Triplet Excited-State Dynamics in Benzothiadiazole-Based Thermally Activated Delayed Fluorescence Compound

The "hot exciton" thermally activated delayed fluorescence (TADF) materials have attracted considerable research interest for their utilization of high-lying triplet excitons. In this work, we reported the mechanism of photoluminescence by revealing the spectral evolution from singlet to triplet states in "hot exciton" TADF molecules by transient absorption (TA) spectra and triplet sensitization experiments. The internal conversion and intersystem crossing are much faster than reverse intersystem crossing (RISC), so that high-lying triplet states (T) are difficult to accumulate to be observed in the transient absorption spectra. In contrast, the emergence of delayed fluorescence in time-resolved emission spectra demonstrates the existence of a high-lying RISC process (hRISC) from T to S₁. Triplet sensitization experiments successfully identified the spectral features of the T₁ state in the TA spectra. This work sheds light on critical factors for the systematic design of these materials to achieve a high emission quantum yield.