学术文献库

We present the results of a theoretical investigation of the linear thermal expansion coefficients (TECs) of BeF$_2$, within a direct Gruneisen formalism where symmetry-preserving deformations are employed. The required physical quantities such as the optimized crystal structures, elastic constants, mode Gruneisen parameters, and phonon density of states are calculated from first-principles. BeF$_2$ shows an extensive polymorphism at low pressures, and the lowest energy phases [$α$-cristobalite with space group (SG) P$4_1 2_1 2$ and its similar phase with SG P$4_3 2_1 2$] are considered in addition to the experimentally observed $α$-quartz phase. For benchmarking purposes, similar calculations are performed for the rutile phase of ZnF$_2$, where the volumetric TEC ($α_v$), derived from the calculated linear TECs along the $a$ ($α_a$) and $c$ ($α_c$) directions, is in very good agreement with experimental data and previous theoretical results. For the considered phases of BeF$_2$, we do not find any negative thermal expansion (NTE). However we observe diverse thermal properties for the distinct phases. The linear TECs are very large, especially $α_c$ of the $α$-cristobalite phase and its similar phase, leading to giant $α_v$ ($\sim 175 \times 10^{-6} {\rm K}^{-1}$ at 300 K). The giant $α_v$ arises from large Gruneisen parameters of low-frequency phonon modes, and the C13 elastic constant that is negatively signed and large in magnitude for the $α$-cristobalite phase. The elastic constants, high-frequency dielectric constants, Born effective charge tensors, and thermal properties of the above phases of BeF$_2$ are reported for the first time and hence serve as predictions.