Rashba effects in lead-free ferroelectric semiconductor [CH3PH3]SnBr3

First-principles density functional theory computations are used to predict Rashba effects cofunctional with ferroelectricity in a recently synthesized lead-free hybrid organic-inorganic perovskite MPSnBr3 (MP=methylphosphonium, [CH3PH3]+). The ground state of the material is polar monoclinic with calculated spontaneous polarization of 3.01?C/cm2. It exhibits near band edges' spin splitting of up to 3.3 meV and Rashba coefficient up to 0.62 eV Å. The spin textures have different topology in the conduction and valence band, which originates from the difference in the spin-momentum coupling strengths. They occur in two orthogonal planes of the Brillouin zone and are coupled to the direction of spontaneous polarization. These features persist at a finite temperature of 293 K. At 333 K, that is, above monoclinic to orthorhombic phase transition, spontaneous polarization is reduced to 0.15?C/cm2, while the maximum spin splitting and Rashba coefficient reduce slightly to the values of 2.9 meV and 0.41 eV Å, respectively. The spin textures remain coupled with the polarization direction. We investigate the dependence of the aforementioned properties on the choice of computational methodology to extend the first-principles predictions to include finite temperature effects. We find that the predictions are sensitive to the methodology. Our study reveals the potential of MPSnBr3 for low-temperature applications in spintronics and quantum computing.