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dc.contributor.authorPeng, Czh_CN
dc.contributor.authorCheng, Xzh_CN
dc.contributor.authorZhang, Yzh_CN
dc.contributor.authorChen, Lzh_CN
dc.contributor.authorFan, QBzh_CN
dc.contributor.author陈亮zh_CN
dc.date.accessioned2013-12-12T02:24:28Z
dc.date.available2013-12-12T02:24:28Z
dc.date.issued2004-04zh_CN
dc.identifier.citationActa Physico-Chimica Sinica, 2004,20(4):436-439zh_CN
dc.identifier.issn1000-6818zh_CN
dc.identifier.otherISI:000220959000023zh_CN
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/65556
dc.description.abstractThe methanol electrooxidation behaviors on commercial carbon supported Pt and PtRu catalysts in acid solution were compared by carrying out electrochemical studies. The potentiodynamic and potentiostatic experimental results showed that the PtRu/C has a higher electrocatalytic activity for the electrocatalytic oxidation of methanol than the Pt/C. Alloy formation of Ru with Pt not only modified the characteristics of H-2 adsorption on the surface of catalyst but also shifted cathodically the reduction peaks of metal oxide on the cathodic sweep with respect to Pt/C. The interaction of CH3OH with Ru is a temperature-activated process requiring elevated temperature.zh_CN
dc.language.isoen_USzh_CN
dc.subjectRU ALLOYSzh_CN
dc.titleComparison of methanol electrooxidation on carbon supported Pt and PtRu catalystszh_CN
dc.typeArticlezh_CN


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