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dc.contributor.authorZhang, C.
dc.contributor.authorSun, L.
dc.contributor.authorRan, R.
dc.contributor.authorShao, Zongping
dc.date.accessioned2017-01-30T15:02:47Z
dc.date.available2017-01-30T15:02:47Z
dc.date.created2016-09-12T08:36:55Z
dc.date.issued2009
dc.identifier.citationZhang, C. and Sun, L. and Ran, R. and Shao, Z. 2009. Activation of a single-chamber solid oxide fuel cell by a simple catalyst-assisted in-situ process. Electrochemistry Communications. 11 (8): pp. 1563-1566.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/42871
dc.identifier.doi10.1016/j.elecom.2009.05.048
dc.description.abstract

Initialization is a critical processing step that has thus far limited the application of the single-chamber solid oxide fuel cell (SC-SOFC). In-situ initialization of a SC-SOFC with a nickel-based anode by methane-air mixtures was investigated. Porous Ru-CeO2 was used as a catalyst layer over a Ni-ScSZ cermet anode. Catalytic testing demonstrated Ru-CeO2 had high activity for methane oxidation. The Ru in the catalyst layer catalyzed the formation of syngas, which successfully reduced the nickel oxide to metallic nickel in the anode. Single cells with a La0.8Sr0.2MnO3 (LSM) cathode, initialized by this in-situ reduction method, delivered peak power densities of 205 and 327 mW cm-2 at 800 °C and 850 °C, respectively. Such performances were better than those of the cell without the Ru-CeO2 catalyst layer that was initialized by an ex-situ reduction method were. © 2009 Elsevier B.V. All rights reserved.

dc.publisherElsevier Inc.
dc.titleActivation of a single-chamber solid oxide fuel cell by a simple catalyst-assisted in-situ process
dc.typeJournal Article
dcterms.source.volume11
dcterms.source.number8
dcterms.source.startPage1563
dcterms.source.endPage1566
dcterms.source.issn1388-2481
dcterms.source.titleElectrochemistry Communications
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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