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dc.contributor.authorZhou, W.
dc.contributor.authorRan, R.
dc.contributor.authorShao, Zongping
dc.contributor.authorZhuang, W.
dc.contributor.authorJia, J.
dc.contributor.authorGu, H.
dc.contributor.authorJin, W.
dc.contributor.authorXu, N.
dc.date.accessioned2017-01-30T12:09:29Z
dc.date.available2017-01-30T12:09:29Z
dc.date.created2016-09-12T08:36:54Z
dc.date.issued2008
dc.identifier.citationZhou, W. and Ran, R. and Shao, Z. and Zhuang, W. and Jia, J. and Gu, H. and Jin, W. et al. 2008. Barium- and strontium-enriched (Ba0.5Sr0.5)1+xCo0.8Fe0.2O3-d oxides as high-performance cathodes for intermediate-temperature solid-oxide fuel cells. Acta Materialia. 56 (12): pp. 2687-2698.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/18709
dc.identifier.doi10.1016/j.actamat.2008.02.002
dc.description.abstract

(Ba0.5Sr0.5)1+xCo0.8Fe0.2O3-d, or BSCF(1 + x), (0 = x = 0.3) oxides were synthesized and investigated as cathodes for intermediate-temperature solid-oxide fuel cells. The A-site cation excess in BSCF(1 + x) resulted in a lattice expansion and the creation of more active sites for oxygen reduction reaction due to the lowered valence states of the B-site ions and the increased oxygen vacancy concentration, which improved the oxygen adsorption process. On the other hand, the A-site excess could also result in higher resistances for oxygen adsorption (due to the formation of BaO and/or SrO impurities), and oxygen-ion transfer (by facilitating the solid-phase reaction between the cathode and the electrolyte). By taking all these factors into account, we found BSCF1.03 to be the optimal composition, which lead to a peak power density of 1026.2 ± 12.7 mW cm-2 at 650 °C for a single cell. © 2008 Acta Materialia Inc.

dc.publisherPergamon Press
dc.titleBarium- and strontium-enriched (Ba0.5Sr0.5)1+xCo0.8Fe0.2O3-d oxides as high-performance cathodes for intermediate-temperature solid-oxide fuel cells
dc.typeJournal Article
dcterms.source.volume56
dcterms.source.number12
dcterms.source.startPage2687
dcterms.source.endPage2698
dcterms.source.issn1359-6454
dcterms.source.titleActa Materialia
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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