Conformational Dynamics Guides Coherent Exciton Migration in Conjugated Polymer Materials: A First-Principles Quantum Dynamical Study

TL;DR

This study uses first-principles quantum simulations to reveal how conformational changes in conjugated polymers facilitate ultrafast, coherent exciton migration, driven by torsional relaxation and exciton-polaron formation.

Contribution

It provides a detailed first-principles analysis of the ultrafast exciton migration mechanism in conjugated polymers, emphasizing the role of conformational dynamics.

Findings

Exciton-polaron formation occurs within tens of femtoseconds.

Torsional relaxation drives exciton migration on a ~300 fs timescale.

Quantum coherence is maintained during ultrafast exciton transfer.

Abstract

We report on high-dimensional quantum dynamical simulations of torsion-induced exciton migration in a single-chain oligothiophene segment comprising twenty repeat units, using a first-principles parametrized Frenkel J-aggregate Hamiltonian. Starting from an initial inter-ring torsional defect, these simulations provide evidence of an ultrafast two-time scale process at low temperatures, involving exciton-polaron formation within tens of femtoseconds, followed by torsional relaxation on a ~300 femtosecond time scale. The second step is the driving force for exciton migration, as initial conjugation breaks are removed by dynamical planarization. The quantum coherent nature of the elementary exciton migration step is consistent with experimental observations highlighting the correlated and vibrationally coherent nature of the dynamics on ultrafast time scales.