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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.accessioned2014-12-08T15:07:50Z-
dc.date.available2014-12-08T15:07:50Z-
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/11536/6167-
dc.description.abstractWe employed an amorphous citrate precursor (ACP) method to synthesize stoichiometric La(0.6)Ca(0.4)Co(0.8)Ru(0.2)O(3) powders. Result from X-ray diffraction demonstrated a perovskite La(0.6)Ca(0.4)CoO(3) lattice, indicating the incorporation of Ru(3+) at the Co(3+) sites. Image from the scanning electron microscope revealed a foamlike microstructure with various pores at 0.5-3 mu m. La(0.6)Ca(0.4)Co(0.8)Ru(0.2)O(3) exhibited a higher H(2)O(2) decomposition rate in KOH solution as opposed to that of ACP-derived La(0.6)Ca(0.4)CoO(3), which suggested an improved catalytic ability for oxygen reduction reaction (ORR). A similar behavior was observed during the ORR current-potential polarization using La(0.6)Ca(0.4)Co(0.8)Ru(0.2)O(3) 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 La(0.6)Ca(0.4)Co(0.8)Ru(0.2)O(3). In galvanostatic measurements and lifetime evaluation, La(0.6)Ca(0.4)Co(0.8)Ru(0.2)O(3) 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 La(0.6)Ca(0.4)Co(0.8)Ru(0.2)O(3) 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.citation.issue6en_US
dc.citation.spageB900en_US
dc.citation.epageB905en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
Appears in Collections:Articles