完整後設資料紀錄
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dc.contributor.authorChang, Yun-Minen_US
dc.contributor.authorWu, Pu-Weien_US
dc.contributor.authorWu, Cheng-Yeouen_US
dc.contributor.authorHsieh, Yi-Fanen_US
dc.contributor.authorChen, Jing-Yuen_US
dc.date.accessioned2014-12-08T15:12:52Z-
dc.date.available2014-12-08T15:12:52Z-
dc.date.issued2008en_US
dc.identifier.issn1099-0062en_US
dc.identifier.urihttp://hdl.handle.net/11536/9920-
dc.identifier.urihttp://dx.doi.org/10.1149/1.2835200en_US
dc.description.abstractLa0.6Ca0.4CoIr0.25O3.5-delta was prepared by a mechanical alloying process from mixtures of La0.6Ca0.4CoO3 and IrO2. Scanning electron microscopy images on the resulting powders exhibited particles with irregular shape at 300-500 nm in size. X-ray diffraction analysis confirmed formation of a perovskite with complete disappearance of rutile signals from IrO2, indicating successful incorporation of Ir4+ at the Co3+ sites. Supported on carbon nanocapsules, the La0.6Ca0.4CoIr0.25O3.5-delta demonstrated superior performance over those of La0.6Ca0.4CoO3 in both charging and discharging current density-voltage polarizations. In addition, galvanostatic charging and discharging measurements at 25 and 100 mA/cm(2) indicated that the electrocatalytic abilities of La0.6Ca0.4CoIr0.25O3.5-delta are stable and sustainable.en_US
dc.language.isoen_USen_US
dc.titleMechanical alloying preparation of La0.6Ca0.4CoIr0.25O3.5-delta as a bifunctional electrocatalyst in alkaline electrolyteen_US
dc.typeArticleen_US
dc.identifier.doi10.1149/1.2835200en_US
dc.identifier.journalELECTROCHEMICAL AND SOLID STATE LETTERSen_US
dc.citation.volume11en_US
dc.citation.issue4en_US
dc.citation.spageB47en_US
dc.citation.epageB50en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000253238000005-
dc.citation.woscount8-
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