Department of Physics and European Theoretical Spectroscopy Facility, Université de Liège, Alleé du 6 août 17, Sart Tilman, B-4000, Liège, Belgium.
Phys Rev Lett. 2013 Jul 12;111(2):025503. doi: 10.1103/PhysRevLett.111.025503. Epub 2013 Jul 10.
In the 32-119 GPa pressure range and at room temperature, a simple cubic phase was reported for calcium in many different experiments. Standard linear response theory, both within density functional perturbation theory and frozen phonon calculations, presents dynamical instabilities for the simple cubic structure in the whole pressure range. Many other possible candidate phases, as well as several possible stabilization mechanisms for the simple cubic phase, have been proposed as the result of ab initio predictions but the role of temperature on the relative stability of the different phases has not been systematically investigated. We revisit the stability of the three most important candidate phases of calcium for the intermediate pressure range and for various temperatures, taking explicitly into account thermal corrections relative to electronic as well as phononic entropy and anharmonic contributions. This corrects the discrepancies among previous theoretical results and experiments and presents a different picture of the temperature driven phase transition, which results from dynamical anharmonic stabilization of simple cubic and destabilization of the tetragonal phase.
在 32-119 GPa 的压力范围和室温下,许多不同的实验都报道了钙的简单立方相。标准线性响应理论,无论是在密度泛函微扰理论还是冻结声子计算中,都呈现出简单立方结构在整个压力范围内的动力学不稳定性。作为从头算预测的结果,提出了许多其他可能的候选相以及几种可能稳定简单立方相的机制,但温度对不同相的相对稳定性的影响尚未得到系统研究。我们重新研究了钙在中间压力范围和各种温度下三种最重要的候选相的稳定性,明确考虑了相对于电子和声子熵以及非谐贡献的热修正。这纠正了以前理论结果与实验之间的差异,并呈现出一个不同的温度驱动相变的图景,这是由于简单立方的动力学非谐稳定和四方相的失稳所致。