Photothermally induced, reversible phase transition in methylammonium lead triiodide

TL;DR

This study uses ultrafast spectroscopy to directly measure the timescale of a reversible phase transition in methylammonium lead triiodide, revealing a tens of nanoseconds transition driven by photothermal effects.

Contribution

It provides the first direct, time-resolved measurement of the phase transition dynamics in methylammonium lead triiodide using cryogenic nanosecond transient absorption spectroscopy.

Findings

Phase transition occurs in tens of nanoseconds.

A significant fraction of the steady-state phase transition is transiently achieved.

Transition times are much slower than inorganic counterparts like VO2.

Abstract

Metal halide perovskites (MHPs) are known to undergo several structural phase transitions, from lower to higher symmetry, upon heating. While structural phase transitions have been investigated by a wide range of optical, thermal and electrical methods, most measurements are quasi-static and hence do not provide direct information regarding the fundamental timescale of phase transitions in this emerging class of semiconductors. Here we investigate the timescale of the orthorhombic-to-tetragonal phase transition in the prototypical metal halide perovskite, methylammonium lead triiodide (CH3NH3PbI3 or MAPbI3) using cryogenic nanosecond transient absorption spectroscopy. By using mid-infrared pump pulses to impulsively heat up the material at slightly below the phase-transition temperature and probing the transient optical response as a function of delay time, we observed a clean signature of a transient, reversible orthorhombic-to-tetragonal phase transition. The forward phase transition is found to proceed at tens of nanoseconds timescale, after which a backward phase transition progresses at a timescale commensurate with heat dissipation from the film to the underlying substrate. A high degree of transient phase transition is observed accounting for one third of the steady-state phase transition. In comparison to fully inorganic phase-change materials such as VO2, the orders of magnitude slower phase transition in MAPbI3 can be attributed to the large energy barrier associated with the strong hydrogen bonding between the organic cation and the inorganic framework. Our approach paves the way for unraveling phase transition dynamics in MHPs and other hybrid semiconducting materials.