Abstract
Abstract The oxygen exchange kinetics of La0.6Sr0.4CoO3-δ was investigated at 700 °C and p(O2) = 0.10 bar by in-situ conductivity relaxation measurements. The experiments were performed for 1000 h in an O2–Ar atmosphere with and without 50 ppm SO2. For post-test analyses, scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDXS) and analytic transmission electron microscopy (TEM) were applied. Elemental depth profiles were obtained by X-ray photoelectron spectroscopy (XPS). The decrease in the chemical oxygen exchange coefficient kchem by a factor of 10 during the course of 1000 h indicated that an accumulation of traces of sulphur (estimated to the range of ppb) in the form of SrSO4 can lead to a significant degradation even in nominally pure O2–Ar. The exposure to 50 ppm of SO2 for 1000 h caused a severe degradation in kchem by a factor of 3000. Post-test analyses showed that the perovskite phase La0.6Sr0.4CoO3-δ is decomposed into SrSO4 and La2O2SO4 within the first 500 nm of the surface, and a nano-crystalline Co-rich phase, which is located in the depth range of 500–1400 nm.
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