Multi Band Gap Electronic Structure in CH3NH3PbI3

Abstract

Organo-lead halide perovskite solar cells represent a revolutionary shift in solar photovoltaics, introducing relatively soft defect containing semiconductors as materials with excellent charge collection for both electrons and holes. Although they are based on the nominally simple cubic perovskite structure, these compounds are in fact very complex. For example, in (CH₃NH₃)PbI₃ the dynamics and ensuing structural fluctuations associated with the (CH₃NH₃)⁺ ions and the interplay with the electronic properties are still not fully understood, despite extensive study. Here, using ab-initio calculations, we show that at room and higher temperature, the rotation of CH₃NH₃ molecules can be viewed as effectively giving local structures that are cubic and tetragonal like from the point of view of the PbI₃ framework, though in fact having lower symmetry. Both of these structures are locally polar, with sizable polarization, ~10 μC/cm² due to the dipoles on the organic. They become energetically degenerate in the volume range, V ~ 250 ų/f.u–265 ų/f.u. We also find very significant dependence of the band gap on the local structure. This type of transition is analogous to a transition between two ferroelectric structures, where in-spite of strong electron phonon coupling, there is strong screening of charged defects which can lead to enhanced mobility and charge collection. The results provide insights into the enhanced light absorption near the band edge and good charge collection in this material.