单斜晶系
拉曼光谱
材料科学
相(物质)
正交晶系
固体氢
分子内力
软化
分子间力
氢
结晶学
氢键
环境压力
相变
分析化学(期刊)
热力学
化学
晶体结构
分子
立体化学
复合材料
物理
有机化学
光学
作者
Xiaoli Huang,Fangfei Li,Yanping Huang,Gang Wu,Xin Li,Qiang Zhou,Bingbing Liu,Tian Cui
出处
期刊:Chinese Physics B
[IOP Publishing]
日期:2016-03-01
卷期号:25 (3): 037401-037401
被引量:15
标识
DOI:10.1088/1674-1056/25/3/037401
摘要
The high-pressure behavior of solid hydrogen has been investigated by in situ Raman spectroscopy upon compression to 300 GPa at ambient temperature. The hydrogen vibron frequency begins to decrease after it initially increases with pressure up to 38 GPa. This softening behavior suggests the weakening of the intramolecular bond and the increased intermolecular interactions. Above 237 GPa, the vibron frequency softens very rapidly with pressure at a much higher rate than that of phase III, corresponding to transformation from phase III into phase IV. The phase transition sequence has been confirmed from phase I to phase III and then to phase IV at 208 and 237 GPa, respectively. Previous theoretical calculations lead to the proposal of an energetically favorable monoclinic C2/c structure for phase III and orthorhombic Pbcn structure for phase IV. Up to 304 GPa, solid hydrogen is not yet an alkali metal since the sample is still transparent.
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