完整後設資料紀錄
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dc.contributor.authorChang, Yun-Minen_US
dc.contributor.authorChang, Yin-Fangen_US
dc.contributor.authorWu, Pu-Weien_US
dc.contributor.authorWu, Cheng-Yeouen_US
dc.contributor.authorLin, Pangen_US
dc.date.accessioned2019-04-02T05:59:35Z-
dc.date.available2019-04-02T05:59:35Z-
dc.date.issued2010-01-01en_US
dc.identifier.issn0013-4651en_US
dc.identifier.urihttp://dx.doi.org/10.1149/1.3384665en_US
dc.identifier.urihttp://hdl.handle.net/11536/149942-
dc.description.abstractWe employed an amorphous citrate precursor (ACP) method to synthesize stoichiometric La0.6Ca0.4Co0.8Ru0.2O3 powders. Result from X-ray diffraction demonstrated a perovskite La0.6Ca0.4CoO3 lattice, indicating the incorporation of Ru3+ at the Co3+ sites. Image from the scanning electron microscope revealed a foamlike microstructure with various pores at 0.5-3 mu m. La0.6Ca0.4Co0.8Ru0.2O3 exhibited a higher H2O2 decomposition rate in KOH solution as opposed to that of ACP-derived La0.6Ca0.4CoO3, which suggested an improved catalytic ability for oxygen reduction reaction (ORR). A similar behavior was observed during the ORR current-potential polarization using La0.6Ca0.4Co0.8Ru0.2O3 supported on Black Pearl 2000 as a gas diffusion electrode. In addition, impedance spectra at the open-circuit voltage and selective cathodic overpotentials also confirmed a smaller charge-transfer resistance for La0.6Ca0.4Co0.8Ru0.2O3. In galvanostatic measurements and lifetime evaluation, La0.6Ca0.4Co0.8Ru0.2O3 demonstrated steady voltage profiles with negligible degradation. (C) 2010 The Electrochemical Society. [DOI: 10.1149/1.3384665] All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleSynthesis and Characterization of La0.6Ca0.4Co0.8Ru0.2O3 for Oxygen Reduction Reaction in an Alkaline Electrolyteen_US
dc.typeArticleen_US
dc.identifier.doi10.1149/1.3384665en_US
dc.identifier.journalJOURNAL OF THE ELECTROCHEMICAL SOCIETYen_US
dc.citation.volume157en_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:000277260200039en_US
dc.citation.woscount7en_US
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