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dc.contributor.authorChen, Chung-Shouen_US
dc.contributor.authorPan, Fu-Mingen_US
dc.date.accessioned2019-04-02T06:00:07Z-
dc.date.available2019-04-02T06:00:07Z-
dc.date.issued2009-09-28en_US
dc.identifier.issn0926-3373en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.apcatb.2009.07.008en_US
dc.identifier.urihttp://hdl.handle.net/11536/149831-
dc.description.abstractPorous TiO2 thin films were prepared on the Si substrate by hydrothermal method, and used as the Pt electrocatalyst support for methanol oxidation study. Well-dispersed Pt nanoparticles with a particle size of 5-7 nm were pulse-electrodeposited on the porous TiO2 support, which was mainly composed of the anatase phase after an annealing at 600 degrees C in vacuum. Cyclic voltammetry (CV) and CO stripping measurements showed that the Pt/TiO2 electrode had a high electrocatalytic activity toward methanol oxidation and an excellent CO tolerance. The excellent electrocatalytic performance of the electrode is ascribed to the synergistic effect of Pt nanoparticles and the porous TiO2 support on CO oxidation. The strong electronic interaction between Pt and the TiO2 support may modify CO chemisorption properties on Pt nanoparticles, thereby facilitating CO oxidation on Pt nanoparticles via the bifunctional mechanism and thus improving the electrocatalytic activity of the Pt catalyst toward methanol oxidation. (C) 2009 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectPorous TiO2en_US
dc.subjectPlatinumen_US
dc.subjectHydrothermal methoden_US
dc.subjectCO oxidationen_US
dc.subjectMethanol electro-oxidationen_US
dc.titleElectrocatalytic activity of Pt nanoparticles deposited on porous TiO2 supports toward methanol oxidationen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.apcatb.2009.07.008en_US
dc.identifier.journalAPPLIED CATALYSIS B-ENVIRONMENTALen_US
dc.citation.volume91en_US
dc.citation.spage663en_US
dc.citation.epage669en_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:000270120600012en_US
dc.citation.woscount78en_US
Appears in Collections:Articles