Приказ основних података о документу

dc.creatorGojković, Snežana Lj.
dc.creatorVidaković, Tanja
dc.creatorDurović, DR
dc.date.accessioned2021-03-10T10:10:27Z
dc.date.available2021-03-10T10:10:27Z
dc.date.issued2003
dc.identifier.issn0013-4686
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/586
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.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.rightsrestrictedAccess
dc.sourceElectrochimica Acta
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.typearticle
dc.rights.licenseARR
dc.citation.epage3614
dc.citation.issue24
dc.citation.other48(24): 3607-3614
dc.citation.rankM22
dc.citation.spage3607
dc.citation.volume48
dc.identifier.doi10.1016/S0013-4686(03)00481-X
dc.identifier.scopus2-s2.0-0141569819
dc.identifier.wos000185674600004
dc.type.versionpublishedVersion


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Приказ основних података о документу