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压力稳定的立方钙钛矿氢氧化物BaScOH

Pressure-Stabilized Cubic Perovskite Oxyhydride BaScOH.

作者信息

Goto Yoshihiro, Tassel Cédric, Noda Yasuto, Hernandez Olivier, Pickard Chris J, Green Mark A, Sakaebe Hikari, Taguchi Noboru, Uchimoto Yoshiharu, Kobayashi Yoji, Kageyama Hiroshi

机构信息

Department of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University , Kyoto 615-8510, Japan.

Division of Chemistry, Graduate School of Science, Kyoto University , Kyoto 606-8502, Japan.

出版信息

Inorg Chem. 2017 May 1;56(9):4840-4845. doi: 10.1021/acs.inorgchem.6b02834. Epub 2017 Apr 11.

Abstract

We report a scandium oxyhydride BaScOH prepared by solid state reaction under high pressure. Rietveld refinements against powder synchrotron X-ray and neutron diffraction data revealed that BaScOH adopts the ideal cubic perovskite structure (Pm3̅m), where oxide (O) and hydride (H) anions are disordered. H nuclear magnetic resonance (NMR) spectroscopy provides a positive chemical shift of about +4.4 ppm, which can be understood by the distance to the nearest (and possibly the next nearest) cation from the H nucleus. A further analysis of the NMR data and calculations based on ab initio random structure searches suggest a partial cis preference in ScOH octahedra. The present oxyhydride, if compositionally or structurally tuned, may become a candidate for H conductors.

摘要

我们报道了一种通过高压固态反应制备的氢氧钪化物BaScOH。基于粉末同步加速器X射线和中子衍射数据的Rietveld精修表明,BaScOH采用理想的立方钙钛矿结构(Pm3̅m),其中氧化物(O)和氢化物(H)阴离子是无序的。氢核磁共振(NMR)光谱给出了约+4.4 ppm的正化学位移,这可以通过氢原子核到最近(可能还有次近)阳离子的距离来理解。对NMR数据的进一步分析以及基于从头算随机结构搜索的计算表明,ScOH八面体中存在部分顺式偏好。如果对这种氢氧钪化物进行成分或结构调整,它可能成为氢导体的候选材料。

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