First-principles study of electronic, vibrational, elastic, and magnetic properties of FeF2as a function of pressure

Abstract

We report systematic ab initio calculations of the electronic band structure, phonon dispersion relation, and the structural characterization of FeF2 in the rutile (P 42/mnm) structure as well as in several high-pressure phases by means of the generalized gradient approximation (GGA) + U approximation. Using the phonon dispersion relations, we calculated the Gibbs free energy and evaluated the phase transitions at 300 K, at which most experimental measurements are performed. Calculated Raman and infrared vibrational modes, lattice parameters, and electronic structure for all considered crystalline structures are compared with available experimental data. Our calculations show that at 5.33 GPa, the FeF2 undergoes a second-order proper ferroelastic phase transition, rutile → CaCl2-type structure. This result is supported by the softening of the elastic shear module Cs in the rutile phase, the softening (hardening) of the B1g (Ag) Raman active mode in the rutile (CaCl2-type) structure near the transition pressure, and the decrease of the square of the spontaneous strain ess from the CaCl2-type structure. This demonstrates that the rutile → CaCl2-type phase transition is driven by the coupling between the Raman active B1g mode and shear modulus Cs. At 8.22 GPa, the CaCl2-type structure undergoes a first-order phase transition to the Pb caphase, a distorted fcc Pa ¯ -3