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Exploring the coordination change of vanadium and structure transformation of metavanadate MgV2O6 under high pressure

机译:高压下钒钒酸盐Mgv2O6钒和结构转化的协调变化

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Raman spectroscopy, synchrotron angle-dispersive X-ray diffraction (ADXRD), first-principles calculations, and electrical resistivity measurements were carried out under high pressure to investigate the structural stability and electrical transport properties of metavanadate MgV2O6. The results have revealed the coordination change of vanadium ions (from 5+1 to 6) at around 4?GPa. In addition, a pressure-induced structure transformation from the C2/m phase to the C2 phase in MgV2O6 was detected above 20?GPa, and both phases coexisted up to the highest pressure. This structural phase transition was induced by the enhanced distortions of MgO6 octahedra and VO6 octahedra under high pressure. Furthermore, the electrical resistivity decreased with pressure but exhibited different slope for these two phases, indicating that the pressure-induced structural phase transitions of MgV2O6 was also accompanied by the obvious changes in its electrical transport behavior.
机译:在高压下进行拉曼光谱,同步辐射角度分散X射线衍射(ADXRD),第一原理计算和电阻率测量,以研究MetavanAdate MgV2O6的结构稳定性和电气传输性能。结果揭示了钒离子(5 + 1至6)的协调变化在约4℃下的GPA。此外,检测到20μlMgv2O6中的C2 / M相的压力诱导的结构转化为MgV2O6中的C2相,并且两个相的两个相位相同至最高压力。这种结构相转变由MgO6 Octahedra和VO6八面体在高压下的增强扭曲引起的诱导。此外,电阻率随压力降低但是对于这两个阶段表现出不同的斜率,表明MgV2O6的压力诱导的结构相转变也伴随着其电气传输行为的明显变化。

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