the reasons of this capacity improvement, the changes in chemical composition of ZTC surface during its pretreatment in sulfuric acid either by simple immersion, or by potentiodynamic polarization, and during subsequent potentiodynamic polarization in KOH solutions, were studied by means of TG/DTA, FTIR spectroscopy and Raman spectroscopy. The results of this study open some novel insights in understanding of very peculiar carbon electrochemistry. The observed changes in surface chemistry include i) fast adsorption of H2O and formation of OH− and epoxide groups on immersion in sulfuric acid, ii) the multiplication of concentration of H2O/OH− and epoxide groups during potentiodynamic cycling in sulfuric acid and iii) the ring-opening of epoxide groups (formed during potentiodynamic cycling in acidic solution) upon its potentiodynamic cycling in alkaline solution, according to a SN2 type mechanism, which results in the formation of aromatic OH-containing diol compounds. © 2018 Elsevier Ltd",
journal = "Carbon",
title = "Mild electrochemical oxidation of zeolite templated carbon in acidic solutions, as a way to boost its charge storage properties in alkaline solutions",
volume = "138",
pages = "369-378",
doi = "10.1016/j.carbon.2018.07.053"
}

Vujković, M., Bajuk-Bogdanović, D. V., Matović, L., Stojmenović, M.,& Mentus, S. V.. (2018). Mild electrochemical oxidation of zeolite templated carbon in acidic solutions, as a way to boost its charge storage properties in alkaline solutions. in Carbon, 138, 369-378.
https://doi.org/10.1016/j.carbon.2018.07.053

Vujković M, Bajuk-Bogdanović DV, Matović L, Stojmenović M, Mentus SV. Mild electrochemical oxidation of zeolite templated carbon in acidic solutions, as a way to boost its charge storage properties in alkaline solutions. in Carbon. 2018;138:369-378.
doi:10.1016/j.carbon.2018.07.053 .

Vujković, Milica, Bajuk-Bogdanović, Danica V., Matović, Ljiljana, Stojmenović, Marija, Mentus, Slavko V., "Mild electrochemical oxidation of zeolite templated carbon in acidic solutions, as a way to boost its charge storage properties in alkaline solutions" in Carbon, 138 (2018):369-378,
https://doi.org/10.1016/j.carbon.2018.07.053 . .

TY  - JOUR
AU  - Vasić, Milica M.
AU  - Čebela, Maria
AU  - Pašti, Igor A.
AU  - Amaral, Luis
AU  - Hercigonja, Radmila V.
AU  - Santos, Diogo M. F.
AU  - Šljukić, Biljana
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1943
AB  - Palladium ion-exchanged zeolite X (PdX) was prepared by zeolite impregnation with palladium acetylacetonate, followed by thermal degradation of the salt. PdX was characterised using SEM-EDS, ICP-OES and XRD. Analysis revealed presence of 7.78 wt.% of Pd in the form of PdO. Subsequently, PdX was tested for hydrogen evolution reaction (HER) in alkaline medium using linear scan voltammetry, chronoamperometry and electrochemical impedance spectroscopy measurements. The influence of addition of carbon black on the materials catalytic performance was also investigated. The HER kinetic parameters, including Tafel slope, exchange current density and activation energy, were determined. In order to provide atomic-level insights, experimental results were complemented by density functional theory calculations. It is suggested that favourable hydrogen adsorption energetics on PdO is responsible for efficient HER catalysis by this novel electrocatalyst. (c) 2017 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Efficient hydrogen evolution electrocatalysis in alkaline medium using Pd-modified zeolite X
VL  - 259
SP  - 882
EP  - 892
DO  - 10.1016/j.electacta.2017.11.020
ER  - 

@article{
author = "Vasić, Milica M. and Čebela, Maria and Pašti, Igor A. and Amaral, Luis and Hercigonja, Radmila V. and Santos, Diogo M. F. and Šljukić, Biljana",
year = "2018",
abstract = "Palladium ion-exchanged zeolite X (PdX) was prepared by zeolite impregnation with palladium acetylacetonate, followed by thermal degradation of the salt. PdX was characterised using SEM-EDS, ICP-OES and XRD. Analysis revealed presence of 7.78 wt.% of Pd in the form of PdO. Subsequently, PdX was tested for hydrogen evolution reaction (HER) in alkaline medium using linear scan voltammetry, chronoamperometry and electrochemical impedance spectroscopy measurements. The influence of addition of carbon black on the materials catalytic performance was also investigated. The HER kinetic parameters, including Tafel slope, exchange current density and activation energy, were determined. In order to provide atomic-level insights, experimental results were complemented by density functional theory calculations. It is suggested that favourable hydrogen adsorption energetics on PdO is responsible for efficient HER catalysis by this novel electrocatalyst. (c) 2017 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Efficient hydrogen evolution electrocatalysis in alkaline medium using Pd-modified zeolite X",
volume = "259",
pages = "882-892",
doi = "10.1016/j.electacta.2017.11.020"
}

Vasić, M. M., Čebela, M., Pašti, I. A., Amaral, L., Hercigonja, R. V., Santos, D. M. F.,& Šljukić, B.. (2018). Efficient hydrogen evolution electrocatalysis in alkaline medium using Pd-modified zeolite X. in Electrochimica Acta, 259, 882-892.
https://doi.org/10.1016/j.electacta.2017.11.020

Vasić MM, Čebela M, Pašti IA, Amaral L, Hercigonja RV, Santos DMF, Šljukić B. Efficient hydrogen evolution electrocatalysis in alkaline medium using Pd-modified zeolite X. in Electrochimica Acta. 2018;259:882-892.
doi:10.1016/j.electacta.2017.11.020 .

Vasić, Milica M., Čebela, Maria, Pašti, Igor A., Amaral, Luis, Hercigonja, Radmila V., Santos, Diogo M. F., Šljukić, Biljana, "Efficient hydrogen evolution electrocatalysis in alkaline medium using Pd-modified zeolite X" in Electrochimica Acta, 259 (2018):882-892,
https://doi.org/10.1016/j.electacta.2017.11.020 . .

TY  - JOUR
AU  - Milikic, Jadranka
AU  - Stoševski, Ivan
AU  - Krstić, Jelena
AU  - Kačarević-Popović, Zorica M.
AU  - Miljanić, Šćepan S.
AU  - Šljukić, Biljana
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1803
AB  - Monitoring bromides (Br-) is of crucial importance since bromates, potential human carcinogens, are formed during ozonation of water containing bromides in concentrations GT 100 mu gL(-1). Within this study, silver (Ag) and four carbon-supported Ag catalysts were synthesized by the gamma-radiation method and their morphology and structure examined using transmission electron microscopy, X-ray diffraction, and UV-Vis analysis. The nanocatalysts were tested for Br- sensing in aqueous media using cyclic voltammetry. All five Ag materials exhibited electroactivity for sensing of Br- ions, with pure Ag catalyst giving the best response to Br- ions presence in terms of the lowest limit of detection. Sensing of bromides was also explored in tap water after addition of bromides suggesting that herein prepared catalysts could be used for bromides detection in real samples. Furthermore, sensing of other halogen ions, namely, chlorides and iodides, was examined, and response due to chloride presence was recorded.
T2  - Journal of Analytical Methods in Chemistry
T1  - Electroanalytical Sensing of Bromides Using Radiolytically Synthesized Silver Nanoparticle Electrocatalysts
DO  - 10.1155/2017/2028417
ER  - 

@article{
author = "Milikic, Jadranka and Stoševski, Ivan and Krstić, Jelena and Kačarević-Popović, Zorica M. and Miljanić, Šćepan S. and Šljukić, Biljana",
year = "2017",
abstract = "Monitoring bromides (Br-) is of crucial importance since bromates, potential human carcinogens, are formed during ozonation of water containing bromides in concentrations GT 100 mu gL(-1). Within this study, silver (Ag) and four carbon-supported Ag catalysts were synthesized by the gamma-radiation method and their morphology and structure examined using transmission electron microscopy, X-ray diffraction, and UV-Vis analysis. The nanocatalysts were tested for Br- sensing in aqueous media using cyclic voltammetry. All five Ag materials exhibited electroactivity for sensing of Br- ions, with pure Ag catalyst giving the best response to Br- ions presence in terms of the lowest limit of detection. Sensing of bromides was also explored in tap water after addition of bromides suggesting that herein prepared catalysts could be used for bromides detection in real samples. Furthermore, sensing of other halogen ions, namely, chlorides and iodides, was examined, and response due to chloride presence was recorded.",
journal = "Journal of Analytical Methods in Chemistry",
title = "Electroanalytical Sensing of Bromides Using Radiolytically Synthesized Silver Nanoparticle Electrocatalysts",
doi = "10.1155/2017/2028417"
}

Milikic, J., Stoševski, I., Krstić, J., Kačarević-Popović, Z. M., Miljanić, Š. S.,& Šljukić, B.. (2017). Electroanalytical Sensing of Bromides Using Radiolytically Synthesized Silver Nanoparticle Electrocatalysts. in Journal of Analytical Methods in Chemistry.
https://doi.org/10.1155/2017/2028417

Milikic J, Stoševski I, Krstić J, Kačarević-Popović ZM, Miljanić ŠS, Šljukić B. Electroanalytical Sensing of Bromides Using Radiolytically Synthesized Silver Nanoparticle Electrocatalysts. in Journal of Analytical Methods in Chemistry. 2017;.
doi:10.1155/2017/2028417 .

Milikic, Jadranka, Stoševski, Ivan, Krstić, Jelena, Kačarević-Popović, Zorica M., Miljanić, Šćepan S., Šljukić, Biljana, "Electroanalytical Sensing of Bromides Using Radiolytically Synthesized Silver Nanoparticle Electrocatalysts" in Journal of Analytical Methods in Chemistry (2017),
https://doi.org/10.1155/2017/2028417 . .

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

@article{
author = "Jovanović, Zoran M. and Holclajtner-Antunović, Ivanka D. and Bajuk-Bogdanović, Danica V. and Jovanović, Sonja and Mravik, Željko and Vujković, Milica",
year = "2017",
abstract = "The influence of thermal treatment in an inert atmosphere on the charge storage properties of graphene oxide (GO)/12-tungstophosphoric acid (WPA) nanocomposite was examined. The transmission electron microscopy analysis revealed high dispersion of WPA on GO matrix, while the surface analysis showed thermal activation of structural changes of WPA and desorption of oxygen functional groups from GO and GO/WPA nanocomposite. Initial GO/WPA nanocomposite had approximately two times higher capacitance compared to initial GO. The thermal treatment of initial GO and GO/WPA to 500 degrees C induced twofold increase of capacitance of GO and 40% increase of GO/WPA, accompanied with significant increase of operating voltage compared to GO (for 300 mV). Above 500 degrees C, a decrease of capacitance of both GO and GO/WPA was observed. The results suggest that understanding of structural changes of components and their interaction is crucial for improvement of electrochemical properties of considered composite.",
journal = "Electrochemistry Communications",
title = "Effect of thermal treatment on the charge storage properties of graphene oxide/12-tungstophosphoric acid nanocomposite",
volume = "83",
pages = "36-40",
doi = "10.1016/j.elecom.2017.08.017"
}

Jovanović, Z. M., Holclajtner-Antunović, I. D., Bajuk-Bogdanović, D. V., Jovanović, S., Mravik, Ž.,& Vujković, M.. (2017). Effect of thermal treatment on the charge storage properties of graphene oxide/12-tungstophosphoric acid nanocomposite. in Electrochemistry Communications, 83, 36-40.
https://doi.org/10.1016/j.elecom.2017.08.017

Jovanović ZM, Holclajtner-Antunović ID, Bajuk-Bogdanović DV, Jovanović S, Mravik Ž, Vujković M. Effect of thermal treatment on the charge storage properties of graphene oxide/12-tungstophosphoric acid nanocomposite. in Electrochemistry Communications. 2017;83:36-40.
doi:10.1016/j.elecom.2017.08.017 .

Jovanović, Zoran M., Holclajtner-Antunović, Ivanka D., Bajuk-Bogdanović, Danica V., Jovanović, Sonja, Mravik, Željko, Vujković, Milica, "Effect of thermal treatment on the charge storage properties of graphene oxide/12-tungstophosphoric acid nanocomposite" in Electrochemistry Communications, 83 (2017):36-40,
https://doi.org/10.1016/j.elecom.2017.08.017 . .

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

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

Jovanović, Z. M., Bajuk-Bogdanović, D. V., Jovanović, S., Mravik, Ž., Kovač, J., Holclajtner-Antunović, I. D.,& Vujković, M.. (2017). The role of surface chemistry in the charge storage properties of graphene oxide. in Electrochimica Acta, 258, 1228-1243.
https://doi.org/10.1016/j.electacta.2017.11.178

Jovanović ZM, Bajuk-Bogdanović DV, Jovanović S, Mravik Ž, Kovač J, Holclajtner-Antunović ID, Vujković M. The role of surface chemistry in the charge storage properties of graphene oxide. in Electrochimica Acta. 2017;258:1228-1243.
doi:10.1016/j.electacta.2017.11.178 .

Jovanović, Zoran M., Bajuk-Bogdanović, Danica V., Jovanović, Sonja, Mravik, Željko, Kovač, Janez, Holclajtner-Antunović, Ivanka D., Vujković, Milica, "The role of surface chemistry in the charge storage properties of graphene oxide" in Electrochimica Acta, 258 (2017):1228-1243,
https://doi.org/10.1016/j.electacta.2017.11.178 . .

TY  - JOUR
AU  - Radoičić, Marija B.
AU  - Ćirić-Marjanović, Gordana N.
AU  - Spasojević, Vuk D.
AU  - Ahrenkiel, Scott Phillip
AU  - Mitrić, Miodrag
AU  - Novaković, Tatjana
AU  - Šaponjić, Zoran
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1597
AB  - A simple bottom-up method for the preparation of novel and very efficient photocatalytic nanocomposite system based on carbonized form of polyaniline (PANI) and colloidal TiO2 nanocrystals has been developed. The carbonized PANI/TiO2 nanocomposites were synthesized in a two-step procedure. Firstly, non-carbonized PANI/TiO2 nanocomposites were synthesized by the chemical oxidative polymerization of aniline (ANI) with ammonium peroxydisulfate, in the presence of colloidal TiO2 nanoparticles (TiO2 NPs) (d 4.5 nm). Initial [TiO2 NANI] mole ratios were 20, 50, and 80. In the second step, following the polymerization process, the carbonization of PANI/TiO2 nanocomposites was performed by thermal treatment in an inert atmosphere at 650 degrees C. The morphological and structural properties of the carbonized nanocomposites were studied using transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray powder diffraction (XRD) and Raman spectroscopy. The accomplishment of complete carbonization of PANI in PANI/TiO2 nanocomposites was confirmed by Raman spectroscopy. The appearance of anatase and rutile crystal forms in TiO2 NPs upon carbonization, with mass ratio depending on the initial molar ratio of ANI and TiO2 NPs was revealed by XRD measurements, TEM, SEM and Raman spectroscopy. The photocatalytic activities of carbonized PANI/TiO2 nanocomposites were evaluated following the photocatalytic degradation processes of Rhodamine B and Methylene blue. Carbonized PANI/TiO2 nanocomposites showed higher photocatalytic efficacy compared to bare TiO2 NPs and non-carbonized PANI/TiO2 nanocomposites. The porosity and surface structure of carbonized PANI/TiO2 nanocomposites, as well as crystalline structure of TiO2, affect photocatalytic activity of nanocomposites. (C) 2017 Elsevier B.V. All rights reserved.
T2  - Applied Catalysis. B: Environmental
T1  - Superior photocatalytic properties of carbonized PANI/TiO2 nanocomposites
VL  - 213
SP  - 155
EP  - 166
DO  - 10.1016/j.apcatb.2017.05.023
ER  - 

@article{
author = "Radoičić, Marija B. and Ćirić-Marjanović, Gordana N. and Spasojević, Vuk D. and Ahrenkiel, Scott Phillip and Mitrić, Miodrag and Novaković, Tatjana and Šaponjić, Zoran",
year = "2017",
abstract = "A simple bottom-up method for the preparation of novel and very efficient photocatalytic nanocomposite system based on carbonized form of polyaniline (PANI) and colloidal TiO2 nanocrystals has been developed. The carbonized PANI/TiO2 nanocomposites were synthesized in a two-step procedure. Firstly, non-carbonized PANI/TiO2 nanocomposites were synthesized by the chemical oxidative polymerization of aniline (ANI) with ammonium peroxydisulfate, in the presence of colloidal TiO2 nanoparticles (TiO2 NPs) (d 4.5 nm). Initial [TiO2 NANI] mole ratios were 20, 50, and 80. In the second step, following the polymerization process, the carbonization of PANI/TiO2 nanocomposites was performed by thermal treatment in an inert atmosphere at 650 degrees C. The morphological and structural properties of the carbonized nanocomposites were studied using transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray powder diffraction (XRD) and Raman spectroscopy. The accomplishment of complete carbonization of PANI in PANI/TiO2 nanocomposites was confirmed by Raman spectroscopy. The appearance of anatase and rutile crystal forms in TiO2 NPs upon carbonization, with mass ratio depending on the initial molar ratio of ANI and TiO2 NPs was revealed by XRD measurements, TEM, SEM and Raman spectroscopy. The photocatalytic activities of carbonized PANI/TiO2 nanocomposites were evaluated following the photocatalytic degradation processes of Rhodamine B and Methylene blue. Carbonized PANI/TiO2 nanocomposites showed higher photocatalytic efficacy compared to bare TiO2 NPs and non-carbonized PANI/TiO2 nanocomposites. The porosity and surface structure of carbonized PANI/TiO2 nanocomposites, as well as crystalline structure of TiO2, affect photocatalytic activity of nanocomposites. (C) 2017 Elsevier B.V. All rights reserved.",
journal = "Applied Catalysis. B: Environmental",
title = "Superior photocatalytic properties of carbonized PANI/TiO2 nanocomposites",
volume = "213",
pages = "155-166",
doi = "10.1016/j.apcatb.2017.05.023"
}

Radoičić, M. B., Ćirić-Marjanović, G. N., Spasojević, V. D., Ahrenkiel, S. P., Mitrić, M., Novaković, T.,& Šaponjić, Z.. (2017). Superior photocatalytic properties of carbonized PANI/TiO2 nanocomposites. in Applied Catalysis. B: Environmental, 213, 155-166.
https://doi.org/10.1016/j.apcatb.2017.05.023

Radoičić MB, Ćirić-Marjanović GN, Spasojević VD, Ahrenkiel SP, Mitrić M, Novaković T, Šaponjić Z. Superior photocatalytic properties of carbonized PANI/TiO2 nanocomposites. in Applied Catalysis. B: Environmental. 2017;213:155-166.
doi:10.1016/j.apcatb.2017.05.023 .

Radoičić, Marija B., Ćirić-Marjanović, Gordana N., Spasojević, Vuk D., Ahrenkiel, Scott Phillip, Mitrić, Miodrag, Novaković, Tatjana, Šaponjić, Zoran, "Superior photocatalytic properties of carbonized PANI/TiO2 nanocomposites" in Applied Catalysis. B: Environmental, 213 (2017):155-166,
https://doi.org/10.1016/j.apcatb.2017.05.023 . .

TY  - JOUR
AU  - Xu, Xiao
AU  - Spasojević-de Bire, Anne
AU  - Ghermani, Nour Eddine
AU  - Wei, Yongge
AU  - Novaković, Slađana B.
AU  - Bošnjaković-Pavlović, Nada
AU  - Wu, Pingfan
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1649
AB  - A high resolution X-ray diffraction study has been carried out on [(C4H9)(4)N](2) [V6O13{(OCH2)(3)CCH2OCCH2CH3}(2)] (V6-C3) at 100 K. The V6 core possesses a negative charge, leading to a strong polarization of the anion. A nucleophilic region localized near the organic moiety and an electrophilic region in the vicinity of the V6 core provide an overall description of charge-transfer behavior.
T2  - Physical Chemistry Chemical Physics
T1  - Experimental evidence of charge transfer in a functionalized hexavanadate: a high resolution X-ray diffraction study
VL  - 19
IS  - 28
SP  - 18162
EP  - 18166
DO  - 10.1039/c7cp01840a
ER  - 

@article{
author = "Xu, Xiao and Spasojević-de Bire, Anne and Ghermani, Nour Eddine and Wei, Yongge and Novaković, Slađana B. and Bošnjaković-Pavlović, Nada and Wu, Pingfan",
year = "2017",
abstract = "A high resolution X-ray diffraction study has been carried out on [(C4H9)(4)N](2) [V6O13{(OCH2)(3)CCH2OCCH2CH3}(2)] (V6-C3) at 100 K. The V6 core possesses a negative charge, leading to a strong polarization of the anion. A nucleophilic region localized near the organic moiety and an electrophilic region in the vicinity of the V6 core provide an overall description of charge-transfer behavior.",
journal = "Physical Chemistry Chemical Physics",
title = "Experimental evidence of charge transfer in a functionalized hexavanadate: a high resolution X-ray diffraction study",
volume = "19",
number = "28",
pages = "18162-18166",
doi = "10.1039/c7cp01840a"
}

Xu, X., Spasojević-de Bire, A., Ghermani, N. E., Wei, Y., Novaković, S. B., Bošnjaković-Pavlović, N.,& Wu, P.. (2017). Experimental evidence of charge transfer in a functionalized hexavanadate: a high resolution X-ray diffraction study. in Physical Chemistry Chemical Physics, 19(28), 18162-18166.
https://doi.org/10.1039/c7cp01840a

Xu X, Spasojević-de Bire A, Ghermani NE, Wei Y, Novaković SB, Bošnjaković-Pavlović N, Wu P. Experimental evidence of charge transfer in a functionalized hexavanadate: a high resolution X-ray diffraction study. in Physical Chemistry Chemical Physics. 2017;19(28):18162-18166.
doi:10.1039/c7cp01840a .

Xu, Xiao, Spasojević-de Bire, Anne, Ghermani, Nour Eddine, Wei, Yongge, Novaković, Slađana B., Bošnjaković-Pavlović, Nada, Wu, Pingfan, "Experimental evidence of charge transfer in a functionalized hexavanadate: a high resolution X-ray diffraction study" in Physical Chemistry Chemical Physics, 19, no. 28 (2017):18162-18166,
https://doi.org/10.1039/c7cp01840a . .

TY  - JOUR
AU  - Vidoeski, Bojan
AU  - Jovanović, Svetlana P.
AU  - Holclajtner-Antunović, Ivanka D.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Budimir, Milica
AU  - Marković, Zoran M.
AU  - Todorović-Marković, Biljana
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1219
AB  - Heteropoly acids (HPAs) have found wide applications, such as in catalysis, energy conversion and storage, analytical chemistry, clinical medicine, materials science and others, but their use is limited due to their low surface area and high solubility in water. One of the possible ways to overcome these obstacles is to use height specific surface area supports for HPAs, such as carbon nanomaterials. Raman spectroscopy was applied for a studying the interaction between HPAs and highly ordered pyrolytic graphite (HOPG) as a model of a support. HOPG was exposed to two different HPAs: 12-tungsto-phosphoric acid and 12-molybodphosphoric acid, at different concentrations. It was noticed that 12-molybodphosphoric acid had stronger effects on the HOPG structure causing a weak doping and an increase of structural disorder. It was supposed that HOPG interacts with especially external oxygen atoms of 12-molybodphosphoric acid. Atomic force microscopy showed that the surface roughness of HOPG treated with 12-molybodphosphoric acid increases with increasing acid concentration, while in the case of HOPG exposed to 12-tungsto-phosphoric acid, the surface roughness concentration independent. The growth trend in the measured surface roughness (RMS) was in the agreement with the changes in the intensity ratio I-D/I-G obtained from the Raman spectra of the HOPG samples treated with 12-molybdophosphoric acid.
T2  - Journal of the Serbian Chemical Society
T1  - Raman study of the interactions between highly ordered pyrolytic graphite (HOPG) and polyoxometalates: The effects of acid concentration
VL  - 81
IS  - 7
SP  - 777
EP  - 787
DO  - 10.2298/JSC160301055V
ER  - 

@article{
author = "Vidoeski, Bojan and Jovanović, Svetlana P. and Holclajtner-Antunović, Ivanka D. and Bajuk-Bogdanović, Danica V. and Budimir, Milica and Marković, Zoran M. and Todorović-Marković, Biljana",
year = "2016",
abstract = "Heteropoly acids (HPAs) have found wide applications, such as in catalysis, energy conversion and storage, analytical chemistry, clinical medicine, materials science and others, but their use is limited due to their low surface area and high solubility in water. One of the possible ways to overcome these obstacles is to use height specific surface area supports for HPAs, such as carbon nanomaterials. Raman spectroscopy was applied for a studying the interaction between HPAs and highly ordered pyrolytic graphite (HOPG) as a model of a support. HOPG was exposed to two different HPAs: 12-tungsto-phosphoric acid and 12-molybodphosphoric acid, at different concentrations. It was noticed that 12-molybodphosphoric acid had stronger effects on the HOPG structure causing a weak doping and an increase of structural disorder. It was supposed that HOPG interacts with especially external oxygen atoms of 12-molybodphosphoric acid. Atomic force microscopy showed that the surface roughness of HOPG treated with 12-molybodphosphoric acid increases with increasing acid concentration, while in the case of HOPG exposed to 12-tungsto-phosphoric acid, the surface roughness concentration independent. The growth trend in the measured surface roughness (RMS) was in the agreement with the changes in the intensity ratio I-D/I-G obtained from the Raman spectra of the HOPG samples treated with 12-molybdophosphoric acid.",
journal = "Journal of the Serbian Chemical Society",
title = "Raman study of the interactions between highly ordered pyrolytic graphite (HOPG) and polyoxometalates: The effects of acid concentration",
volume = "81",
number = "7",
pages = "777-787",
doi = "10.2298/JSC160301055V"
}

Vidoeski, B., Jovanović, S. P., Holclajtner-Antunović, I. D., Bajuk-Bogdanović, D. V., Budimir, M., Marković, Z. M.,& Todorović-Marković, B.. (2016). Raman study of the interactions between highly ordered pyrolytic graphite (HOPG) and polyoxometalates: The effects of acid concentration. in Journal of the Serbian Chemical Society, 81(7), 777-787.
https://doi.org/10.2298/JSC160301055V

Vidoeski B, Jovanović SP, Holclajtner-Antunović ID, Bajuk-Bogdanović DV, Budimir M, Marković ZM, Todorović-Marković B. Raman study of the interactions between highly ordered pyrolytic graphite (HOPG) and polyoxometalates: The effects of acid concentration. in Journal of the Serbian Chemical Society. 2016;81(7):777-787.
doi:10.2298/JSC160301055V .

Vidoeski, Bojan, Jovanović, Svetlana P., Holclajtner-Antunović, Ivanka D., Bajuk-Bogdanović, Danica V., Budimir, Milica, Marković, Zoran M., Todorović-Marković, Biljana, "Raman study of the interactions between highly ordered pyrolytic graphite (HOPG) and polyoxometalates: The effects of acid concentration" in Journal of the Serbian Chemical Society, 81, no. 7 (2016):777-787,
https://doi.org/10.2298/JSC160301055V . .

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

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

Vujković, M., Vidoeski, B., Jovanović, S. P., Bajuk-Bogdanović, D. V., Budimir, M., Marković, Z. M., Pavlović, V. B., Todorović-Marković, B.,& Holclajtner-Antunović, I. D.. (2016). Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices. in Electrochimica Acta, 217, 34-46.
https://doi.org/10.1016/j.electacta.2016.09.067

Vujković M, Vidoeski B, Jovanović SP, Bajuk-Bogdanović DV, Budimir M, Marković ZM, Pavlović VB, Todorović-Marković B, Holclajtner-Antunović ID. Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices. in Electrochimica Acta. 2016;217:34-46.
doi:10.1016/j.electacta.2016.09.067 .

Vujković, Milica, Vidoeski, Bojan, Jovanović, Svetlana P., Bajuk-Bogdanović, Danica V., Budimir, Milica, Marković, Zoran M., Pavlović, Vladimir B., Todorović-Marković, Biljana, Holclajtner-Antunović, Ivanka D., "Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices" in Electrochimica Acta, 217 (2016):34-46,
https://doi.org/10.1016/j.electacta.2016.09.067 . .

TY  - JOUR
AU  - Xu, Xiao
AU  - Bošnjaković-Pavlović, Nada
AU  - Čolović, Mirjana B.
AU  - Krstić, Danijela Z.
AU  - Vasić, Vesna M.
AU  - Gillet, Jean-Michel
AU  - Wu, Pingfan
AU  - Wei, Yongge
AU  - Spasojević-de Bire, Anne
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1158
AB  - In vitro influence of five synthesized functionalized hexavanadates (V-6) on commercial porcine cerebral cortex Na+/K+-ATPase activity has been studied. Dose dependent Na+/K+-ATPase inhibition was obtained for all investigated compounds. Calculated half maximal inhibitory concentration IC50 values, in mol/L, for Na+/K+-ATPase were 7.6 x 10(-5), 1.8 x 10(-5), 2.9 x 10(-5), 5.5 x 10(-5) for functionalized hexavanadates (V-6) with tetrabutylammonium (TBA) [V-6-CH3][TBA](2), [V-6-NO2][TBA](2), [V-6-OH][TBA](2) and [V-6-C-3][TBA](2) respectively. [V-6-OH][Na](2) inhibited Na+/K+-ATPase activity up to 30% at maximal investigated concentration 1 x 10(-3) mol/L. This reactivity has been interpreted using a study of the non-covalent interactions of functionalized hexavanadate hybrids through Cambridge Structural Database (CSD) analysis. Bibliographic searching has led to 18 different structures and 99 contacts. We have observed that C-H center dot center dot center dot O contacts consolidate the structures. We have also performed density functional theory (DFT) calculations and have determined electrostatic potential values at the molecular surface on a series of functionalized V-6. These results enlightened their chemical reactivity and their potential biological applications such as the inhibition of the ATPase. (C) 2016 Elsevier Inc. All rights reserved.
T2  - Journal of Inorganic Biochemistry
T1  - A combined crystallographic analysis and ab initio calculations to interpret the reactivity of functionalized hexavanadates and their inhibitor potency toward Na+/K+-ATPase
VL  - 161
SP  - 27
EP  - 36
DO  - 10.1016/j.jinorgbio.2016.04.029
ER  - 

@article{
author = "Xu, Xiao and Bošnjaković-Pavlović, Nada and Čolović, Mirjana B. and Krstić, Danijela Z. and Vasić, Vesna M. and Gillet, Jean-Michel and Wu, Pingfan and Wei, Yongge and Spasojević-de Bire, Anne",
year = "2016",
abstract = "In vitro influence of five synthesized functionalized hexavanadates (V-6) on commercial porcine cerebral cortex Na+/K+-ATPase activity has been studied. Dose dependent Na+/K+-ATPase inhibition was obtained for all investigated compounds. Calculated half maximal inhibitory concentration IC50 values, in mol/L, for Na+/K+-ATPase were 7.6 x 10(-5), 1.8 x 10(-5), 2.9 x 10(-5), 5.5 x 10(-5) for functionalized hexavanadates (V-6) with tetrabutylammonium (TBA) [V-6-CH3][TBA](2), [V-6-NO2][TBA](2), [V-6-OH][TBA](2) and [V-6-C-3][TBA](2) respectively. [V-6-OH][Na](2) inhibited Na+/K+-ATPase activity up to 30% at maximal investigated concentration 1 x 10(-3) mol/L. This reactivity has been interpreted using a study of the non-covalent interactions of functionalized hexavanadate hybrids through Cambridge Structural Database (CSD) analysis. Bibliographic searching has led to 18 different structures and 99 contacts. We have observed that C-H center dot center dot center dot O contacts consolidate the structures. We have also performed density functional theory (DFT) calculations and have determined electrostatic potential values at the molecular surface on a series of functionalized V-6. These results enlightened their chemical reactivity and their potential biological applications such as the inhibition of the ATPase. (C) 2016 Elsevier Inc. All rights reserved.",
journal = "Journal of Inorganic Biochemistry",
title = "A combined crystallographic analysis and ab initio calculations to interpret the reactivity of functionalized hexavanadates and their inhibitor potency toward Na+/K+-ATPase",
volume = "161",
pages = "27-36",
doi = "10.1016/j.jinorgbio.2016.04.029"
}

Xu, X., Bošnjaković-Pavlović, N., Čolović, M. B., Krstić, D. Z., Vasić, V. M., Gillet, J., Wu, P., Wei, Y.,& Spasojević-de Bire, A.. (2016). A combined crystallographic analysis and ab initio calculations to interpret the reactivity of functionalized hexavanadates and their inhibitor potency toward Na+/K+-ATPase. in Journal of Inorganic Biochemistry, 161, 27-36.
https://doi.org/10.1016/j.jinorgbio.2016.04.029

Xu X, Bošnjaković-Pavlović N, Čolović MB, Krstić DZ, Vasić VM, Gillet J, Wu P, Wei Y, Spasojević-de Bire A. A combined crystallographic analysis and ab initio calculations to interpret the reactivity of functionalized hexavanadates and their inhibitor potency toward Na+/K+-ATPase. in Journal of Inorganic Biochemistry. 2016;161:27-36.
doi:10.1016/j.jinorgbio.2016.04.029 .

Xu, Xiao, Bošnjaković-Pavlović, Nada, Čolović, Mirjana B., Krstić, Danijela Z., Vasić, Vesna M., Gillet, Jean-Michel, Wu, Pingfan, Wei, Yongge, Spasojević-de Bire, Anne, "A combined crystallographic analysis and ab initio calculations to interpret the reactivity of functionalized hexavanadates and their inhibitor potency toward Na+/K+-ATPase" in Journal of Inorganic Biochemistry, 161 (2016):27-36,
https://doi.org/10.1016/j.jinorgbio.2016.04.029 . .

TY  - CONF
AU  - Bogdanović, Una
AU  - Vodnik, Vesna
AU  - Pašti, Igor A.
AU  - Ćirić-Marjanović, Gordana N.
AU  - Mitrić, Miodrag
AU  - Ahrenkiel, Scott Phillip
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9178
AB  - Gold‒polyaniline (AuPANI) nanocomposite, with granular morphology  of PANI and rod‒like Au nanoparticles (NPs) as dominate structure distributed in  it,  was  prepared  by  interfacial  polymerization  method  in  an  immiscible water/toluene     biphasic     system.     Simultaneously     with     the     aniline polymerization to polyaniline (PANI) by HAuCl4, as an oxidant, AuNPs are formed. AuPANI composite as green precipitate is collected from aqueous phase.  Polyaniline  in  the  composite  is  in  the  conductive  emeraldine  salt form  (PANIES),  with  high  amount  of  Au  (28.85  wt  %).  Nanocomposite showed   great   electrocatalytic   activity   towards   the   electrochemical   O2reduction   reaction   (ORR),   with   high   ORR   onset   potential   and   high selectivity  for  O2reduction  to  water.  This  makes  it  a  good  candidate  for  a new class of Pt‒free ORR catalyst.
PB  - Society of Physical Chemists of Serbia
C3  - Physical chemistry 2016 : 13th international conference on fundamental and applied aspects of physical chemistry
T1  - Electrocatalityc application of gold-polyaniline nanocomposite
SP  - 391
EP  - 394
UR  - https://hdl.handle.net/21.15107/rcub_vinar_9178
ER  - 

@conference{
author = "Bogdanović, Una and Vodnik, Vesna and Pašti, Igor A. and Ćirić-Marjanović, Gordana N. and Mitrić, Miodrag and Ahrenkiel, Scott Phillip",
year = "2016",
abstract = "Gold‒polyaniline (AuPANI) nanocomposite, with granular morphology  of PANI and rod‒like Au nanoparticles (NPs) as dominate structure distributed in  it,  was  prepared  by  interfacial  polymerization  method  in  an  immiscible water/toluene     biphasic     system.     Simultaneously     with     the     aniline polymerization to polyaniline (PANI) by HAuCl4, as an oxidant, AuNPs are formed. AuPANI composite as green precipitate is collected from aqueous phase.  Polyaniline  in  the  composite  is  in  the  conductive  emeraldine  salt form  (PANIES),  with  high  amount  of  Au  (28.85  wt  %).  Nanocomposite showed   great   electrocatalytic   activity   towards   the   electrochemical   O2reduction   reaction   (ORR),   with   high   ORR   onset   potential   and   high selectivity  for  O2reduction  to  water.  This  makes  it  a  good  candidate  for  a new class of Pt‒free ORR catalyst.",
publisher = "Society of Physical Chemists of Serbia",
journal = "Physical chemistry 2016 : 13th international conference on fundamental and applied aspects of physical chemistry",
title = "Electrocatalityc application of gold-polyaniline nanocomposite",
pages = "391-394",
url = "https://hdl.handle.net/21.15107/rcub_vinar_9178"
}

Bogdanović, U., Vodnik, V., Pašti, I. A., Ćirić-Marjanović, G. N., Mitrić, M.,& Ahrenkiel, S. P.. (2016). Electrocatalityc application of gold-polyaniline nanocomposite. in Physical chemistry 2016 : 13th international conference on fundamental and applied aspects of physical chemistry
Society of Physical Chemists of Serbia., 391-394.
https://hdl.handle.net/21.15107/rcub_vinar_9178

Bogdanović U, Vodnik V, Pašti IA, Ćirić-Marjanović GN, Mitrić M, Ahrenkiel SP. Electrocatalityc application of gold-polyaniline nanocomposite. in Physical chemistry 2016 : 13th international conference on fundamental and applied aspects of physical chemistry. 2016;:391-394.
https://hdl.handle.net/21.15107/rcub_vinar_9178 .

Bogdanović, Una, Vodnik, Vesna, Pašti, Igor A., Ćirić-Marjanović, Gordana N., Mitrić, Miodrag, Ahrenkiel, Scott Phillip, "Electrocatalityc application of gold-polyaniline nanocomposite" in Physical chemistry 2016 : 13th international conference on fundamental and applied aspects of physical chemistry (2016):391-394,
https://hdl.handle.net/21.15107/rcub_vinar_9178 .

TY  - JOUR
AU  - Ležaić Janošević, Aleksandra 
AU  - Bajuk-Bogdanović, Danica V.
AU  - Radoičić, Marija B.
AU  - Mirsky, Vladimir M.
AU  - Ćirić-Marjanović, Gordana N.
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1027
AB  - Nanofibrous polyanilines (PANIs) were synthesized by several oxidative polymerization pathways that have in common the presence of excess oxidant(s) (ammonium peroxydisulfate and its mixture with hydrogen peroxide), the absence of added acid, and the absence of external template (self-assembly process). Conducting forms of the synthesized PANI nanofibers (re)doped with various acids were further used as precursors for carbonization process to obtain nanofibrous carbonaceous materials (Carb-PANIs). Morphology, molecular structure, surface properties and electrical characteristics of PANI nanofibrous precursors and their carbonized counterparts were studied by scanning electron microscopy, Raman spectroscopy, by measurements of zeta-potential and determination of isoelectric points, as well as by measurements of electrical conductivity. (C) 2016 Elsevier B.V. All rights reserved.
PB  - Elsevier
T2  - Synthetic Metals
T1  - Influence of synthetic conditions on the structure and electrical properties of nanofibrous polyanilines and their nanofibrous carbonized forms
VL  - 214
SP  - 35
EP  - 44
DO  - 10.1016/j.synthmet.2016.01.015
ER  - 

@article{
author = "Ležaić Janošević, Aleksandra  and Bajuk-Bogdanović, Danica V. and Radoičić, Marija B. and Mirsky, Vladimir M. and Ćirić-Marjanović, Gordana N.",
year = "2016",
abstract = "Nanofibrous polyanilines (PANIs) were synthesized by several oxidative polymerization pathways that have in common the presence of excess oxidant(s) (ammonium peroxydisulfate and its mixture with hydrogen peroxide), the absence of added acid, and the absence of external template (self-assembly process). Conducting forms of the synthesized PANI nanofibers (re)doped with various acids were further used as precursors for carbonization process to obtain nanofibrous carbonaceous materials (Carb-PANIs). Morphology, molecular structure, surface properties and electrical characteristics of PANI nanofibrous precursors and their carbonized counterparts were studied by scanning electron microscopy, Raman spectroscopy, by measurements of zeta-potential and determination of isoelectric points, as well as by measurements of electrical conductivity. (C) 2016 Elsevier B.V. All rights reserved.",
publisher = "Elsevier",
journal = "Synthetic Metals",
title = "Influence of synthetic conditions on the structure and electrical properties of nanofibrous polyanilines and their nanofibrous carbonized forms",
volume = "214",
pages = "35-44",
doi = "10.1016/j.synthmet.2016.01.015"
}

Ležaić Janošević, A., Bajuk-Bogdanović, D. V., Radoičić, M. B., Mirsky, V. M.,& Ćirić-Marjanović, G. N.. (2016). Influence of synthetic conditions on the structure and electrical properties of nanofibrous polyanilines and their nanofibrous carbonized forms. in Synthetic Metals
Elsevier., 214, 35-44.
https://doi.org/10.1016/j.synthmet.2016.01.015

Ležaić Janošević A, Bajuk-Bogdanović DV, Radoičić MB, Mirsky VM, Ćirić-Marjanović GN. Influence of synthetic conditions on the structure and electrical properties of nanofibrous polyanilines and their nanofibrous carbonized forms. in Synthetic Metals. 2016;214:35-44.
doi:10.1016/j.synthmet.2016.01.015 .

Ležaić Janošević, Aleksandra , Bajuk-Bogdanović, Danica V., Radoičić, Marija B., Mirsky, Vladimir M., Ćirić-Marjanović, Gordana N., "Influence of synthetic conditions on the structure and electrical properties of nanofibrous polyanilines and their nanofibrous carbonized forms" in Synthetic Metals, 214 (2016):35-44,
https://doi.org/10.1016/j.synthmet.2016.01.015 . .

TY  - JOUR
AU  - Jovic, Aleksandar
AU  - Đorđević, Aleksandar R.
AU  - Čebela, Maria
AU  - Stojković-Simatović, Ivana
AU  - Hercigonja, Radmila V.
AU  - Šljukić, Biljana
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1263
AB  - Electrodes based on composites of zeolites with carbonized polyaniline prepared in the presence of 5-sulfosalicylic acid are evaluated for both qualitative and quantitative determination of phenols in aqueous solutions. Zeolites used included NaX and NaY, as well as their transition metal (Mn and Cu) cation-exchanged forms, and they were all characterized usingXRPD, FTIR and SEM. Cyclic voltammetry was used to study composites electrochemical response in the presence of p-nitrophenol, phenol and 5-aminophenol in acidic, neutral and al- kaline media. Linear dependence of current on p-nitrophenol concentration in acidic media was obtained in 0.11 mM concentration range. The comparative evaluation of the electrochemical response of NaX/carbonized polyaniline composite and its individual components revealed significantly lower limit of detection obtained using composite electrode (1.27 mu M) compared to that obtained using pure zeolite (135 mu M) or pure carbonized polyaniline (94.5 mu M) electrode. Composite electrode gave response to p-nitrophenol presence in neutral media as well, but it quickly disappeared with continuous scanning, while no clear response could be seen in highly alkaline media. Thus, this work demonstrates benefits of using novel composite based on zeolites and carbonized polyaniline for sensing of phenols in acidic aqueous solutions. (C) 2016 Elsevier B.V. All rights reserved.
T2  - Journal of Electroanalytical Chemistry
T1  - Composite zeolite/carbonized polyaniline electrodes for p-nitrophenol sensing
VL  - 778
SP  - 137
EP  - 147
DO  - 10.1016/j.jelechem.2016.08.025
ER  - 

@article{
author = "Jovic, Aleksandar and Đorđević, Aleksandar R. and Čebela, Maria and Stojković-Simatović, Ivana and Hercigonja, Radmila V. and Šljukić, Biljana",
year = "2016",
abstract = "Electrodes based on composites of zeolites with carbonized polyaniline prepared in the presence of 5-sulfosalicylic acid are evaluated for both qualitative and quantitative determination of phenols in aqueous solutions. Zeolites used included NaX and NaY, as well as their transition metal (Mn and Cu) cation-exchanged forms, and they were all characterized usingXRPD, FTIR and SEM. Cyclic voltammetry was used to study composites electrochemical response in the presence of p-nitrophenol, phenol and 5-aminophenol in acidic, neutral and al- kaline media. Linear dependence of current on p-nitrophenol concentration in acidic media was obtained in 0.11 mM concentration range. The comparative evaluation of the electrochemical response of NaX/carbonized polyaniline composite and its individual components revealed significantly lower limit of detection obtained using composite electrode (1.27 mu M) compared to that obtained using pure zeolite (135 mu M) or pure carbonized polyaniline (94.5 mu M) electrode. Composite electrode gave response to p-nitrophenol presence in neutral media as well, but it quickly disappeared with continuous scanning, while no clear response could be seen in highly alkaline media. Thus, this work demonstrates benefits of using novel composite based on zeolites and carbonized polyaniline for sensing of phenols in acidic aqueous solutions. (C) 2016 Elsevier B.V. All rights reserved.",
journal = "Journal of Electroanalytical Chemistry",
title = "Composite zeolite/carbonized polyaniline electrodes for p-nitrophenol sensing",
volume = "778",
pages = "137-147",
doi = "10.1016/j.jelechem.2016.08.025"
}

Jovic, A., Đorđević, A. R., Čebela, M., Stojković-Simatović, I., Hercigonja, R. V.,& Šljukić, B.. (2016). Composite zeolite/carbonized polyaniline electrodes for p-nitrophenol sensing. in Journal of Electroanalytical Chemistry, 778, 137-147.
https://doi.org/10.1016/j.jelechem.2016.08.025

Jovic A, Đorđević AR, Čebela M, Stojković-Simatović I, Hercigonja RV, Šljukić B. Composite zeolite/carbonized polyaniline electrodes for p-nitrophenol sensing. in Journal of Electroanalytical Chemistry. 2016;778:137-147.
doi:10.1016/j.jelechem.2016.08.025 .

Jovic, Aleksandar, Đorđević, Aleksandar R., Čebela, Maria, Stojković-Simatović, Ivana, Hercigonja, Radmila V., Šljukić, Biljana, "Composite zeolite/carbonized polyaniline electrodes for p-nitrophenol sensing" in Journal of Electroanalytical Chemistry, 778 (2016):137-147,
https://doi.org/10.1016/j.jelechem.2016.08.025 . .

TY  - JOUR
AU  - Bogdanović, Una
AU  - Pašti, Igor A.
AU  - Ćirić-Marjanović, Gordana N.
AU  - Mitrić, Miodrag
AU  - Ahrenkiel, Scott Phillip
AU  - Vodnik, Vesna
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/922
AB  - Gold-polyaniline (Au-PANI) nanocomposite was prepared using a simple interfacial polymerization method, performed in an immiscible water/toluene biphasic system using tetrachloroaurate, AuCl4- as an oxidant. The formation of Au+ nanoparticles (AuNPs) or Au-PANI nanocomposite can be controlled to a certain degree by varying the ratio of initial Au+ and aniline concentrations. Under optimal condition (HAuCl4/aniline ratio is 1:2), green dispersion of Au-PANI nanocomposite is produced in aqueous phase, whose morphology, structure and physicochemical properties are investigated in details. The nanocomposite shows granular morphology with mostly rodlike AuNPs embedded in polymer. It was found that polyaniline in the composite is in the conducting emeraldine salt form, containing high amount of Au (28.85 wt %). Furthermore, the electrical conductivity of the nanocomposite was found to be four-fold higher than that of the polymer itself. In addition, the nanocomposite powder, isolated from the as-prepared aqueous dispersion, can later be easily redispersed in water and further used for various applications. Moreover, the obtained Au-PANI nanocomposite showed excellent electrocatalytic performance toward the electrochemical oxygen reduction reaction (ORR), with high ORR onset potential and good selectivity. This makes it a promising candidate for a new class of Pt-free ORR. catalyst.
T2  - ACS Applied Materials and Interfaces
T1  - Interfacial Synthesis of Gold-Polyaniline Nanocomposite and Its Electrocatalytic Application
VL  - 7
IS  - 51
SP  - 28393
EP  - 28403
DO  - 10.1021/acsami.5b09145
ER  - 

@article{
author = "Bogdanović, Una and Pašti, Igor A. and Ćirić-Marjanović, Gordana N. and Mitrić, Miodrag and Ahrenkiel, Scott Phillip and Vodnik, Vesna",
year = "2015",
abstract = "Gold-polyaniline (Au-PANI) nanocomposite was prepared using a simple interfacial polymerization method, performed in an immiscible water/toluene biphasic system using tetrachloroaurate, AuCl4- as an oxidant. The formation of Au+ nanoparticles (AuNPs) or Au-PANI nanocomposite can be controlled to a certain degree by varying the ratio of initial Au+ and aniline concentrations. Under optimal condition (HAuCl4/aniline ratio is 1:2), green dispersion of Au-PANI nanocomposite is produced in aqueous phase, whose morphology, structure and physicochemical properties are investigated in details. The nanocomposite shows granular morphology with mostly rodlike AuNPs embedded in polymer. It was found that polyaniline in the composite is in the conducting emeraldine salt form, containing high amount of Au (28.85 wt %). Furthermore, the electrical conductivity of the nanocomposite was found to be four-fold higher than that of the polymer itself. In addition, the nanocomposite powder, isolated from the as-prepared aqueous dispersion, can later be easily redispersed in water and further used for various applications. Moreover, the obtained Au-PANI nanocomposite showed excellent electrocatalytic performance toward the electrochemical oxygen reduction reaction (ORR), with high ORR onset potential and good selectivity. This makes it a promising candidate for a new class of Pt-free ORR. catalyst.",
journal = "ACS Applied Materials and Interfaces",
title = "Interfacial Synthesis of Gold-Polyaniline Nanocomposite and Its Electrocatalytic Application",
volume = "7",
number = "51",
pages = "28393-28403",
doi = "10.1021/acsami.5b09145"
}

Bogdanović, U., Pašti, I. A., Ćirić-Marjanović, G. N., Mitrić, M., Ahrenkiel, S. P.,& Vodnik, V.. (2015). Interfacial Synthesis of Gold-Polyaniline Nanocomposite and Its Electrocatalytic Application. in ACS Applied Materials and Interfaces, 7(51), 28393-28403.
https://doi.org/10.1021/acsami.5b09145

Bogdanović U, Pašti IA, Ćirić-Marjanović GN, Mitrić M, Ahrenkiel SP, Vodnik V. Interfacial Synthesis of Gold-Polyaniline Nanocomposite and Its Electrocatalytic Application. in ACS Applied Materials and Interfaces. 2015;7(51):28393-28403.
doi:10.1021/acsami.5b09145 .

Bogdanović, Una, Pašti, Igor A., Ćirić-Marjanović, Gordana N., Mitrić, Miodrag, Ahrenkiel, Scott Phillip, Vodnik, Vesna, "Interfacial Synthesis of Gold-Polyaniline Nanocomposite and Its Electrocatalytic Application" in ACS Applied Materials and Interfaces, 7, no. 51 (2015):28393-28403,
https://doi.org/10.1021/acsami.5b09145 . .

TY  - JOUR
AU  - Jovanović, Dragana J.
AU  - Dugandžić, Ivan
AU  - Ćirić-Marjanović, Gordana N.
AU  - Radetić, Tamara
AU  - Ahrenkiel, Scott Phillip
AU  - Milošević, Olivera
AU  - Nedeljković, Jovan
AU  - Šaponjić, Zoran
AU  - Mančić, Lidija
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/771
AB  - We report on the possibility to build hierarchically organized three-dimensional (3D) titania spherical particles having high surface-to-volume-ratio, by aerosol processing of nanotubular building blocks. Morphology and crystal structure of titania based spherical assemblies, obtained in the temperature range from 150 to 650 degrees C, were characterized by means of scanning and transmission electron microscopy, x-ray powder diffraction and Raman spectroscopy. Initial shape of 1D building units, nanotubes, was well preserved in the spherical assemblies processed at 150 and 450 degrees C. Processing at 650 degrees C resulted in a collapse of the nanotubular building blocks and formation of the assemblies of irregularly shaped TiO2 nanoparticles. Structural analysis revealed several phase transitions in titania spherical assemblies in course with the temperature increase indicating possibility of in-situ phase composition adjustment during aerosol processing. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
T2  - Ceramics International
T1  - Spherical assemblies of titania nanotubes generated through aerosol processing
VL  - 41
IS  - 10
SP  - 14754
EP  - 14759
DO  - 10.1016/j.ceramint.2015.07.205
ER  - 

@article{
author = "Jovanović, Dragana J. and Dugandžić, Ivan and Ćirić-Marjanović, Gordana N. and Radetić, Tamara and Ahrenkiel, Scott Phillip and Milošević, Olivera and Nedeljković, Jovan and Šaponjić, Zoran and Mančić, Lidija",
year = "2015",
abstract = "We report on the possibility to build hierarchically organized three-dimensional (3D) titania spherical particles having high surface-to-volume-ratio, by aerosol processing of nanotubular building blocks. Morphology and crystal structure of titania based spherical assemblies, obtained in the temperature range from 150 to 650 degrees C, were characterized by means of scanning and transmission electron microscopy, x-ray powder diffraction and Raman spectroscopy. Initial shape of 1D building units, nanotubes, was well preserved in the spherical assemblies processed at 150 and 450 degrees C. Processing at 650 degrees C resulted in a collapse of the nanotubular building blocks and formation of the assemblies of irregularly shaped TiO2 nanoparticles. Structural analysis revealed several phase transitions in titania spherical assemblies in course with the temperature increase indicating possibility of in-situ phase composition adjustment during aerosol processing. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.",
journal = "Ceramics International",
title = "Spherical assemblies of titania nanotubes generated through aerosol processing",
volume = "41",
number = "10",
pages = "14754-14759",
doi = "10.1016/j.ceramint.2015.07.205"
}

Jovanović, D. J., Dugandžić, I., Ćirić-Marjanović, G. N., Radetić, T., Ahrenkiel, S. P., Milošević, O., Nedeljković, J., Šaponjić, Z.,& Mančić, L.. (2015). Spherical assemblies of titania nanotubes generated through aerosol processing. in Ceramics International, 41(10), 14754-14759.
https://doi.org/10.1016/j.ceramint.2015.07.205

Jovanović DJ, Dugandžić I, Ćirić-Marjanović GN, Radetić T, Ahrenkiel SP, Milošević O, Nedeljković J, Šaponjić Z, Mančić L. Spherical assemblies of titania nanotubes generated through aerosol processing. in Ceramics International. 2015;41(10):14754-14759.
doi:10.1016/j.ceramint.2015.07.205 .

Jovanović, Dragana J., Dugandžić, Ivan, Ćirić-Marjanović, Gordana N., Radetić, Tamara, Ahrenkiel, Scott Phillip, Milošević, Olivera, Nedeljković, Jovan, Šaponjić, Zoran, Mančić, Lidija, "Spherical assemblies of titania nanotubes generated through aerosol processing" in Ceramics International, 41, no. 10 (2015):14754-14759,
https://doi.org/10.1016/j.ceramint.2015.07.205 . .