# Triplet harvesting in the polaritonic regime: a variational polaron approach

## TL;DR

This paper investigates how microcavities can enhance electroluminescence efficiency in molecular emitters by analyzing population dynamics and vibrational effects using a variational polaron approach.

## Contribution

It introduces a variationally optimized master equation to explore electroluminescence in molecular emitters under different vibrational and coupling regimes.

## Key findings

- Strong coupling can improve efficiency when the singlet-triplet transition is in the inverted Marcus regime.
- Vibrational relaxation into polaritons enhances photoluminescence for small emitter numbers.
- Delocalization of polaritons across many molecules can reduce electroluminescence efficiency.

## Abstract

We explore the electroluminescence efficiency for a quantum mechanical model of a large number of molecular emitters embedded in an optical microcavity. We characterize the circumstances under which a microcavity enhances harvesting of triplet excitons via reverse intersystem-crossing (R-ISC) into singlet populations that can emit light. For that end, we develop a time-local master equation in a variationally optimized frame which allows for the exploration of the population dynamics of chemically relevant species in different regimes of emitter coupling to the condensed phase vibrational bath and to the microcavity photonic mode. For a vibrational bath that equilibrates faster than R-ISC (in emitters with weak singlet-triplet mixing), our results reveal that significant improvements in efficiencies with respect to the cavity-free counterpart can be obtained for strong coupling of the singlet exciton to a photonic mode, as long as the singlet to triplet exciton transition is within the inverted Marcus regime; under these circumstances, we show the possibility to overcome the detrimental delocalization of the polariton states across a macroscopic number of molecules. On the other hand, for a vibrational bath that equilibrates slower than R-ISC (i.e., emitters with strong singlet-triplet mixing), we find that while enhancemnents in photoluminiscence can be obtained via vibrational relaxation into polaritons, this only occurs for small number of emitters coupled to the photon mode, with delocalization of the polaritons across many emitters eventually being detrimental to electroluminescence efficiency. These findings provide insight on the tunability of optoelectronic processes in molecular materials due to weak and strong light-matter coupling.