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dc.contributor.authorHsieh, Yu-Chien_US
dc.contributor.authorChang, Li-Chungen_US
dc.contributor.authorWu, Pu-Weien_US
dc.contributor.authorChang, Yun-Minen_US
dc.contributor.authorLee, Jyh-Fuen_US
dc.date.accessioned2014-12-08T15:11:55Z-
dc.date.available2014-12-08T15:11:55Z-
dc.date.issued2011-03-14en_US
dc.identifier.issn0926-3373en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.apcatb.2011.01.017en_US
dc.identifier.urihttp://hdl.handle.net/11536/9147-
dc.description.abstractThe displacement reaction of Pt on Ru to form a Ru core and Pt shell (Ru@Pt) bimetallic structure is investigated by immersing the carbon-supported Ru nanoparticles in hexachloroplatinic acids with pH of 1,2.2. and 8, followed by a hydrogen reduction treatment. Results from inductively coupled plasma mass spectrometry suggest that the dissolution of Ru is mostly caused by the reduction of Pt cations. Images from transmission electron microscopy demonstrate a uniform distribution of Ru@Pt in size of 3-5 nm. Spectra from X-ray absorption near edge structure and extended X-ray absorption fine structure confirm that the pH value of hexachloroplatinic acid determines the type of ligands complexing the Pt cations that affects their activity and consequently the severity of displacement reaction and alloying degree of Ru@Pt nanoparticles. As a result, the samples from pH 1 bath reveal a desirable core-shell structure that displays a reduced onset potential in CO stripping and stable catalytic performance for H(2) oxidation while the samples from pH 8 bath indicate the formation of Pt clusters on the Ru surface that leads to poor CO stripping and H(2) oxidation characteristics. (C) 2011 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectDisplacement reactionen_US
dc.subjectPtRu bimetallic nanoparticlesen_US
dc.subjectHexachloroplatinic aciden_US
dc.subjectMethanol oxidationen_US
dc.subjectX-ray absorption spectroscopyen_US
dc.titleDisplacement reaction of Pt on carbon-supported Ru nanoparticles in hexachloroplatinic acidsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.apcatb.2011.01.017en_US
dc.identifier.journalAPPLIED CATALYSIS B-ENVIRONMENTALen_US
dc.citation.volume103en_US
dc.citation.issue1-2en_US
dc.citation.spage116en_US
dc.citation.epage127en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.department加速器光源科技與應用學位學程zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.contributor.departmentMaster and Ph.D. Program for Science and Technology of Accelrrator Light Sourceen_US
dc.identifier.wosnumberWOS:000288884500015-
dc.citation.woscount15-
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