Pressure-Induced Structural and Electronic Properties of Inorganic Halide Perovskite Cspbbr3

Abstract

In this paper, density functional theory (DFT) based on first principles is used to study the influence of pressure on the structural and electronic properties of the cubic and orthorhombic phases of halogen perovskite CsPbBr3. We observe that the lattice constant of the cubic phase shows a monotonically decreasing trend in a wide pressure range, while the Pb-Br irregular octahedron of the orthorhombic phase rotates under pressure and distorts at 67 and 70GPa pressure points, respectively. Moreover, the pressure has a good adjustment effect on the band gap of the cubic and orthorhombic phases. The band gap of the orthorhombic phase changes between the direct band gap and the indirect band gap under pressure. The charge difference density and density of states are calculated to study the type of bonds between internal atoms and the effect of pressure on the distribution of orbital electrons. The study of the overlap population and lattice energy of the electron cloud shows that the pressure has a significant adjustment effect on the strength of the Pb-Br covalent bond and the Cs-Br ionic bond. These results provide a comprehensive reference and guidance for the further research and application of perovskite material pressure engineering.

Keywords: pressure, CsPbBr3, First-principles calculation, Structural and electronic properties