Pressure-induced structural phase transition in BaHCl

被引:1
作者
Ubukata, Hiroki [1 ]
Ishida, Kohdai [1 ]
Higo, Yuji [2 ]
Tange, Yoshinori [2 ]
Broux, Thibault [1 ]
Tassel, Cedric [1 ]
Kageyama, Hiroshi [1 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
[2] Japan Synchrotron Radiat Res Inst, SPring 8, Sayo, Hyogo 6795198, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
Mixed anion; Hydride-chlorides; Phase transition; High pressure; PbFCl-type materials; BOND-VALENCE PARAMETERS; CRYSTAL-STRUCTURE; CONDUCTION;
D O I
10.1016/j.jssc.2022.123253
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
We have investigated the structural evolution of BaHCl under high pressure using in-situ synchrotron X-ray diffraction up to 30 GPa. The in-situ observation found that the ambient pressure BaHCl phase crystallizing in the PbFCl-type structure (P4/nmm) is transformed into an orthorhombic phase at 29 GPa and 300 K. Rietveld refinements of synchrotron X-ray and neutron diffraction data for the quenched sample revealed that BaHCl adopts PbCl2-type structure (Pnma), which consists of a distorted hcp framework of Ba2+ ions, with H- and Cl- ions at tetrahedral and octahedral interstitials, respectively. The complete ordering of anions in the PbCl2-type BaHCl contrasts with the partial ordering in the PbCl2-type AHF (A =1/4 alkali earth metal). This result may promote further exploration of hydride-based mixed anion materials and understanding and control of anion order/disorder.
引用
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页数:6
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