Persistent Enhancement of Exciton Diffusivity in CsPbBr3 Nanocrystal Solids

TL;DR

This study reveals that exciton diffusivity in CsPbBr3 nanocrystal solids can be persistently enhanced by recent excitation, due to an intrinsic lattice response, leading to significantly faster exciton transport than previously observed.

Contribution

It demonstrates a novel, intrinsic, excitation-dependent enhancement of exciton diffusivity in CsPbBr3 nanocrystals, independent of nonlinear interactions or surface effects.

Findings

Exciton diffusivity can be increased by recent excitation history.

The enhanced diffusivity persists for microseconds at room temperature.

The observed diffusivity exceeds 0.15 cm²/s, indicating strong excitonic coupling.

Abstract

In semiconductors, exciton or charge carrier diffusivity is typically described as an inherent material property. Here, we show that the transport of excitons (i.e., bound electron-hole pairs) in CsPbBr3 perovskite nanocrystals (NCs) depends markedly on how recently those NCs were occupied by a previous exciton. Using fluence- and repetition-rate-dependent transient photoluminescence microscopy, we visualize the effect of excitation frequency on exciton transport in CsPbBr3 NC solids. Surprisingly, we observe a striking dependence of the apparent exciton diffusivity on excitation laser power that does not arise from nonlinear exciton-exciton interactions nor from thermal heating of the sample. We interpret our observations with a model in which excitons cause NCs to undergo a transition to a metastable configuration that admits faster exciton transport by roughly an order of magnitude. This metastable configuration persists for ~microseconds at room temperature, and does not depend on the identity of surface ligands or presence of an oxide shell, suggesting that it is an intrinsic response of the perovskite lattice to electronic excitation. The exciton diffusivity observed here (>0.15 cm2/s) is considerably higher than that observed in other NC systems on similar timescales, revealing unusually strong excitonic coupling in a NC material. The finding of a persistent enhancement in excitonic coupling between NCs may help explain other extraordinary photophysical behaviors observed in CsPbBr3 NC arrays, such as superfluorescence. Additionally, faster exciton diffusivity under higher photoexcitation intensity is likely to provide practical insights for optoelectronic device engineering.