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dc.contributor.authorHe, Beibei
dc.contributor.authorZhao, Ling
dc.contributor.authorSong, S.
dc.contributor.authorLiu, T.
dc.contributor.authorChen, F.
dc.contributor.authorXia, C.
dc.date.accessioned2017-01-30T10:45:12Z
dc.date.available2017-01-30T10:45:12Z
dc.date.created2015-03-03T20:16:20Z
dc.date.issued2012
dc.identifier.citationHe, B. and Zhao, L. and Song, S. and Liu, T. and Chen, F. and Xia, C. 2012. Sr2Fe1.5Mo0.5O6-δ - Sm0.2Ce0.8O1.9 Composite Anodes for Intermediate-Temperature Solid Oxide Fuel Cells. Journal of the Electrochemical Society. 159 (5): pp. B619-B626.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/5305
dc.identifier.doi10.1149/2.020206jes
dc.description.abstract

Sr2Fe1.5Mo0.5O6−δ (SFM) perovskite is carefully investigated as an anode material for solid oxide fuel cells with LaGaO3-based electrolytes. Its electronic conductivity under anodic atmosphere is measured with four-probe method while its ionic conductivity is determined with oxygen permeation measurement. Samaria doped ceria (SDC) is incorporated into SFM electrode to improve the anodic performance. A strong relation is observed between SDC addition and polarization losses, suggesting that the internal SFM-SDC contacts are active for H2 oxidation. The best electrode performance is achieved for the composite with 30 wt% SDC addition, resulting in an interfacial polarization resistance of 0.258 Ω cm2 at 700°C for La0.8Sr0.2Ga0.8Mg0.2O3−δ supported single cells. Electrochemical impedance spectroscopy analysis indicates that the high performance of SFM-SDC composite anodes is likely due to the high ionic conductivity and electro-catalytic activity of SDC by promoting the ionic exchange processes. Redox cycle treatment shows that SDC addition can even improve the redox tolerance of SFM anodes.

dc.publisherThe Electrochemical Society, Inc
dc.titleSr2Fe1.5Mo0.5O6-δ - Sm0.2Ce0.8O1.9 Composite Anodes for Intermediate-Temperature Solid Oxide Fuel Cells
dc.typeJournal Article
dcterms.source.volume159
dcterms.source.startPageB619
dcterms.source.endPageB626
dcterms.source.issn0013-4651
dcterms.source.titleJournal of the Electrochemical Society
curtin.accessStatusFulltext not available


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