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dc.contributor.authorChen, Chung-Shouen_US
dc.contributor.authorPan, Fu-Mingen_US
dc.contributor.authorYu, Hsin-Jungen_US
dc.date.accessioned2014-12-08T15:11:32Z-
dc.date.available2014-12-08T15:11:32Z-
dc.date.issued2011-05-18en_US
dc.identifier.issn0926-3373en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.apcatb.2011.03.002en_US
dc.identifier.urihttp://hdl.handle.net/11536/8848-
dc.description.abstractThe study prepared rugged Ni thin films for the study on electrocatalytic methanol oxidation reaction (MOR) in alkaline solutions. The rugged Ni thin film has a karst-like morphology, which provides a large surface area for Pt nanoparticle loading by pulse electrodeposition. Cyclic voltammetry measurements showed that the Pt/karst-Ni electrode had a high electrocatalytic activity toward MOR and CO tolerance in the KOH electrolyte. Ni(OH)(2) formed on the Ni support during the potential scan can enhance CO tolerance of Pt nanoparticles via the bi-functional mechanism. The Langmuir-Hinshelwood and the Eley-Rideal mechanisms are used to elucidate the role of OH surface groups on the Ni support and OH- ions in the electrolyte, respectively, in the enhancement of the CO tolerance. XPS analysis indicates that negative charges transfer from the Ni support to Pt nanoparticles. The electronic interaction may modify adsorption properties of CO adspecies on the Pt catalyst; the modification allows easy CO electro-oxidation by OH species surrounding the Pt nanoparticles, either from the Ni support or from the alkaline solution. The synergistic effect of the bifunctional mechanism and the electronic interaction makes the Pt/karst-Ni structure a good catalytic electrode for MOR in the KOH solution. (C) 2011 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectNickelen_US
dc.subjectPlatinum nanoparticlesen_US
dc.subjectDMFCen_US
dc.subjectCO toleranceen_US
dc.subjectAlkaline solutionen_US
dc.titleElectrocatalytic activity of Pt nanoparticles on a karst-like Ni thin film toward methanol oxidation in alkaline solutionsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.apcatb.2011.03.002en_US
dc.identifier.journalAPPLIED CATALYSIS B-ENVIRONMENTALen_US
dc.citation.volume104en_US
dc.citation.issue3-4en_US
dc.citation.spage382en_US
dc.citation.epage389en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000291182100023-
dc.citation.woscount16-
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