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Performance stability of strontium-doped lanthanum cobaltite ceramic cathode synthesized by a wet chemical method

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dc.contributor.authorPark, Jun-Sik-
dc.contributor.authorBae, Jiwoong-
dc.contributor.authorKim, Young-Beom-
dc.date.accessioned2021-07-30T04:58:49Z-
dc.date.available2021-07-30T04:58:49Z-
dc.date.created2021-05-12-
dc.date.issued2016-08-
dc.identifier.issn0272-8842-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/2535-
dc.description.abstractPorous strontium-doped lanthanum cobaltite (La0.5Sr0.5CoO3-delta, LSC) thin film electrodes were deposited by a metal-organic chemical solution deposition method. These films were used as cathodic electrodes replacing precious metal electrodes for low-temperature solid oxide fuel cell (LT-SOFC) applications. They were characterized electrochemically and compared with devices that had platinum (Pt) cathodes. Pt was prepared by a DC magnetron sputtering method and LSC-YSZ-Pt and Pt-YSZ-Pt (cathode-electrolyte anode) SOFC unit cells were fabricated. The performance of each cell was continuously evaluated under operating conditions and the performance of fuel cells with a Pt cathode was superior to those using a LSC cathode at the initial stages of operation; however, the output power density started to decrease as a function of time due to the degradation that comes from the heat vulnerability of Pt. As a consequence, the performance of Pt-YSZ-Pt was significantly lower than LSC-YSZ-Pt, and the electrode resistance grew to be about four times larger compared to before operation. In contrast, neither the output power density nor the electrode resistance of LSC-YSZ-Pt changed during operation. These results imply that LSC has better long-term performance stability compared to Pt and feasibility of using ceramic electrode for low temperature solid oxide fuel cells.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCI LTD-
dc.titlePerformance stability of strontium-doped lanthanum cobaltite ceramic cathode synthesized by a wet chemical method-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Young-Beom-
dc.identifier.doi10.1016/j.ceramint.2016.05.050-
dc.identifier.scopusid2-s2.0-84969699843-
dc.identifier.wosid000378952100041-
dc.identifier.bibliographicCitationCERAMICS INTERNATIONAL, v.42, no.11, pp.12853 - 12859-
dc.relation.isPartOfCERAMICS INTERNATIONAL-
dc.citation.titleCERAMICS INTERNATIONAL-
dc.citation.volume42-
dc.citation.number11-
dc.citation.startPage12853-
dc.citation.endPage12859-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Ceramics-
dc.subject.keywordPlusOXIDE FUEL-CELLS-
dc.subject.keywordPlusTRIPLE-PHASE-BOUNDARY-
dc.subject.keywordPlusATOMIC LAYER DEPOSITION-
dc.subject.keywordPlusTHIN-FILM ELECTROLYTE-
dc.subject.keywordPlusZIRCONIA ELECTROLYTE-
dc.subject.keywordPlusPOROUS PLATINUM-
dc.subject.keywordPlusINTERMEDIATE-
dc.subject.keywordPlusFABRICATION-
dc.subject.keywordPlusSOFCS-
dc.subject.keywordPlusMICROSTRUCTURE-
dc.subject.keywordAuthorCeramic electrode-
dc.subject.keywordAuthorStrontium-doped lanthanum cobaltite-
dc.subject.keywordAuthorMetal organic chemical solution deposition-
dc.subject.keywordAuthorSolid oxide fuel cell-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0272884216306575?via%3Dihub-
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