TY  - JOUR
AU  - Mitrović, Dejan
AU  - Panić, Vladimir
AU  - Dekanski, Aleksandar
AU  - Milonjić, Slobodan K.
AU  - Atanasoski, Radoslav
AU  - Nikolić, Branislav
PY  - 2001
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/26
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.
AB  - U radu je ispitivan uticaj metanola, etanola, 1-propanola i 2-propanola, dodatih u disperznu sredinu RuO2-TiO2 smeše solova, na elektrohemijski aktivnu površinu i elektrokatalitičku aktivnost za reakciju izdvajanja hlora (RIH) RuO2-TiO2/Ti elektroda dobijenih sol-gel postupkom. Elektrohemijski aktivna površina ispitivana je metodom ciklične voltametrije, dok je aktivnost za RIH ispitivana polarizacionim merenjima. Takođe je i ubrzanim testom stabilnosti ispitivana postojanost dobijenih oksidnih prevlaka. Utvrđeno je da osobine dobijenih anoda zavise od broja ugljenikovih atoma u molekulu dodatog alkohola i vremena proteklog od pripreme smeše alkohola i solova do nanošenja smeše na titanski nosač. Uočeno je da dodatak alkohola prouzrokuje povećanje aktivnosti anoda za RIH u odnosu na anode dobijene bez dodavanja alkohola. Istovremeno, anode dobijene dodavanjem alkohola su manje stabilne od anoda dobijenih bez dodavanja alkohola.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - The effect of the composition of the dispersing medium of oxide sols on the electrocatalytic activity of sol-gel obtained RuO2-TiO2/Ti anodes
T1  - Uticaj sastava disperzne sredine oksidnih solova na elektrokatalitičku aktivnost RuO2-TiO2/Ti anoda dobijenih sol-gel postupkom
VL  - 66
IS  - 11-12
SP  - 847
EP  - 857
UR  - https://hdl.handle.net/21.15107/rcub_cer_26
ER  - 

@article{
author = "Mitrović, Dejan and Panić, Vladimir and Dekanski, Aleksandar and Milonjić, Slobodan K. and Atanasoski, Radoslav and Nikolić, Branislav",
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., U radu je ispitivan uticaj metanola, etanola, 1-propanola i 2-propanola, dodatih u disperznu sredinu RuO2-TiO2 smeše solova, na elektrohemijski aktivnu površinu i elektrokatalitičku aktivnost za reakciju izdvajanja hlora (RIH) RuO2-TiO2/Ti elektroda dobijenih sol-gel postupkom. Elektrohemijski aktivna površina ispitivana je metodom ciklične voltametrije, dok je aktivnost za RIH ispitivana polarizacionim merenjima. Takođe je i ubrzanim testom stabilnosti ispitivana postojanost dobijenih oksidnih prevlaka. Utvrđeno je da osobine dobijenih anoda zavise od broja ugljenikovih atoma u molekulu dodatog alkohola i vremena proteklog od pripreme smeše alkohola i solova do nanošenja smeše na titanski nosač. Uočeno je da dodatak alkohola prouzrokuje povećanje aktivnosti anoda za RIH u odnosu na anode dobijene bez dodavanja alkohola. Istovremeno, anode dobijene dodavanjem alkohola su manje stabilne od anoda dobijenih bez dodavanja alkohola.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "The effect of the composition of the dispersing medium of oxide sols on the electrocatalytic activity of sol-gel obtained RuO2-TiO2/Ti anodes, Uticaj sastava disperzne sredine oksidnih solova na elektrokatalitičku aktivnost RuO2-TiO2/Ti anoda dobijenih sol-gel postupkom",
volume = "66",
number = "11-12",
pages = "847-857",
url = "https://hdl.handle.net/21.15107/rcub_cer_26"
}

Mitrović, D., Panić, V., Dekanski, A., Milonjić, S. K., Atanasoski, R.,& Nikolić, B.. (2001). The effect of the composition of the dispersing medium of oxide sols on the electrocatalytic activity of sol-gel obtained RuO2-TiO2/Ti anodes. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 66(11-12), 847-857.
https://hdl.handle.net/21.15107/rcub_cer_26

Mitrović D, Panić V, Dekanski A, Milonjić SK, Atanasoski R, Nikolić B. The effect of the composition of the dispersing medium of oxide sols on the electrocatalytic 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_cer_26 .

Mitrović, Dejan, Panić, Vladimir, Dekanski, Aleksandar, Milonjić, Slobodan K., Atanasoski, Radoslav, Nikolić, Branislav, "The effect of the composition of the dispersing medium of oxide sols on the electrocatalytic 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_cer_26 .

TY  - JOUR
AU  - Panić, Vesna
AU  - Dekanski, Aleksandar
AU  - Milonjić, Slobodan K.
AU  - Atanasoski, Radoslav
AU  - Nikolić, B.
PY  - 2000
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/17
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.
AB  - U radu je ispitivan uticaj dodavanja etanola odnosno izopropanola u disperznu sredinu smeše solova TiO2 i RuO2 na morfologiju i elektrohemijske osobine aktiviranih titanskih anoda dobijenih sol-gel postupkom. Osobine ovako dobijenih anoda su poređene kako međusobno tako i sa osobinama anoda dobijenih termičkim postupkom iz hlorida rutenijuma i titana. Morfologija anodnih prevlaka ispitivana je skenirajućom tunelskom mikroskopijom, a elektrohemijsko ponašanje cikličnom voltametrijom i polarizacionim merenjima. Stabilnost anoda u paralelnim reakcijama izdvajanja kiseonika i hlora ispitivana je ubrzanim testom stabilnosti. Uočeno je da morfologija, elektrokatalitička aktivnost i stabilnost dobijenih anoda zavisi od vrste dodatog alkohola.
PB  - Serbian Chemical Society
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
T1  - Uticaj prisustva alkohola u disperznoj sredini oksidnih solova ha osobine RuO2-TiO2/Ti anoda dobijenih sol-gel postupkom
VL  - 65
IS  - 9
SP  - 649
EP  - 660
DO  - 10.2298/JSC0009649P
ER  - 

@article{
author = "Panić, Vesna and Dekanski, Aleksandar and Milonjić, Slobodan K. and Atanasoski, Radoslav and Nikolić, B.",
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., U radu je ispitivan uticaj dodavanja etanola odnosno izopropanola u disperznu sredinu smeše solova TiO2 i RuO2 na morfologiju i elektrohemijske osobine aktiviranih titanskih anoda dobijenih sol-gel postupkom. Osobine ovako dobijenih anoda su poređene kako međusobno tako i sa osobinama anoda dobijenih termičkim postupkom iz hlorida rutenijuma i titana. Morfologija anodnih prevlaka ispitivana je skenirajućom tunelskom mikroskopijom, a elektrohemijsko ponašanje cikličnom voltametrijom i polarizacionim merenjima. Stabilnost anoda u paralelnim reakcijama izdvajanja kiseonika i hlora ispitivana je ubrzanim testom stabilnosti. Uočeno je da morfologija, elektrokatalitička aktivnost i stabilnost dobijenih anoda zavisi od vrste dodatog alkohola.",
publisher = "Serbian Chemical Society",
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, Uticaj prisustva alkohola u disperznoj sredini oksidnih solova ha osobine RuO2-TiO2/Ti anoda dobijenih sol-gel postupkom",
volume = "65",
number = "9",
pages = "649-660",
doi = "10.2298/JSC0009649P"
}

Panić, V., Dekanski, A., Milonjić, S. K., Atanasoski, R.,& Nikolić, B.. (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
Serbian Chemical Society., 65(9), 649-660.
https://doi.org/10.2298/JSC0009649P

Panić V, Dekanski A, Milonjić SK, Atanasoski R, Nikolić B. 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.
doi:10.2298/JSC0009649P .

Panić, Vesna, Dekanski, Aleksandar, Milonjić, Slobodan K., Atanasoski, Radoslav, Nikolić, B., "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://doi.org/10.2298/JSC0009649P . .

TY  - JOUR
AU  - Panić, Vladimir
AU  - Dekanski, Aleksandar
AU  - Milonjić, Slobodan
AU  - Atanasoski, Radoslav
AU  - Nikolić, Branislav
PY  - 2000
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4089
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.
PB  - Elsevier
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
SP  - 415
EP  - 421
DO  - 10.1016/S0013-4686(00)00600-9
ER  - 

@article{
author = "Panić, Vladimir and Dekanski, Aleksandar and Milonjić, Slobodan and Atanasoski, Radoslav and Nikolić, Branislav",
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.",
publisher = "Elsevier",
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",
pages = "415-421",
doi = "10.1016/S0013-4686(00)00600-9"
}

Panić, V., Dekanski, A., Milonjić, S., Atanasoski, R.,& Nikolić, B.. (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
Elsevier., 46, 415-421.
https://doi.org/10.1016/S0013-4686(00)00600-9

Panić V, Dekanski A, Milonjić S, Atanasoski R, Nikolić B. 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;46:415-421.
doi:10.1016/S0013-4686(00)00600-9 .

Panić, Vladimir, Dekanski, Aleksandar, Milonjić, Slobodan, Atanasoski, Radoslav, Nikolić, Branislav, "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 (2000):415-421,
https://doi.org/10.1016/S0013-4686(00)00600-9 . .

TY  - JOUR
AU  - Panić, Vladimir
AU  - Dekanski, Aleksandar
AU  - Milonjić, Slobodan K.
AU  - Atanasoski, Radoslav
AU  - Nikolić, Branislav Ž.
PY  - 1999
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4078
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 X-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.
PB  - Elsevier
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 = "Panić, Vladimir and Dekanski, Aleksandar and Milonjić, Slobodan K. and Atanasoski, Radoslav 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 X-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.",
publisher = "Elsevier",
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"
}

Panić, V., Dekanski, A., 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
Elsevier., 157(1-3), 269-274.
https://doi.org/10.1016/S0927-7757(99)00094-1

Panić V, Dekanski A, 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 .

Panić, Vladimir, Dekanski, Aleksandar, Milonjić, Slobodan K., Atanasoski, Radoslav, 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 . .

TY  - JOUR
AU  - Jovanović, Vladislava M.
AU  - Dekanski, Aleksandar
AU  - Despotov, P.
AU  - Nikolić, Branislav Ž.
AU  - Atanasoski, Radoslav T.
PY  - 1992
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3659
AB  - Electrocatalytic oxide coatings with variable concentration profiles of RuO2 as the active component were obtained through a combination of separately applied layers of RuO2, TiO2, IrO2, RuO2 + TiO2 and RuO2 + IrO2 on titanium and glassy carbon substrates. The stability of the samples was examined by accelerated tests performed at high anodic current densities. Electrochemical techniques, cyclic voltammetry for assessing the charge associated with the coating, polarization measurements for assessing the electrocatalytic activity, and Auger electron spectroscopy to register surface composition of the coatings, were applied to follow changes due to the stability experiments. The stability and the charge depended strongly on the sequence of layers in the RuO2-TiO2 coating, with the samples having the RuO2 + TiO2 layer facing the electrolyte exhibiting the highest values for both properties. In contrast to this, the stability of the RuO2-IrO2 coatings, besides being lower than the stability of RuO2-TiO2 coatings, showed no dependence on the sequence of the applied layers. Much lower stability was exhibited by the coatings applied on glassy carbon rather than on titanium. A mechanism of the stability of the coatings based on the interaction of lower than four valency state titanium with higher than four valency ruthenium, proposed for single-crystal surfaces, is corroborated. Finally, during the thermal treatment a diffusion of titanium originating in the titanium substrate through the coating was established.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T2  - Journal of Electroanalytical ChemistryJ Electroanal Chem
T1  - The roles of the ruthenium concentration profile, the stabilizing component and the substrate on the stability of oxide coatings
VL  - 339
IS  - 1-2
SP  - 147
EP  - 165
DO  - 10.1016/0022-0728(92)80449-E
ER  - 

@article{
author = "Jovanović, Vladislava M. and Dekanski, Aleksandar and Despotov, P. and Nikolić, Branislav Ž. and Atanasoski, Radoslav T.",
year = "1992",
abstract = "Electrocatalytic oxide coatings with variable concentration profiles of RuO2 as the active component were obtained through a combination of separately applied layers of RuO2, TiO2, IrO2, RuO2 + TiO2 and RuO2 + IrO2 on titanium and glassy carbon substrates. The stability of the samples was examined by accelerated tests performed at high anodic current densities. Electrochemical techniques, cyclic voltammetry for assessing the charge associated with the coating, polarization measurements for assessing the electrocatalytic activity, and Auger electron spectroscopy to register surface composition of the coatings, were applied to follow changes due to the stability experiments. The stability and the charge depended strongly on the sequence of layers in the RuO2-TiO2 coating, with the samples having the RuO2 + TiO2 layer facing the electrolyte exhibiting the highest values for both properties. In contrast to this, the stability of the RuO2-IrO2 coatings, besides being lower than the stability of RuO2-TiO2 coatings, showed no dependence on the sequence of the applied layers. Much lower stability was exhibited by the coatings applied on glassy carbon rather than on titanium. A mechanism of the stability of the coatings based on the interaction of lower than four valency state titanium with higher than four valency ruthenium, proposed for single-crystal surfaces, is corroborated. Finally, during the thermal treatment a diffusion of titanium originating in the titanium substrate through the coating was established.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry, Journal of Electroanalytical ChemistryJ Electroanal Chem",
title = "The roles of the ruthenium concentration profile, the stabilizing component and the substrate on the stability of oxide coatings",
volume = "339",
number = "1-2",
pages = "147-165",
doi = "10.1016/0022-0728(92)80449-E"
}

Jovanović, V. M., Dekanski, A., Despotov, P., Nikolić, B. Ž.,& Atanasoski, R. T.. (1992). The roles of the ruthenium concentration profile, the stabilizing component and the substrate on the stability of oxide coatings. in Journal of Electroanalytical Chemistry
Elsevier., 339(1-2), 147-165.
https://doi.org/10.1016/0022-0728(92)80449-E

Jovanović VM, Dekanski A, Despotov P, Nikolić BŽ, Atanasoski RT. The roles of the ruthenium concentration profile, the stabilizing component and the substrate on the stability of oxide coatings. in Journal of Electroanalytical Chemistry. 1992;339(1-2):147-165.
doi:10.1016/0022-0728(92)80449-E .

Jovanović, Vladislava M., Dekanski, Aleksandar, Despotov, P., Nikolić, Branislav Ž., Atanasoski, Radoslav T., "The roles of the ruthenium concentration profile, the stabilizing component and the substrate on the stability of oxide coatings" in Journal of Electroanalytical Chemistry, 339, no. 1-2 (1992):147-165,
https://doi.org/10.1016/0022-0728(92)80449-E . .

TY  - JOUR
AU  - Ragoisha, Genady
AU  - Jovanović, Vladislava M.
AU  - Avramov Ivić, Milka
AU  - Atanasoski, Radoslav T.
AU  - Smyrl, William H.
PY  - 1991
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3658
AB  - Small organic molecules (HCOOH, C,H,(OH),, CH,OH, CH,O, etc.) have become more interesting with the possibility of their application in fuel cells. Therefore, the anodic oxidation of such molecules has been studied on a number of noble metals. The present paper is intended to expand these investigations by introducing glassy carbon as an electrode material and/or a support to enhance the catalytic activity of silver deposited on its surface.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T2  - Journal of Electroanalytical Chemistry
T1  - Anodic oxidation of small organic molecules on silver modified glassy carbon electrodes
VL  - 319
IS  - 1-2
SP  - 373
EP  - 379
DO  - 10.1016/0022-0728(91)87094-K
ER  - 

@article{
author = "Ragoisha, Genady and Jovanović, Vladislava M. and Avramov Ivić, Milka and Atanasoski, Radoslav T. and Smyrl, William H.",
year = "1991",
abstract = "Small organic molecules (HCOOH, C,H,(OH),, CH,OH, CH,O, etc.) have become more interesting with the possibility of their application in fuel cells. Therefore, the anodic oxidation of such molecules has been studied on a number of noble metals. The present paper is intended to expand these investigations by introducing glassy carbon as an electrode material and/or a support to enhance the catalytic activity of silver deposited on its surface.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry, Journal of Electroanalytical Chemistry",
title = "Anodic oxidation of small organic molecules on silver modified glassy carbon electrodes",
volume = "319",
number = "1-2",
pages = "373-379",
doi = "10.1016/0022-0728(91)87094-K"
}

Ragoisha, G., Jovanović, V. M., Avramov Ivić, M., Atanasoski, R. T.,& Smyrl, W. H.. (1991). Anodic oxidation of small organic molecules on silver modified glassy carbon electrodes. in Journal of Electroanalytical Chemistry
Elsevier., 319(1-2), 373-379.
https://doi.org/10.1016/0022-0728(91)87094-K

Ragoisha G, Jovanović VM, Avramov Ivić M, Atanasoski RT, Smyrl WH. Anodic oxidation of small organic molecules on silver modified glassy carbon electrodes. in Journal of Electroanalytical Chemistry. 1991;319(1-2):373-379.
doi:10.1016/0022-0728(91)87094-K .

Ragoisha, Genady, Jovanović, Vladislava M., Avramov Ivić, Milka, Atanasoski, Radoslav T., Smyrl, William H., "Anodic oxidation of small organic molecules on silver modified glassy carbon electrodes" in Journal of Electroanalytical Chemistry, 319, no. 1-2 (1991):373-379,
https://doi.org/10.1016/0022-0728(91)87094-K . .

TY  - JOUR
AU  - Atanasoska, Ljiljana
AU  - Atanasoski, Radoslav
AU  - Trasatti, Sergio
PY  - 1990
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4088
AB  - The surface composition of RuO2+IrO2 mixed oxide layers (1-2 μm thick) deposited on titanium by thermal degradation of the corresponding chlorides in aqueous or isopropanol solutions has been investigated. A surface enrichment with Ir, more pronounced for the layers obtained from isopropanol, has always been found. Electrochemical data reflecting the surface properties of RuO2+IrO2 at the surface.
PB  - Elsevier
T2  - Vaccum
T1  - XPS and AES study of mixed layers of RuO2 and IrO2
VL  - 40
IS  - 1-2
SP  - 91
EP  - 94
DO  - 10.1016/0042-207X(90)90127-K
ER  - 

@article{
author = "Atanasoska, Ljiljana and Atanasoski, Radoslav and Trasatti, Sergio",
year = "1990",
abstract = "The surface composition of RuO2+IrO2 mixed oxide layers (1-2 μm thick) deposited on titanium by thermal degradation of the corresponding chlorides in aqueous or isopropanol solutions has been investigated. A surface enrichment with Ir, more pronounced for the layers obtained from isopropanol, has always been found. Electrochemical data reflecting the surface properties of RuO2+IrO2 at the surface.",
publisher = "Elsevier",
journal = "Vaccum",
title = "XPS and AES study of mixed layers of RuO2 and IrO2",
volume = "40",
number = "1-2",
pages = "91-94",
doi = "10.1016/0042-207X(90)90127-K"
}

Atanasoska, L., Atanasoski, R.,& Trasatti, S.. (1990). XPS and AES study of mixed layers of RuO2 and IrO2. in Vaccum
Elsevier., 40(1-2), 91-94.
https://doi.org/10.1016/0042-207X(90)90127-K

Atanasoska L, Atanasoski R, Trasatti S. XPS and AES study of mixed layers of RuO2 and IrO2. in Vaccum. 1990;40(1-2):91-94.
doi:10.1016/0042-207X(90)90127-K .

Atanasoska, Ljiljana, Atanasoski, Radoslav, Trasatti, Sergio, "XPS and AES study of mixed layers of RuO2 and IrO2" in Vaccum, 40, no. 1-2 (1990):91-94,
https://doi.org/10.1016/0042-207X(90)90127-K . .

TY  - JOUR
AU  - Kozlowski, Mark R.
AU  - Smyrl, William H.
AU  - Atanasoska, Ljiljana L.
AU  - Atanasoski, Radoslav T.
PY  - 1989
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4202
AB  - Auger depth profiling was used to determine the local film thickness of a thin anodic oxide grown on a polycrystalline Ti substrate. The oxide thickness was studied as a function of substrate crystallography and final growth voltage. These results were related to local photocurrent measurements obtained using photoelectrochemical microscopy. Variations in the film thickness are too small to account for the non-uniform photocurrent response. The non-uniform photoresponse is instead attributed to variations in the defect density of the oxide
PB  - Elsevier
T2  - Electrochimica Acta
T1  - Local film thickness and photoresponse of thin anodic TiO2 films on polycrystalline titanium
VL  - 34
IS  - 12
SP  - 1763
EP  - 1768
DO  - 10.1016/0013-4686(89)85062-5
ER  - 

@article{
author = "Kozlowski, Mark R. and Smyrl, William H. and Atanasoska, Ljiljana L. and Atanasoski, Radoslav T.",
year = "1989",
abstract = "Auger depth profiling was used to determine the local film thickness of a thin anodic oxide grown on a polycrystalline Ti substrate. The oxide thickness was studied as a function of substrate crystallography and final growth voltage. These results were related to local photocurrent measurements obtained using photoelectrochemical microscopy. Variations in the film thickness are too small to account for the non-uniform photocurrent response. The non-uniform photoresponse is instead attributed to variations in the defect density of the oxide",
publisher = "Elsevier",
journal = "Electrochimica Acta",
title = "Local film thickness and photoresponse of thin anodic TiO2 films on polycrystalline titanium",
volume = "34",
number = "12",
pages = "1763-1768",
doi = "10.1016/0013-4686(89)85062-5"
}

Kozlowski, M. R., Smyrl, W. H., Atanasoska, L. L.,& Atanasoski, R. T.. (1989). Local film thickness and photoresponse of thin anodic TiO2 films on polycrystalline titanium. in Electrochimica Acta
Elsevier., 34(12), 1763-1768.
https://doi.org/10.1016/0013-4686(89)85062-5

Kozlowski MR, Smyrl WH, Atanasoska LL, Atanasoski RT. Local film thickness and photoresponse of thin anodic TiO2 films on polycrystalline titanium. in Electrochimica Acta. 1989;34(12):1763-1768.
doi:10.1016/0013-4686(89)85062-5 .

Kozlowski, Mark R., Smyrl, William H., Atanasoska, Ljiljana L., Atanasoski, Radoslav T., "Local film thickness and photoresponse of thin anodic TiO2 films on polycrystalline titanium" in Electrochimica Acta, 34, no. 12 (1989):1763-1768,
https://doi.org/10.1016/0013-4686(89)85062-5 . .

TY  - JOUR
AU  - Atanasoska, Ljiljana L.
AU  - O'Grady, William E.
AU  - Atanasoski, Radoslav T.
AU  - Pollak, Fred Hugo
PY  - 1988
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4213
AB  - The (110) and the (100) surfaces of RuO2 show well defined LEED patterns. The surface lattice dimensions agree within 5% with the values predicted from X-ray diffraction. Both surfaces undergo a series of reversible surface reconstructions which result in well defined LEED patterns. These states come about from the loss of surface oxygen and each oxygen and each state is characterized by a well defined O Ru ratio. The final state is an overlayer of Ru metal. Furthermore, nearly equal concentrations of RuO3 are observed on all of the surfaces regardless of the structure which is present. This suggests that RuO3 plays a significant role in the stability of RuO2 surfaces.
PB  - Elsevier
T2  - Surface Science
T1  - The surface structure of RuO2: A leed, auger and XPS study of the (110) and (100) faces
VL  - 202
IS  - 1-2
SP  - 142
EP  - 166
DO  - 10.1016/0039-6028(88)90066-0
ER  - 

@article{
author = "Atanasoska, Ljiljana L. and O'Grady, William E. and Atanasoski, Radoslav T. and Pollak, Fred Hugo",
year = "1988",
abstract = "The (110) and the (100) surfaces of RuO2 show well defined LEED patterns. The surface lattice dimensions agree within 5% with the values predicted from X-ray diffraction. Both surfaces undergo a series of reversible surface reconstructions which result in well defined LEED patterns. These states come about from the loss of surface oxygen and each oxygen and each state is characterized by a well defined O Ru ratio. The final state is an overlayer of Ru metal. Furthermore, nearly equal concentrations of RuO3 are observed on all of the surfaces regardless of the structure which is present. This suggests that RuO3 plays a significant role in the stability of RuO2 surfaces.",
publisher = "Elsevier",
journal = "Surface Science",
title = "The surface structure of RuO2: A leed, auger and XPS study of the (110) and (100) faces",
volume = "202",
number = "1-2",
pages = "142-166",
doi = "10.1016/0039-6028(88)90066-0"
}

Atanasoska, L. L., O'Grady, W. E., Atanasoski, R. T.,& Pollak, F. H.. (1988). The surface structure of RuO2: A leed, auger and XPS study of the (110) and (100) faces. in Surface Science
Elsevier., 202(1-2), 142-166.
https://doi.org/10.1016/0039-6028(88)90066-0

Atanasoska LL, O'Grady WE, Atanasoski RT, Pollak FH. The surface structure of RuO2: A leed, auger and XPS study of the (110) and (100) faces. in Surface Science. 1988;202(1-2):142-166.
doi:10.1016/0039-6028(88)90066-0 .

Atanasoska, Ljiljana L., O'Grady, William E., Atanasoski, Radoslav T., Pollak, Fred Hugo, "The surface structure of RuO2: A leed, auger and XPS study of the (110) and (100) faces" in Surface Science, 202, no. 1-2 (1988):142-166,
https://doi.org/10.1016/0039-6028(88)90066-0 . .

TY  - JOUR
AU  - Kozlowski, Mark R.
AU  - Tyler, Paul S.
AU  - Smyrl, William H.
AU  - Atanasoski, Radoslav T.
PY  - 1988
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4217
AB  - Thin electrochemically grown oxide films on polycrystalline titanium substrates were examined by photoelectrochemical and electron diffraction techniques. Photoelectrochemical microscopy, based on illumination by a focused laser beam, was used to measure the local photoresponse of the oxide films. For oxide films grown slowly (1 nm/h)if, by ramping the electrode potential at 0.1 mV/s, the oxide photoresponse was found to map the grain structure of the underlying substrate. As the oxide growth rate was increased the photoresponse became more homogeneous and the average photocurrent decreased. The photoresponse heterogeneities were associated with variations in the structure of the oxide film. Electron diffraction studies showed that for slowly grown films, an ordered oxide structure was present with a preferential growth direction of [110] occurring on some substrate grains. As the oxide growth rate was increased the film structure became more homogeneous and the average oxide crystalline size decreased. The decrease in oxide crystallinity with increase in oxide growth rate was also observed in photospectroscopy measurements as a loss of the 3.7 eV direct bandgap. For all oxide films studied here, rutile was the only identifiable phase.
PB  - Elsevier
T2  - Surface Science
T1  - Photoelectrochemical microscopy of oxide films on metals: Ti/TiO2 interface
VL  - 194
IS  - 3
SP  - 505
EP  - 530
DO  - 10.1016/0039-6028(88)90866-7
ER  - 

@article{
author = "Kozlowski, Mark R. and Tyler, Paul S. and Smyrl, William H. and Atanasoski, Radoslav T.",
year = "1988",
abstract = "Thin electrochemically grown oxide films on polycrystalline titanium substrates were examined by photoelectrochemical and electron diffraction techniques. Photoelectrochemical microscopy, based on illumination by a focused laser beam, was used to measure the local photoresponse of the oxide films. For oxide films grown slowly (1 nm/h)if, by ramping the electrode potential at 0.1 mV/s, the oxide photoresponse was found to map the grain structure of the underlying substrate. As the oxide growth rate was increased the photoresponse became more homogeneous and the average photocurrent decreased. The photoresponse heterogeneities were associated with variations in the structure of the oxide film. Electron diffraction studies showed that for slowly grown films, an ordered oxide structure was present with a preferential growth direction of [110] occurring on some substrate grains. As the oxide growth rate was increased the film structure became more homogeneous and the average oxide crystalline size decreased. The decrease in oxide crystallinity with increase in oxide growth rate was also observed in photospectroscopy measurements as a loss of the 3.7 eV direct bandgap. For all oxide films studied here, rutile was the only identifiable phase.",
publisher = "Elsevier",
journal = "Surface Science",
title = "Photoelectrochemical microscopy of oxide films on metals: Ti/TiO2 interface",
volume = "194",
number = "3",
pages = "505-530",
doi = "10.1016/0039-6028(88)90866-7"
}

Kozlowski, M. R., Tyler, P. S., Smyrl, W. H.,& Atanasoski, R. T.. (1988). Photoelectrochemical microscopy of oxide films on metals: Ti/TiO2 interface. in Surface Science
Elsevier., 194(3), 505-530.
https://doi.org/10.1016/0039-6028(88)90866-7

Kozlowski MR, Tyler PS, Smyrl WH, Atanasoski RT. Photoelectrochemical microscopy of oxide films on metals: Ti/TiO2 interface. in Surface Science. 1988;194(3):505-530.
doi:10.1016/0039-6028(88)90866-7 .

Kozlowski, Mark R., Tyler, Paul S., Smyrl, William H., Atanasoski, Radoslav T., "Photoelectrochemical microscopy of oxide films on metals: Ti/TiO2 interface" in Surface Science, 194, no. 3 (1988):505-530,
https://doi.org/10.1016/0039-6028(88)90866-7 . .

TY  - JOUR
AU  - Angelinetta, Claudio
AU  - Trasatti, Sergio P.
AU  - Atanasoska, Ljiljana L.
AU  - Atanasoski, Radoslav T.
PY  - 1986
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4158
AB  - The surface properties of RuO2 + IrO2 mixed oxide layers deposited on Ti by thermal decomposition of the corresponding chlorides in aqueous solutions have been investigated by means of cyclic voltammetry and ex situ UHV (AES and XPS) techniques. The data obtained have shown that the surface is enriched with Ir and also that the bulk composition is likely to be inhomogenous. The surface composition estimated on the basis of the voltammetric curves has been found to agree excellently with the results of ex situ surface analysis. Finally, the samples have been found to "absorb" protons from the solution through a mechanism which does not interfere with the estimation of the electrochemically active surface area on the basis of the voltammetric charge.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Surface properties of RuO2 + IrO2 mixed oxide electrodes
VL  - 214
IS  - 1-2
SP  - 535
EP  - 546
DO  - 10.1016/0022-0728(86)80122-X
ER  - 

@article{
author = "Angelinetta, Claudio and Trasatti, Sergio P. and Atanasoska, Ljiljana L. and Atanasoski, Radoslav T.",
year = "1986",
abstract = "The surface properties of RuO2 + IrO2 mixed oxide layers deposited on Ti by thermal decomposition of the corresponding chlorides in aqueous solutions have been investigated by means of cyclic voltammetry and ex situ UHV (AES and XPS) techniques. The data obtained have shown that the surface is enriched with Ir and also that the bulk composition is likely to be inhomogenous. The surface composition estimated on the basis of the voltammetric curves has been found to agree excellently with the results of ex situ surface analysis. Finally, the samples have been found to "absorb" protons from the solution through a mechanism which does not interfere with the estimation of the electrochemically active surface area on the basis of the voltammetric charge.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Surface properties of RuO2 + IrO2 mixed oxide electrodes",
volume = "214",
number = "1-2",
pages = "535-546",
doi = "10.1016/0022-0728(86)80122-X"
}

Angelinetta, C., Trasatti, S. P., Atanasoska, L. L.,& Atanasoski, R. T.. (1986). Surface properties of RuO2 + IrO2 mixed oxide electrodes. in Journal of Electroanalytical Chemistry
Elsevier., 214(1-2), 535-546.
https://doi.org/10.1016/0022-0728(86)80122-X

Angelinetta C, Trasatti SP, Atanasoska LL, Atanasoski RT. Surface properties of RuO2 + IrO2 mixed oxide electrodes. in Journal of Electroanalytical Chemistry. 1986;214(1-2):535-546.
doi:10.1016/0022-0728(86)80122-X .

Angelinetta, Claudio, Trasatti, Sergio P., Atanasoska, Ljiljana L., Atanasoski, Radoslav T., "Surface properties of RuO2 + IrO2 mixed oxide electrodes" in Journal of Electroanalytical Chemistry, 214, no. 1-2 (1986):535-546,
https://doi.org/10.1016/0022-0728(86)80122-X . .

TY  - JOUR
AU  - Dražić, Dragutin M.
AU  - Zečević, Strahinja K.
AU  - Atanasoski, Radoslav
AU  - Despić, Aleksandar
PY  - 1983
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4415
AB  - Aluminum has been known to exhibit widely different electrochemical properties in different aqueous electrolytes. Thus, OH- ions in strongly alkaline solutions reveal its strong affinity to water by dissolving its protective oxide film. The metal establishes a very negative electrode potential, undergoing violent corrosion resulting in the evolution of hydrogen and the formation of aluminate ions. In this communication, some experiments on the effect of activity promoting anions are presented and a model is forwarded for a possible explanation of the observed phenomena.
PB  - Elsevier
T2  - Electrochimica Acta
T1  - The effect of anions on the electrochemical behaviour of aluminium
VL  - 28
IS  - 5
SP  - 751
EP  - 755
DO  - 10.1016/0013-4686(83)85076-2
ER  - 

@article{
author = "Dražić, Dragutin M. and Zečević, Strahinja K. and Atanasoski, Radoslav and Despić, Aleksandar",
year = "1983",
abstract = "Aluminum has been known to exhibit widely different electrochemical properties in different aqueous electrolytes. Thus, OH- ions in strongly alkaline solutions reveal its strong affinity to water by dissolving its protective oxide film. The metal establishes a very negative electrode potential, undergoing violent corrosion resulting in the evolution of hydrogen and the formation of aluminate ions. In this communication, some experiments on the effect of activity promoting anions are presented and a model is forwarded for a possible explanation of the observed phenomena.",
publisher = "Elsevier",
journal = "Electrochimica Acta",
title = "The effect of anions on the electrochemical behaviour of aluminium",
volume = "28",
number = "5",
pages = "751-755",
doi = "10.1016/0013-4686(83)85076-2"
}

Dražić, D. M., Zečević, S. K., Atanasoski, R.,& Despić, A.. (1983). The effect of anions on the electrochemical behaviour of aluminium. in Electrochimica Acta
Elsevier., 28(5), 751-755.
https://doi.org/10.1016/0013-4686(83)85076-2

Dražić DM, Zečević SK, Atanasoski R, Despić A. The effect of anions on the electrochemical behaviour of aluminium. in Electrochimica Acta. 1983;28(5):751-755.
doi:10.1016/0013-4686(83)85076-2 .

Dražić, Dragutin M., Zečević, Strahinja K., Atanasoski, Radoslav, Despić, Aleksandar, "The effect of anions on the electrochemical behaviour of aluminium" in Electrochimica Acta, 28, no. 5 (1983):751-755,
https://doi.org/10.1016/0013-4686(83)85076-2 . .

TY  - JOUR
AU  - Despić, Aleksandar
AU  - Dražić, Dragutin M.
AU  - Zečević, Strahinja K.
AU  - Atanasoski, Radoslav
PY  - 1981
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4414
AB  - Two types of anodic oxidation of aluminum have been recognized in the past: a) oxidation requiring a steady increase of voltage drop across the interface up to a few hundred volts in order to overcome the resistance of increasingly thick compact oxide layer and maintain a steady oxidation current, and b) a porous oxide layer forming oxidation resulting in layers of significant thickness, rather regular structure and with good adsorbing qualities (representing the basis of decorative anodization processes). The third type of oxidation is recognized, following seemingly normal anodic dissolution kinetics. This type of dissolution has been obtained in chloride, chlorate, and perchlorate solution and in some other electrolytes. In this third type, it has been found recently, however, that a careful elimination of pseudo-ohmic overpotential leads to an unusual type of polarization behavior, whereby after reaching some current density range, the polarization of the aluminum-electrolyte interface alone, decreases with increasing current density in an approximately linear. It is the purpose of this short communication to report in more detail about this phenomenon which is tantamount to the appearance of negative equivalent resistance at the surface.
PB  - Elsevier
T2  - Electrochimica Acta
T1  - Abnormal polarization change in anodic dissolution of aluminium at high current densities
VL  - 26
IS  - 1
SP  - 173
EP  - 177
DO  - 10.1016/0013-4686(81)80021-7
ER  - 

@article{
author = "Despić, Aleksandar and Dražić, Dragutin M. and Zečević, Strahinja K. and Atanasoski, Radoslav",
year = "1981",
abstract = "Two types of anodic oxidation of aluminum have been recognized in the past: a) oxidation requiring a steady increase of voltage drop across the interface up to a few hundred volts in order to overcome the resistance of increasingly thick compact oxide layer and maintain a steady oxidation current, and b) a porous oxide layer forming oxidation resulting in layers of significant thickness, rather regular structure and with good adsorbing qualities (representing the basis of decorative anodization processes). The third type of oxidation is recognized, following seemingly normal anodic dissolution kinetics. This type of dissolution has been obtained in chloride, chlorate, and perchlorate solution and in some other electrolytes. In this third type, it has been found recently, however, that a careful elimination of pseudo-ohmic overpotential leads to an unusual type of polarization behavior, whereby after reaching some current density range, the polarization of the aluminum-electrolyte interface alone, decreases with increasing current density in an approximately linear. It is the purpose of this short communication to report in more detail about this phenomenon which is tantamount to the appearance of negative equivalent resistance at the surface.",
publisher = "Elsevier",
journal = "Electrochimica Acta",
title = "Abnormal polarization change in anodic dissolution of aluminium at high current densities",
volume = "26",
number = "1",
pages = "173-177",
doi = "10.1016/0013-4686(81)80021-7"
}

Despić, A., Dražić, D. M., Zečević, S. K.,& Atanasoski, R.. (1981). Abnormal polarization change in anodic dissolution of aluminium at high current densities. in Electrochimica Acta
Elsevier., 26(1), 173-177.
https://doi.org/10.1016/0013-4686(81)80021-7

Despić A, Dražić DM, Zečević SK, Atanasoski R. Abnormal polarization change in anodic dissolution of aluminium at high current densities. in Electrochimica Acta. 1981;26(1):173-177.
doi:10.1016/0013-4686(81)80021-7 .

Despić, Aleksandar, Dražić, Dragutin M., Zečević, Strahinja K., Atanasoski, Radoslav, "Abnormal polarization change in anodic dissolution of aluminium at high current densities" in Electrochimica Acta, 26, no. 1 (1981):173-177,
https://doi.org/10.1016/0013-4686(81)80021-7 . .

TY  - JOUR
AU  - Adžić, Radoslav R.
AU  - Tripković, Amalija
AU  - Atanasoski, Radoslav
PY  - 1978
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2756
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T2  - Journal of Electroanalytical Chemistry
T1  - Oxygen reduction of electrode surfaces modified by foreign metal adatoms
VL  - 94
IS  - 3
SP  - 231
EP  - 235
DO  - 10.1016/S0022-0728(78)80318-0
ER  - 

@article{
author = "Adžić, Radoslav R. and Tripković, Amalija and Atanasoski, Radoslav",
year = "1978",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry, Journal of Electroanalytical Chemistry",
title = "Oxygen reduction of electrode surfaces modified by foreign metal adatoms",
volume = "94",
number = "3",
pages = "231-235",
doi = "10.1016/S0022-0728(78)80318-0"
}

Adžić, R. R., Tripković, A.,& Atanasoski, R.. (1978). Oxygen reduction of electrode surfaces modified by foreign metal adatoms. in Journal of Electroanalytical Chemistry
Elsevier., 94(3), 231-235.
https://doi.org/10.1016/S0022-0728(78)80318-0

Adžić RR, Tripković A, Atanasoski R. Oxygen reduction of electrode surfaces modified by foreign metal adatoms. in Journal of Electroanalytical Chemistry. 1978;94(3):231-235.
doi:10.1016/S0022-0728(78)80318-0 .

Adžić, Radoslav R., Tripković, Amalija, Atanasoski, Radoslav, "Oxygen reduction of electrode surfaces modified by foreign metal adatoms" in Journal of Electroanalytical Chemistry, 94, no. 3 (1978):231-235,
https://doi.org/10.1016/S0022-0728(78)80318-0 . .

TY  - JOUR
AU  - Atanasoski, Radoslav
AU  - Nikolić, B. Ž.
AU  - Jakšić, M. M.
AU  - Despić, Aleksandar R.
PY  - 1975
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3158
AB  - The use of dimensionally stable titanium anodes activated with Pt, Ir or ruthenium oxide for electrolytic chlorate production has been investigated. Simultaneous measurements were made of the amount of noble metal at the surface and of electrode activity, as functions of time of electrolysis at constant current and temperature. After more than 400 days of operation, an electrode with 7 g m−2 of surface of noble metals exhibits good polarization characteristics as well as freedom from corrosion of the coating.
PB  - Springer Science and Business Media LLC
T2  - Journal of Applied Electrochemistry
T1  - Platinum-iridium catalyzed titanium anode. I. Properties and use in chlorate electrolysis
VL  - 5
IS  - 2
SP  - 155
EP  - 158
DO  - 10.1007/BF00613220
ER  - 

@article{
author = "Atanasoski, Radoslav and Nikolić, B. Ž. and Jakšić, M. M. and Despić, Aleksandar R.",
year = "1975",
abstract = "The use of dimensionally stable titanium anodes activated with Pt, Ir or ruthenium oxide for electrolytic chlorate production has been investigated. Simultaneous measurements were made of the amount of noble metal at the surface and of electrode activity, as functions of time of electrolysis at constant current and temperature. After more than 400 days of operation, an electrode with 7 g m−2 of surface of noble metals exhibits good polarization characteristics as well as freedom from corrosion of the coating.",
publisher = "Springer Science and Business Media LLC",
journal = "Journal of Applied Electrochemistry",
title = "Platinum-iridium catalyzed titanium anode. I. Properties and use in chlorate electrolysis",
volume = "5",
number = "2",
pages = "155-158",
doi = "10.1007/BF00613220"
}

Atanasoski, R., Nikolić, B. Ž., Jakšić, M. M.,& Despić, A. R.. (1975). Platinum-iridium catalyzed titanium anode. I. Properties and use in chlorate electrolysis. in Journal of Applied Electrochemistry
Springer Science and Business Media LLC., 5(2), 155-158.
https://doi.org/10.1007/BF00613220

Atanasoski R, Nikolić BŽ, Jakšić MM, Despić AR. Platinum-iridium catalyzed titanium anode. I. Properties and use in chlorate electrolysis. in Journal of Applied Electrochemistry. 1975;5(2):155-158.
doi:10.1007/BF00613220 .

Atanasoski, Radoslav, Nikolić, B. Ž., Jakšić, M. M., Despić, Aleksandar R., "Platinum-iridium catalyzed titanium anode. I. Properties and use in chlorate electrolysis" in Journal of Applied Electrochemistry, 5, no. 2 (1975):155-158,
https://doi.org/10.1007/BF00613220 . .