Abstract

The oxygen nonstoichiometry of La0.6Sr0.4CoO3−δ has been the topic of various reports in the literature, but has been exclusively measured at high oxygen partial pressures, pO2, and/or elevated temperatures. For applications of La0.6Sr0.4CoO3−δ, such as solid oxide fuel cell cathodes or oxygen permeation membranes, knowledge of the oxygen nonstoichiometry and thermo-chemical stability over a wide range of pO2 is crucial, as localized low pO2 could trigger failure of the material and device. By employing coulometric titration combined with thermogravimetry, the oxygen nonstoichiometry of La0.6Sr0.4CoO3−δ was measured at high and intermediate pO2 until the material decomposed (at log(pO2/bar)≈−4.5 at 1073K). For a gradually reduced sample, an offset in oxygen content suggests that La0.6Sr0.4CoO3−δ forms a “super-reduced” solid solution before decomposing. When the sample underwent alternate reduction–oxidation, a hysteresis-like pO2 dependence of the oxygen content in the decomposition pO2 range was attributed to the reversible formation of ABO3 and A2BO4 phases. Reduction enthalpy and entropy were determined for the single-phase region and confirmed interpolated values from the literature.

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