Dekanski, Aleksandar B.

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orcid::0000-0003-3122-8342
  • Dekanski, Aleksandar B. (17)
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Author's Bibliography

The effect of the addition of colloidal iridium oxide into sol-gel obtained titanium and ruthenium oxide coatings on titanium on their electrochemical properties

Panić, Vladimir V.; Dekanski, Aleksandar B.; Mitrić, Miodrag; Milonjić, Slobodan K.; Mišković-Stanković, Vesna B.; Nikolić, Branislav Ž.

(2010)

TY  - JOUR
AU  - Panić, Vladimir V.
AU  - Dekanski, Aleksandar B.
AU  - Mitrić, Miodrag
AU  - Milonjić, Slobodan K.
AU  - Mišković-Stanković, Vesna B.
AU  - Nikolić, Branislav Ž.
PY  - 2010
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4030
AB  - Electrochemical properties of sol-gel processed Ti(0.6)Ir(0.4)O(2) and Ti(0.6)Ru(0.3)Ir(0.1)O(2) coatings on titanium substrate were investigated using cyclic voltammetry, polarization measurements and electrochemical impedance spectroscopy and compared to the properties of Ti(0.6)Ru(0.4)O(2) coating. The role of iridium oxide in the improvement of the electrocatalytic, capacitive and stability properties of titanium anodes activated by a RuO(2)-TiO(2) coating is discussed. The oxide sols were prepared by forced hydrolysis of the metal chlorides. The characterization by dynamic light scattering and X-ray diffraction showed that polydisperse oxide sols were obtained with the particles tending to form agglomerates. The presence of IrO(2) causes a suppression of the X-ray diffraction peaks of TiO(2) and RuO(2) in the sol-gel prepared Ti(0.6)Ir(0.4)O(2) and Ti(0.6)Ru(0.3)Ir(0.1)O(2) coatings. The IrO(2)-containing coatings had an enhanced charge storage ability and activity for the oxygen evolution reaction (OER) in comparison to Ti(0.6)Ru(0.4)O(2) coating. The voltammogram of the Ti(0.6)Ir(0.4)O(2)/Ti electrode showed well-resolved peaks related to Ir redox transitions, which are responsible for the enhanced charge storage ability of IrO(2)-containing coatings. Redox transitions of Ir were also registered in the high-frequency domain of the ac impedance spectra of the coatings as a semicircle with characteristics insensitive to the electrolyte composition and to the electrode potential prior to OER. However, the semicircle characteristics were different for the two IrO(2)-containing coatings, as well as at potentials outside the OER in comparison to those at which the OER occurs.
T2  - Physical Chemistry Chemical Physics
T1  - The effect of the addition of colloidal iridium oxide into sol-gel obtained titanium and ruthenium oxide coatings on titanium on their electrochemical properties
VL  - 12
IS  - 27
SP  - 7521
EP  - 7528
DO  - 10.1039/b921582d
ER  - 
@article{
author = "Panić, Vladimir V. and Dekanski, Aleksandar B. and Mitrić, Miodrag and Milonjić, Slobodan K. and Mišković-Stanković, Vesna B. and Nikolić, Branislav Ž.",
year = "2010",
abstract = "Electrochemical properties of sol-gel processed Ti(0.6)Ir(0.4)O(2) and Ti(0.6)Ru(0.3)Ir(0.1)O(2) coatings on titanium substrate were investigated using cyclic voltammetry, polarization measurements and electrochemical impedance spectroscopy and compared to the properties of Ti(0.6)Ru(0.4)O(2) coating. The role of iridium oxide in the improvement of the electrocatalytic, capacitive and stability properties of titanium anodes activated by a RuO(2)-TiO(2) coating is discussed. The oxide sols were prepared by forced hydrolysis of the metal chlorides. The characterization by dynamic light scattering and X-ray diffraction showed that polydisperse oxide sols were obtained with the particles tending to form agglomerates. The presence of IrO(2) causes a suppression of the X-ray diffraction peaks of TiO(2) and RuO(2) in the sol-gel prepared Ti(0.6)Ir(0.4)O(2) and Ti(0.6)Ru(0.3)Ir(0.1)O(2) coatings. The IrO(2)-containing coatings had an enhanced charge storage ability and activity for the oxygen evolution reaction (OER) in comparison to Ti(0.6)Ru(0.4)O(2) coating. The voltammogram of the Ti(0.6)Ir(0.4)O(2)/Ti electrode showed well-resolved peaks related to Ir redox transitions, which are responsible for the enhanced charge storage ability of IrO(2)-containing coatings. Redox transitions of Ir were also registered in the high-frequency domain of the ac impedance spectra of the coatings as a semicircle with characteristics insensitive to the electrolyte composition and to the electrode potential prior to OER. However, the semicircle characteristics were different for the two IrO(2)-containing coatings, as well as at potentials outside the OER in comparison to those at which the OER occurs.",
journal = "Physical Chemistry Chemical Physics",
title = "The effect of the addition of colloidal iridium oxide into sol-gel obtained titanium and ruthenium oxide coatings on titanium on their electrochemical properties",
volume = "12",
number = "27",
pages = "7521-7528",
doi = "10.1039/b921582d"
}
Panić, V. V., Dekanski, A. B., Mitrić, M., Milonjić, S. K., Mišković-Stanković, V. B.,& Nikolić, B. Ž.. (2010). The effect of the addition of colloidal iridium oxide into sol-gel obtained titanium and ruthenium oxide coatings on titanium on their electrochemical properties. in Physical Chemistry Chemical Physics, 12(27), 7521-7528.
https://doi.org/10.1039/b921582d
Panić VV, Dekanski AB, Mitrić M, Milonjić SK, Mišković-Stanković VB, Nikolić BŽ. The effect of the addition of colloidal iridium oxide into sol-gel obtained titanium and ruthenium oxide coatings on titanium on their electrochemical properties. in Physical Chemistry Chemical Physics. 2010;12(27):7521-7528.
doi:10.1039/b921582d .
Panić, Vladimir V., Dekanski, Aleksandar B., Mitrić, Miodrag, Milonjić, Slobodan K., Mišković-Stanković, Vesna B., Nikolić, Branislav Ž., "The effect of the addition of colloidal iridium oxide into sol-gel obtained titanium and ruthenium oxide coatings on titanium on their electrochemical properties" in Physical Chemistry Chemical Physics, 12, no. 27 (2010):7521-7528,
https://doi.org/10.1039/b921582d . .
17
17
19

Differences in the electrochemical behavior of ruthenium and iridium oxide in electrocatalytic coatings of activated titanium anodes prepared by the sol-gel procedure

Panić, Vladimir V.; Dekanski, Aleksandar B.; Mišković-Stanković, Vesna B.; Milonjić, Slobodan K.; Nikolić, Branislav Ž.

(2010)

TY  - JOUR
AU  - Panić, Vladimir V.
AU  - Dekanski, Aleksandar B.
AU  - Mišković-Stanković, Vesna B.
AU  - Milonjić, Slobodan K.
AU  - Nikolić, Branislav Ž.
PY  - 2010
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4138
AB  - The electrochemical characteristics of Ti(0.6)Ir(0.4)O(2)/Ti and Ti(0.6)Ru(0.4)O(2)/Ti anodes prepared by the sol gel procedure from the corresponding oxide sols, obtained by force hydrolysis of the corresponding metal chlorides, were compared. The voltammetric properties in H(2)SO(4) solution indicate that Ti(0.6)Ir(0.4)O(2)/Ti has more pronounced pseudocapacitive characteristics, caused by proton-assisted, solid state surface redox transitions of the oxide. At potentials negative to 0.0 V(SCE), this electrode is of poor conductivity and activity, while the voltammetric behavior of the Ti(0.6)Ru(0.4)O(2)/Ti electrode is governed by proton injection/ejection into the oxide structure. The Ti(0.6)Ir(0.4)O(2)/Ti electrode had a higher electrocatalytical activity for oxygen evolution, while the investigated anodes were of similar activity for chlorine evolution. The potential dependence of the impedance characteristics showed that the Ti(0.6)Ru(0.4)O(2)/Ti electrode behaved like a capacitor over a wider potential range than the Ti(0.6)Ir(0.4)O(2)/Ti electrode, with fully-developed pseudocapacitive properties at. potentials positive to 0.60 V(SCE). However, the impedance characteristics of the Ti(0.6)Ir(0.4)O(2)/Ti electrode changed with increasing potential from resistor-like to capacitor-like behavior.
T2  - Journal of the Serbian Chemical Society
T1  - Differences in the electrochemical behavior of ruthenium and iridium oxide in electrocatalytic coatings of activated titanium anodes prepared by the sol-gel procedure
VL  - 75
IS  - 10
SP  - 1413
EP  - 1420
DO  - 10.2298/JSC100310078P
ER  - 
@article{
author = "Panić, Vladimir V. and Dekanski, Aleksandar B. and Mišković-Stanković, Vesna B. and Milonjić, Slobodan K. and Nikolić, Branislav Ž.",
year = "2010",
abstract = "The electrochemical characteristics of Ti(0.6)Ir(0.4)O(2)/Ti and Ti(0.6)Ru(0.4)O(2)/Ti anodes prepared by the sol gel procedure from the corresponding oxide sols, obtained by force hydrolysis of the corresponding metal chlorides, were compared. The voltammetric properties in H(2)SO(4) solution indicate that Ti(0.6)Ir(0.4)O(2)/Ti has more pronounced pseudocapacitive characteristics, caused by proton-assisted, solid state surface redox transitions of the oxide. At potentials negative to 0.0 V(SCE), this electrode is of poor conductivity and activity, while the voltammetric behavior of the Ti(0.6)Ru(0.4)O(2)/Ti electrode is governed by proton injection/ejection into the oxide structure. The Ti(0.6)Ir(0.4)O(2)/Ti electrode had a higher electrocatalytical activity for oxygen evolution, while the investigated anodes were of similar activity for chlorine evolution. The potential dependence of the impedance characteristics showed that the Ti(0.6)Ru(0.4)O(2)/Ti electrode behaved like a capacitor over a wider potential range than the Ti(0.6)Ir(0.4)O(2)/Ti electrode, with fully-developed pseudocapacitive properties at. potentials positive to 0.60 V(SCE). However, the impedance characteristics of the Ti(0.6)Ir(0.4)O(2)/Ti electrode changed with increasing potential from resistor-like to capacitor-like behavior.",
journal = "Journal of the Serbian Chemical Society",
title = "Differences in the electrochemical behavior of ruthenium and iridium oxide in electrocatalytic coatings of activated titanium anodes prepared by the sol-gel procedure",
volume = "75",
number = "10",
pages = "1413-1420",
doi = "10.2298/JSC100310078P"
}
Panić, V. V., Dekanski, A. B., Mišković-Stanković, V. B., Milonjić, S. K.,& Nikolić, B. Ž.. (2010). Differences in the electrochemical behavior of ruthenium and iridium oxide in electrocatalytic coatings of activated titanium anodes prepared by the sol-gel procedure. in Journal of the Serbian Chemical Society, 75(10), 1413-1420.
https://doi.org/10.2298/JSC100310078P
Panić VV, Dekanski AB, Mišković-Stanković VB, Milonjić SK, Nikolić BŽ. Differences in the electrochemical behavior of ruthenium and iridium oxide in electrocatalytic coatings of activated titanium anodes prepared by the sol-gel procedure. in Journal of the Serbian Chemical Society. 2010;75(10):1413-1420.
doi:10.2298/JSC100310078P .
Panić, Vladimir V., Dekanski, Aleksandar B., Mišković-Stanković, Vesna B., Milonjić, Slobodan K., Nikolić, Branislav Ž., "Differences in the electrochemical behavior of ruthenium and iridium oxide in electrocatalytic coatings of activated titanium anodes prepared by the sol-gel procedure" in Journal of the Serbian Chemical Society, 75, no. 10 (2010):1413-1420,
https://doi.org/10.2298/JSC100310078P . .
11
10
13

Activity and stability of RuO2-coated titanium anodes prepared via the alkoxide route

Panić, Vladimir; Dekanski, Aleksandar B.; Milonjić, Slobodan K.; Mišković-Stanković, Vesna B.; Nikolić, Branislav Ž.

(2006)

TY  - JOUR
AU  - Panić, Vladimir
AU  - Dekanski, Aleksandar B.
AU  - Milonjić, Slobodan K.
AU  - Mišković-Stanković, Vesna B.
AU  - Nikolić, Branislav Ž.
PY  - 2006
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3143
AB  - Titanium anodes with an active RuO2 coating of two different thicknesses were prepared from the oxide suspended in ethanol (ink method), while the oxide itself was synthesized by the hydrolysis of ruthenium ethoxide in ail ethanolic solution (alkoxide route). The morphology of prepared oxide was examined by scanning electron microscopy. The electrochemical propel-ties of the prepared Ti/RuO2 anodes, involving their cyclic voltammetric behavior in H2SO4 and NaCl solutions, activity in the chlorine and oxygen evolution reaction, impedance behavior in H2SO4, and stability during electrolysis in dilute chloride solutions, were investigated. The performances of the anodes are compared to those of a Ti/RuO2 anode prepared by the sol-gel procedure from an oxide sol obtained by the forced hydrolysis of ruthenium chloride in acid solution. The anodes prepared via the alkoxide route showed a higher capacitance and activity for the chlorine evolution reaction than the anode prepared by the inorganic sol-gel procedure. The results of the stability test showed that the utilization of the coating active material is better when the anodes were prepared via the alkoxide route than via the inorganic sol-gel procedure, particularly for anodes with a smaller mass of coating. The different rates of loss of activity indicate a degradation mechanism for the anodes prepared via the alkoxide route in which electrochemical dissolution of RuO2 from the coating surface prevails over the growth of an insulating TiO2 layer in the coating/Ti substrate interphase. The effect of RuO2 dissolution from the coating surface increases with increasing coating mass.
T2  - Journal of the Serbian Chemical Society
T1  - Activity and stability of RuO2-coated titanium anodes prepared via the alkoxide route
VL  - 71
IS  - 11
SP  - 1173
EP  - 1186
DO  - 10.2298/JSC0611173P
ER  - 
@article{
author = "Panić, Vladimir and Dekanski, Aleksandar B. and Milonjić, Slobodan K. and Mišković-Stanković, Vesna B. and Nikolić, Branislav Ž.",
year = "2006",
abstract = "Titanium anodes with an active RuO2 coating of two different thicknesses were prepared from the oxide suspended in ethanol (ink method), while the oxide itself was synthesized by the hydrolysis of ruthenium ethoxide in ail ethanolic solution (alkoxide route). The morphology of prepared oxide was examined by scanning electron microscopy. The electrochemical propel-ties of the prepared Ti/RuO2 anodes, involving their cyclic voltammetric behavior in H2SO4 and NaCl solutions, activity in the chlorine and oxygen evolution reaction, impedance behavior in H2SO4, and stability during electrolysis in dilute chloride solutions, were investigated. The performances of the anodes are compared to those of a Ti/RuO2 anode prepared by the sol-gel procedure from an oxide sol obtained by the forced hydrolysis of ruthenium chloride in acid solution. The anodes prepared via the alkoxide route showed a higher capacitance and activity for the chlorine evolution reaction than the anode prepared by the inorganic sol-gel procedure. The results of the stability test showed that the utilization of the coating active material is better when the anodes were prepared via the alkoxide route than via the inorganic sol-gel procedure, particularly for anodes with a smaller mass of coating. The different rates of loss of activity indicate a degradation mechanism for the anodes prepared via the alkoxide route in which electrochemical dissolution of RuO2 from the coating surface prevails over the growth of an insulating TiO2 layer in the coating/Ti substrate interphase. The effect of RuO2 dissolution from the coating surface increases with increasing coating mass.",
journal = "Journal of the Serbian Chemical Society",
title = "Activity and stability of RuO2-coated titanium anodes prepared via the alkoxide route",
volume = "71",
number = "11",
pages = "1173-1186",
doi = "10.2298/JSC0611173P"
}
Panić, V., Dekanski, A. B., Milonjić, S. K., Mišković-Stanković, V. B.,& Nikolić, B. Ž.. (2006). Activity and stability of RuO2-coated titanium anodes prepared via the alkoxide route. in Journal of the Serbian Chemical Society, 71(11), 1173-1186.
https://doi.org/10.2298/JSC0611173P
Panić V, Dekanski AB, Milonjić SK, Mišković-Stanković VB, Nikolić BŽ. Activity and stability of RuO2-coated titanium anodes prepared via the alkoxide route. in Journal of the Serbian Chemical Society. 2006;71(11):1173-1186.
doi:10.2298/JSC0611173P .
Panić, Vladimir, Dekanski, Aleksandar B., Milonjić, Slobodan K., Mišković-Stanković, Vesna B., Nikolić, Branislav Ž., "Activity and stability of RuO2-coated titanium anodes prepared via the alkoxide route" in Journal of the Serbian Chemical Society, 71, no. 11 (2006):1173-1186,
https://doi.org/10.2298/JSC0611173P . .
7
8
8

Electrocatalytic activity of sol-gel-prepared RuO2/Ti anode in chlorine and oxygen evolution reactions

Panić, Vesna V.; Dekanski, Aleksandar B.; Milonjić, Slobodan K.; Miskovic-Stankovic, V. B.; Nikolić, Branislav Ž.

(2006)

TY  - JOUR
AU  - Panić, Vesna V.
AU  - Dekanski, Aleksandar B.
AU  - Milonjić, Slobodan K.
AU  - Miskovic-Stankovic, V. B.
AU  - Nikolić, Branislav Ž.
PY  - 2006
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6629
AB  - Electrocatalytic properties of RuO2/Ti anode with different coating masses, which are prepared by the alkoxide sol-gel procedure, are investigated in chlorine and oxygen evolution reactions by polarization measurements and electrochemical impedance spectroscopy in H2SO4 and NaCl electrolytes. According to polarization measurements, the activity of anodes at overpotentials below 100 mV is independent of coating mass. However, impedance measurements above 100 mV reveal changes in the activity of anodes in chlorine evolution reaction for different coating masses. The diffusion limitations related to the evolved chlorine are registered in low-frequency domain at 1.10 V (SCE), diminishing with the increase in potential to the 1.15 V (SCE). The observed impedance behavior is discussed with respect to the activity model for activated titanium anodes in chlorine evolution reaction involving formation of gas channels within porous coating structure. Gas channels enhance the mass transfer rate similarly to the forced convection, which also increases the activity of anode. This is more pronounced for the anode of greater coating mass due to its more compact surface structure. The more compact structure appears to be beneficial for gas channels formation.
T2  - Russian Journal of Electrochemistry
T1  - Electrocatalytic activity of sol-gel-prepared RuO2/Ti anode in chlorine and oxygen evolution reactions
VL  - 42
IS  - 10
SP  - 1055
EP  - 1060
DO  - 10.1134/S1023193506100107
ER  - 
@article{
author = "Panić, Vesna V. and Dekanski, Aleksandar B. and Milonjić, Slobodan K. and Miskovic-Stankovic, V. B. and Nikolić, Branislav Ž.",
year = "2006",
abstract = "Electrocatalytic properties of RuO2/Ti anode with different coating masses, which are prepared by the alkoxide sol-gel procedure, are investigated in chlorine and oxygen evolution reactions by polarization measurements and electrochemical impedance spectroscopy in H2SO4 and NaCl electrolytes. According to polarization measurements, the activity of anodes at overpotentials below 100 mV is independent of coating mass. However, impedance measurements above 100 mV reveal changes in the activity of anodes in chlorine evolution reaction for different coating masses. The diffusion limitations related to the evolved chlorine are registered in low-frequency domain at 1.10 V (SCE), diminishing with the increase in potential to the 1.15 V (SCE). The observed impedance behavior is discussed with respect to the activity model for activated titanium anodes in chlorine evolution reaction involving formation of gas channels within porous coating structure. Gas channels enhance the mass transfer rate similarly to the forced convection, which also increases the activity of anode. This is more pronounced for the anode of greater coating mass due to its more compact surface structure. The more compact structure appears to be beneficial for gas channels formation.",
journal = "Russian Journal of Electrochemistry",
title = "Electrocatalytic activity of sol-gel-prepared RuO2/Ti anode in chlorine and oxygen evolution reactions",
volume = "42",
number = "10",
pages = "1055-1060",
doi = "10.1134/S1023193506100107"
}
Panić, V. V., Dekanski, A. B., Milonjić, S. K., Miskovic-Stankovic, V. B.,& Nikolić, B. Ž.. (2006). Electrocatalytic activity of sol-gel-prepared RuO2/Ti anode in chlorine and oxygen evolution reactions. in Russian Journal of Electrochemistry, 42(10), 1055-1060.
https://doi.org/10.1134/S1023193506100107
Panić VV, Dekanski AB, Milonjić SK, Miskovic-Stankovic VB, Nikolić BŽ. Electrocatalytic activity of sol-gel-prepared RuO2/Ti anode in chlorine and oxygen evolution reactions. in Russian Journal of Electrochemistry. 2006;42(10):1055-1060.
doi:10.1134/S1023193506100107 .
Panić, Vesna V., Dekanski, Aleksandar B., Milonjić, Slobodan K., Miskovic-Stankovic, V. B., Nikolić, Branislav Ž., "Electrocatalytic activity of sol-gel-prepared RuO2/Ti anode in chlorine and oxygen evolution reactions" in Russian Journal of Electrochemistry, 42, no. 10 (2006):1055-1060,
https://doi.org/10.1134/S1023193506100107 . .
15
15
15

Morphology and capacitive properties of [RuOxHy/low-surface area carbon black] composite materials prepared by sol-gel procedure

Panic, V; Dekanski, Aleksandar B.; Gojković, S; Milonjić, Slobodan K.; Mišković-Stanković, Vesna B.; Nikolić, Branislav Ž.

(2005)

TY  - JOUR
AU  - Panic, V
AU  - Dekanski, Aleksandar B.
AU  - Gojković, S
AU  - Milonjić, Slobodan K.
AU  - Mišković-Stanković, Vesna B.
AU  - Nikolić, Branislav Ž.
PY  - 2005
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6529
AB  - The morphology and the capacitive properties of carbon supported hydrous ruthenium oxide (RuOxHy/C), prepared by impregnation of low-surface area carbon black Vulcano (R) XC-72 R with solid phase of RuOxHy sol, were investigated by scanning electron microscopy, cyclic voltammetry and electrochemical impedance spectroscopy. The oxide sols of different ageing times, prepared by forced hydrolysis of RuCl3, were used for composite preparation. The prepared composites show considerably higher capacitance values in acid electrolyte if compared to carbon black support. Microscopic investigations show that the extent of impregnation and the composite surface appearance depend on ageing time. The composite capacitance increases with ageing time of oxide sol. A gradual decrease in capacitance of thermally untreated composite with charging/discharging cycles was registered, which appears to be related to the extent of impregnation, too. Electrochemical impedance spectroscopy measurements indicate an in-depth capacitance distribution through the composite layer. It was found that Nafion (R) layer, used to ensure the adhesion of the composite layer to the current collector, influenced the composite impedance behavior, especially on the oxide-rich parts of the composite surface.
T2  - Materials Science Forum
T1  - Morphology and capacitive properties of [RuOxHy/low-surface area carbon black] composite materials prepared by sol-gel procedure
VL  - 494
SP  - 235
EP  - 240
DO  - 10.4028/www.scientific.net/MSF.494.235
ER  - 
@article{
author = "Panic, V and Dekanski, Aleksandar B. and Gojković, S and Milonjić, Slobodan K. and Mišković-Stanković, Vesna B. and Nikolić, Branislav Ž.",
year = "2005",
abstract = "The morphology and the capacitive properties of carbon supported hydrous ruthenium oxide (RuOxHy/C), prepared by impregnation of low-surface area carbon black Vulcano (R) XC-72 R with solid phase of RuOxHy sol, were investigated by scanning electron microscopy, cyclic voltammetry and electrochemical impedance spectroscopy. The oxide sols of different ageing times, prepared by forced hydrolysis of RuCl3, were used for composite preparation. The prepared composites show considerably higher capacitance values in acid electrolyte if compared to carbon black support. Microscopic investigations show that the extent of impregnation and the composite surface appearance depend on ageing time. The composite capacitance increases with ageing time of oxide sol. A gradual decrease in capacitance of thermally untreated composite with charging/discharging cycles was registered, which appears to be related to the extent of impregnation, too. Electrochemical impedance spectroscopy measurements indicate an in-depth capacitance distribution through the composite layer. It was found that Nafion (R) layer, used to ensure the adhesion of the composite layer to the current collector, influenced the composite impedance behavior, especially on the oxide-rich parts of the composite surface.",
journal = "Materials Science Forum",
title = "Morphology and capacitive properties of [RuOxHy/low-surface area carbon black] composite materials prepared by sol-gel procedure",
volume = "494",
pages = "235-240",
doi = "10.4028/www.scientific.net/MSF.494.235"
}
Panic, V., Dekanski, A. B., Gojković, S., Milonjić, S. K., Mišković-Stanković, V. B.,& Nikolić, B. Ž.. (2005). Morphology and capacitive properties of [RuOxHy/low-surface area carbon black] composite materials prepared by sol-gel procedure. in Materials Science Forum, 494, 235-240.
https://doi.org/10.4028/www.scientific.net/MSF.494.235
Panic V, Dekanski AB, Gojković S, Milonjić SK, Mišković-Stanković VB, Nikolić BŽ. Morphology and capacitive properties of [RuOxHy/low-surface area carbon black] composite materials prepared by sol-gel procedure. in Materials Science Forum. 2005;494:235-240.
doi:10.4028/www.scientific.net/MSF.494.235 .
Panic, V, Dekanski, Aleksandar B., Gojković, S, Milonjić, Slobodan K., Mišković-Stanković, Vesna B., Nikolić, Branislav Ž., "Morphology and capacitive properties of [RuOxHy/low-surface area carbon black] composite materials prepared by sol-gel procedure" in Materials Science Forum, 494 (2005):235-240,
https://doi.org/10.4028/www.scientific.net/MSF.494.235 . .
4
9

On the deactivation mechanism of RuO2-TiO2/Ti anodes prepared by the sol-gel procedure

Panic, V; Dekanski, Aleksandar B.; Mišković-Stanković, Vesna B.; Milonjić, Slobodan K.; Nikolić, Branislav Ž.

(2005)

TY  - JOUR
AU  - Panic, V
AU  - Dekanski, Aleksandar B.
AU  - Mišković-Stanković, Vesna B.
AU  - Milonjić, Slobodan K.
AU  - Nikolić, Branislav Ž.
PY  - 2005
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2883
AB  - The deactivation process that leads to the end of titanium supported RuO2-TiO2 coating service life, for anodes prepared from RuO2 and TiO2 sols, as well as by the conventional thermal decomposition of RuCl3 and TiCl3, was investigated. The loss of electrocatalytic activity was registered by an accelerated stability test in 0.50 mol dm(-3) NaCl electrolyte, while the changes in the electrochemical properties were monitored during the stability test by cyclic voltammetry, polarization measurements and electrochemical impedance spectroscopy in 1.0 mol dm(-3) HClO4 and in 0.50 mol dm(-3) NaCl. The changes in anode behavior suggest that the essential cause for the deactivation of the anode prepared by the sol-gel procedure is the formation of an insulating TiO2-rich layer at the coating surface due to the continuous dissolution of the Ru active species. However, the growth of the insulating TiO2 layer in the coating/Ti substrate interphase mainly causes deactivation of the thermally prepared anode. The deactivation mechanism appeared to be the consequence of the different morphology of the coatings prepared by two different procedures. (c) 2005 Elsevier B.V. All rights reserved.
T2  - Journal of Electroanalytical Chemistry
T1  - On the deactivation mechanism of RuO2-TiO2/Ti anodes prepared by the sol-gel procedure
VL  - 579
IS  - 1
SP  - 67
EP  - 76
DO  - 10.1016/j.jelechem.2005.01.026
ER  - 
@article{
author = "Panic, V and Dekanski, Aleksandar B. and Mišković-Stanković, Vesna B. and Milonjić, Slobodan K. and Nikolić, Branislav Ž.",
year = "2005",
abstract = "The deactivation process that leads to the end of titanium supported RuO2-TiO2 coating service life, for anodes prepared from RuO2 and TiO2 sols, as well as by the conventional thermal decomposition of RuCl3 and TiCl3, was investigated. The loss of electrocatalytic activity was registered by an accelerated stability test in 0.50 mol dm(-3) NaCl electrolyte, while the changes in the electrochemical properties were monitored during the stability test by cyclic voltammetry, polarization measurements and electrochemical impedance spectroscopy in 1.0 mol dm(-3) HClO4 and in 0.50 mol dm(-3) NaCl. The changes in anode behavior suggest that the essential cause for the deactivation of the anode prepared by the sol-gel procedure is the formation of an insulating TiO2-rich layer at the coating surface due to the continuous dissolution of the Ru active species. However, the growth of the insulating TiO2 layer in the coating/Ti substrate interphase mainly causes deactivation of the thermally prepared anode. The deactivation mechanism appeared to be the consequence of the different morphology of the coatings prepared by two different procedures. (c) 2005 Elsevier B.V. All rights reserved.",
journal = "Journal of Electroanalytical Chemistry",
title = "On the deactivation mechanism of RuO2-TiO2/Ti anodes prepared by the sol-gel procedure",
volume = "579",
number = "1",
pages = "67-76",
doi = "10.1016/j.jelechem.2005.01.026"
}
Panic, V., Dekanski, A. B., Mišković-Stanković, V. B., Milonjić, S. K.,& Nikolić, B. Ž.. (2005). On the deactivation mechanism of RuO2-TiO2/Ti anodes prepared by the sol-gel procedure. in Journal of Electroanalytical Chemistry, 579(1), 67-76.
https://doi.org/10.1016/j.jelechem.2005.01.026
Panic V, Dekanski AB, Mišković-Stanković VB, Milonjić SK, Nikolić BŽ. On the deactivation mechanism of RuO2-TiO2/Ti anodes prepared by the sol-gel procedure. in Journal of Electroanalytical Chemistry. 2005;579(1):67-76.
doi:10.1016/j.jelechem.2005.01.026 .
Panic, V, Dekanski, Aleksandar B., Mišković-Stanković, Vesna B., Milonjić, Slobodan K., Nikolić, Branislav Ž., "On the deactivation mechanism of RuO2-TiO2/Ti anodes prepared by the sol-gel procedure" in Journal of Electroanalytical Chemistry, 579, no. 1 (2005):67-76,
https://doi.org/10.1016/j.jelechem.2005.01.026 . .
3
66
63
77

The role of sol-gel procedure conditions in electrochemical behavior and corrosion stability of Ti/[RuO2-TiO2] anodes

Panic, V; Dekanski, Aleksandar B.; Mišković-Stanković, Vesna B.; Nikolić, Branislav Ž.; Milonjić, Slobodan K.

(2005)

TY  - JOUR
AU  - Panic, V
AU  - Dekanski, Aleksandar B.
AU  - Mišković-Stanković, Vesna B.
AU  - Nikolić, Branislav Ž.
AU  - Milonjić, Slobodan K.
PY  - 2005
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2853
AB  - Using a sol-gel procedure, RuO2-TiO2 active coatings were formed on a titanium support. The conditions of preparation of the RuO2 and TiO2 sols were investigated and the sols were characterized by transmission electron microscopy (TEM) and X-ray diffraction technique. Prepared anodes were investigated from the standpoint of morphology (scanning tunneling and electron microscopy) and electrochemical behavior (cyclic voltammetry, polarization measurements, and electrochemical impedance spectroscopy). The service life of the RuO2-TiO2 active coatings was examined by an accelerated corrosion stability test in 0.5 mol dm(-3) NaCl solution. In order to resolve the role of TiO2 in the deactivation mechanism of the active coating, additional TiO2 layers were introduced in the support/coating interface or on the surface of the coating. The behavior of these anodes with the TiO2-enriched coating layer was compared with the behavior of anodes with regular RuO2-TiO2 coatings. The results show that the loss of coating electrocatalytic activity is caused by dissolution of active Ru species and TiO2 enrichment in the coating. It is also observed that the sol-gel preparation procedure favors the formation of the TiO2 layer at the surface of the RuO2-TiO2 coating.
T2  - Materials and Manufacturing Processes
T1  - The role of sol-gel procedure conditions in electrochemical behavior and corrosion stability of Ti/[RuO2-TiO2] anodes
VL  - 20
IS  - 1
SP  - 89
EP  - 103
DO  - 10.1081/AMP-200041645
ER  - 
@article{
author = "Panic, V and Dekanski, Aleksandar B. and Mišković-Stanković, Vesna B. and Nikolić, Branislav Ž. and Milonjić, Slobodan K.",
year = "2005",
abstract = "Using a sol-gel procedure, RuO2-TiO2 active coatings were formed on a titanium support. The conditions of preparation of the RuO2 and TiO2 sols were investigated and the sols were characterized by transmission electron microscopy (TEM) and X-ray diffraction technique. Prepared anodes were investigated from the standpoint of morphology (scanning tunneling and electron microscopy) and electrochemical behavior (cyclic voltammetry, polarization measurements, and electrochemical impedance spectroscopy). The service life of the RuO2-TiO2 active coatings was examined by an accelerated corrosion stability test in 0.5 mol dm(-3) NaCl solution. In order to resolve the role of TiO2 in the deactivation mechanism of the active coating, additional TiO2 layers were introduced in the support/coating interface or on the surface of the coating. The behavior of these anodes with the TiO2-enriched coating layer was compared with the behavior of anodes with regular RuO2-TiO2 coatings. The results show that the loss of coating electrocatalytic activity is caused by dissolution of active Ru species and TiO2 enrichment in the coating. It is also observed that the sol-gel preparation procedure favors the formation of the TiO2 layer at the surface of the RuO2-TiO2 coating.",
journal = "Materials and Manufacturing Processes",
title = "The role of sol-gel procedure conditions in electrochemical behavior and corrosion stability of Ti/[RuO2-TiO2] anodes",
volume = "20",
number = "1",
pages = "89-103",
doi = "10.1081/AMP-200041645"
}
Panic, V., Dekanski, A. B., Mišković-Stanković, V. B., Nikolić, B. Ž.,& Milonjić, S. K.. (2005). The role of sol-gel procedure conditions in electrochemical behavior and corrosion stability of Ti/[RuO2-TiO2] anodes. in Materials and Manufacturing Processes, 20(1), 89-103.
https://doi.org/10.1081/AMP-200041645
Panic V, Dekanski AB, Mišković-Stanković VB, Nikolić BŽ, Milonjić SK. The role of sol-gel procedure conditions in electrochemical behavior and corrosion stability of Ti/[RuO2-TiO2] anodes. in Materials and Manufacturing Processes. 2005;20(1):89-103.
doi:10.1081/AMP-200041645 .
Panic, V, Dekanski, Aleksandar B., Mišković-Stanković, Vesna B., Nikolić, Branislav Ž., Milonjić, Slobodan K., "The role of sol-gel procedure conditions in electrochemical behavior and corrosion stability of Ti/[RuO2-TiO2] anodes" in Materials and Manufacturing Processes, 20, no. 1 (2005):89-103,
https://doi.org/10.1081/AMP-200041645 . .
7
8
8

The properties of carbon-supported hydrous ruthenium oxide obtained from RuOxHy sol

Panic, V; Vidakovic, T; Gojković, S; Dekanski, Aleksandar B.; Milonjić, Slobodan K.; Nikolić, Branislav Ž.

(2003)

TY  - JOUR
AU  - Panic, V
AU  - Vidakovic, T
AU  - Gojković, S
AU  - Dekanski, Aleksandar B.
AU  - Milonjić, Slobodan K.
AU  - Nikolić, Branislav Ž.
PY  - 2003
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6385
AB  - Preparation of RuOxHy/carbon black nanocomposite material was performed by the impregnation method starting from RuOxHy sol as a precursor. Black Pearls 2000(R) (BP) and Vulcan(R) XC-72 R (XC) were used as supporting materials. Samples of the composite were calcined in nitrogen atmosphere at temperatures from 130 to 450 degreesC. Chemical and structural characterization of the precursor and the composites was performed by using energy-dispersive X-ray fluorescence spectroscopy (EDXRFS), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). These techniques showed that the oxide impregnated into carbon support is hydrous and amorphous. The amorphous structure is maintained if the composite is calcined up to 300 degreesC, while the lowintensity peak at 2theta position that corresponds to the most intensive peak of the rutile structure was registered at 450 degreesC. The capacitance of the composite was determined using cyclic voltammetry. It was found that the capacitance is dependent on calcination temperature and surface area of the carbon black support. The highest specific capacitance of about 700 F g(-1) of composite was registered for RuOxHy supported on BP and calcined at 300 degreesC while four times lower values was obtained for RuOxHy supported on XC. The capacitance measurements indicated that XC-supported RuOXHy composite is highly porous while BP-supported one is more compact. (C) 2003 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - The properties of carbon-supported hydrous ruthenium oxide obtained from RuOxHy sol
VL  - 48
IS  - 25-26
SP  - 3805
EP  - 3813
DO  - 10.1016/S0013-4686(03)00514-0
ER  - 
@article{
author = "Panic, V and Vidakovic, T and Gojković, S and Dekanski, Aleksandar B. and Milonjić, Slobodan K. and Nikolić, Branislav Ž.",
year = "2003",
abstract = "Preparation of RuOxHy/carbon black nanocomposite material was performed by the impregnation method starting from RuOxHy sol as a precursor. Black Pearls 2000(R) (BP) and Vulcan(R) XC-72 R (XC) were used as supporting materials. Samples of the composite were calcined in nitrogen atmosphere at temperatures from 130 to 450 degreesC. Chemical and structural characterization of the precursor and the composites was performed by using energy-dispersive X-ray fluorescence spectroscopy (EDXRFS), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). These techniques showed that the oxide impregnated into carbon support is hydrous and amorphous. The amorphous structure is maintained if the composite is calcined up to 300 degreesC, while the lowintensity peak at 2theta position that corresponds to the most intensive peak of the rutile structure was registered at 450 degreesC. The capacitance of the composite was determined using cyclic voltammetry. It was found that the capacitance is dependent on calcination temperature and surface area of the carbon black support. The highest specific capacitance of about 700 F g(-1) of composite was registered for RuOxHy supported on BP and calcined at 300 degreesC while four times lower values was obtained for RuOxHy supported on XC. The capacitance measurements indicated that XC-supported RuOXHy composite is highly porous while BP-supported one is more compact. (C) 2003 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "The properties of carbon-supported hydrous ruthenium oxide obtained from RuOxHy sol",
volume = "48",
number = "25-26",
pages = "3805-3813",
doi = "10.1016/S0013-4686(03)00514-0"
}
Panic, V., Vidakovic, T., Gojković, S., Dekanski, A. B., Milonjić, S. K.,& Nikolić, B. Ž.. (2003). The properties of carbon-supported hydrous ruthenium oxide obtained from RuOxHy sol. in Electrochimica Acta, 48(25-26), 3805-3813.
https://doi.org/10.1016/S0013-4686(03)00514-0
Panic V, Vidakovic T, Gojković S, Dekanski AB, Milonjić SK, Nikolić BŽ. The properties of carbon-supported hydrous ruthenium oxide obtained from RuOxHy sol. in Electrochimica Acta. 2003;48(25-26):3805-3813.
doi:10.1016/S0013-4686(03)00514-0 .
Panic, V, Vidakovic, T, Gojković, S, Dekanski, Aleksandar B., Milonjić, Slobodan K., Nikolić, Branislav Ž., "The properties of carbon-supported hydrous ruthenium oxide obtained from RuOxHy sol" in Electrochimica Acta, 48, no. 25-26 (2003):3805-3813,
https://doi.org/10.1016/S0013-4686(03)00514-0 . .
62
64
71

The role of titanium oxide concentration profile of titanium oxide of RuO2-TiO2 coatings obtained by the sol-gel procedure on its electrochemical behavior

Panic, VV; Dekanski, Aleksandar B.; Mišković-Stanković, Vesna B.; Milonjić, Slobodan K.; Nikolić, Branislav Ž.

(2003)

TY  - JOUR
AU  - Panic, VV
AU  - Dekanski, Aleksandar B.
AU  - Mišković-Stanković, Vesna B.
AU  - Milonjić, Slobodan K.
AU  - Nikolić, Branislav Ž.
PY  - 2003
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2700
AB  - In order to understand the rule of TiO2 in the deactivation mechanism of an active RuO2-TiO2 coating, an additional TiO2 laver was introduced in the support\coating interphase of regular Ti//[RuO2-TiO2] anode in one case and on the surface of the coating in the other. The electrochemical behavior of these, with TiO2 enriched, anodes was compared with the behavior of anodes with regular RuO2-TiO2 coatings. which were subjected to an accelerated stability test. A high-frequency semicircle in the complex plane plot, obtained by electrochemical impedance spectroscopy, for a regular RuO2-TiO2 coating corresponds to TiO2 enrichment in the coating as a consequence of anode corrosion. In the case of the coatings with additional TiO2 layers, a high-frequency semicircle was not observed The additional TiO2 layers increase the coating overall resistance and influence the coating impedance behavior at low frequencies. Similar equivalent electrical circuits were used to analyze the impedance behavior of coatings having an additional TO, layer at different position within RuO2-TiO2 coating.
T2  - Journal of the Serbian Chemical Society
T1  - The role of titanium oxide concentration profile of titanium oxide of RuO2-TiO2 coatings obtained by the sol-gel procedure on its electrochemical behavior
VL  - 68
IS  - 12
SP  - 979
EP  - 988
DO  - 10.2298/0352-51390312979P
ER  - 
@article{
author = "Panic, VV and Dekanski, Aleksandar B. and Mišković-Stanković, Vesna B. and Milonjić, Slobodan K. and Nikolić, Branislav Ž.",
year = "2003",
abstract = "In order to understand the rule of TiO2 in the deactivation mechanism of an active RuO2-TiO2 coating, an additional TiO2 laver was introduced in the support\coating interphase of regular Ti//[RuO2-TiO2] anode in one case and on the surface of the coating in the other. The electrochemical behavior of these, with TiO2 enriched, anodes was compared with the behavior of anodes with regular RuO2-TiO2 coatings. which were subjected to an accelerated stability test. A high-frequency semicircle in the complex plane plot, obtained by electrochemical impedance spectroscopy, for a regular RuO2-TiO2 coating corresponds to TiO2 enrichment in the coating as a consequence of anode corrosion. In the case of the coatings with additional TiO2 layers, a high-frequency semicircle was not observed The additional TiO2 layers increase the coating overall resistance and influence the coating impedance behavior at low frequencies. Similar equivalent electrical circuits were used to analyze the impedance behavior of coatings having an additional TO, layer at different position within RuO2-TiO2 coating.",
journal = "Journal of the Serbian Chemical Society",
title = "The role of titanium oxide concentration profile of titanium oxide of RuO2-TiO2 coatings obtained by the sol-gel procedure on its electrochemical behavior",
volume = "68",
number = "12",
pages = "979-988",
doi = "10.2298/0352-51390312979P"
}
Panic, V., Dekanski, A. B., Mišković-Stanković, V. B., Milonjić, S. K.,& Nikolić, B. Ž.. (2003). The role of titanium oxide concentration profile of titanium oxide of RuO2-TiO2 coatings obtained by the sol-gel procedure on its electrochemical behavior. in Journal of the Serbian Chemical Society, 68(12), 979-988.
https://doi.org/10.2298/0352-51390312979P
Panic V, Dekanski AB, Mišković-Stanković VB, Milonjić SK, Nikolić BŽ. The role of titanium oxide concentration profile of titanium oxide of RuO2-TiO2 coatings obtained by the sol-gel procedure on its electrochemical behavior. in Journal of the Serbian Chemical Society. 2003;68(12):979-988.
doi:10.2298/0352-51390312979P .
Panic, VV, Dekanski, Aleksandar B., Mišković-Stanković, Vesna B., Milonjić, Slobodan K., Nikolić, Branislav Ž., "The role of titanium oxide concentration profile of titanium oxide of RuO2-TiO2 coatings obtained by the sol-gel procedure on its electrochemical behavior" in Journal of the Serbian Chemical Society, 68, no. 12 (2003):979-988,
https://doi.org/10.2298/0352-51390312979P . .
12

Morphology of RuO2-TiO2 coatings and TEM characterization of oxide sols used for their preparation

Panic, V; Dekanski, Aleksandar B.; Wang, G; Fedoroff, M; Milonjić, Slobodan K.; Nikolić, Branislav Ž.

(2003)

TY  - JOUR
AU  - Panic, V
AU  - Dekanski, Aleksandar B.
AU  - Wang, G
AU  - Fedoroff, M
AU  - Milonjić, Slobodan K.
AU  - Nikolić, Branislav Ž.
PY  - 2003
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2641
AB  - Characterization of RuO2 and TiO2 sols of different aging times, obtained by forced hydrolysis of appropriate chloride salts, was performed by transmission electron microscopy (TEM). The aging time of TiO2 sols was observed to affect the size of particles as well as the crystallinity of the solid phase of the sols. The surface morphology of RuO2-TiO2 coatings on titanium, obtained by the sol-gel procedure using TiO2 sols of different aging times and RuO2 sol of fixed aging time, was investigated by scanning tunneling microscopy (STM) at three different scan sizes. The STM data indicated uniform microdistribution of the coating material (small microroughness) and an increase in nanoroughness with the aging time of the TiO2 sol. The observed increase in real coating surface area with increasing TiO2 particle size confirms the earlier cyclic voltammetry results. (C) 2003 Elsevier Science (USA). All rights reserved.
T2  - Journal of Colloid and Interface Science
T1  - Morphology of RuO2-TiO2 coatings and TEM characterization of oxide sols used for their preparation
VL  - 263
IS  - 1
SP  - 68
EP  - 73
DO  - 10.1016/S0021-9797(03)00261-3
ER  - 
@article{
author = "Panic, V and Dekanski, Aleksandar B. and Wang, G and Fedoroff, M and Milonjić, Slobodan K. and Nikolić, Branislav Ž.",
year = "2003",
abstract = "Characterization of RuO2 and TiO2 sols of different aging times, obtained by forced hydrolysis of appropriate chloride salts, was performed by transmission electron microscopy (TEM). The aging time of TiO2 sols was observed to affect the size of particles as well as the crystallinity of the solid phase of the sols. The surface morphology of RuO2-TiO2 coatings on titanium, obtained by the sol-gel procedure using TiO2 sols of different aging times and RuO2 sol of fixed aging time, was investigated by scanning tunneling microscopy (STM) at three different scan sizes. The STM data indicated uniform microdistribution of the coating material (small microroughness) and an increase in nanoroughness with the aging time of the TiO2 sol. The observed increase in real coating surface area with increasing TiO2 particle size confirms the earlier cyclic voltammetry results. (C) 2003 Elsevier Science (USA). All rights reserved.",
journal = "Journal of Colloid and Interface Science",
title = "Morphology of RuO2-TiO2 coatings and TEM characterization of oxide sols used for their preparation",
volume = "263",
number = "1",
pages = "68-73",
doi = "10.1016/S0021-9797(03)00261-3"
}
Panic, V., Dekanski, A. B., Wang, G., Fedoroff, M., Milonjić, S. K.,& Nikolić, B. Ž.. (2003). Morphology of RuO2-TiO2 coatings and TEM characterization of oxide sols used for their preparation. in Journal of Colloid and Interface Science, 263(1), 68-73.
https://doi.org/10.1016/S0021-9797(03)00261-3
Panic V, Dekanski AB, Wang G, Fedoroff M, Milonjić SK, Nikolić BŽ. Morphology of RuO2-TiO2 coatings and TEM characterization of oxide sols used for their preparation. in Journal of Colloid and Interface Science. 2003;263(1):68-73.
doi:10.1016/S0021-9797(03)00261-3 .
Panic, V, Dekanski, Aleksandar B., Wang, G, Fedoroff, M, Milonjić, Slobodan K., Nikolić, Branislav Ž., "Morphology of RuO2-TiO2 coatings and TEM characterization of oxide sols used for their preparation" in Journal of Colloid and Interface Science, 263, no. 1 (2003):68-73,
https://doi.org/10.1016/S0021-9797(03)00261-3 . .
25
25
28

The effect of the composition of the dispersing medium of oxide sols on the electro catalytic activity of sol-gel obtained RuO2-TiO2/Ti anodes

Mitrovic, D; Panic, V; Dekanski, Aleksandar B.; Milonjić, Slobodan K.; Atanasoski, R; Nikolić, Branislav Ž.

(2001)

TY  - JOUR
AU  - Mitrovic, D
AU  - Panic, V
AU  - Dekanski, Aleksandar B.
AU  - Milonjić, Slobodan K.
AU  - Atanasoski, R
AU  - Nikolić, Branislav Ž.
PY  - 2001
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2485
AB  - The influence of the addition of methanol, ethanol, 1-propanol and 2-propanol to the dispersing medium of a mixture of RuO2 and TiO2 sols on the electrochemically active surface area for proton exchange, as well as on the electrocatalytic activity for the chlorine evolution reaction (CER) of RuO2-TiO2/Ti electrode obtained by sol-gel procedure was investigated. The electrochemically active surface area was examined by cyclic voltammetry, while the analysis of the activity for the CER was performed by polarization measurements. The stability of the obtained anode coatings was also checked by an accelerated stability test. The anode properties depend on the number of C atoms in the alcohol molecule, as well as on the elapsed time between the preparation of the sols/alcohol mixture and its application onto the titanium support. The addition of alcohol increased the activity of the anodes for the CER, compared to those prepared without the addition, but their stability was smaller.
T2  - Journal of the Serbian Chemical Society
T1  - The effect of the composition of the dispersing medium of oxide sols on the electro catalytic activity of sol-gel obtained RuO2-TiO2/Ti anodes
VL  - 66
IS  - 11-12
SP  - 847
EP  - 857
UR  - https://hdl.handle.net/21.15107/rcub_vinar_2485
ER  - 
@article{
author = "Mitrovic, D and Panic, V and Dekanski, Aleksandar B. and Milonjić, Slobodan K. and Atanasoski, R and Nikolić, Branislav Ž.",
year = "2001",
abstract = "The influence of the addition of methanol, ethanol, 1-propanol and 2-propanol to the dispersing medium of a mixture of RuO2 and TiO2 sols on the electrochemically active surface area for proton exchange, as well as on the electrocatalytic activity for the chlorine evolution reaction (CER) of RuO2-TiO2/Ti electrode obtained by sol-gel procedure was investigated. The electrochemically active surface area was examined by cyclic voltammetry, while the analysis of the activity for the CER was performed by polarization measurements. The stability of the obtained anode coatings was also checked by an accelerated stability test. The anode properties depend on the number of C atoms in the alcohol molecule, as well as on the elapsed time between the preparation of the sols/alcohol mixture and its application onto the titanium support. The addition of alcohol increased the activity of the anodes for the CER, compared to those prepared without the addition, but their stability was smaller.",
journal = "Journal of the Serbian Chemical Society",
title = "The effect of the composition of the dispersing medium of oxide sols on the electro catalytic activity of sol-gel obtained RuO2-TiO2/Ti anodes",
volume = "66",
number = "11-12",
pages = "847-857",
url = "https://hdl.handle.net/21.15107/rcub_vinar_2485"
}
Mitrovic, D., Panic, V., Dekanski, A. B., Milonjić, S. K., Atanasoski, R.,& Nikolić, B. Ž.. (2001). The effect of the composition of the dispersing medium of oxide sols on the electro catalytic activity of sol-gel obtained RuO2-TiO2/Ti anodes. in Journal of the Serbian Chemical Society, 66(11-12), 847-857.
https://hdl.handle.net/21.15107/rcub_vinar_2485
Mitrovic D, Panic V, Dekanski AB, Milonjić SK, Atanasoski R, Nikolić BŽ. The effect of the composition of the dispersing medium of oxide sols on the electro catalytic activity of sol-gel obtained RuO2-TiO2/Ti anodes. in Journal of the Serbian Chemical Society. 2001;66(11-12):847-857.
https://hdl.handle.net/21.15107/rcub_vinar_2485 .
Mitrovic, D, Panic, V, Dekanski, Aleksandar B., Milonjić, Slobodan K., Atanasoski, R, Nikolić, Branislav Ž., "The effect of the composition of the dispersing medium of oxide sols on the electro catalytic activity of sol-gel obtained RuO2-TiO2/Ti anodes" in Journal of the Serbian Chemical Society, 66, no. 11-12 (2001):847-857,
https://hdl.handle.net/21.15107/rcub_vinar_2485 .
7

The influence of the aging time of RuO2 sol on the electrochemical properties of the activated titanium anodes obtained by sol-gel procedure

Panic, V; Dekanski, Aleksandar B.; Milonjić, Slobodan K.; Atanasoski, R; Nikolić, Branislav Ž.

(2000)

TY  - JOUR
AU  - Panic, V
AU  - Dekanski, Aleksandar B.
AU  - Milonjić, Slobodan K.
AU  - Atanasoski, R
AU  - Nikolić, Branislav Ž.
PY  - 2000
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6305
AB  - The influence of the aging time of RuO2 sol on the electrochemical properties and behaviour in chlorine evolution reaction of RuO2/Ti and (40%RuO2 + 60%TiO2)/Ti anodes obtained by sol-gel procedure was studied. The electrochemically active surface area of the anode coatings was examined by cyclic voltammetry. The electrocatalytic activity and anode stability in chlorine evolution reaction were investigated by polarization measurements and accelerated stability test. The dependence of electrochemical properties of obtained activated titanium anodes on RuO2 particle size was established.
T2  - Materials Science Forum
T1  - The influence of the aging time of RuO2 sol on the electrochemical properties of the activated titanium anodes obtained by sol-gel procedure
VL  - 352
SP  - 117
EP  - 122
DO  - 10.4028/www.scientific.net/MSF.352.117
ER  - 
@article{
author = "Panic, V and Dekanski, Aleksandar B. and Milonjić, Slobodan K. and Atanasoski, R and Nikolić, Branislav Ž.",
year = "2000",
abstract = "The influence of the aging time of RuO2 sol on the electrochemical properties and behaviour in chlorine evolution reaction of RuO2/Ti and (40%RuO2 + 60%TiO2)/Ti anodes obtained by sol-gel procedure was studied. The electrochemically active surface area of the anode coatings was examined by cyclic voltammetry. The electrocatalytic activity and anode stability in chlorine evolution reaction were investigated by polarization measurements and accelerated stability test. The dependence of electrochemical properties of obtained activated titanium anodes on RuO2 particle size was established.",
journal = "Materials Science Forum",
title = "The influence of the aging time of RuO2 sol on the electrochemical properties of the activated titanium anodes obtained by sol-gel procedure",
volume = "352",
pages = "117-122",
doi = "10.4028/www.scientific.net/MSF.352.117"
}
Panic, V., Dekanski, A. B., Milonjić, S. K., Atanasoski, R.,& Nikolić, B. Ž.. (2000). The influence of the aging time of RuO2 sol on the electrochemical properties of the activated titanium anodes obtained by sol-gel procedure. in Materials Science Forum, 352, 117-122.
https://doi.org/10.4028/www.scientific.net/MSF.352.117
Panic V, Dekanski AB, Milonjić SK, Atanasoski R, Nikolić BŽ. The influence of the aging time of RuO2 sol on the electrochemical properties of the activated titanium anodes obtained by sol-gel procedure. in Materials Science Forum. 2000;352:117-122.
doi:10.4028/www.scientific.net/MSF.352.117 .
Panic, V, Dekanski, Aleksandar B., Milonjić, Slobodan K., Atanasoski, R, Nikolić, Branislav Ž., "The influence of the aging time of RuO2 sol on the electrochemical properties of the activated titanium anodes obtained by sol-gel procedure" in Materials Science Forum, 352 (2000):117-122,
https://doi.org/10.4028/www.scientific.net/MSF.352.117 . .
7
9

The effect of the presence of alcohol in the dispersing phase of oxide sols on the properties of RuO2-TiO2/Ti anodes obtained by the sol-gel procedure

Panic, V; Dekanski, Aleksandar B.; Milonjić, Slobodan K.; Atanasoski, R; Nikolić, Branislav Ž.

(2000)

TY  - JOUR
AU  - Panic, V
AU  - Dekanski, Aleksandar B.
AU  - Milonjić, Slobodan K.
AU  - Atanasoski, R
AU  - Nikolić, Branislav Ž.
PY  - 2000
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2375
AB  - The effect of the addition of ethanol and 2-propanol to the dispersing phase of TiO2 and RuO2 sols mixture on the morphology and, consequently, on the electrochemical properties of the sol-gel obtained activated titanium anodes was investigated. The properties of the obtained anodes were compared to those obtained by the thermal decomposition of appropriate chloride salts. The morphology of the anode coatings was examined by scanning tunneling microscopy. The electrochemical behaviour was investigated by cyclic voltammetry and by polarization measurements. An accelerated stability test was used for the examination of the stability of the anodes under simultaneous oxygen and chlorine evolution reaction. A dependence of the anode stability on the type of added alcohol is indicated.
T2  - Journal of the Serbian Chemical Society
T1  - The effect of the presence of alcohol in the dispersing phase of oxide sols on the properties of RuO2-TiO2/Ti anodes obtained by the sol-gel procedure
VL  - 65
IS  - 9
SP  - 649
EP  - 660
UR  - https://hdl.handle.net/21.15107/rcub_vinar_2375
ER  - 
@article{
author = "Panic, V and Dekanski, Aleksandar B. and Milonjić, Slobodan K. and Atanasoski, R and Nikolić, Branislav Ž.",
year = "2000",
abstract = "The effect of the addition of ethanol and 2-propanol to the dispersing phase of TiO2 and RuO2 sols mixture on the morphology and, consequently, on the electrochemical properties of the sol-gel obtained activated titanium anodes was investigated. The properties of the obtained anodes were compared to those obtained by the thermal decomposition of appropriate chloride salts. The morphology of the anode coatings was examined by scanning tunneling microscopy. The electrochemical behaviour was investigated by cyclic voltammetry and by polarization measurements. An accelerated stability test was used for the examination of the stability of the anodes under simultaneous oxygen and chlorine evolution reaction. A dependence of the anode stability on the type of added alcohol is indicated.",
journal = "Journal of the Serbian Chemical Society",
title = "The effect of the presence of alcohol in the dispersing phase of oxide sols on the properties of RuO2-TiO2/Ti anodes obtained by the sol-gel procedure",
volume = "65",
number = "9",
pages = "649-660",
url = "https://hdl.handle.net/21.15107/rcub_vinar_2375"
}
Panic, V., Dekanski, A. B., Milonjić, S. K., Atanasoski, R.,& Nikolić, B. Ž.. (2000). The effect of the presence of alcohol in the dispersing phase of oxide sols on the properties of RuO2-TiO2/Ti anodes obtained by the sol-gel procedure. in Journal of the Serbian Chemical Society, 65(9), 649-660.
https://hdl.handle.net/21.15107/rcub_vinar_2375
Panic V, Dekanski AB, Milonjić SK, Atanasoski R, Nikolić BŽ. The effect of the presence of alcohol in the dispersing phase of oxide sols on the properties of RuO2-TiO2/Ti anodes obtained by the sol-gel procedure. in Journal of the Serbian Chemical Society. 2000;65(9):649-660.
https://hdl.handle.net/21.15107/rcub_vinar_2375 .
Panic, V, Dekanski, Aleksandar B., Milonjić, Slobodan K., Atanasoski, R, Nikolić, Branislav Ž., "The effect of the presence of alcohol in the dispersing phase of oxide sols on the properties of RuO2-TiO2/Ti anodes obtained by the sol-gel procedure" in Journal of the Serbian Chemical Society, 65, no. 9 (2000):649-660,
https://hdl.handle.net/21.15107/rcub_vinar_2375 .
8

The influence of the aging time of RuO2 and TiO2 sols on the electrochemical properties and behavior for the chlorine evolution reaction of activated titanium anodes obtained by the sol-gel procedure

Panic, V; Dekanski, Aleksandar B.; Milonjić, Slobodan K.; Atanasoski, R; Nikolić, Branislav Ž.

(2000)

TY  - JOUR
AU  - Panic, V
AU  - Dekanski, Aleksandar B.
AU  - Milonjić, Slobodan K.
AU  - Atanasoski, R
AU  - Nikolić, Branislav Ž.
PY  - 2000
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6298
AB  - The influence of the aging time of RuO2 and TiO2 sols used for the preparation of (40% RuO2 + 60% TiO2)/Ti anodes by the sol-gel procedure on the electrochemical properties and behavior for the chlorine evolution reaction of obtained anodes was studied. The electrochemical (active) surface area of the anode coatings was examined by cyclic voltammetry. The electrocatalytic activity and stability of obtained anodes for the chlorine evolution reaction were investigated by polarization measurements and accelerated stability test. The dependence of electrochemical properties of obtained activated titanium anodes on RuO2 and TiO2 sol particle size was established. (C) 2000 Elsevier Science Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - The influence of the aging time of RuO2 and TiO2 sols on the electrochemical properties and behavior for the chlorine evolution reaction of activated titanium anodes obtained by the sol-gel procedure
VL  - 46
IS  - 2-3
SP  - 415
EP  - 421
DO  - 10.1016/S0013-4686(00)00600-9
ER  - 
@article{
author = "Panic, V and Dekanski, Aleksandar B. and Milonjić, Slobodan K. and Atanasoski, R and Nikolić, Branislav Ž.",
year = "2000",
abstract = "The influence of the aging time of RuO2 and TiO2 sols used for the preparation of (40% RuO2 + 60% TiO2)/Ti anodes by the sol-gel procedure on the electrochemical properties and behavior for the chlorine evolution reaction of obtained anodes was studied. The electrochemical (active) surface area of the anode coatings was examined by cyclic voltammetry. The electrocatalytic activity and stability of obtained anodes for the chlorine evolution reaction were investigated by polarization measurements and accelerated stability test. The dependence of electrochemical properties of obtained activated titanium anodes on RuO2 and TiO2 sol particle size was established. (C) 2000 Elsevier Science Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "The influence of the aging time of RuO2 and TiO2 sols on the electrochemical properties and behavior for the chlorine evolution reaction of activated titanium anodes obtained by the sol-gel procedure",
volume = "46",
number = "2-3",
pages = "415-421",
doi = "10.1016/S0013-4686(00)00600-9"
}
Panic, V., Dekanski, A. B., Milonjić, S. K., Atanasoski, R.,& Nikolić, B. Ž.. (2000). The influence of the aging time of RuO2 and TiO2 sols on the electrochemical properties and behavior for the chlorine evolution reaction of activated titanium anodes obtained by the sol-gel procedure. in Electrochimica Acta, 46(2-3), 415-421.
https://doi.org/10.1016/S0013-4686(00)00600-9
Panic V, Dekanski AB, Milonjić SK, Atanasoski R, Nikolić BŽ. The influence of the aging time of RuO2 and TiO2 sols on the electrochemical properties and behavior for the chlorine evolution reaction of activated titanium anodes obtained by the sol-gel procedure. in Electrochimica Acta. 2000;46(2-3):415-421.
doi:10.1016/S0013-4686(00)00600-9 .
Panic, V, Dekanski, Aleksandar B., Milonjić, Slobodan K., Atanasoski, R, Nikolić, Branislav Ž., "The influence of the aging time of RuO2 and TiO2 sols on the electrochemical properties and behavior for the chlorine evolution reaction of activated titanium anodes obtained by the sol-gel procedure" in Electrochimica Acta, 46, no. 2-3 (2000):415-421,
https://doi.org/10.1016/S0013-4686(00)00600-9 . .
55
57
69

RuO2-TiO2 coated titanium anodes obtained by the sol-gel procedure and their electrochemical behaviour in the chlorine evolution reaction

Panic, VV; Dekanski, Aleksandar B.; Milonjić, Slobodan K.; Atanasoski, RT; Nikolić, Branislav Ž.

(1999)

TY  - JOUR
AU  - Panic, VV
AU  - Dekanski, Aleksandar B.
AU  - Milonjić, Slobodan K.
AU  - Atanasoski, RT
AU  - Nikolić, Branislav Ž.
PY  - 1999
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6285
AB  - TiO2 and RuO2 sols were obtained from RuCl3 and TiCl3 aqueous solutions by condensation and forced hydrolysis at elevated temperature. The Ti supported coatings were obtained by the sol-gel method using a sol mixture in which the metal content was Ru(40%)-Ti(60%). The crystal structure of the solid phase of the sols and their mixtures was examined by S-ray diffraction. The surface and morphology of the coatings were characterized by scanning electron microscopy and scanning tunneling microscopy. Polarization measurements and cyclic voltammetry were used to obtain information about the electrochemical properties of the obtained anodes. An accelerated corrosion test was applied to quantify the anode stability for the chlorine evolution reaction. A stability comparison of the anodes shows a considerably higher lifetime for sol-gel coated anodes than for those obtained by the usual thermal decomposition method. (C) 1999 Elsevier Science B.V. All rights reserved.
T2  - Colloids and Surfaces. A: Physicochemical and Engineering Aspects
T1  - RuO2-TiO2 coated titanium anodes obtained by the sol-gel procedure and their electrochemical behaviour in the chlorine evolution reaction
VL  - 157
IS  - 1-3
SP  - 269
EP  - 274
DO  - 10.1016/S0927-7757(99)00094-1
ER  - 
@article{
author = "Panic, VV and Dekanski, Aleksandar B. and Milonjić, Slobodan K. and Atanasoski, RT and Nikolić, Branislav Ž.",
year = "1999",
abstract = "TiO2 and RuO2 sols were obtained from RuCl3 and TiCl3 aqueous solutions by condensation and forced hydrolysis at elevated temperature. The Ti supported coatings were obtained by the sol-gel method using a sol mixture in which the metal content was Ru(40%)-Ti(60%). The crystal structure of the solid phase of the sols and their mixtures was examined by S-ray diffraction. The surface and morphology of the coatings were characterized by scanning electron microscopy and scanning tunneling microscopy. Polarization measurements and cyclic voltammetry were used to obtain information about the electrochemical properties of the obtained anodes. An accelerated corrosion test was applied to quantify the anode stability for the chlorine evolution reaction. A stability comparison of the anodes shows a considerably higher lifetime for sol-gel coated anodes than for those obtained by the usual thermal decomposition method. (C) 1999 Elsevier Science B.V. All rights reserved.",
journal = "Colloids and Surfaces. A: Physicochemical and Engineering Aspects",
title = "RuO2-TiO2 coated titanium anodes obtained by the sol-gel procedure and their electrochemical behaviour in the chlorine evolution reaction",
volume = "157",
number = "1-3",
pages = "269-274",
doi = "10.1016/S0927-7757(99)00094-1"
}
Panic, V., Dekanski, A. B., Milonjić, S. K., Atanasoski, R.,& Nikolić, B. Ž.. (1999). RuO2-TiO2 coated titanium anodes obtained by the sol-gel procedure and their electrochemical behaviour in the chlorine evolution reaction. in Colloids and Surfaces. A: Physicochemical and Engineering Aspects, 157(1-3), 269-274.
https://doi.org/10.1016/S0927-7757(99)00094-1
Panic V, Dekanski AB, Milonjić SK, Atanasoski R, Nikolić BŽ. RuO2-TiO2 coated titanium anodes obtained by the sol-gel procedure and their electrochemical behaviour in the chlorine evolution reaction. in Colloids and Surfaces. A: Physicochemical and Engineering Aspects. 1999;157(1-3):269-274.
doi:10.1016/S0927-7757(99)00094-1 .
Panic, VV, Dekanski, Aleksandar B., Milonjić, Slobodan K., Atanasoski, RT, Nikolić, Branislav Ž., "RuO2-TiO2 coated titanium anodes obtained by the sol-gel procedure and their electrochemical behaviour in the chlorine evolution reaction" in Colloids and Surfaces. A: Physicochemical and Engineering Aspects, 157, no. 1-3 (1999):269-274,
https://doi.org/10.1016/S0927-7757(99)00094-1 . .
3
64
57
63

Boron and phosphorus doped glassy carbon: I. Surface properties

Đurkić, Tatjana M.; Perić, Aleksandra A.; Laušević, Mila D.; Dekanski, Aleksandar B.; Nešković, Olivera M.; Veljković, Miomir V.; Laušević, Zoran

(1997)

TY  - JOUR
AU  - Đurkić, Tatjana M.
AU  - Perić, Aleksandra A.
AU  - Laušević, Mila D.
AU  - Dekanski, Aleksandar B.
AU  - Nešković, Olivera M.
AU  - Veljković, Miomir V.
AU  - Laušević, Zoran
PY  - 1997
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2103
AB  - The effects of boron and phosphorus incorporation in phenolic resin precursor on the surface properties of glassy carbon (GC) have been studied. Characterization of the surface properties using X-ray photoelectron spectroscopy and mass spectrometry analysis of desorption products showed that boron and phosphorus doped GC contained more carbon-oxygen complexes on the surface than undoped GC. The thermal decomposition of the surface oxide species, resulting in desorption of CO and CO2 as major gas products, showed that the presence of heteroatoms affects the nature of the surface oxide species and contributes to their increased stability. The presence of stable surface oxide species promotes the increased oxidation resistance of doped GC samples. (C) 1997 Elsevier Science Ltd.
T2  - Carbon
T1  - Boron and phosphorus doped glassy carbon: I. Surface properties
VL  - 35
IS  - 10-11
SP  - 1567
EP  - 1572
DO  - 10.1016/S0008-6223(97)00113-9
ER  - 
@article{
author = "Đurkić, Tatjana M. and Perić, Aleksandra A. and Laušević, Mila D. and Dekanski, Aleksandar B. and Nešković, Olivera M. and Veljković, Miomir V. and Laušević, Zoran",
year = "1997",
abstract = "The effects of boron and phosphorus incorporation in phenolic resin precursor on the surface properties of glassy carbon (GC) have been studied. Characterization of the surface properties using X-ray photoelectron spectroscopy and mass spectrometry analysis of desorption products showed that boron and phosphorus doped GC contained more carbon-oxygen complexes on the surface than undoped GC. The thermal decomposition of the surface oxide species, resulting in desorption of CO and CO2 as major gas products, showed that the presence of heteroatoms affects the nature of the surface oxide species and contributes to their increased stability. The presence of stable surface oxide species promotes the increased oxidation resistance of doped GC samples. (C) 1997 Elsevier Science Ltd.",
journal = "Carbon",
title = "Boron and phosphorus doped glassy carbon: I. Surface properties",
volume = "35",
number = "10-11",
pages = "1567-1572",
doi = "10.1016/S0008-6223(97)00113-9"
}
Đurkić, T. M., Perić, A. A., Laušević, M. D., Dekanski, A. B., Nešković, O. M., Veljković, M. V.,& Laušević, Z.. (1997). Boron and phosphorus doped glassy carbon: I. Surface properties. in Carbon, 35(10-11), 1567-1572.
https://doi.org/10.1016/S0008-6223(97)00113-9
Đurkić TM, Perić AA, Laušević MD, Dekanski AB, Nešković OM, Veljković MV, Laušević Z. Boron and phosphorus doped glassy carbon: I. Surface properties. in Carbon. 1997;35(10-11):1567-1572.
doi:10.1016/S0008-6223(97)00113-9 .
Đurkić, Tatjana M., Perić, Aleksandra A., Laušević, Mila D., Dekanski, Aleksandar B., Nešković, Olivera M., Veljković, Miomir V., Laušević, Zoran, "Boron and phosphorus doped glassy carbon: I. Surface properties" in Carbon, 35, no. 10-11 (1997):1567-1572,
https://doi.org/10.1016/S0008-6223(97)00113-9 . .
3
64
58
63

Surface characterization of oxidized activated carbon cloth

Polovina, Mirjana J.; Babić, Biljana M.; Kaluđerović, Branka V.; Dekanski, Aleksandar B.

(1997)

TY  - JOUR
AU  - Polovina, Mirjana J.
AU  - Babić, Biljana M.
AU  - Kaluđerović, Branka V.
AU  - Dekanski, Aleksandar B.
PY  - 1997
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2082
AB  - Cellulose based activated carbon cloth has been oxidized by air, nitric acid, hydrogen peroxide and iron nitrate cristallohydrate melt treatments. Thermogravimetric analysis, selective neutralization, X-ray photoelectron spectroscopy and electrical resistance measurements have been applied to characterize the products. The amount and type of oxygen surface groups have been determined for the different oxidation procedures. The amount of surface groups formed decrease with oxidation procedure in the order: iron nitrate, nitric acid, air and hydrogen peroxide. (C) 1997 Elsevier Science Ltd.
T2  - Carbon
T1  - Surface characterization of oxidized activated carbon cloth
VL  - 35
IS  - 8
SP  - 1047
EP  - 1052
DO  - 10.1016/S0008-6223(97)00057-2
ER  - 
@article{
author = "Polovina, Mirjana J. and Babić, Biljana M. and Kaluđerović, Branka V. and Dekanski, Aleksandar B.",
year = "1997",
abstract = "Cellulose based activated carbon cloth has been oxidized by air, nitric acid, hydrogen peroxide and iron nitrate cristallohydrate melt treatments. Thermogravimetric analysis, selective neutralization, X-ray photoelectron spectroscopy and electrical resistance measurements have been applied to characterize the products. The amount and type of oxygen surface groups have been determined for the different oxidation procedures. The amount of surface groups formed decrease with oxidation procedure in the order: iron nitrate, nitric acid, air and hydrogen peroxide. (C) 1997 Elsevier Science Ltd.",
journal = "Carbon",
title = "Surface characterization of oxidized activated carbon cloth",
volume = "35",
number = "8",
pages = "1047-1052",
doi = "10.1016/S0008-6223(97)00057-2"
}
Polovina, M. J., Babić, B. M., Kaluđerović, B. V.,& Dekanski, A. B.. (1997). Surface characterization of oxidized activated carbon cloth. in Carbon, 35(8), 1047-1052.
https://doi.org/10.1016/S0008-6223(97)00057-2
Polovina MJ, Babić BM, Kaluđerović BV, Dekanski AB. Surface characterization of oxidized activated carbon cloth. in Carbon. 1997;35(8):1047-1052.
doi:10.1016/S0008-6223(97)00057-2 .
Polovina, Mirjana J., Babić, Biljana M., Kaluđerović, Branka V., Dekanski, Aleksandar B., "Surface characterization of oxidized activated carbon cloth" in Carbon, 35, no. 8 (1997):1047-1052,
https://doi.org/10.1016/S0008-6223(97)00057-2 . .
6
190
169
200