Abstract

Strong light-matter coupling provides the means to challenge the traditional rules of chemistry. In particular, an energy inversion of singlet and triplet excited states would be fundamentally remarkable since it would violate the classical Hund’s rule. An organic chromophore possessing a lower singlet excited state can effectively harvest the dark triplet states, thus enabling 100% internal quantum efficiency in electrically pumped light-emitting diodes and lasers. Here we demonstrate unambiguously an inversion of singlet and triplet excited states of a prototype molecule by strong coupling to an optical cavity. The inversion not only implies that the polaritonic state lies at a lower energy, but also a direct energy pathway between the triplet and polaritonic states is opened. The intrinsic photophysics of reversed-intersystem crossing are thereby completely overturned from an endothermic process to an exothermic one. By doing so, we show that it is possible to break the limit of Hund’s rule and manipulate the energy flow in molecular systems by strong light-matter coupling. Our results will directly promote the development of organic light-emitting diodes based on reversed-intersystem crossing. Moreover, we anticipate that it provides the pathway to the creation of electrically pumped polaritonic lasers in organic systems.

Highlights

  • Strong light-matter coupling provides the means to challenge the traditional rules of chemistry

  • Thermally activated delayed fluorescence (TADF) has aroused tremendous interest as it harvests the energy of triplet states through reversed-intersystem crossing (RISC) to the corresponding emissive singlet state

  • We show that the formed polaritonic state is energetically inverted with the molecular triplet state by measuring prompt and delayed emission

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Summary

Introduction

Strong light-matter coupling provides the means to challenge the traditional rules of chemistry. The triplet state (T1) always possesses a lower energy than the corresponding singlet state (S1) due to subtle electron-electron interactions This phenomena is commonly referred as Hund’s rule[1], and it results in energy transfer from T1 to S1 being an endothermic process. Thermally activated delayed fluorescence (TADF) has aroused tremendous interest as it harvests the energy of triplet states through reversed-intersystem crossing (RISC) to the corresponding emissive singlet state. This process requires a small energy gap (ΔE) between T1 and S1. The connection is lost with a too low matter contribution to the lower polariton, which could be an explanation to earlier observations

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