Abstract

We report the crystal growth of well-faceted single crystals of methylammonium lead iodide, CH3NH3PbI3, and detailed single crystal neutron diffraction structural studies aimed at elucidating the orientation of the methylammonium (CH3NH3+) cation in the tetragonal and cubic phases of the hybrid inorganic–organic perovskite. Room temperature experiments reveal a tetragonal structure where the protonated amine substituent (−NH3+) of the cation is disordered in four positions, each preferentially located near the neighboring iodine of the [PbI6] octahedra, while the methyl substituent (−CH3) is disordered in eight positions located near the body position of the unit cell. High temperature experiments show a cubic structure where the cation aligns along the [011] (edge), the [111] (diagonal), and the [100] (face) directions of the unit cell. The resulting site occupancy ratio suggests the CH3NH3+ cation resides primarily along the [011] direction, in agreement with reported DFT calculations. One important fea...

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