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dc.contributor.authorNiu, Y.
dc.contributor.authorSunarso, J.
dc.contributor.authorLiang, F.
dc.contributor.authorZhou, W.
dc.contributor.authorZhu, Z.
dc.contributor.authorShao, Zongping
dc.date.accessioned2017-01-30T10:41:31Z
dc.date.available2017-01-30T10:41:31Z
dc.date.created2015-10-29T04:09:53Z
dc.date.issued2011
dc.identifier.citationNiu, Y. and Sunarso, J. and Liang, F. and Zhou, W. and Zhu, Z. and Shao, Z. 2011. A comparative study of oxygen reduction reaction on Bi-and La-doped SrFeO3-d perovskite cathodes. Journal of the Electrochemical Society. 158 (2): pp. B132-B138.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/4751
dc.identifier.doi10.1149/1.3521316
dc.description.abstract

In this work the oxygen reduction reaction on Bi0.5 Sr 0.5 FeO3-d (BSF) and La0.5 Sr 0.5 Fe O3-d (LSF) as cathodes for intermediate temperature solid oxide fuel cells (600-750°C) is compared in detail. Partial substitution of Sr in SrFe O3-d with 50 mole % of Bi or La results in the distinct structural features which strongly impact its electrochemical characteristics due to the presence of a lone electron pair in Bi3+, which is not available in La3+. Cubic structure for BSF favours higher ionic conductivity and enhanced formation of oxygen vacancies relative to rhombohedral structure for LSF. Large oxygen nonstoichiometry for BSF, nevertheless, leads to the dominance of Fe3+ and subsequent low electronic conductivity relative to LSF. It was found that upon cathodic polarization, the oxygen vacancies are created on LSF which helps reducing its interfacial resistance afterward, which is not the case for BSF. Overall, BSF demonstrates good electrochemical performance which can be further optimized by enhancing its electronic conductivity. © 2010 The Electrochemical Society.

dc.titleA comparative study of oxygen reduction reaction on Bi-and La-doped SrFeO3-d perovskite cathodes
dc.typeJournal Article
dcterms.source.volume158
dcterms.source.number2
dcterms.source.startPageB132
dcterms.source.endPageB138
dcterms.source.issn0013-4651
dcterms.source.titleJournal of the Electrochemical Society
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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