完整後設資料紀錄
DC 欄位語言
dc.contributor.authorChen, Chung-Shouen_US
dc.contributor.authorPan, Fu-Mingen_US
dc.date.accessioned2014-12-08T15:08:41Z-
dc.date.available2014-12-08T15:08:41Z-
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/11536/6655-
dc.description.abstractPorous TiO(2) 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 TiO(2) 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/TiO(2) 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 TiO(2) support on CO oxidation. The strong electronic interaction between Pt and the TiO(2) 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.titleElectrocatalytic activity of Pt nanoparticles deposited on porous TiO(2) 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.issue3-4en_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
顯示於類別:期刊論文