La2−xSrxCoO4−δ (x = 0.9, 1.0, 1.1) Ruddlesden-Popper-type layered cobaltites as cathode materials for IT-SOFC application
La2−xSrxCoO4−δ (x = 0.9, 1.0, 1.1) compounds with Ruddlesden-Popper K2NiF4-type structure have been investigated as potential cathode materials for IT-SOFC application. Materials have been prepared by citrate-nitrate combustion method. Structural evolution analysed by XRD shows a shortened Co–O–Co b...
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Veröffentlicht in: | International journal of hydrogen energy 2013-03, Vol.38 (7), p.3064-3072 |
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Sprache: | eng |
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Zusammenfassung: | La2−xSrxCoO4−δ (x = 0.9, 1.0, 1.1) compounds with Ruddlesden-Popper K2NiF4-type structure have been investigated as potential cathode materials for IT-SOFC application. Materials have been prepared by citrate-nitrate combustion method. Structural evolution analysed by XRD shows a shortened Co–O–Co bond length within the perovskite layer as Sr substitution increases, while the interlayer distance at the same time increases. An oxygen stoichiometry close to 4 has been found for all compositions at room temperature. Thermal expansion coefficients have been obtained from temperature-dependent XRD analysis and show large values (>20 × 10−6 K−1) compared to the currently utilized electrolyte materials. Electrochemical characterisation has been performed by means of impedance spectroscopy on symmetric cells with CGO electrolyte. Pure electrodes have a high Area Specific Resistance, probably due to limited oxygen ion diffusion. By using composite electrode (50 wt.% CGO), an Area Specific Resistance of 0.25 Ω cm2 is obtained at approximately 700 °C for all the three compounds suggesting promising electrochemical properties for IT-SOFCs.
► La2−xSrxCoO4−δ cathode materials for solid oxide cells are studied. ► The oxygen stoichiometry at rom temperature is close to 4. ► Thermal expansion is greater than 20 × 10−6 K−1 ► Pure electrode materials present a high Area Specific Resistance. ► Composite electrodes show a low ASR of 0.25 Ω.cm2 at 700 °C. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2012.12.047 |