首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Postperovskite Phase Transition of ZnGeO_3: Comparative Crystal Chemistry of Postperovskite Phase Transition from Germanate Perovskites
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Postperovskite Phase Transition of ZnGeO_3: Comparative Crystal Chemistry of Postperovskite Phase Transition from Germanate Perovskites

机译:ZnGeO_3的钙钛矿后相变:锗酸盐钙钛矿中钙钛矿后相变的比较晶体化学

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摘要

The postperovskite phase of ZnGeO_3 was confirmed by laser heating experiments of the perovskite phase under 110-130 GPa at high temperature. Ab initio calculations indicated that the phase transition occurs at 133 GPa at 0 K. This postperovskite transition pressure is significantly higher than those reported for other germanates, such as MnGeO_3 and MgGeO_3. The comparative crystal chemistry of the perovskite-to-postperovskite transition suggests that a relatively elongated b-axis in the low-pressure range resulted in the delay in the transition to the postperovskite phase. Similar to most GdFeO_3-type perovskites that transform to the CaIrO_3-type postperovskite phase, ZnGeO_3 perovskite eventually transformed to the CaIrO_3-type postperovskite phase at a critical rotational angle of the GeO_6 octahedron. The formation of the postperovskite structure at a very low critical rotational angle for MnGeO_3 suggests that relatively large divalent cations likely break down the cornersharing GeO_6 frameworks without a large rotation of GeO_6 to form the postperovskite phase.
机译:ZnGeO_3的钙钛矿后相通过110-130 GPa高温下钙钛矿相的激光加热实验确定。从头算计算表明,在0 K下,相变发生在133 GPa处。该钙钛矿后的转变压力显着高于其他锗酸盐(如MnGeO_3和MgGeO_3)的报道压力。钙钛矿过渡到钙钛矿后过渡的比较晶体化学表明,低压范围内相对较长的b轴导致过渡到钙钛矿后过渡的延迟。与大多数转变为CaIrO_3型钙钛矿后相的GdFeO_3型钙钛矿相类似,ZnGeO_3钙钛矿最终以GeO_6八面体的临界旋转角转变为CaIrO_3型钙钛矿后相。对于MnGeO_3,在非常低的临界旋转角处形成钙钛矿后结构,表明相对较大的二价阳离子可能会破坏边角共享的GeO_6骨架,而不会大量旋转GeO_6形成钙钛矿后相。

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