Institute of Chemical Technologies and Analytics, Vienna University of Technology, Getreidemarkt 9, Vienna, A-1060, Austria.
Phys Chem Chem Phys. 2018 May 3;20(17):12016-12026. doi: 10.1039/c7cp07845e.
La0.6Sr0.4FeO3-δ (LSF) thin films of different thickness were prepared by pulsed laser deposition on yttria stabilized zirconia (YSZ) and characterized by using three electrode impedance spectroscopy. Electrochemical film capacitance was analyzed in relation to oxygen partial pressure (0.25 mbar to 1 bar), DC polarization (0 m to -600 m) and temperature (500 to 650 °C). For most measurement parameters, the chemical bulk capacitance dominates the overall capacitive properties and the corresponding defect chemical state depends solely on the oxygen chemical potential inside the film, independent of atmospheric oxygen pressure and DC polarization. Thus, defect chemical properties (defect concentrations and defect formation enthalpies) could be deduced from such measurements. Comparison with LSF defect chemical bulk data from the literature showed good agreement for vacancy formation energies but suggested larger electronic defect concentrations in the films. From thickness-dependent measurements at lower oxygen chemical potentials, an additional capacitive contribution could be identified and attributed to the LSF|YSZ interface. Deviations from simple chemical capacitance models at high pressures are most probably due to defect interactions.
采用脉冲激光沉积法在氧化钇稳定的氧化锆(YSZ)上制备了不同厚度的 La0.6Sr0.4FeO3-δ(LSF)薄膜,并通过三电极阻抗谱进行了表征。分析了电化学薄膜电容与氧分压(0.25 毫巴至 1 巴)、直流极化(0 毫伏至-600 毫伏)和温度(500 至 650°C)的关系。对于大多数测量参数,化学体相电容主导着整体电容特性,相应的缺陷化学状态仅取决于薄膜内的氧化学势,与大气氧分压和直流极化无关。因此,可以从这些测量中推断出缺陷化学性质(缺陷浓度和缺陷形成焓)。与文献中 LSF 缺陷化学体相数据的比较表明,空位形成能的吻合较好,但薄膜中的电子缺陷浓度较大。从较低氧化学势下的厚度依赖性测量中,可以识别出一个额外的电容贡献,并归因于 LSF|YSZ 界面。在高压下偏离简单的化学电容模型可能是由于缺陷相互作用所致。