Abstract

Layered 2D halide perovskites with their alternating organic and inorganic atomic layers that form a self‐assembled quantum well system are analogues of the purely inorganic 2D transition metal dichalcogenides. Within their periodic structures lie a hotbed of photophysical phenomena such as dielectric confinement effect, optical Stark effect, strong exciton–photon coupling, etc. Detailed understanding into the strong light–matter interactions in these hybrid organic–inorganic semiconductor systems remains modest. Herein, the intricate coherent interplay of exciton, spin, and phonon dynamics in (C6H5C2H4NH3)2PbI4 thin films using transient optical spectroscopy is explicated. New insights into the hotly debated origins of transient spectral features, relaxation pathways, ultrafast spin relaxation via exchange interaction, and strong coherent exciton–phonon coupling are revealed from the detailed phenomenological modeling. Importantly, this work unravels the complex interplay of spin–quasiparticle interactions in these layered 2D halide perovskites with large spin–orbit coupling.

Highlights

  • There are growing interests in 2D perovskites due to their revealed from the detailed phenomenological modeling

  • Halide perovskites are in the limelight due to their outstanding tronic applications

  • We developed a phenomenological model which could satisfactorily replicate the experimental transient dynamics in PEPI

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Summary

Introduction

The intricate coherent interplay of exciton, spin, and dichalcogenide monolayers and can be phonon dynamics in (C6H5C2H4NH3)2PbI4 thin films using transient optical spectroscopy is explicated. We explicate the origins of the transient spectral features, coherent interactions, and dynamics between the photoexcited excitons, their spin and phonon subsystems in solution-processed (C6H5C2H4NH3)2PbI4 perovskite (hereafter termed PEPI) thin films using femtosecond (fs) transient absorption (TA) spectroscopy.

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