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dc.contributor.authorNagai, Tsukasa
dc.contributor.authorFujiwara, Naoko
dc.contributor.authorKitta, Mitsunori
dc.contributor.authorAsahi, Masafumi
dc.contributor.authorYamazaki, Shin
dc.contributor.authorSiroma, Zyun
dc.contributor.authorIoroi, Tsutomu
dc.date.accessioned2017-05-09T01:19:22Z
dc.date.available2017-05-09T01:19:22Z
dc.date.issued2015
dc.identifier.issn2381-6872
dc.identifier.otherfc_012_02_021007.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl/handle/yetl/158373
dc.description.abstractA nanosized perovskitetype oxide supported on carbon black (perovskite/C) was prepared by the polyvinyl pyrrolidone (PVP) addition method and subsequent mechanical milling with carbon black. Transmission electron microscope (TEM) observation and scanning transmission electron microscope (STEM)–energy dispersive Xray (EDX) mapping clearly revealed that the oxide prepared by the PVP method was small (ca. 20 nm) and highly dispersed on the carbon support. The oxygen reduction reaction (ORR) activity on the perovskite/C catalyst was investigated with rotating ringdisk electrode (RRDE) measurement in an alkaline solution at 25 آ°C. The prepared perovskite/C catalyst showed enhanced activity compared to catalysts obtained by the conventional solid state reaction and citrate process; i.e., a positive shift of the onset potential and increased ORR current at a disk electrode. The present catalyst was also associated with decreased ring current.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleOxygen Reduction Activity on a Nanosized Perovskite Type Oxide Prepared by Polyvinyl Pyrrolidone Method
dc.typeJournal Paper
dc.journal.volume12
dc.journal.issue2
dc.journal.titleJournal of Fuel Cell Science and Technology
dc.identifier.doi10.1115/1.4029424
dc.journal.fristpage21007
dc.journal.lastpage21007
dc.identifier.eissn2381-6910
dc.treeJournal of Fuel Cell Science and Technology:;2015:;volume( 012 ):;issue: 002
dc.contenttypeFulltext


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