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dc.contributor.authorCao, X.
dc.contributor.authorJiang, San Ping
dc.date.accessioned2017-01-30T13:31:19Z
dc.date.available2017-01-30T13:31:19Z
dc.date.created2015-04-09T09:08:03Z
dc.date.issued2014
dc.identifier.citationCao, X. and Jiang, S.P. 2014. Effect of Sr and Al or Fe co-doping on the sinterability and conductivity of lanthanum silicateoxyapatite electrolytes for solid oxide fuel cells. International Journal of Hydrogen Energy. 39: pp. 19093-19101.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/32514
dc.identifier.doi10.1016/j.ijhydene.2014.09.092
dc.description.abstract

The effect of co-doping of Sr and Al or Fe on the microstructure, sinterability and oxide-ion conductivity of lanthanum silicate oxyapatites is investigated in detail at 300–800 °C by the electrochemical impedance spectroscopy. The oxide-ion conductivity is 1.46 × 10−2 S cm−1 for La9.5Sr0.5Si5.5Fe0.5O26.5 (LSSFO) and 1.34 × 10−2 S cm−1 at 800 °C for La9.5Sr0.5Si5.5Al0.5O26.5 (LSSAO), respectively, which is one order of magnitude higher than 6.16 × 10−3 S cm−1 measured on La9.67Si6O26.5 (LSO) oxyapatite under the identical test conditions. The grain bulk and grain boundary resistances of co-doped oxyapatite are significantly smaller than that of LSO oxyapatite, and decrease significantly with the increase of the sintering temperature. LSSFO and LSSAO also show significantly higher density as compared to that of LSO. The results indicate that co-doping of Sr and Al or Fe significantly improves the densification, sinterability and oxide-ion conductivity of lanthanum silicate oxyapatites.

dc.publisherElsevier Ltd
dc.subjectSolid oxide fuel cells' Electrolyte' Lanthanum silicate oxyapatite
dc.subjectCo-doping' Oxide-ion conductivity
dc.titleEffect of Sr and Al or Fe co-doping on the sinterability and conductivity of lanthanum silicateoxyapatite electrolytes for solid oxide fuel cells
dc.typeJournal Article
dcterms.source.volume39
dcterms.source.startPage19093
dcterms.source.endPage19101
dcterms.source.issn0360-3199
dcterms.source.titleInternational Journal of Hydrogen Energy
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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