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Highly Efficient Oxygen Evolution Activity of Ca2IrO4 in an Acidic Environment due to Its CrystalConfiguration

机译:Ca2IrO4的结晶性使其在酸性环境中具有高效的析氧活性组态

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摘要

We systematically characterized the perovskite-like oxides Ca2IrO4 and CaIrO3 as the oxygen evolution reaction (OER) catalysts. Compared with IrO2, universally accepted as the current state-of-the-art OER catalyst, Ca2IrO4 showed an excellent OER catalytic activity in an acidic environment, whereas CaIrO3 did not. X-ray photoelectron spectroscopy (XPS) spectra showed that the oxidation of iridium in Ca2IrO4 and CaIrO3 was slightly beyond +4. X-ray absorption near-edge structure (XANES) spectra illustrated that the IrO6 octahedral geometric structure in Ca2IrO4 and CaIrO3 showed differences. The IrO6 octahedral is asymmetrically distorted and uniformly compressed in Ca2IrO4 and CaIrO3. Therefore, we propose that the IrO6 octahedral distortion plays an important role in the OER activities.
机译:我们系统地将钙钛矿状氧化物Ca2IrO4和CaIrO3表征为析氧反应(OER)催化剂。与普遍公认的当前最先进的OER催化剂IrO2相比,Ca2IrO4在酸性环境中显示出优异的OER催化活性,而CaIrO3没有。 X射线光电子能谱(XPS)表明,Ca2IrO4和CaIrO3中铱的氧化程度略高于+4。 X射线吸收近边缘结构(XANES)光谱表明,Ca2IrO4和CaIrO3中的IrO6八面体几何结构存在差异。 IrO6八面体在Ca2IrO 4 和CaIrO 3 中不对称变形并均匀压缩。因此,我们提出IrO 6 八面体畸变在OER活动中起重要作用。

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