Using Fluorescence Detected Two-Dimensional Spectroscopy to Investigate Initial Exciton Delocalization Between Coupled Chromophores

TL;DR

This paper demonstrates how Fluorescence Detected Two-Dimensional Spectroscopy can detect initial exciton delocalization and coherence between coupled chromophores, challenging traditional assumptions of incoherent energy transfer in molecular systems.

Contribution

It provides a theoretical framework using fourth order perturbation theory to identify conditions for observing donor-acceptor coherence at zero waiting time in FD2DS.

Findings

Identifies conditions for coherence-induced cross-peaks at zero waiting time.

Provides an analytical solution for a heterodimer model.

Challenges the assumption of immediate incoherent energy transfer.

Abstract

F\"orster theory describes electronic exciton energy migration in molecular assemblies as an incoherent hopping process between donor and acceptor molecules. The rate is expressed in terms of the overlap integral between donor fluorescence and acceptor absorption spectra. Typical time scales for systems like photosynthetic antennae are on the order of a few picoseconds. Prior to transfer it is assumed that the initially excited donor molecule has equilibrated with respect to the local environment. However, upon excitation and during the equilibration phase the state of the system needs to be described by the full density matrix, including coherences between donor and acceptor states. While being intuitively clear, addressing this regime experimentally has been a challenge until the recently reported advances in Fluorescence Detected Two-Dimensional Spectroscopy (FD2DS). Here, we demonstrate using fourth order perturbation theory, the conditions for the presence of donor-acceptor coherence induced cross-peaks at zero waiting time between the first and the second pair of pulses. The approach is illustrated for a heterodimer model which facilitates an analytical solution.