Defect structure, electronic conductivity and expansion of properties of (La1−xSrx)sCo1−yNiyO3−δ

Publication: Research - peer-reviewJournal article – Annual report year: 2010

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This study reports on oxygen nonstoichiometry, electronic conductivity and lattice expansion of three compositions as function of T and PO2 in the (La1−xSrx)sCo1−yNiyO3−δ (x=0.1, y=0.4; x=0.1, y=0.3; x=0.2, y=0.2) materials system. The nonstoichiometry data were successfully fitted using the itinerant electron model which indicates the existence of delocalized electronic states. This was also reflected in the high electronic conductivities, above 1000 S cm−1, measured for all three compositions. The electronic conductivity was shown to decrease linearly with the oxygen nonstoichiometry parameter, δ, supporting that the conductivity is dependent on p-type charge carriers. Comparing calculated p-type mobilities with data reported in literature on La1−xSrxCoO3 indicated that Ni-substitution into (La1−xSrx)sCoO3−δ increases the p-type mobility. The electronic conductivity was also found to be dependent on intrinsic charge related to spin excitations and Ni substitution rather than the p-type charge. A conductivity mechanism is hypothesized including a metallic like conductivity of the p-type charge and a small polaron conductivity of the intrinsic charge. Lattice expansion as function of T and δ was successfully described using first and second order thermal and chemical expansion coefficients. Substituting 10% Co with Ni in (La0.6Sr0.4)0.99CoO3−δ was found to decrease the apparent thermal expansion with about 25%.
Original languageEnglish
JournalJournal of Solid State Chemistry
Publication date2010
Volume183
Issue8
Pages1853-1862
ISSN0022-4596
DOIs
StatePublished
CitationsWeb of Science® Times Cited: 9

Keywords

  • Solid Oxide Fuel Cells, Fuel Cells and hydrogen
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