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In Situ XANES/XPS Investigation of Doped Manganese Perovskite Catalysts

机译:掺杂钙钛矿型锰催化剂的原位XANES / XPS研究

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Studying catalysts in situ is of high interest for understanding their surface structure and electronic states in operation. Herein, we present a study of epitaxial manganite perovskite thin films (Pr1−xCaxMnO3) active for the oxygen evolution reaction (OER) from electro-catalytic water splitting. X-ray absorption near-edge spectroscopy (XANES) at the Mn L- and O K-edges, as well as X-ray photoemission spectroscopy (XPS) of the O 1s and Ca 2p states have been performed in ultra-high vacuum and in water vapor under positive applied bias at room temperature. It is shown that under the oxidizing conditions of the OER a reduced Mn2+ species is generated at the catalyst surface. The Mn valence shift is accompanied by the formation of surface oxygen vacancies. Annealing of the catalysts in O2 atmosphere at 120 °C restores the virgin surfaces.
机译:现场研究催化剂对于了解催化剂的表面结构和运行中的电子态具有极大的兴趣。本文中,我们研究了对氧析出反应具有活性的外延锰酸钙钙钛矿薄膜(Pr 1-x Ca x MnO 3 ) OER)由电催化水分解产生。已经在超高真空下进行了Mn L边缘和O K边缘的X射线吸收近边缘光谱(XANES)以及O 1s和Ca 2p态的X射线光发射光谱(XPS)。在室温下施加正偏压的水蒸气中。结果表明,在OER的氧化条件下,催化剂表面会生成还原的Mn 2 + 物种。 Mn价态转变伴随着表面氧空位的形成。在O 2 气氛中于120°C进行催化剂退火可恢复原始表面。

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