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dc.contributor.authorLi Fangen_US
dc.contributor.authorJinlu Heen_US
dc.contributor.authorSurin Saipanyaen_US
dc.contributor.authorXiaoping Huangen_US
dc.date.accessioned2018-09-04T10:11:19Z-
dc.date.available2018-09-04T10:11:19Z-
dc.date.issued2015-01-01en_US
dc.identifier.issn14523981en_US
dc.identifier.other2-s2.0-84936766279en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84936766279&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/54298-
dc.description.abstract© 2015 The Authors. Rh<inf>5</inf>@Pt<inf>x</inf>/C core-shell nanoparticles were prepared by a two-step hydrogen reduction process and characterized by cyclic voltammetry (CV) combined with X-ray diffraction (XRD) and transmission electron microscopy (TEM). The effects of the thickness of Pt shell on the catalytic performance for ethanol oxidation were investigated for activity performance evaluation. It was also found that Rh core was practically covered by Pt shell with a strong interaction between Rh and Pt although there was no PtRh alloy formation at the surface of the Pt shell during the deposition process for the catalyst preparation. The Rh core remarkably enhanced the catalytic activity of Pt shell and promoted the breaking of C-C bonds of ethanol resulting in relatively lower potential for the ethanol reaction. It can also be concluded that the current density of the oxidation peak on h<inf>5</inf>@Pt<inf>5</inf>/C was ca. 64 % higher than that on Pt<inf>5</inf>/C although they both showed rather similar characteristic peaks.en_US
dc.subjectChemistryen_US
dc.titlePreparation of Rh&lt;inf&gt;5&lt;/inf&gt;@Pt&lt;inf&gt;x&lt;/inf&gt;/C core-shell nanoparticles for electrocatalytic oxidation of ethanolen_US
dc.typeJournalen_US
article.title.sourcetitleInternational Journal of Electrochemical Scienceen_US
article.volume10en_US
article.stream.affiliationsShanxi Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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