材料科学
介电谱
电解
电极
电容
阳极
氧化物
退火(玻璃)
极化(电化学)
分析化学(期刊)
多孔性
电化学
化学工程
复合材料
冶金
化学
电解质
工程类
物理化学
色谱法
作者
Martin Krammer,Alexander Schmid,Andreas Nenning,Andreas E. Bumberger,Matthäus Siebenhofer,Christopher Herzig,Andreas Limbeck,Christoph Rameshan,Markus Kubicek,Jürgen Fleig
标识
DOI:10.1021/acsami.2c20731
摘要
Electrochemical impedance spectroscopy was used to investigate the chemical capacitance of La0.6Sr0.4CoO3-δ (LSC) thin-film electrodes under anodic polarization (i.e., in the electrolysis mode). For this purpose, electrodes with different microstructures were prepared via pulsed-laser deposition. Analysis of dense electrodes and electrodes with open porosity revealed decreasing chemical capacitances with increasing anodic overpotentials, as expected from defect chemical considerations. However, extremely high chemical capacitance peaks with values in the range of 104 F/cm3 at overpotentials of >140 mV were obtained after annealing for several hours in synthetic air and/or after applying high anodic bias voltages of >750 mV. From the results of several surface analysis techniques and transmission electron microscopy, it is concluded that closed pores develop upon both of these treatments: (i) During annealing, initially open pores get closed by SrSO4, which forms due to strontium segregation in measurement gases with minute traces of sulfur. (ii) The bias treatment causes mechanical failure and morphological changes including closed pores in the bulk of dense films. Under anodic polarization, high-pressure oxygen accumulates in those closed pores, and this causes the capacitance peak. Model calculations based on a real-gas equation allow us to properly predict the experimentally obtained capacitance increase. We demonstrate that analysis of the chemical capacitance of oxygen electrodes in solid oxide electrolysis cells can thus be used as a nondestructive observation tool to detect and quantify closed porosity with a lower detection limit between 10-4 and 10-3.
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