Pressure-induced ferroelectric-like transition creates a polar metal in defect antiperovskites Hg₃Te₂X₂ (X = Cl, Br).

ABSTRACT: Ferroelectricity is typically suppressed under hydrostatic compression because the short-range repulsions, which favor the nonpolar phase, increase more rapidly than the long-range interactions, which prefer the ferroelectric phase. Here, based on single-crystal X-ray diffraction and density-functional theory, we provide evidence of a ferroelectric-like transition from phase I2₁3 to R3 induced by pressure in two isostructural defect antiperovskites Hg₃Te₂Cl₂ (15.5 GPa) and Hg₃Te₂Br₂ (17.5 GPa). First-principles calculations show that this transition is attributed to pressure-induced softening of the infrared phonon mode Γ₄, similar to the archetypal ferroelectric material BaTiO₃ at ambient pressure. Additionally, we observe a gradual band-gap closing from ~2.5 eV to metallic-like state of Hg₃Te₂Br₂ with an unexpectedly stable R3 phase even after semiconductor-to-metal transition. This study demonstrates the possibility of emergence of polar metal under pressure in this class of materials and establishes the possibility of pressure-induced ferroelectric-like transition in perovskite-related systems.

SUBMITTER: Cai W 

PROVIDER: S-EPMC7940478 | biostudies-literature |

REPOSITORIES: biostudies-literature