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dc.contributor.authorChang, Yun-Minen_US
dc.contributor.authorHsieh, Yu-Chien_US
dc.contributor.authorWu, Pu-Weien_US
dc.contributor.authorLai, Chun-Hanen_US
dc.contributor.authorChang, Tin-Yuen_US
dc.date.accessioned2014-12-08T15:10:46Z-
dc.date.available2014-12-08T15:10:46Z-
dc.date.issued2008-10-15en_US
dc.identifier.issn0167-577Xen_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.matlet.2008.06.040en_US
dc.identifier.urihttp://hdl.handle.net/11536/8244-
dc.description.abstractLa0.6Ca0.4Co0.8Ir0.2O3 was prepared by solid state reaction synthesis from mixtures of La(NO3)(3)center dot 6H(2)O, Ca (NO3)(2)center dot 4H(2)O, Co(NO3)(3)center dot 6H(2)O, and IrO2 at stoichiometric ratio. Images from scanning electron microscopy on the as-synthesized powders exhibited particles in irregular shape at 100-250 nm in size. X-ray diffraction analysis confirmed the formation of perovskite without the rutile signals from IrO2, suggesting successful incorporation of Ir4+ at the Co cation sites. The carbon nanocapsules (CNCs) were used as an electrocatalyst support. Electrodes for electrochemical measurements were fabricated by depositing mixtures of CNCs, La0.6Ca0.4Co0.8Ir0.2O3 and polymeric binders on commercially available noncatalyzed gas diffusion electrodes. In alkaline electrolyte, the La0.6Ca0.4Co0.8Ir0.2O3/CNCs demonstrated superior performances than those of La0.6Ca0.4Co0.8Ir0.2O3/CNCs and IrO2/CNCs in both charging and discharging current-potential polarization measurements. (c) 2008 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectperovskitesen_US
dc.subjectcatalystsen_US
dc.subjectbifunctional abilitiesen_US
dc.subjectalkaline electrolyteen_US
dc.titleEnhancement of bifunctional catalysis by Ir doping of La0.6Ca0.4CoO3 perovskitesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.matlet.2008.06.040en_US
dc.identifier.journalMATERIALS LETTERSen_US
dc.citation.volume62en_US
dc.citation.issue26en_US
dc.citation.spage4220en_US
dc.citation.epage4222en_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:000258908600015-
dc.citation.woscount6-
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