Chemical stability and compatibility of double perovskite anode materials for SOFCs

Double perovskites with composition Sr2BMoO6−δ (B=Mg, Ni and Co) and Sr2Fe1.5Mo0.5O6−δ have been proposed as potential anode material for direct hydrocarbon oxidation in solid oxide fuel cells (SOFCs). However, the phase stability under different atmospheres (H2 and CO2) and the chemical compatibili...

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Veröffentlicht in:Solid state ionics 2013-05, Vol.239, p.1-7
Hauptverfasser: dos Santos-Gómez, L., León-Reina, L., Porras-Vázquez, J.M., Losilla, E.R., Marrero-López, D.
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Sprache:eng
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Zusammenfassung:Double perovskites with composition Sr2BMoO6−δ (B=Mg, Ni and Co) and Sr2Fe1.5Mo0.5O6−δ have been proposed as potential anode material for direct hydrocarbon oxidation in solid oxide fuel cells (SOFCs). However, the phase stability under different atmospheres (H2 and CO2) and the chemical compatibility with different electrolytes of most of these materials have not been previously studied. The chemical compatibility studies carried out by X-ray powder diffraction (XRPD) revealed high reactivity between these electrodes and zirconia based electrolytes, Zr0.84Y0.16O2−δ, at temperatures as low as 800°C with the formation of SrMoO4 and SrZrO3 as main reaction products; however, lower chemical reactivity was found with Ce0.8Gd0.2O2−δ. Sr2CoMoO6−δ and Sr2NiMoO6−δ phases resulted to be unstable under reducing atmosphere above 800°C, decomposing partially into Sr3MoO6 and Co/Ni metals respectively. These two materials also exhibited low resistance to carbonation in the intermediate temperature range 600–800°C. Nevertheless, Sr2Fe1.5Mo0.5O6−δ is stable under H2 and pure CO2 atmospheres. Furthermore, area specific resistances of these anode materials in symmetrical cells were determined in order to compare their electrochemical efficiency. •Partial decomposition of Sr2CoMoO6−δ and Sr2NiMoO6−δ structures was observed under H2 and CO2 atmospheres.•Sr2Fe1.5Mo0.5O6−δ is stable under H2 and pure CO2.•Reactivity between YSZ and the double perovskite anode materials was observed at 800°C.•Lower chemical reactivity was found with LSGM and CGO electrolytes.
ISSN:0167-2738
1872-7689
DOI:10.1016/j.ssi.2013.03.005