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

We present an ab initio molecular dynamics study of the temperature-induced phases of methylammonium lead bromide (MAPbBr(3)). 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 Pm (3) over barm 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 center dot center dot center dot 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.

Automated summary

In this study, we investigated the temperature-induced phases of methylammonium lead bromide using ab initio molecular dynamics simulations. We found that the low-temperature phase is not ferroelectric and the distortions in this phase originate from octahedral scissoring modes. However, these distortions disappear at room temperature. The predicted timescales of methylammonium (MA) motion matched well with experimental estimates, indicating dynamic disordering of the molecular dipoles at room temperature. We also identified the key modes of the inorganic and organic sublattices that are coupled through hydrogen bonding, which showed a strong connection between the organic-inorganic hybrid perovskites and the lifetimes of the hydrogen bonds.