Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/49968
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dc.contributor.authorLi Fangen_US
dc.contributor.authorXiao Xiao Guoen_US
dc.contributor.authorYue Peng Liuen_US
dc.contributor.authorXiao Ping Huangen_US
dc.contributor.authorSurin Saipanyaen_US
dc.date.accessioned2018-09-04T04:21:04Z-
dc.date.available2018-09-04T04:21:04Z-
dc.date.issued2011-06-06en_US
dc.identifier.issn10226680en_US
dc.identifier.other2-s2.0-79957844823en_US
dc.identifier.other10.4028/www.scientific.net/AMR.236-238.1073en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79957844823&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/49968-
dc.description.abstractBimetallic catalysts PtRh@Pt 5/C with different deposit structures were prepared by force deposition followed calcination at 400°C and characterized by cyclic voltammetry (CV) combined with XRD. The activity of the obtained catalysts was examined in methanol electrooxidation by CV. It was found that PtRh@Pt 5/C catalysts achieved higher catalytic activity and better tolerance to CO compared with Pt 5/C. The surfaces of PtRh@Pt 5/C derived from sandwich-like deposit structure was composed of crystallites and amorphous of PtRh alloys, showing exceptional catalytic activity in methanol oxidation with peak potential shifting 0.03V negatively and 90% increase in current density. © (2011) Trans Tech Publications.en_US
dc.subjectEngineeringen_US
dc.titlePtRh@Pt 5C/catalyst preparation for methanol electrooxidationen_US
dc.typeBook Seriesen_US
article.title.sourcetitleAdvanced Materials Researchen_US
article.volume236-238en_US
article.stream.affiliationsShanxi Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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