Zhang Huichao, Tóth Ondrej, Liu Xiao-Di, Bini Roberto, Gregoryanz Eugene, Dalladay-Simpson Philip, De Panfilis Simone, Santoro Mario, Gorelli Federico Aiace, Martoňák Roman
Key Laboratory of Materials Physics, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 230031, China.
University of Science and Technology of China, Hefei 230026, China.
Proc Natl Acad Sci U S A. 2020 Apr 21;117(16):8736-8742. doi: 10.1073/pnas.1917749117. Epub 2020 Apr 3.
We report here the pressure-induced amorphization and reversible structural transformation between two amorphous forms of SO: molecular amorphous and polymeric amorphous, with the transition found at 26 GPa over a broad temperature regime, 77 K to 300 K. The transformation was observed by both Raman spectroscopy and X-ray diffraction in a diamond anvil cell. The results were corroborated by ab initio molecular dynamics simulations, where both forward and reverse transitions were detected, opening a window to detailed analysis of the respective local structures. The high-pressure polymeric amorphous form was found to consist mainly of disordered polymeric chains made of three-coordinated sulfur atoms connected via oxygen atoms, with few residual intact molecules. This study provides an example of polyamorphism in a system consisting of simple molecules with multiple bonds.
我们在此报告压力诱导的SO的非晶化以及两种非晶形式(分子非晶和聚合物非晶)之间的可逆结构转变,该转变在26 GPa下于77 K至300 K的宽温度范围内被发现。在金刚石对顶砧中通过拉曼光谱和X射线衍射观察到了这种转变。从头算分子动力学模拟证实了该结果,其中检测到了正向和反向转变,为详细分析各自的局部结构打开了一扇窗口。发现高压聚合物非晶形式主要由通过氧原子连接的三配位硫原子构成的无序聚合物链组成,几乎没有残留的完整分子。这项研究提供了一个由具有多个键的简单分子组成的系统中多晶型现象的例子。