Department of Physics, Oakland University , Rochester, Michigan, 48309, United States.
J Phys Chem A. 2014 Mar 6;118(9):1713-20. doi: 10.1021/jp4124666. Epub 2014 Feb 19.
The high-pressure structural and vibrational properties of Bi2S3 have been probed up to 65 GPa with a combination of experimental and theoretical methods. The ambient-pressure Pnma structure is found to persist up to 50 GPa; further compression leads to structural disorder. Closer inspection of our structural and Raman spectroscopic results reveals notable compressibility changes in specific structural parameters of the Pnma phase beyond 4-6 GPa. By taking the available literature into account, we speculate that a second-order isostructural transition is realized near that pressure, originating probably from a topological modification of the Bi2S3 electronic structure near that pressure. Finally, the Bi(3+) lone-electron pair (LEP) stereochemical activity decreases against pressure increase; an utter vanishing, however, is not expected until 1 Mbar. This persistence of the Bi(3+) LEP activity in Bi2S3 can explain the absence of any structural transitions toward higher crystalline symmetries in the investigated pressure range.
采用实验和理论相结合的方法研究了 Bi2S3 的高压结构和振动特性,研究压力高达 65 GPa。常压下的 Pnma 结构在 50 GPa 之前保持稳定;进一步的压缩导致结构无序。对我们的结构和拉曼光谱结果的仔细检查表明,在 4-6 GPa 以上,Pnma 相的某些特定结构参数具有明显的可压缩性变化。考虑到现有文献,我们推测在该压力附近实现了二阶同构转变,可能源于该压力附近 Bi2S3 电子结构的拓扑修饰。最后,Bi(3+)孤对电子对(LEP)的立体化学活性随着压力的增加而降低;然而,预计在 1 Mbar 之前不会完全消失。Bi2S3 中 Bi(3+) LEP 活性的持续存在可以解释在研究的压力范围内,没有任何结构转变为更高的晶体对称性。