Electrical conductivity of Sr2−xVMoO6−y (x = 0.0, 0.1, 0.2) double perovskites

Electrical conductivity of Sr2-xVMoO6-y (x = 0.0, 0.1, 0.2) double perovskites has been investigated in a reducing atmosphere at temperatures up to 800 °C. This material has a key application in solid oxide fuel cell anodes as a mixed ion and electron conductor. A solid state synthesis technique was...

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Veröffentlicht in:Journal of applied physics 2013-06, Vol.113 (24)
Hauptverfasser: Childs, Nicholas B., Weisenstein, Adam, Smith, Richard, Sofie, Stephen, Key, Camas
Format: Artikel
Sprache:eng
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Zusammenfassung:Electrical conductivity of Sr2-xVMoO6-y (x = 0.0, 0.1, 0.2) double perovskites has been investigated in a reducing atmosphere at temperatures up to 800 °C. This material has a key application in solid oxide fuel cell anodes as a mixed ion and electron conductor. A solid state synthesis technique was used to fabricate materials and crystal structure was verified through x-ray diffraction. Subsequent to conventional sintering in a reducing environment, elemental valence states were indentified through x-ray photoemission spectroscopy on the double perovskite material before and after annealing in a hydrogen environment. Samples exhibited metallic like conduction with electrical conductivities of 1250 S/cm (Sr2VMoO6-y′), 2530 S/cm (Sr1.8VMoO6-y″), and 3610 S/cm (Sr1.9VMoO6-y‴) at 800 °C in 5% H2/95% N2, with a substantial increase in conductivity upon cooling to room temperature. Room temperature electrical conductivity values for Sr1.9VMoO6-y‴ make it a candidate as the highest electrically conductive oxide known. Highly insulating secondary surface phases, Sr3V2O8, and SrMoO4, begin to reduce at 400 °C in a hydrogen environment, as confirmed by X-ray photoemission and thermal gravimetric analysis. This reduction, from V5+ and Mo6+ to lower valence states, leads to a large increase in sample electrical conductivity.
ISSN:0021-8979
1089-7550
DOI:10.1063/1.4811715