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Change in compression in M$$^{3+}$$OOH oxyhydroxide and implication for hydrogen bond symmetrization

M$$^{3+}$$OOH水酸化物における圧縮挙動の変化と水素結合対称化

佐野 亜沙美   ; 八木 健彦*; 岡田 卓*; 後藤 弘匡*; 鍵 裕之*; 永井 隆哉*; 亀卦川 卓美*

Sano, Asami; Yagi, Takehiko*; Okada, Taku*; Goto, Hirotada*; Kagi, Hiroyuki*; Nagai, Takaya*; Kikegawa, Takumi*

InOOH-type M$$^{3+}$$OOH with distorted rutile structure is one of the densest polymorph among oxyhydroxide, and has a strong hydrogen bond. Previous X-ray diffraction study on aluminum oxyhydroxide, $$delta$$-AlOOH(D), reported the change in axial compressibility and axial ratio at high pressure. This change has been attributed to the transition from the structure with asymmetric hydrogen bond (spacegroup P2$$_{1}$$nm) to disordered or symmetric hydrogen bond (Pnnm), that is previously predicted by theoretical and neutron studies. To investigate the detail of the change in compression mechanism in InOOH-type M$$^{3+}$$OOH, we conducted compression experiments on InOOH-type GaOOH (P2$$_{1}$$nm) and CrOOH (guyanaite; Pnnm). In GaOOH, similar behavior to $$delta$$-AlOOH was obtained: b/c decreases rapidly as pressure increases to 10 GPa, but it increases at the pressure range from about 10 to 30 GPa. On the other hand, b/c of CrOOH simply increases to 31 GPa.

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