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RESEARCH PRODUCT
Solid-state compatibility of Ca:LaNbO4 with perovskite cathodes: Evidences from X-ray microspectroscopy
Candida PipitoneAlessandro LongoAlessandro ChiaraAntonino MartoranaGiovanna CanuFrancesco Giannicisubject
cathodeMaterials scienceAbsorption spectroscopyGeneral Chemical EngineeringNiobiumchemistry.chemical_elementPositive ionelectrolyteinterfaceschemistry.chemical_compoundchemical compatibilityLanthanumscheelitesolid oxide fuel cellElectrochemistryLanthanumx-ray microspectroscopySOFClanthanum strontium cobaltiteperovskitePerovskite (structure)Compatibility (geochemistry)CobaltiteChemical statechemistryChemical engineeringNiobium compoundStrontiumSettore CHIM/03 - Chimica Generale E InorganicaLaNbO4X ray absorption spectroscopylanthanum strontium ferriteCalciumCobaltlanthanum niobatedescription
The solid-state compatibility between calcium-doped lanthanum niobate and three perovskite cathode materials was investigated using two X-ray microbeam techniques, micro X-ray fluorescence and micro X-ray absorption spectroscopy. The cathode powders (lanthanum strontium ferrite, either cobalt or copper-doped, and lanthanum strontium cobaltite) in contact with the dense electrolyte pellet were annealed at 1150 degrees C for 12-144 h to simulate the effect of thermal stresses due to fabrication and long-term operation. As a result, several interdiffusion phenomena were then observed on the bilayer cross-sections: in particular, the chemical state and coordination environment of calcium, iron, niobium and lanthanum were probed with space-resolved X-ray absorption spectroscopy. The ab initio modeling of the near-edge X-ray absorption spectra reveal that the cation interdiffusion is facilitated by the structural flexibility of the perovskite structure, which is able to accommodate a variety of foreign cations in different oxidation states. Limited stability at high-temperatures was found for all candidate perovskite compositions in contact with lanthanum niobate. (C) 2021 Elsevier Ltd. All rights reserved.
year | journal | country | edition | language |
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2022-01-01 |