Modified strontium titanates : from defect chemistry to SOFC anodes
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Modified strontium titanates have received much attention recently for their potential as anode material in solid oxide fuel cells (SOFC). Their inherent redox stability and superior tolerance to sulphur poisoning and coking as compared to Ni based cermet anodes could improve durability of SOFC systems dramatically. Various substitution strategies can be deployed to optimise materials properties in these strontium titanates, such as electronic conductivity, electrocatalytic activity, chemical stability and sinterability, and thus mechanical strength. Substitution strategies not only cover choice and amount of substituent, but also perovskite defect chemistry, distinguishing between A-site deficiency (A1-xBO3) and cation-stoichiometry (ABO3+δ). Literature suggests distinct differences in the materials properties between the latter two compositional approaches. After discussing the defect chemistry of modified strontium titanates, this paper reviews three different A-site deficient donor (La, Y, Nb) substituted strontium titanates for their electrical behaviour and fuel cell performance. Promising performances in both electrolyte as well as anode supported cell designs have been obtained, when using hydrogen as fuel. Performances are retained after numerous redox cycles. Long term stability in sulphur and carbon containing fuels still needs to be explored in greater detail.
Verbraeken , M C , Ramos , T , Agersted , K , Ma , Q , Savaniu , C D , Sudireddy , B R , Irvine , J T S , Holtappels , P & Tietz , F 2015 , ' Modified strontium titanates : from defect chemistry to SOFC anodes ' Royal Society of Chemistry Advances , vol 5 , no. 2 , pp. 1168-1180 . DOI: 10.1039/c4ra09751c
Royal Society of Chemistry Advances
© Royal Society of Chemistry 2014. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at http://dx.doi.org/10.1039/C4RA09751C
DescriptionThe authors acknowledge funding from the Fuel Cells and Hydrogen Joint Undertaking under grant agreement no. 256730.
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