Deciphering the Nature of Temperature-Induced Phases of MAPbBr3 by Ab Initio Molecular Dynamics

Abstract

We present an ab initio molecular dynamics study of the temperature-induced phases of methylammonium lead bromide (MAPbBr3). We confirm that the low-temperature phase is not ferroelectric and rule out the presence of any overall polarization arising from the motion of the individual sublattices. Our simulations at room temperature resulted in a cubic Pm3̅m phase with no discernible local orthorhombic distortions. At low temperatures, such distortions are shown to originate from octahedral scissoring modes, but they vanish at room temperature. The predicted timescales of MA motion agree very well with experimental estimates, establishing dynamic disordering of the molecular dipoles over several orientational minima at room temperature. We also identify the key modes of the inorganic and organic sublattices that are coupled at all temperatures, mainly through the N–H···Br hydrogen bonds. Estimated lifetimes of the H bonds correlate well with MA dynamics, indicating a strong connection between these two aspects of organic–inorganic hybrid perovskites. We also confirm that, in addition to the disordering of MA orientations, the transition to the cubic phase is also associated with displacive characteristics arising from both MA and Br ions in the lattice.