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dc.creatorGojković, SL
dc.creatorVidakovic, TR
dc.creatorDurovic, DR
dc.date.accessioned2018-03-01T19:19:53Z
dc.date.available2018-03-01T19:19:53Z
dc.date.issued2003
dc.identifier.issn0013-4686
dc.identifier.issn1873-3859
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/2674
dc.description.abstractMethanol electrooxidation was investigated on the carbon-supported PtRu electrocatalyst (1:1 atomic ratio) in acid media. X-ray diffraction measurement indicated alloying of Pt and Ru. Cyclic voltammetry of the sample reflects the amount of Ruin the catalyst and its ability to adsorb OH radicals. Tafel plots for the oxidation of 0.02-3 M methanol in the solutions containing 0.05-1 M HClO4 and in the temperature range 27-40 degreesC showed reasonably well-defined linear region with the slope of about 115 mV dec(-1) at the low currents, irrespective of the experimental conditions employed. Reaction order with respect to methanol was found to be 0.5. A correlation between methanol oxidation rate and pseudocapacitive current of OH adsorption on Ru sites was established. It was proposed that bifunctional mechanism is operative with the reaction between methanol residues adsorbed on Pt sites and OH radicals adsorbed on Ru sites as the rate-determining step. (C) 2003 Elsevier Ltd. All rights reserved.en
dc.rightsrestrictedAccessen
dc.sourceElectrochimica Actaen
dc.subjectelectrochemical oxidationen
dc.subjectmethanolen
dc.subjectplatinum-ruthenium-supported catalysten
dc.subjectfuel cell catalysten
dc.titleKinetic study of methanol oxidation on carbon-supported PtRu electrocatalysten
dc.typearticleen
dcterms.abstractГојковиц, СЛ; Видаковиц, ТР; Дуровиц, ДР;
dc.citation.volume48
dc.citation.issue24
dc.citation.spage3607
dc.citation.epage3614
dc.identifier.wos000185674600004
dc.identifier.doi10.1016/S0013-4686(03)00481-X
dc.citation.rankM23
dc.identifier.scopus2-s2.0-0141569819


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