TY  - JOUR
AU  - Lović, Jelena
AU  - Obradović, Maja
AU  - Tripković, Dušan
AU  - Popović, Ksenija
AU  - Jovanović, Vladislava M.
AU  - Gojković, Snežana Lj.
AU  - Tripković, Amalija
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2148
AB  - Formic acid oxidation was studied on a new prepared Pt2Bi characterized by X-ray diffraction spectroscopy (phase composition), scanning tunneling microscopy (STM) (surface morphology), and COads stripping voltammetry (surface composition). Bulk composition of Pt2Bi revealed two phases-55% PtBi alloy and 45% Pt. Estimated contribution of pure Pt on the Pt2Bi surface (43.5%) determined by COads stripping voltammetry corresponds closely to bulk composition. Pt2Bi reveals high activity and stability in formic acid oxidation. High activity originates from the fact that formic acid oxidation proceeds completely through dehydrogenation path based on an ensemble effect. The high stability of Pt2Bi surface is induced by the suppression of Bi leaching as it was evidenced by insignificant changes of surface morphology and surface roughness shown by STM images before and after electrochemical treatment in formic acid containing solution. Pt2Bi is found to be powerful catalyst exhibiting up to two orders of magnitude larger current densities at 0.0 V and onset potential shifted for similar to 0.2 V to more negative value relative to Pt under steady-state condition.
PB  - Springer, New York
T2  - Electrocatalysis
T1  - High Activity and Stability of Pt2Bi Catalyst in Formic Acid Oxidation
EP  - 352
IS  - 3-4
SP  - 346
VL  - 3
DO  - 10.1007/s12678-012-0099-9
ER  - 

@article{
author = "Lović, Jelena and Obradović, Maja and Tripković, Dušan and Popović, Ksenija and Jovanović, Vladislava M. and Gojković, Snežana Lj. and Tripković, Amalija",
year = "2012",
abstract = "Formic acid oxidation was studied on a new prepared Pt2Bi characterized by X-ray diffraction spectroscopy (phase composition), scanning tunneling microscopy (STM) (surface morphology), and COads stripping voltammetry (surface composition). Bulk composition of Pt2Bi revealed two phases-55% PtBi alloy and 45% Pt. Estimated contribution of pure Pt on the Pt2Bi surface (43.5%) determined by COads stripping voltammetry corresponds closely to bulk composition. Pt2Bi reveals high activity and stability in formic acid oxidation. High activity originates from the fact that formic acid oxidation proceeds completely through dehydrogenation path based on an ensemble effect. The high stability of Pt2Bi surface is induced by the suppression of Bi leaching as it was evidenced by insignificant changes of surface morphology and surface roughness shown by STM images before and after electrochemical treatment in formic acid containing solution. Pt2Bi is found to be powerful catalyst exhibiting up to two orders of magnitude larger current densities at 0.0 V and onset potential shifted for similar to 0.2 V to more negative value relative to Pt under steady-state condition.",
publisher = "Springer, New York",
journal = "Electrocatalysis",
title = "High Activity and Stability of Pt2Bi Catalyst in Formic Acid Oxidation",
pages = "352-346",
number = "3-4",
volume = "3",
doi = "10.1007/s12678-012-0099-9"
}

Lović, J., Obradović, M., Tripković, D., Popović, K., Jovanović, V. M., Gojković, S. Lj.,& Tripković, A.. (2012). High Activity and Stability of Pt2Bi Catalyst in Formic Acid Oxidation. in Electrocatalysis
Springer, New York., 3(3-4), 346-352.
https://doi.org/10.1007/s12678-012-0099-9

Lović J, Obradović M, Tripković D, Popović K, Jovanović VM, Gojković SL, Tripković A. High Activity and Stability of Pt2Bi Catalyst in Formic Acid Oxidation. in Electrocatalysis. 2012;3(3-4):346-352.
doi:10.1007/s12678-012-0099-9 .

Lović, Jelena, Obradović, Maja, Tripković, Dušan, Popović, Ksenija, Jovanović, Vladislava M., Gojković, Snežana Lj., Tripković, Amalija, "High Activity and Stability of Pt2Bi Catalyst in Formic Acid Oxidation" in Electrocatalysis, 3, no. 3-4 (2012):346-352,
https://doi.org/10.1007/s12678-012-0099-9 . .

TY  - JOUR
AU  - Obradović, Maja
AU  - Tripković, Amalija
AU  - Gojković, Snežana Lj.
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2234
AB  - Bulk Pt3Co and nanosized Pt3Co and PtCo alloys supported on high area carbon were investigated as the electrocatalysts for the COads and HCOOH oxidation. Pt3Co alloy with Co electrochemically leached from the surface (Pt skeleton) was employed to separate electronic from ensemble and bifunctional effects of Co. Cyclic voltammetry in 0.1 M HClO4 showed reduced amount of adsorbed hydrogen on Pt sites on Pt3Co alloy compared to pure Pt. However, no significant difference in hydrogen adsorption/desorption and Pt-oxide reduction features between Pt3Co with Pt skeleton structure and bulk Pt was observed. The oxidation of COads on Pt3Co alloy commenced earlier than on Pt, but this effect on Pt3Co with Pt skeleton structure was minor indicating that bifunctional mechanism is stronger than the electronic modification of Pt by Co. The HCOOH oxidation rate on Pt3Co alloy was about seven times higher than on bulk Pt when the reaction rates were compared at 0.4 V, i.e., in the middle of the potential range for the HCOOH oxidation. Like in the case of COads oxidation, Pt skeleton showed similar activity as bulk Pt indicating that the ensemble effect is responsible for the enhanced activity of Pt3Co alloy toward HCOOH oxidation. The comparison of COads and HCOOH oxidation on Pt3Co/C and PtCo/C with the same reaction on Pt/C were qualitatively the same as on bulk materials.
PB  - Springer, New York
T2  - Journal of Solid State Electrochemistry
T1  - Oxidation of carbon monoxide and formic acid on bulk and nanosized Pt-Co alloys
EP  - 595
IS  - 2
SP  - 587
VL  - 16
DO  - 10.1007/s10008-011-1389-5
ER  - 

@article{
author = "Obradović, Maja and Tripković, Amalija and Gojković, Snežana Lj.",
year = "2012",
abstract = "Bulk Pt3Co and nanosized Pt3Co and PtCo alloys supported on high area carbon were investigated as the electrocatalysts for the COads and HCOOH oxidation. Pt3Co alloy with Co electrochemically leached from the surface (Pt skeleton) was employed to separate electronic from ensemble and bifunctional effects of Co. Cyclic voltammetry in 0.1 M HClO4 showed reduced amount of adsorbed hydrogen on Pt sites on Pt3Co alloy compared to pure Pt. However, no significant difference in hydrogen adsorption/desorption and Pt-oxide reduction features between Pt3Co with Pt skeleton structure and bulk Pt was observed. The oxidation of COads on Pt3Co alloy commenced earlier than on Pt, but this effect on Pt3Co with Pt skeleton structure was minor indicating that bifunctional mechanism is stronger than the electronic modification of Pt by Co. The HCOOH oxidation rate on Pt3Co alloy was about seven times higher than on bulk Pt when the reaction rates were compared at 0.4 V, i.e., in the middle of the potential range for the HCOOH oxidation. Like in the case of COads oxidation, Pt skeleton showed similar activity as bulk Pt indicating that the ensemble effect is responsible for the enhanced activity of Pt3Co alloy toward HCOOH oxidation. The comparison of COads and HCOOH oxidation on Pt3Co/C and PtCo/C with the same reaction on Pt/C were qualitatively the same as on bulk materials.",
publisher = "Springer, New York",
journal = "Journal of Solid State Electrochemistry",
title = "Oxidation of carbon monoxide and formic acid on bulk and nanosized Pt-Co alloys",
pages = "595-587",
number = "2",
volume = "16",
doi = "10.1007/s10008-011-1389-5"
}

Obradović, M., Tripković, A.,& Gojković, S. Lj.. (2012). Oxidation of carbon monoxide and formic acid on bulk and nanosized Pt-Co alloys. in Journal of Solid State Electrochemistry
Springer, New York., 16(2), 587-595.
https://doi.org/10.1007/s10008-011-1389-5

Obradović M, Tripković A, Gojković SL. Oxidation of carbon monoxide and formic acid on bulk and nanosized Pt-Co alloys. in Journal of Solid State Electrochemistry. 2012;16(2):587-595.
doi:10.1007/s10008-011-1389-5 .

Obradović, Maja, Tripković, Amalija, Gojković, Snežana Lj., "Oxidation of carbon monoxide and formic acid on bulk and nanosized Pt-Co alloys" in Journal of Solid State Electrochemistry, 16, no. 2 (2012):587-595,
https://doi.org/10.1007/s10008-011-1389-5 . .

TY  - JOUR
AU  - Obradović, Maja
AU  - Rogan, Jelena
AU  - Babić, Biljana M.
AU  - Tripković, Amalija
AU  - Gautam, A. R. S.
AU  - Radmilović, Velimir R.
AU  - Gojković, Snežana Lj.
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2242
AB  - Pt-Au nanoparticles supported on high area carbon were prepared by simultaneous reduction of Au and Pt precursors and by reduction of Pt precursor on already prepared Au nanoparticles. The first method produced a solid solution of Pt in Au containing similar to 5% Pt with the remaining Pt on the nanoparticles' surface. For the Pt:Au precursor ratio of 1:4 and 1:9, the surface ratio was found to be 0.70:0.30 and 0.55:0.45, respectively. By the second method with the Pt:Au precursors ratio of 1:12, the surface ratio was 0.30:0.70. The voltammetric peaks of Pt-oxide reduction and CO(ads) oxidation demonstrated electronic modification of Pt by Au in all catalysts. With decreasing Pt:Au surface ratio the activity for HCOOH oxidation increases and surface coverage by CO(ads) decreases. The highest activity under potentiodynamic and quasi steady-state conditions without poisoning by CO(ads) was observed for the catalyst with the lowest Pt:Au surface ratio. Chronoamperometic test showed that its high catalytic activity is associated with a high deactivation rate. It was postulated that too strong adsorption of a reactive or non-reactive intermediate caused by electron modification of Pt by underlying Au, is responsible for the deactivation. This result stresses that high Pt dispersion, necessary for promotion of the dehydrogenation path in HCOOH oxidation, can produce too strong adsorption of intermediates causing deactivation of the catalyst.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Power Sources
T1  - Formic acid oxidation on Pt-Au nanoparticles: Relation between the catalyst activity and the poisoning rate
EP  - 79
SP  - 72
VL  - 197
DO  - 10.1016/j.jpowsour.2011.09.043
ER  - 

@article{
author = "Obradović, Maja and Rogan, Jelena and Babić, Biljana M. and Tripković, Amalija and Gautam, A. R. S. and Radmilović, Velimir R. and Gojković, Snežana Lj.",
year = "2012",
abstract = "Pt-Au nanoparticles supported on high area carbon were prepared by simultaneous reduction of Au and Pt precursors and by reduction of Pt precursor on already prepared Au nanoparticles. The first method produced a solid solution of Pt in Au containing similar to 5% Pt with the remaining Pt on the nanoparticles' surface. For the Pt:Au precursor ratio of 1:4 and 1:9, the surface ratio was found to be 0.70:0.30 and 0.55:0.45, respectively. By the second method with the Pt:Au precursors ratio of 1:12, the surface ratio was 0.30:0.70. The voltammetric peaks of Pt-oxide reduction and CO(ads) oxidation demonstrated electronic modification of Pt by Au in all catalysts. With decreasing Pt:Au surface ratio the activity for HCOOH oxidation increases and surface coverage by CO(ads) decreases. The highest activity under potentiodynamic and quasi steady-state conditions without poisoning by CO(ads) was observed for the catalyst with the lowest Pt:Au surface ratio. Chronoamperometic test showed that its high catalytic activity is associated with a high deactivation rate. It was postulated that too strong adsorption of a reactive or non-reactive intermediate caused by electron modification of Pt by underlying Au, is responsible for the deactivation. This result stresses that high Pt dispersion, necessary for promotion of the dehydrogenation path in HCOOH oxidation, can produce too strong adsorption of intermediates causing deactivation of the catalyst.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Power Sources",
title = "Formic acid oxidation on Pt-Au nanoparticles: Relation between the catalyst activity and the poisoning rate",
pages = "79-72",
volume = "197",
doi = "10.1016/j.jpowsour.2011.09.043"
}

Obradović, M., Rogan, J., Babić, B. M., Tripković, A., Gautam, A. R. S., Radmilović, V. R.,& Gojković, S. Lj.. (2012). Formic acid oxidation on Pt-Au nanoparticles: Relation between the catalyst activity and the poisoning rate. in Journal of Power Sources
Elsevier Science Bv, Amsterdam., 197, 72-79.
https://doi.org/10.1016/j.jpowsour.2011.09.043

Obradović M, Rogan J, Babić BM, Tripković A, Gautam ARS, Radmilović VR, Gojković SL. Formic acid oxidation on Pt-Au nanoparticles: Relation between the catalyst activity and the poisoning rate. in Journal of Power Sources. 2012;197:72-79.
doi:10.1016/j.jpowsour.2011.09.043 .

Obradović, Maja, Rogan, Jelena, Babić, Biljana M., Tripković, Amalija, Gautam, A. R. S., Radmilović, Velimir R., Gojković, Snežana Lj., "Formic acid oxidation on Pt-Au nanoparticles: Relation between the catalyst activity and the poisoning rate" in Journal of Power Sources, 197 (2012):72-79,
https://doi.org/10.1016/j.jpowsour.2011.09.043 . .

TY  - JOUR
AU  - Stevanović, Sanja
AU  - Tripković, Dušan
AU  - Rogan, Jelena
AU  - Popović, Ksenija
AU  - Lović, Jelena
AU  - Tripković, Amalija
AU  - Jovanović, Vladislava M.
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2173
AB  - High surface area carbon-supported Pt, PtRh, and PtSn catalysts were synthesized by microwave-assisted polyol procedure and tested for ethanol oxidation in perchloric acid. The catalysts were characterized by thermogravimetric analysis (TGA), X-ray diffraction (XRD), scanning tunnelling microscopy (STM), TEM, and EDX techniques. STM analysis of unsupported catalysts shows that small particles (similar to 2 nm) with a narrow size distribution are obtained. TEM and XRD examinations of supported catalysts revealed an increase in particle size upon deposition on carbon support (diameter similar to aEuro parts per thousand 3 nm). The diffraction peaks of the bimetallic catalysts in X-ray diffraction patterns are slightly shifted to lower (PtSn/C) or higher (PtRh/C) 2 theta values with respect to the corresponding peaks at Pt/C catalyst as a consequence of alloy formation. Oxidation of ethanol is significantly improved at PtSn/C with the onset potential shifted for similar to aEuro parts per thousand 150 mV to more negative values and the increase of activity for approximately three times in comparison to Pt/C catalyst. This is the lowest onset potential found for ethanol oxidation at PtSn catalysts with a similar composition. Chronoamperometric measurements confirmed that PtSn/C is notably less poisoned than Pt/C catalyst. PtRh/C catalyst exhibited mild enhancement of overall electrochemical reaction in comparison to Pt/C.
PB  - Springer, New York
T2  - Journal of Solid State Electrochemistry
T1  - Microwave-assisted polyol synthesis of carbon-supported platinum-based bimetallic catalysts for ethanol oxidation
EP  - 3157
IS  - 10
SP  - 3147
VL  - 16
DO  - 10.1007/s10008-012-1755-y
ER  - 

@article{
author = "Stevanović, Sanja and Tripković, Dušan and Rogan, Jelena and Popović, Ksenija and Lović, Jelena and Tripković, Amalija and Jovanović, Vladislava M.",
year = "2012",
abstract = "High surface area carbon-supported Pt, PtRh, and PtSn catalysts were synthesized by microwave-assisted polyol procedure and tested for ethanol oxidation in perchloric acid. The catalysts were characterized by thermogravimetric analysis (TGA), X-ray diffraction (XRD), scanning tunnelling microscopy (STM), TEM, and EDX techniques. STM analysis of unsupported catalysts shows that small particles (similar to 2 nm) with a narrow size distribution are obtained. TEM and XRD examinations of supported catalysts revealed an increase in particle size upon deposition on carbon support (diameter similar to aEuro parts per thousand 3 nm). The diffraction peaks of the bimetallic catalysts in X-ray diffraction patterns are slightly shifted to lower (PtSn/C) or higher (PtRh/C) 2 theta values with respect to the corresponding peaks at Pt/C catalyst as a consequence of alloy formation. Oxidation of ethanol is significantly improved at PtSn/C with the onset potential shifted for similar to aEuro parts per thousand 150 mV to more negative values and the increase of activity for approximately three times in comparison to Pt/C catalyst. This is the lowest onset potential found for ethanol oxidation at PtSn catalysts with a similar composition. Chronoamperometric measurements confirmed that PtSn/C is notably less poisoned than Pt/C catalyst. PtRh/C catalyst exhibited mild enhancement of overall electrochemical reaction in comparison to Pt/C.",
publisher = "Springer, New York",
journal = "Journal of Solid State Electrochemistry",
title = "Microwave-assisted polyol synthesis of carbon-supported platinum-based bimetallic catalysts for ethanol oxidation",
pages = "3157-3147",
number = "10",
volume = "16",
doi = "10.1007/s10008-012-1755-y"
}

Stevanović, S., Tripković, D., Rogan, J., Popović, K., Lović, J., Tripković, A.,& Jovanović, V. M.. (2012). Microwave-assisted polyol synthesis of carbon-supported platinum-based bimetallic catalysts for ethanol oxidation. in Journal of Solid State Electrochemistry
Springer, New York., 16(10), 3147-3157.
https://doi.org/10.1007/s10008-012-1755-y

Stevanović S, Tripković D, Rogan J, Popović K, Lović J, Tripković A, Jovanović VM. Microwave-assisted polyol synthesis of carbon-supported platinum-based bimetallic catalysts for ethanol oxidation. in Journal of Solid State Electrochemistry. 2012;16(10):3147-3157.
doi:10.1007/s10008-012-1755-y .

Stevanović, Sanja, Tripković, Dušan, Rogan, Jelena, Popović, Ksenija, Lović, Jelena, Tripković, Amalija, Jovanović, Vladislava M., "Microwave-assisted polyol synthesis of carbon-supported platinum-based bimetallic catalysts for ethanol oxidation" in Journal of Solid State Electrochemistry, 16, no. 10 (2012):3147-3157,
https://doi.org/10.1007/s10008-012-1755-y . .

TY  - JOUR
AU  - Stevanović, Sanja
AU  - Tripković, Dušan
AU  - Poleti, Dejan
AU  - Rogan, Jelena
AU  - Tripković, Amalija
AU  - Jovanović, Vladislava M.
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1798
AB  - Carbon-supported Pt and Pt-Rh-Sn catalysts were synthesized by the microwave-polyol method in ethylene glycol solution and were investigated in the ethanol electro-oxidation reaction. The catalysts were characterized in terms of structure, morphology and composition employing the X-ray diffraction (XRD), scanning tunneling microscopy and energy-dispersive X-ray spectroscopy techniques. The STM analysis indicated rather uniform particles and particle sizes below 2 nm for both catalysts. The XRD analysis of the Pt/C catalyst revealed two phases, one with the main characteristic peaks of the face-centered cubic crystal structure (fcc) of platinum and the other related to the graphite-like structure of the carbon support, Vulcan XC-72R. However, in the XRD pattern of the Pt-Rh-Sn/C catalyst, diffraction peaks for Pt, Rh or Sn could not be resolved, indicating extremely low crystallinity. The small particle sizes and homogeneous size distributions of both catalysts could be attributed to the advantages of the microwave-assisted modified polyol process in ethylene glycol solution. The Pt-Rh-Sn/C catalyst was highly active for ethanol oxidation with the onset potential shifted by more than 150 mV to more negative values and with currents nearly 5 times higher in comparison to the Pt/C catalyst. The stability tests of the catalysts, as studied by chronoamperometric experiments, revealed that the Pt-Rh-Sn/C catalyst was evidently less poisoned than the Pt/C catalyst. The increased activity of Pt-Rh-Sn/C in comparison to Pt/C catalyst was most probably promoted by the bi-functional mechanism and the electronic effect of the alloyed metals.
AB  - Pt i Pt-Rh-Sn katalizatori na ugljeniku razvijene površine su sintetizovani poliol-mikrotalasnim postupkom u rastvoru etilenglikola i ispitivani za reakciju eletrohemijske oksidacije etanola u kiseloj sredini. Katalizatori su okarakterisani strukturno, morfološki i po sastavu korišćenjem XRD, STM i EDX tehnika. STM analiza je potvrdila da su Pt i Pt-Rh-Sn čestice uniformne veličine i prečnika manjeg od 2 nm. XRD analiza Pt/C katalizatora pokazala je prisustvo dve faze, jedne sa glavnim karakterističnim pikovima za pljosno-centriranu kubnu kristalnu strukturu platine (111, 200, 220 i 311) i druge sa difrakcionim pikom na 2q oko 25° karakterističnim za heksagonalnu strukturu vulkana XC-72R (ugljeničnog nosača). XRD analiza Pt-Rh-Sn/C katalizatora nije pokazala karakteristične pikove, što je indikacija veoma male kristaličnosti katalizatora. Aktivnost katalizatora ispitivana je potenciodinamičkim i hronoamperometrijskim merenjima. Pt-Rh-Sn/C katalizator je veoma aktivan za oksidaciju etanola sa početkom reakcije na potencijalima za oko 150 mV pomerenim ka negativnijim vrednostima i strujama koje su oko pet puta veće u poređenju sa Pt/C katalizatorom. Stabilnost katalizatora ispitivana hronoamperometrijski pokazala je da se Pt-Rh-Sn/C katalizator manje truje od Pt/C katalizatora. Mala veličina i homogena distribucija čestica mogu se pripisati prednostima mikrotalasne sinteze i modifikovanog poliol postupka u rastvoru etilenglikola. Veća aktivnost Pt-Rh-Sn/C katalizatora u poređenju sa Pt/C katalizatorom posledica je bi-funkcionalnog mehanizma i elektronskog (ligand) efekta metala u sintetizovanoj leguri.
PB  - Serbian Chemical Society, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Microwave synthesis and characterization of Pt and Pt-Rh-Sn electrocatalysts for ethanol oxidation
T1  - Mikrotalasna sinteza i karakterizacija Pt i Pt-Rh-Sn katalizatora za oksidaciju etanola
EP  - 1685
IS  - 12
SP  - 1673
VL  - 76
UR  - https://hdl.handle.net/21.15107/rcub_technorep_1798
ER  - 

@article{
author = "Stevanović, Sanja and Tripković, Dušan and Poleti, Dejan and Rogan, Jelena and Tripković, Amalija and Jovanović, Vladislava M.",
year = "2011",
abstract = "Carbon-supported Pt and Pt-Rh-Sn catalysts were synthesized by the microwave-polyol method in ethylene glycol solution and were investigated in the ethanol electro-oxidation reaction. The catalysts were characterized in terms of structure, morphology and composition employing the X-ray diffraction (XRD), scanning tunneling microscopy and energy-dispersive X-ray spectroscopy techniques. The STM analysis indicated rather uniform particles and particle sizes below 2 nm for both catalysts. The XRD analysis of the Pt/C catalyst revealed two phases, one with the main characteristic peaks of the face-centered cubic crystal structure (fcc) of platinum and the other related to the graphite-like structure of the carbon support, Vulcan XC-72R. However, in the XRD pattern of the Pt-Rh-Sn/C catalyst, diffraction peaks for Pt, Rh or Sn could not be resolved, indicating extremely low crystallinity. The small particle sizes and homogeneous size distributions of both catalysts could be attributed to the advantages of the microwave-assisted modified polyol process in ethylene glycol solution. The Pt-Rh-Sn/C catalyst was highly active for ethanol oxidation with the onset potential shifted by more than 150 mV to more negative values and with currents nearly 5 times higher in comparison to the Pt/C catalyst. The stability tests of the catalysts, as studied by chronoamperometric experiments, revealed that the Pt-Rh-Sn/C catalyst was evidently less poisoned than the Pt/C catalyst. The increased activity of Pt-Rh-Sn/C in comparison to Pt/C catalyst was most probably promoted by the bi-functional mechanism and the electronic effect of the alloyed metals., Pt i Pt-Rh-Sn katalizatori na ugljeniku razvijene površine su sintetizovani poliol-mikrotalasnim postupkom u rastvoru etilenglikola i ispitivani za reakciju eletrohemijske oksidacije etanola u kiseloj sredini. Katalizatori su okarakterisani strukturno, morfološki i po sastavu korišćenjem XRD, STM i EDX tehnika. STM analiza je potvrdila da su Pt i Pt-Rh-Sn čestice uniformne veličine i prečnika manjeg od 2 nm. XRD analiza Pt/C katalizatora pokazala je prisustvo dve faze, jedne sa glavnim karakterističnim pikovima za pljosno-centriranu kubnu kristalnu strukturu platine (111, 200, 220 i 311) i druge sa difrakcionim pikom na 2q oko 25° karakterističnim za heksagonalnu strukturu vulkana XC-72R (ugljeničnog nosača). XRD analiza Pt-Rh-Sn/C katalizatora nije pokazala karakteristične pikove, što je indikacija veoma male kristaličnosti katalizatora. Aktivnost katalizatora ispitivana je potenciodinamičkim i hronoamperometrijskim merenjima. Pt-Rh-Sn/C katalizator je veoma aktivan za oksidaciju etanola sa početkom reakcije na potencijalima za oko 150 mV pomerenim ka negativnijim vrednostima i strujama koje su oko pet puta veće u poređenju sa Pt/C katalizatorom. Stabilnost katalizatora ispitivana hronoamperometrijski pokazala je da se Pt-Rh-Sn/C katalizator manje truje od Pt/C katalizatora. Mala veličina i homogena distribucija čestica mogu se pripisati prednostima mikrotalasne sinteze i modifikovanog poliol postupka u rastvoru etilenglikola. Veća aktivnost Pt-Rh-Sn/C katalizatora u poređenju sa Pt/C katalizatorom posledica je bi-funkcionalnog mehanizma i elektronskog (ligand) efekta metala u sintetizovanoj leguri.",
publisher = "Serbian Chemical Society, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Microwave synthesis and characterization of Pt and Pt-Rh-Sn electrocatalysts for ethanol oxidation, Mikrotalasna sinteza i karakterizacija Pt i Pt-Rh-Sn katalizatora za oksidaciju etanola",
pages = "1685-1673",
number = "12",
volume = "76",
url = "https://hdl.handle.net/21.15107/rcub_technorep_1798"
}

Stevanović, S., Tripković, D., Poleti, D., Rogan, J., Tripković, A.,& Jovanović, V. M.. (2011). Microwave synthesis and characterization of Pt and Pt-Rh-Sn electrocatalysts for ethanol oxidation. in Journal of the Serbian Chemical Society
Serbian Chemical Society, Belgrade., 76(12), 1673-1685.
https://hdl.handle.net/21.15107/rcub_technorep_1798

Stevanović S, Tripković D, Poleti D, Rogan J, Tripković A, Jovanović VM. Microwave synthesis and characterization of Pt and Pt-Rh-Sn electrocatalysts for ethanol oxidation. in Journal of the Serbian Chemical Society. 2011;76(12):1673-1685.
https://hdl.handle.net/21.15107/rcub_technorep_1798 .

Stevanović, Sanja, Tripković, Dušan, Poleti, Dejan, Rogan, Jelena, Tripković, Amalija, Jovanović, Vladislava M., "Microwave synthesis and characterization of Pt and Pt-Rh-Sn electrocatalysts for ethanol oxidation" in Journal of the Serbian Chemical Society, 76, no. 12 (2011):1673-1685,
https://hdl.handle.net/21.15107/rcub_technorep_1798 .

TY  - JOUR
AU  - Stevanović, Sanja
AU  - Tripković, Dušan
AU  - Rogan, Jelena
AU  - Minić, Dragica M.
AU  - Gavrilović, Aleksandra
AU  - Tripković, Amalija
AU  - Jovanović, Vladislava M.
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1899
AB  - High surface area carbon supported Pt and Pt3Sn catalysts were synthesized by microwave irradiation and investigated in the ethanol electro-oxidation reaction. The catalysts were obtained using a modified polyol method in an ethylene glycol solution and were characterized in terms of structure, morphology and composition by employing XRD, STM and EDX techniques. The diffraction peaks of Pt3Sn/C catalyst in XRD patterns are shifted to lower 2 theta values with respect to the corresponding peaks at Pt/C catalyst as a consequence of alloy formation between Pt and Sn. Particle size analysis from STM and XRD shows that Pt and Pt3Sn clusters are of a small diameter (similar to 2 nm) with a narrow size distribution. Pt3Sn/C catalyst is highly active in ethanol oxidation with the onset potential shifted for similar to 150 mV to more negative values and with similar to 2 times higher currents in comparison to Pt/C.
PB  - Maik Nauka/Interperiodica/Springer, New York
T2  - Russian Journal of Physical Chemistry A
T1  - Enhanced activity in ethanol oxidation of Pt3Sn electrocatalysts synthesized by microwave irradiation
EP  - 2304
IS  - 13
SP  - 2299
VL  - 85
DO  - 10.1134/S0036024411130309
ER  - 

@article{
author = "Stevanović, Sanja and Tripković, Dušan and Rogan, Jelena and Minić, Dragica M. and Gavrilović, Aleksandra and Tripković, Amalija and Jovanović, Vladislava M.",
year = "2011",
abstract = "High surface area carbon supported Pt and Pt3Sn catalysts were synthesized by microwave irradiation and investigated in the ethanol electro-oxidation reaction. The catalysts were obtained using a modified polyol method in an ethylene glycol solution and were characterized in terms of structure, morphology and composition by employing XRD, STM and EDX techniques. The diffraction peaks of Pt3Sn/C catalyst in XRD patterns are shifted to lower 2 theta values with respect to the corresponding peaks at Pt/C catalyst as a consequence of alloy formation between Pt and Sn. Particle size analysis from STM and XRD shows that Pt and Pt3Sn clusters are of a small diameter (similar to 2 nm) with a narrow size distribution. Pt3Sn/C catalyst is highly active in ethanol oxidation with the onset potential shifted for similar to 150 mV to more negative values and with similar to 2 times higher currents in comparison to Pt/C.",
publisher = "Maik Nauka/Interperiodica/Springer, New York",
journal = "Russian Journal of Physical Chemistry A",
title = "Enhanced activity in ethanol oxidation of Pt3Sn electrocatalysts synthesized by microwave irradiation",
pages = "2304-2299",
number = "13",
volume = "85",
doi = "10.1134/S0036024411130309"
}

Stevanović, S., Tripković, D., Rogan, J., Minić, D. M., Gavrilović, A., Tripković, A.,& Jovanović, V. M.. (2011). Enhanced activity in ethanol oxidation of Pt3Sn electrocatalysts synthesized by microwave irradiation. in Russian Journal of Physical Chemistry A
Maik Nauka/Interperiodica/Springer, New York., 85(13), 2299-2304.
https://doi.org/10.1134/S0036024411130309

Stevanović S, Tripković D, Rogan J, Minić DM, Gavrilović A, Tripković A, Jovanović VM. Enhanced activity in ethanol oxidation of Pt3Sn electrocatalysts synthesized by microwave irradiation. in Russian Journal of Physical Chemistry A. 2011;85(13):2299-2304.
doi:10.1134/S0036024411130309 .

Stevanović, Sanja, Tripković, Dušan, Rogan, Jelena, Minić, Dragica M., Gavrilović, Aleksandra, Tripković, Amalija, Jovanović, Vladislava M., "Enhanced activity in ethanol oxidation of Pt3Sn electrocatalysts synthesized by microwave irradiation" in Russian Journal of Physical Chemistry A, 85, no. 13 (2011):2299-2304,
https://doi.org/10.1134/S0036024411130309 . .

TY  - JOUR
AU  - Obradović, Maja
AU  - Tripković, Amalija
AU  - Gojković, Snežana Lj.
PY  - 2009
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1417
AB  - We have investigated the oxidation of HCOOH on Au-modified Pt (Au"Pt) and Pt-modified Au (Pt")/Au) electrodes to establish the role of the ensemble and the electronic effect in the catalysis of this reaction. The surfaces were modified by the electrodeposition of sub-monolayers. Cyclic voltammetry in the supporting electrolyte and COads stripping have shown that the electronic Pt-Au interactions are insignificant on Au"Pt. but considerable on Pt"Au. oxidation of COads on Au"Pt commenced at the same potentials as on bare Pt, whereas on Pt"Au the oxidation was delayed for similar to 0.2 V. Both types of Pt-Au surfaces were found to be more active toward the oxidation of HCOOH compared to bare Pt, exhibiting the maximum activity at Pt fraction between 0.15 and 0.25 with the enhancement factor of more than two orders of magnitude. On bimetallic surfaces the amount of COads formed by HCOOH dehydration was low and decreased with decreasing Pt fraction. it was concluded that the high activity of Pt-Au surfaces is caused by the increased selectivity toward the HCOOH dehydrogenation. Similar behavior of Pt-Au surfaces in the HCOOH oxidation, regardless on the Pt-Au electronic interactions, leads to the conclusion that the ensemble effect plays dominant role in the catalysis of HCOOH oxidation.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Electrochimica Acta
T1  - The origin of high activity of Pt-Au surfaces in the formic acid oxidation
EP  - 209
IS  - 1
SP  - 204
VL  - 55
DO  - 10.1016/j.electacta.2009.08.038
ER  - 

@article{
author = "Obradović, Maja and Tripković, Amalija and Gojković, Snežana Lj.",
year = "2009",
abstract = "We have investigated the oxidation of HCOOH on Au-modified Pt (Au"Pt) and Pt-modified Au (Pt")/Au) electrodes to establish the role of the ensemble and the electronic effect in the catalysis of this reaction. The surfaces were modified by the electrodeposition of sub-monolayers. Cyclic voltammetry in the supporting electrolyte and COads stripping have shown that the electronic Pt-Au interactions are insignificant on Au"Pt. but considerable on Pt"Au. oxidation of COads on Au"Pt commenced at the same potentials as on bare Pt, whereas on Pt"Au the oxidation was delayed for similar to 0.2 V. Both types of Pt-Au surfaces were found to be more active toward the oxidation of HCOOH compared to bare Pt, exhibiting the maximum activity at Pt fraction between 0.15 and 0.25 with the enhancement factor of more than two orders of magnitude. On bimetallic surfaces the amount of COads formed by HCOOH dehydration was low and decreased with decreasing Pt fraction. it was concluded that the high activity of Pt-Au surfaces is caused by the increased selectivity toward the HCOOH dehydrogenation. Similar behavior of Pt-Au surfaces in the HCOOH oxidation, regardless on the Pt-Au electronic interactions, leads to the conclusion that the ensemble effect plays dominant role in the catalysis of HCOOH oxidation.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Electrochimica Acta",
title = "The origin of high activity of Pt-Au surfaces in the formic acid oxidation",
pages = "209-204",
number = "1",
volume = "55",
doi = "10.1016/j.electacta.2009.08.038"
}

Obradović, M., Tripković, A.,& Gojković, S. Lj.. (2009). The origin of high activity of Pt-Au surfaces in the formic acid oxidation. in Electrochimica Acta
Pergamon-Elsevier Science Ltd, Oxford., 55(1), 204-209.
https://doi.org/10.1016/j.electacta.2009.08.038

Obradović M, Tripković A, Gojković SL. The origin of high activity of Pt-Au surfaces in the formic acid oxidation. in Electrochimica Acta. 2009;55(1):204-209.
doi:10.1016/j.electacta.2009.08.038 .

Obradović, Maja, Tripković, Amalija, Gojković, Snežana Lj., "The origin of high activity of Pt-Au surfaces in the formic acid oxidation" in Electrochimica Acta, 55, no. 1 (2009):204-209,
https://doi.org/10.1016/j.electacta.2009.08.038 . .

TY  - JOUR
AU  - Gojković, Snežana Lj.
AU  - Tripković, Amalija
AU  - Stevanović, Rade M.
PY  - 2007
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1108
AB  - The electrochemical oxidation of methanol, 2-propanol, and their mixtures was investigated on a Pt/C thin film electrode in acid solution. It was confirmed that the oxidation of 2-propanol commences at less positive potentials than that of methanol and exhibits significantly higher oxidation current densities at low potentials. When both methanol and 2-propanol were present in the solution, the onset of the oxidation current was the same as for the oxidation of pure 2-propanol. Although both alcohols inhibit the oxidation reaction of each other to a certain extent, steady-state polarization measurements showed that their mixture provides higher current densities than single alcohols over the entire potential region from the hydrogen region to oxide formation on the Pt surface. This implies that the addition of 2-propanol into the fuel may extend the operational range of direct methanol fuel cells.
AB  - Isptivana je elektrohemijska oksidacija metanola, 2-propanola i njihovih smeša na tankom filmu Pt/C katalizatora u kiseloj sredini. Potvrđeno je da oksidacija 2-propanola počinje na manje pozitivnim potencijalima nego oksidacija metanola i da daje znatno veće gustine struja pri nižim potencijalima. Kada su i metanol i 2-propanol prisutni u rastvoru, struja oksidacije se pojavljuje na istom potencijalu kao u slučaju čistog 2-propanola. Mada oba alkohola inhibiraju oksidaciju onog drugog u izvesnoj meri, stacionarma merenja su pokazala da njihova smeša daje veće gustine struja od pojedinačnih alkohola u celoj oblasti potencijala od vodonične oblasti pa do formiranja oksida na platini. To ukazuje da se radni opseg gorivog sprega sa metanolom može povećati dodatkom 2-propanola u gorivo.
PB  - Serbian Chemical Society, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Mixtures of methanol and 2-propanol as a potential fuel for direct alcohol fuel cells
T1  - Smeša metanola i 2-propanola kao potencijalno gorivo u gorivim spregovima sa alkoholom
EP  - 1425
IS  - 12
SP  - 1419
VL  - 72
UR  - https://hdl.handle.net/21.15107/rcub_technorep_1108
ER  - 

@article{
author = "Gojković, Snežana Lj. and Tripković, Amalija and Stevanović, Rade M.",
year = "2007",
abstract = "The electrochemical oxidation of methanol, 2-propanol, and their mixtures was investigated on a Pt/C thin film electrode in acid solution. It was confirmed that the oxidation of 2-propanol commences at less positive potentials than that of methanol and exhibits significantly higher oxidation current densities at low potentials. When both methanol and 2-propanol were present in the solution, the onset of the oxidation current was the same as for the oxidation of pure 2-propanol. Although both alcohols inhibit the oxidation reaction of each other to a certain extent, steady-state polarization measurements showed that their mixture provides higher current densities than single alcohols over the entire potential region from the hydrogen region to oxide formation on the Pt surface. This implies that the addition of 2-propanol into the fuel may extend the operational range of direct methanol fuel cells., Isptivana je elektrohemijska oksidacija metanola, 2-propanola i njihovih smeša na tankom filmu Pt/C katalizatora u kiseloj sredini. Potvrđeno je da oksidacija 2-propanola počinje na manje pozitivnim potencijalima nego oksidacija metanola i da daje znatno veće gustine struja pri nižim potencijalima. Kada su i metanol i 2-propanol prisutni u rastvoru, struja oksidacije se pojavljuje na istom potencijalu kao u slučaju čistog 2-propanola. Mada oba alkohola inhibiraju oksidaciju onog drugog u izvesnoj meri, stacionarma merenja su pokazala da njihova smeša daje veće gustine struja od pojedinačnih alkohola u celoj oblasti potencijala od vodonične oblasti pa do formiranja oksida na platini. To ukazuje da se radni opseg gorivog sprega sa metanolom može povećati dodatkom 2-propanola u gorivo.",
publisher = "Serbian Chemical Society, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Mixtures of methanol and 2-propanol as a potential fuel for direct alcohol fuel cells, Smeša metanola i 2-propanola kao potencijalno gorivo u gorivim spregovima sa alkoholom",
pages = "1425-1419",
number = "12",
volume = "72",
url = "https://hdl.handle.net/21.15107/rcub_technorep_1108"
}

Gojković, S. Lj., Tripković, A.,& Stevanović, R. M.. (2007). Mixtures of methanol and 2-propanol as a potential fuel for direct alcohol fuel cells. in Journal of the Serbian Chemical Society
Serbian Chemical Society, Belgrade., 72(12), 1419-1425.
https://hdl.handle.net/21.15107/rcub_technorep_1108

Gojković SL, Tripković A, Stevanović RM. Mixtures of methanol and 2-propanol as a potential fuel for direct alcohol fuel cells. in Journal of the Serbian Chemical Society. 2007;72(12):1419-1425.
https://hdl.handle.net/21.15107/rcub_technorep_1108 .

Gojković, Snežana Lj., Tripković, Amalija, Stevanović, Rade M., "Mixtures of methanol and 2-propanol as a potential fuel for direct alcohol fuel cells" in Journal of the Serbian Chemical Society, 72, no. 12 (2007):1419-1425,
https://hdl.handle.net/21.15107/rcub_technorep_1108 .

TY  - JOUR
AU  - Tripković, Amalija
AU  - Gojković, Snežana Lj.
AU  - Popović, Ksenija
AU  - Lović, Jelena
AU  - Kowal, Andrzej
PY  - 2007
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1147
AB  - Electrochemical oxidation of HCOOH in H2SO4 and HCIO4 solutions was examined on thin film Pt2RU3/C electrode. XRD pattern revealed that Pt2RU3 alloy consisted of the solid solution of Ru in Pt and the small amount of Ru or solid solution of Pt in Ru. According to STM images, Pt2RU3 particles size was between 2 and 6 nm. It was established that electrochemical oxidation of HCOOH commenced at -0.1 V versus SCE at Pt sites in the catalyst. Kinetic parameters indicated that dehydrogenation path was predominant. Dehydration occurs in parallel, but without significant poisoning by COad dowing to oxidative removal by OH species on Ru atoms. The coverage Of Pt2RU3 surface by CO preadsorbed from the solution was found to be 24% lower when the surface was modified by irreversibly adsorbed Bi. Modification by Bi also shifted the onset potential for HCOOH oxidation for about 50 m V towards more negative values and consequently, increased the reaction rate for a factor of two. It was proposed that Ru acts through bifunctional mechanism, i.e. OH species adsorbed on Ru oxidizes COad from Pt sites, while Bi hinders the adsorption of CO on Pt sites via electronic and/or ensemble effects.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Electrochimica Acta
T1  - Study of the kinetics and the influence of Bi-irr, on formic acid oxidation at Pt2RU3/C
EP  - 893
IS  - 2
SP  - 887
VL  - 53
DO  - 10.1016/j.electacta.2007.07.073
ER  - 

@article{
author = "Tripković, Amalija and Gojković, Snežana Lj. and Popović, Ksenija and Lović, Jelena and Kowal, Andrzej",
year = "2007",
abstract = "Electrochemical oxidation of HCOOH in H2SO4 and HCIO4 solutions was examined on thin film Pt2RU3/C electrode. XRD pattern revealed that Pt2RU3 alloy consisted of the solid solution of Ru in Pt and the small amount of Ru or solid solution of Pt in Ru. According to STM images, Pt2RU3 particles size was between 2 and 6 nm. It was established that electrochemical oxidation of HCOOH commenced at -0.1 V versus SCE at Pt sites in the catalyst. Kinetic parameters indicated that dehydrogenation path was predominant. Dehydration occurs in parallel, but without significant poisoning by COad dowing to oxidative removal by OH species on Ru atoms. The coverage Of Pt2RU3 surface by CO preadsorbed from the solution was found to be 24% lower when the surface was modified by irreversibly adsorbed Bi. Modification by Bi also shifted the onset potential for HCOOH oxidation for about 50 m V towards more negative values and consequently, increased the reaction rate for a factor of two. It was proposed that Ru acts through bifunctional mechanism, i.e. OH species adsorbed on Ru oxidizes COad from Pt sites, while Bi hinders the adsorption of CO on Pt sites via electronic and/or ensemble effects.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Electrochimica Acta",
title = "Study of the kinetics and the influence of Bi-irr, on formic acid oxidation at Pt2RU3/C",
pages = "893-887",
number = "2",
volume = "53",
doi = "10.1016/j.electacta.2007.07.073"
}

Tripković, A., Gojković, S. Lj., Popović, K., Lović, J.,& Kowal, A.. (2007). Study of the kinetics and the influence of Bi-irr, on formic acid oxidation at Pt2RU3/C. in Electrochimica Acta
Pergamon-Elsevier Science Ltd, Oxford., 53(2), 887-893.
https://doi.org/10.1016/j.electacta.2007.07.073

Tripković A, Gojković SL, Popović K, Lović J, Kowal A. Study of the kinetics and the influence of Bi-irr, on formic acid oxidation at Pt2RU3/C. in Electrochimica Acta. 2007;53(2):887-893.
doi:10.1016/j.electacta.2007.07.073 .

Tripković, Amalija, Gojković, Snežana Lj., Popović, Ksenija, Lović, Jelena, Kowal, Andrzej, "Study of the kinetics and the influence of Bi-irr, on formic acid oxidation at Pt2RU3/C" in Electrochimica Acta, 53, no. 2 (2007):887-893,
https://doi.org/10.1016/j.electacta.2007.07.073 . .

TY  - JOUR
AU  - Gojković, Snežana Lj.
AU  - Tripković, Amalija
AU  - Stevanović, Rade M.
AU  - Krstajić, Nedeljko V.
PY  - 2007
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1153
AB  - Surface processes on Pt4Mo alloy well-defined by X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) were studied in acid solution by cyclic voltammetry. It was established that Mo in the alloy is much more resistant toward electrochemical dissolution than pure Mo. During the potential cycling of Pt4Mo surfaces in completely quiescent electrolyte, hydrous Mo-oxide could be generated on Mo sites. Investigation of the formic acid oxidation revealed that this type of Mo-oxide enhances the reaction rate by more than I order of magnitude with respect to pure Pt. Surface poisoning by COads is significantly lower on Pt4Mo alloy than on pure Pt. The effect of hydrous Mo-oxide on the HCOOH oxidation rate was explained through the facilitated removal of the poisoning species and through its possible influence on the intrinsic rate of the direct reaction path.
PB  - Amer Chemical Soc, Washington
T2  - Langmuir
T1  - High activity of Pt4Mo alloy for the electrochemical oxidation of formic acid
EP  - 12764
IS  - 25
SP  - 12760
VL  - 23
DO  - 10.1021/la702344s
ER  - 

@article{
author = "Gojković, Snežana Lj. and Tripković, Amalija and Stevanović, Rade M. and Krstajić, Nedeljko V.",
year = "2007",
abstract = "Surface processes on Pt4Mo alloy well-defined by X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) were studied in acid solution by cyclic voltammetry. It was established that Mo in the alloy is much more resistant toward electrochemical dissolution than pure Mo. During the potential cycling of Pt4Mo surfaces in completely quiescent electrolyte, hydrous Mo-oxide could be generated on Mo sites. Investigation of the formic acid oxidation revealed that this type of Mo-oxide enhances the reaction rate by more than I order of magnitude with respect to pure Pt. Surface poisoning by COads is significantly lower on Pt4Mo alloy than on pure Pt. The effect of hydrous Mo-oxide on the HCOOH oxidation rate was explained through the facilitated removal of the poisoning species and through its possible influence on the intrinsic rate of the direct reaction path.",
publisher = "Amer Chemical Soc, Washington",
journal = "Langmuir",
title = "High activity of Pt4Mo alloy for the electrochemical oxidation of formic acid",
pages = "12764-12760",
number = "25",
volume = "23",
doi = "10.1021/la702344s"
}

Gojković, S. Lj., Tripković, A., Stevanović, R. M.,& Krstajić, N. V.. (2007). High activity of Pt4Mo alloy for the electrochemical oxidation of formic acid. in Langmuir
Amer Chemical Soc, Washington., 23(25), 12760-12764.
https://doi.org/10.1021/la702344s

Gojković SL, Tripković A, Stevanović RM, Krstajić NV. High activity of Pt4Mo alloy for the electrochemical oxidation of formic acid. in Langmuir. 2007;23(25):12760-12764.
doi:10.1021/la702344s .

Gojković, Snežana Lj., Tripković, Amalija, Stevanović, Rade M., Krstajić, Nedeljko V., "High activity of Pt4Mo alloy for the electrochemical oxidation of formic acid" in Langmuir, 23, no. 25 (2007):12760-12764,
https://doi.org/10.1021/la702344s . .

TY  - JOUR
AU  - Tripković, Amalija
AU  - Gojković, Snežana Lj.
AU  - Popović, Ksenija
AU  - Lović, Jelena
PY  - 2006
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/954
AB  - Methanol oxidation in acid solution was studied at platinum single crystals, Pt(hkl), as the model catalyst, and at nanostructural platinum supported on high surface area carbon, Pt/C, as the real catalyst. The linear extrapolation method was used to determine the beginning of hydroxyl anion adsorption. Structural sensitivity of the adsorption was proved and a correlation with the onset of the methanol oxidation current was established at all catalysts. Bisulfate and chloride anions were found to decrease the methanol oxidation rate, but probably did not influence the reaction parth. The specific activity for the reaction increased in the sequence Pt(110)  lt Pt/C  lt  Pt(111), suggesting that the activity of the supported Pt catalyst can be correlated with the activities of the dominating crystal planes on its surface.
AB  - Oksidacija metanola ispitivana je na niskoindeksnim Pt monokristalnim elektrodama (model katalizator) i na nanokatalizatoru Pt dispergovanom na aktivnom uglju kao nosaču (realni katalizator) u kiseloj sredini. Metoda linearne ekstrapolacije krivih zavisnosti količine naelektrisanja adsorpcije kiseoničnih čestica od potencijala korišćena je za određivanje početka adsorpcije OH anjona. Potvrđeno je da je adsorpcija OH čestica strukturno osetljiva reakcija i pokazana je korelacija sa početkom reakcije oksidacije metanola. Utvrđeno je da bisulfatni i hloridni anjoni iz nosećeg elektrolita smanjuju brzinu oksidacije metanola, ali verovatno ne utiču na reakcioni put. Elektrokatalitička aktivnost ispitivanih katalizatora rasla je u nizu Pt(110)  lt  Pt/C  lt  Pt(111) ukazujući na to da se aktivnost Pt nanokatalizatora može povezati sa udelima niskoindeksnih ravni na površini Pt nanočestice.
PB  - Serbian Chemical Society, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Methanol oxidation at platinum electrodes in acid solution: Comparison between model and real catalysts
T1  - Oksidacija metanola na platinskim elektrodama u kiseloj sredini - poređenje model i realnih katalizatora
EP  - 1343
IS  - 12
SP  - 1333
VL  - 71
UR  - https://hdl.handle.net/21.15107/rcub_technorep_954
ER  - 

@article{
author = "Tripković, Amalija and Gojković, Snežana Lj. and Popović, Ksenija and Lović, Jelena",
year = "2006",
abstract = "Methanol oxidation in acid solution was studied at platinum single crystals, Pt(hkl), as the model catalyst, and at nanostructural platinum supported on high surface area carbon, Pt/C, as the real catalyst. The linear extrapolation method was used to determine the beginning of hydroxyl anion adsorption. Structural sensitivity of the adsorption was proved and a correlation with the onset of the methanol oxidation current was established at all catalysts. Bisulfate and chloride anions were found to decrease the methanol oxidation rate, but probably did not influence the reaction parth. The specific activity for the reaction increased in the sequence Pt(110)  lt Pt/C  lt  Pt(111), suggesting that the activity of the supported Pt catalyst can be correlated with the activities of the dominating crystal planes on its surface., Oksidacija metanola ispitivana je na niskoindeksnim Pt monokristalnim elektrodama (model katalizator) i na nanokatalizatoru Pt dispergovanom na aktivnom uglju kao nosaču (realni katalizator) u kiseloj sredini. Metoda linearne ekstrapolacije krivih zavisnosti količine naelektrisanja adsorpcije kiseoničnih čestica od potencijala korišćena je za određivanje početka adsorpcije OH anjona. Potvrđeno je da je adsorpcija OH čestica strukturno osetljiva reakcija i pokazana je korelacija sa početkom reakcije oksidacije metanola. Utvrđeno je da bisulfatni i hloridni anjoni iz nosećeg elektrolita smanjuju brzinu oksidacije metanola, ali verovatno ne utiču na reakcioni put. Elektrokatalitička aktivnost ispitivanih katalizatora rasla je u nizu Pt(110)  lt  Pt/C  lt  Pt(111) ukazujući na to da se aktivnost Pt nanokatalizatora može povezati sa udelima niskoindeksnih ravni na površini Pt nanočestice.",
publisher = "Serbian Chemical Society, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Methanol oxidation at platinum electrodes in acid solution: Comparison between model and real catalysts, Oksidacija metanola na platinskim elektrodama u kiseloj sredini - poređenje model i realnih katalizatora",
pages = "1343-1333",
number = "12",
volume = "71",
url = "https://hdl.handle.net/21.15107/rcub_technorep_954"
}

Tripković, A., Gojković, S. Lj., Popović, K.,& Lović, J.. (2006). Methanol oxidation at platinum electrodes in acid solution: Comparison between model and real catalysts. in Journal of the Serbian Chemical Society
Serbian Chemical Society, Belgrade., 71(12), 1333-1343.
https://hdl.handle.net/21.15107/rcub_technorep_954

Tripković A, Gojković SL, Popović K, Lović J. Methanol oxidation at platinum electrodes in acid solution: Comparison between model and real catalysts. in Journal of the Serbian Chemical Society. 2006;71(12):1333-1343.
https://hdl.handle.net/21.15107/rcub_technorep_954 .

Tripković, Amalija, Gojković, Snežana Lj., Popović, Ksenija, Lović, Jelena, "Methanol oxidation at platinum electrodes in acid solution: Comparison between model and real catalysts" in Journal of the Serbian Chemical Society, 71, no. 12 (2006):1333-1343,
https://hdl.handle.net/21.15107/rcub_technorep_954 .

TY  - JOUR
AU  - Lović, Jelena
AU  - Gojković, Snežana Lj.
AU  - Popović, Ksenija
AU  - Tripković, D. V.
AU  - Tripković, Amalija
PY  - 2006
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/987
AB  - Formic acid oxidation was studied at low-index Pt single crystals (model systems) as well as at the platinum catalyst supported on high area carbon (real catalyst) in HClO4. The Pt single crystals were characterized by LEED. The LEED patterns obtained after a mild heating of flame-annealed crystals have shown clean, well ordered unreconstructured surfaces. Pt-C supported catalyst was analyzed by AFM and STM in air and by XRD. AFM and STM images revealed the presence of Pt-C agglomerates of several tenth of nm consisting of Pt particles ranged from 2 nm to 6 nm. The electrocatalytic activity of these catalysts in formic acid oxidation increased in a sequence: Pt(100)  lt  Pt(110)  lt  Pt-C/GC  lt  Pt(111).
PB  - Trans Tech Publications Ltd, Durnten-Zurich
T2  - Recent Developments in Advanced Materials and Processes
T1  - Structural effects in electrocatalysis: Formic acid oxidation at model and real Pt catalysts
EP  - 264
SP  - 259
VL  - 518
DO  - 10.4028/www.scientific.net/MSF.518.259
ER  - 

@article{
author = "Lović, Jelena and Gojković, Snežana Lj. and Popović, Ksenija and Tripković, D. V. and Tripković, Amalija",
year = "2006",
abstract = "Formic acid oxidation was studied at low-index Pt single crystals (model systems) as well as at the platinum catalyst supported on high area carbon (real catalyst) in HClO4. The Pt single crystals were characterized by LEED. The LEED patterns obtained after a mild heating of flame-annealed crystals have shown clean, well ordered unreconstructured surfaces. Pt-C supported catalyst was analyzed by AFM and STM in air and by XRD. AFM and STM images revealed the presence of Pt-C agglomerates of several tenth of nm consisting of Pt particles ranged from 2 nm to 6 nm. The electrocatalytic activity of these catalysts in formic acid oxidation increased in a sequence: Pt(100)  lt  Pt(110)  lt  Pt-C/GC  lt  Pt(111).",
publisher = "Trans Tech Publications Ltd, Durnten-Zurich",
journal = "Recent Developments in Advanced Materials and Processes",
title = "Structural effects in electrocatalysis: Formic acid oxidation at model and real Pt catalysts",
pages = "264-259",
volume = "518",
doi = "10.4028/www.scientific.net/MSF.518.259"
}

Lović, J., Gojković, S. Lj., Popović, K., Tripković, D. V.,& Tripković, A.. (2006). Structural effects in electrocatalysis: Formic acid oxidation at model and real Pt catalysts. in Recent Developments in Advanced Materials and Processes
Trans Tech Publications Ltd, Durnten-Zurich., 518, 259-264.
https://doi.org/10.4028/www.scientific.net/MSF.518.259

Lović J, Gojković SL, Popović K, Tripković DV, Tripković A. Structural effects in electrocatalysis: Formic acid oxidation at model and real Pt catalysts. in Recent Developments in Advanced Materials and Processes. 2006;518:259-264.
doi:10.4028/www.scientific.net/MSF.518.259 .

Lović, Jelena, Gojković, Snežana Lj., Popović, Ksenija, Tripković, D. V., Tripković, Amalija, "Structural effects in electrocatalysis: Formic acid oxidation at model and real Pt catalysts" in Recent Developments in Advanced Materials and Processes, 518 (2006):259-264,
https://doi.org/10.4028/www.scientific.net/MSF.518.259 . .

TY  - JOUR
AU  - Lović, Jelena
AU  - Tripković, Amalija
AU  - Gojković, Snežana Lj.
AU  - Popović, Ksenija
AU  - Tripković, Dušan
AU  - Olszewski, Piotr K.
AU  - Kowal, Andrzej
PY  - 2005
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/781
AB  - Oxidation of formic acid on the platinum catalyst supported on high area carbon was investigated by potent iodynamic and quasi-steady-state polarization measurements. It was found that the poisoning of the reaction occurred both in the hydrogen region and in the double-layer region, but poisons were formed faster at lower potentials. Kinetics of the reaction was consistent with the dual path mechanism. At lower potentials HCOOH was oxidized to CO, at the Pt sites uncovered by COads. If high coverage by the poisoning species was attained, the reaction reached the limiting current plateau and further increase of the Current densities started at the potential of COads oxidation. Kinetic parameters of the HCOOH oxidation suggested that the rate determining step was the transfer of the first electron from HCOOHads, which was adsorbed under the Temkin conditions, Oxidation of formic acid became pH-dependent reaction in the electrolytes of pH  lt  1 with the reaction order with respect to H+ ions of about - 0.8.
PB  - Elsevier Science Sa, Lausanne
T2  - Journal of Electroanalytical Chemistry
T1  - Kinetic study of formic acid oxidation on carbon-supported platinum electrocatalyst
EP  - 302
IS  - 2
SP  - 294
VL  - 581
DO  - 10.1016/j.jelechem.2005.05.002
ER  - 

@article{
author = "Lović, Jelena and Tripković, Amalija and Gojković, Snežana Lj. and Popović, Ksenija and Tripković, Dušan and Olszewski, Piotr K. and Kowal, Andrzej",
year = "2005",
abstract = "Oxidation of formic acid on the platinum catalyst supported on high area carbon was investigated by potent iodynamic and quasi-steady-state polarization measurements. It was found that the poisoning of the reaction occurred both in the hydrogen region and in the double-layer region, but poisons were formed faster at lower potentials. Kinetics of the reaction was consistent with the dual path mechanism. At lower potentials HCOOH was oxidized to CO, at the Pt sites uncovered by COads. If high coverage by the poisoning species was attained, the reaction reached the limiting current plateau and further increase of the Current densities started at the potential of COads oxidation. Kinetic parameters of the HCOOH oxidation suggested that the rate determining step was the transfer of the first electron from HCOOHads, which was adsorbed under the Temkin conditions, Oxidation of formic acid became pH-dependent reaction in the electrolytes of pH  lt  1 with the reaction order with respect to H+ ions of about - 0.8.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Journal of Electroanalytical Chemistry",
title = "Kinetic study of formic acid oxidation on carbon-supported platinum electrocatalyst",
pages = "302-294",
number = "2",
volume = "581",
doi = "10.1016/j.jelechem.2005.05.002"
}

Lović, J., Tripković, A., Gojković, S. Lj., Popović, K., Tripković, D., Olszewski, P. K.,& Kowal, A.. (2005). Kinetic study of formic acid oxidation on carbon-supported platinum electrocatalyst. in Journal of Electroanalytical Chemistry
Elsevier Science Sa, Lausanne., 581(2), 294-302.
https://doi.org/10.1016/j.jelechem.2005.05.002

Lović J, Tripković A, Gojković SL, Popović K, Tripković D, Olszewski PK, Kowal A. Kinetic study of formic acid oxidation on carbon-supported platinum electrocatalyst. in Journal of Electroanalytical Chemistry. 2005;581(2):294-302.
doi:10.1016/j.jelechem.2005.05.002 .

Lović, Jelena, Tripković, Amalija, Gojković, Snežana Lj., Popović, Ksenija, Tripković, Dušan, Olszewski, Piotr K., Kowal, Andrzej, "Kinetic study of formic acid oxidation on carbon-supported platinum electrocatalyst" in Journal of Electroanalytical Chemistry, 581, no. 2 (2005):294-302,
https://doi.org/10.1016/j.jelechem.2005.05.002 . .

TY  - JOUR
AU  - Tripković, Amalija
AU  - Popović, Ksenija
AU  - Grgur, Branimir
AU  - Blizanac, B.
AU  - Ross, P.N.
AU  - Marković, Nenad M.
PY  - 2002
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/456
AB  - The kinetics of methanol oxidation on supported 47.5 wt.% Pt and 54 wt.% Pt-Ru (with nominal Pt:Ru ratios of 2:3) catalysts are measured in 0.5 M H2SO4 and 0.1 NaOH at 295 and 333 K using thin-film rotating disk electrode (RDE) method. It was found that the activity of Pt and Pt-Ru for methanol oxidation is a strong function of pH of solution and temperature. The kinetics are much higher in alkaline than in acid solution; at 333 K, a factor of 30 for Pt and a factor of 20 for Pt2Ru3 at 0.5 V. The pH effect is attributed to the pH competitive adsorption of oxygenated species with anions from supporting electrolytes. The activity of Pt and Pt2Ru3 catalysts at 333 K is higher (a factor of 5) than at 295 K. Irrespective of pH, only negligible differences in the kinetics are observed between Pt and on high Ru content Pt alloys, presumably owing to a slow rate of methanol dehydrogenation on the Rurich surface and insufficient number of Pt sites required for dissociative chemisorption of methanol.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Electrochimica Acta
T1  - Methanol electrooxidation on supported Pt and PtRu catalysts in acid and alkaline solutions
EP  - 3714
IS  - 22-23
SP  - 3707
VL  - 47
DO  - 10.1016/S0013-4686(02)00340-7
ER  - 

@article{
author = "Tripković, Amalija and Popović, Ksenija and Grgur, Branimir and Blizanac, B. and Ross, P.N. and Marković, Nenad M.",
year = "2002",
abstract = "The kinetics of methanol oxidation on supported 47.5 wt.% Pt and 54 wt.% Pt-Ru (with nominal Pt:Ru ratios of 2:3) catalysts are measured in 0.5 M H2SO4 and 0.1 NaOH at 295 and 333 K using thin-film rotating disk electrode (RDE) method. It was found that the activity of Pt and Pt-Ru for methanol oxidation is a strong function of pH of solution and temperature. The kinetics are much higher in alkaline than in acid solution; at 333 K, a factor of 30 for Pt and a factor of 20 for Pt2Ru3 at 0.5 V. The pH effect is attributed to the pH competitive adsorption of oxygenated species with anions from supporting electrolytes. The activity of Pt and Pt2Ru3 catalysts at 333 K is higher (a factor of 5) than at 295 K. Irrespective of pH, only negligible differences in the kinetics are observed between Pt and on high Ru content Pt alloys, presumably owing to a slow rate of methanol dehydrogenation on the Rurich surface and insufficient number of Pt sites required for dissociative chemisorption of methanol.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Electrochimica Acta",
title = "Methanol electrooxidation on supported Pt and PtRu catalysts in acid and alkaline solutions",
pages = "3714-3707",
number = "22-23",
volume = "47",
doi = "10.1016/S0013-4686(02)00340-7"
}

Tripković, A., Popović, K., Grgur, B., Blizanac, B., Ross, P.N.,& Marković, N. M.. (2002). Methanol electrooxidation on supported Pt and PtRu catalysts in acid and alkaline solutions. in Electrochimica Acta
Pergamon-Elsevier Science Ltd, Oxford., 47(22-23), 3707-3714.
https://doi.org/10.1016/S0013-4686(02)00340-7

Tripković A, Popović K, Grgur B, Blizanac B, Ross P, Marković NM. Methanol electrooxidation on supported Pt and PtRu catalysts in acid and alkaline solutions. in Electrochimica Acta. 2002;47(22-23):3707-3714.
doi:10.1016/S0013-4686(02)00340-7 .

Tripković, Amalija, Popović, Ksenija, Grgur, Branimir, Blizanac, B., Ross, P.N., Marković, Nenad M., "Methanol electrooxidation on supported Pt and PtRu catalysts in acid and alkaline solutions" in Electrochimica Acta, 47, no. 22-23 (2002):3707-3714,
https://doi.org/10.1016/S0013-4686(02)00340-7 . .