Time-Domain Observation of Ultrafast Self-Trapped Exciton Formation in Lead-Free Double Halide Perovskites

Self-trapped excitons (STEs), which have one or both carriers spatially trapped by a lattice distortion, are associated with broadband emission and a large Stokes shift that is desirable for many applications. The fundamental physical processes that lead to their formation are difficult to observe, mainly due to the ultrafast time scales involved and the low oscillator strength of STE transitions. Here, we employ ultrafast transient absorption spectroscopy with sub-20 fs temporal resolution in the ultraviolet to study the STE formation process in a pair of lead-free double perovskites, Cs2AgInCl6 and Cs2(Ag0.6Na0.4)InCl6. Using first-principles calculations, we assign a broad photoinduced absorption band in Cs2AgInCl6 to an intraband transition in the valence band that tracks the initial 70 fs hot-hole cooling step. Furthermore, exciton-phonon coupling calculations unravel the phonon modes that couple strongly with excitons in the lowest absorption peak to cause self-trapping. The transient absorption data shows the buildup of a stimulated emission band from the STE on a 200 fs time scale and long-lived coherent oscillations corresponding to the phonons of the lattice modified by the STE formation process.