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Cathodic Activity and Interfacial Stability of Y0.8Ca0.2Co1–xFexO3/YSZ Electrodes for Solid Oxide Fuel Cells

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dc.contributor.authorLee, Hee Y.-
dc.contributor.authorJang, Jong H.-
dc.contributor.authorOh, Seung M.-
dc.date.accessioned2009-07-17T05:40:00Z-
dc.date.available2009-07-17T05:40:00Z-
dc.date.issued1999-05-
dc.identifier.citationJ. Electrochem. Soc., 146, 1707 (1999)en
dc.identifier.issn0013-4651-
dc.identifier.urihttps://hdl.handle.net/10371/5703-
dc.description.abstractThe Fe-doped cobaltates, Y0.8Ca0.2Co1–xFexO3– (x = 0.1–0.7), were prepared and their high-temperature phase stability and cathodic activity were investigated. The perovskite/yttria-stabilized zirconia (YSZ) electrodes were fabricated via a silk printing technique. It was found that the undoped cobaltate (x = 0) is so thermally unstable that the preparation of pure perovskite phase was unsuccessful. The partial Fe-doping to Co (x = 0.1–0.7), however, gave us highly crystalline perovskite powders of an orthorhombic lattice. Among those samples of x = 0.1–0.7, the Y0.8Ca0.2Co0.7Fe0.3O3– showed the best cathodic activity which is superior to La0.9Sr0.1MnO3. The thermal expansion coefficient of this material (10.5 × 10–6 cm/cm-K at 25–1000°C) was very close to that of 8 mol % YSZ (10.8 × 10–6 cm/cm-K). As a result of interfacial reaction between Y0.8Ca0.2Co0.7Fe0.3O3– and YSZ electrolyte, a spinel-type oxide was produced. But the interfacial product formation proceeded mainly during the electrode adhesion period (1200°C) whereas its growth during the cell operation (900–1000°C) was negligible.en
dc.description.sponsorshipThis work was supported by Ssangyong Cement Industry and Korea Science and Engineering Foundation (966-0304-005-2).en
dc.language.isoenen
dc.publisherElectrochemical Societyen
dc.titleCathodic Activity and Interfacial Stability of Y0.8Ca0.2Co1–xFexO3/YSZ Electrodes for Solid Oxide Fuel Cellsen
dc.typeArticleen
dc.contributor.AlternativeAuthor이희영-
dc.contributor.AlternativeAuthor오승모-
dc.identifier.doi10.1149/1.1391830-
dc.citation.journaltitleJournal of the electrochemical society-
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