Abstract
Chemically tuned organic-inorganic hybrid halide perovskites based on bromide and chloride anions CH(NH2)2Pb(Br1 − xClx)3 (CH(NH2)2+: formamidinium ion, FA) have been crystallized and investigated by neutron powder diffraction (NPD), single crystal X-ray diffraction (SCXRD), scanning electron microscopy (SEM) and UV-vis spectroscopy. CH(NH2)2PbBr3 and CH(NH2)2PbCl3 experience successive phase transitions upon cooling, lowering the symmetry from cubic to orthorhombic phases; however, these transitions are suppressed for the mixed halide phases, probably due to compositional disorder. The band-gap engineering brought about by the chemical doping of CH(NH2)2Pb(Br1 − xClx)3 perovskites (x = 0.0, 0.33, 0.5, 0.66 and 1.0) can be controllably tuned: the gap progressively increases with the concentration of Cl− ions from 2.17 to 2.91 eV at room temperature, presenting a nonlinear behavior. This study provides an improved understanding of the structural and optical properties of these appealing hybrid perovskites.