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dc.contributor.authorSuwit Suthirakunen_US
dc.contributor.authorThapanee Sarakonsrien_US
dc.contributor.authorSuparerk Aukkaravittayapunen_US
dc.contributor.authorThiraphat Vilaithongen_US
dc.date.accessioned2018-09-10T03:19:20Z-
dc.date.available2018-09-10T03:19:20Z-
dc.date.issued2009-10-26en_US
dc.identifier.issn12299162en_US
dc.identifier.other2-s2.0-70350148242en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70350148242&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/59686-
dc.description.abstractIn this study, Pt and PtRu supported on N 2 plasma treated carbon were prepared by a simple microwave-assisted solution method using ethylene glycol as both a reducing agent and the solvent. The N 2 plasma treatment of the carbon supporter provided C-N and C = N functional groups on the surface of the carbon support which are the active sites for hydrogen oxidation and oxygen reduction reactions. Moreover, by employing microwave heated polyol, Pt and PtRu solutions can be reduced by ethylene glycol and become Pt metal or PtRu alloy on the carbon support. Depending on these procedures and physical and electrochemical characterizations, Pt and PtRu supported on plasma treated carbon were obtained and their catalytic activity studied. X-ray diffraction patterns of the catalysts prepared indicated the crystallographic structure of Pt/C and PtRu/C. TEM images of the catalysts prepared showed the particle size of Pt/C catalysts to be about 1.67 nm and for the PtRu/C catalyst it was about 1.04 nm. The catalysts prepared were homogeneously distributed on the carbon supports. Among the catalysts prepared and commercial Pt catalysts, PtRu catalyst supported on plasma treated carbon showed the highest electrochemical activity.en_US
dc.subjectMaterials Scienceen_US
dc.titlePlasma modified carbon supported Pt and PtRu electrocatalyst materials for PEMFCsen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Ceramic Processing Researchen_US
article.volume10en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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