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Reversal of the Lattice Structure in SrCoOx Epitaxial Thin Films Studied by Real-Time Optical Spectroscopy and First-Principles Calculations

机译:实时光谱法和第一性原理研究的SrCoOx外延薄膜晶格结构的反转

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摘要

Using real-time spectroscopic ellipsometry, we directly observed a reversible lattice and electronic structure evolution in SrCoOx (x = 2.5-3) epitaxial thin films. Drastically different electronic ground states, which are extremely susceptible to the oxygen content x, are found in the two topotactic phases: i.e., the brownmillerite SrCoO2.5 and the perovskite SrCoO3. First-principles calculations confirmed substantial differences in the electronic structure, including a metal-insulator transition, which originate from the modification in the Co valence states and crystallographic structures. More interestingly, the two phases can be reversibly controlled by changing the ambient pressure at greatly reduced temperatures. Our finding provides an important pathway to understanding the novel oxygen-content-dependent phase transition uniquely found in multivalent transition metal oxides
机译:使用实时光谱椭偏仪,我们直接观察到SrCoOx(x = 2.5-3)外延薄膜中的可逆晶格和电子结构演变。在两个定势相中发现了完全不同的电子基态,这些基态对氧含量x极度敏感:即,棕褐色SrCoO2.5和钙钛矿SrCoO3。第一性原理的计算证实了电子结构的重大差异,包括金属-绝缘体的跃迁,这是由共价态和晶体结构的变化引起的。更有趣的是,可以通过在大大降低的温度下改变环境压力来可逆地控制这两相。我们的发现为理解多价过渡金属氧化物中独特的新型氧含量依赖性相变提供了重要途径

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