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dc.creatorGojković, Snežana Lj.
dc.creatorBabić, Biljana M.
dc.creatorRadmilovíć, Velimir R.
dc.creatorKrstajic, N. V.
dc.date.accessioned2018-03-01T21:06:59Z
dc.date.available2018-03-01T21:06:59Z
dc.date.issued2010
dc.identifier.issn1572-6657
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/3924
dc.description.abstractTiO2 doped by 0.5% Nb was synthesized by the acid-catalyzed sol-gel method. BET surface area was determined to be 72 m(2) g(-1). XRD measurements showed that TiO2 has structure of anatase with similar to 13 nm average crystallite size. Using Nb-TiO2 as a support, Pt/Nb-TiO2 and Pt-Ru/Nb-TiO2 were prepared by borohydride reduction method. TEM imaging of Pt-Ru/Nb-TiO2 revealed rather uniform distribution of the metallic particles on the support with a mean diameter of 3.8 nm. According to XRD analysis, Pt-Ru particles consist of the solid solution of Ru in Pt (40 at.% Ru) and a small amount of RuO2. Cyclic voltammetry of Pt/Nb-TiO2 and Pt-Ru/Nb-TiO2 indicated good conductivity of the supporting material. Oxidation of pre-adsorbed CO and methanol on Pt-Ru/Nb-TiO2 was faster than on Pt/Nb-TiO2. However, when the activities of Pt/Nb-TiO2 and Pt-Ru/Nb-TiO2 for methanol oxidation were compared to those of Pt/XC-72 and Pt-Ru/XC-72, no significant difference was observed. This means that Nb-TiO2 is a promising replacement for high area carbon supports in PEMFC anodes, but without the influence on the reaction kinetics. (C) 2009 Elsevier B.V. All rights reserved.en
dc.relationMinistry of Science and Development, Republic of Serbia [142038]
dc.rightsrestrictedAccessen
dc.sourceJournal of Electroanalytical Chemistryen
dc.subjectOxide supporten
dc.subjectTiO2en
dc.subjectPt-Ru nanocatalysten
dc.subjectMethanol oxidationen
dc.subjectPolymer electrolyte membrane fuel cellen
dc.titleNb-doped TiO2 as a support of Pt and Pt-Ru anode catalyst for PEMFCsen
dc.typearticleen
dcterms.abstractГојковиц, С. Љ.; Бабиц, Б. М.; Радмиловиц, В. Р.; Крстајиц, Н. В.;
dc.citation.volume639
dc.citation.issue1-2
dc.citation.spage161
dc.citation.epage166
dc.identifier.wos000275137400023
dc.identifier.doi10.1016/j.jelechem.2009.12.004
dc.citation.rankM21
dc.identifier.scopus2-s2.0-75349102327


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