Photoinduced metastable cation disorder in metal halide double perovskites

TL;DR

This study uncovers a photoinduced metastable phase in Cs2AgInCl6 double perovskites, driven by B-site disorder and STE formation, leading to prolonged transient states with potential optoelectronic applications.

Contribution

It reveals a new photoinduced disorder mechanism in lead-free double perovskites, supported by experimental and theoretical analysis, expanding understanding of their excited-state dynamics.

Findings

Identification of a long-lived metastable phase with millisecond lifetime.

B-site (Ag-In) disorder reduces the optical bandgap significantly.

Photogenerated STEs oxidize Ag+ to Ag2+, facilitating disorder transition.

Abstract

Lead-free perovskites have emerged as environmentally benign alternatives to lead-halide counterparts for optoelectronics. Among them, the double perovskite Cs2AgInCl6 family exhibits remarkable white-light emission with proper composition engineering, enabled by strong electron-phonon coupling and the formation of self-trapped excitons (STEs). Despite these advantages, the fundamental photo- and structural dynamics governing their excited-state behavior remain poorly understood. Here, we report a long-lived metastable phase in the Cs2AgInCl6 double perovskite family and unravel this process and the concomitant electronic and structural evolution using a suite of tools including transient optical spectroscopy, time-resolved X-ray diffraction (TR-XRD) and X-ray absorption (TR-XAS). We show that the photoinduced, transient metastable phase is associated with B-site (Ag-In) disorder, which induces a dramatically reduced optical bandgap. Supported by TR-XRD and first-principles calculations, the Ag-In disorder drives the formation of Ag-rich and In-rich domains with millisecond lifetimes, with lifetimes increasing at lower temperatures. TR-XAS further reveals that photogenerated STEs oxidize Ag+ to Ag2+, facilitating this highly temporally asymmetric order-disorder transition. Our findings demonstrate a new mechanism, mediated by hole-localized STE formation, that enables prolongation of transient light-induced states to the multi-millisecond regime in double perovskites, opening possibilities to harvesting the functional properties of metastable phases of these materials.