Photo-excited charge carrier lifetime enhanced by slow cation molecular dynamics in lead iodide perovskite FAPbI$_3$

Abstract

Using muon spin relaxation ($\mu$SR) measurements on formamidinium lead iodide [FAPbI$_3$, where FA denotes HC(NH$_2)_2$] we show that, among the five structurally distinct phases of FAPbI$_3$ exhibited through two different temperature hysteresis, the reorientation motion of FA molecules is quasi-static below $\approx50$ K over the time scale of 10$^{-6}$ s in the low-temperature (LT) hexagonal (Hex-LT, $<160$ K) phase which has relatively longer photo-excited charge carrier lifetime ($\tau_{\rm c}\sim$10$^{-6}$ s). In contrast, a sharp increase in the FA molecular motion was found above $\approx50$ K in the Hex-LT phase, LT-tetragonal phase (Tet-LT, $<140$ K), the high-temperature (HT) hexagonal phase (Hex-HT, 160-380 K), and the HT-tetragonal phase (Tet-HT, 140-280 K) where $\tau_{\rm c}$ decreases with increasing temperature. More interestingly, the reorientation motion is further promoted in the cubic phase at higher temperatures ($>380/280$ K), while $\tau_{\rm c}$ is recovered to comparable or larger than that of the LT phases. These results indicate that there are two factors that determine $\tau_{\rm c}$, one related to the local reorientation of cationic molecules that is not unencumbered by phonons, and the other to the high symmetry of the bulk crystal structure.