Unveiling the TADF Emitters with Apparent Negative Singlet‐Triplet Gaps: Implications for Exciton Harvesting and OLED Performance

Abstract Intramolecular through‐space charge transfer thermally activated delayed fluorescence (TSCT‐TADF) has attracted much attention recently as it can achieve both small energy splitting and high emission efficiency. However, the relationship of excited states between TSCT and through‐bond charge transfer (TBCT) remains a challenge in the TSCT‐TADF molecules. Herein, three compounds DPS‐ m ‐bAc, DPS‐ p ‐bAc, and DPS‐OAc that possess emissive TSCT and/or TBCT states are prepared. Interestingly, a so‐called inverted energy gap is found for both DPS‐ m ‐bAc and DPS‐ p ‐bAc in toluene solution, which results from the different charge transfer states of ICT high and ICT low , as proved by the detailed transient photoluminescence and calculated results. Intense emission from blue to yellow associated with high photoluminescence quantum yields of 70–100% are measured in doped polymethyl(methacrylate) (PMMA) films. Notably, compound DPS‐ m ‐bAc achieves the highest reverse intersystem crossing rate constant ( k RISC ) of over 10 7 s −1 in a PMMA film, benefiting from close‐lying TSCT and TBCT states. The solution‐processed device with DPS‐ m ‐bAc displays a maximum external quantum efficiency of 21.7% and a relatively small efficiency roll‐off ( EQE of 20.2% @ 100 cd m −2 ). Overall, this work demonstrates how with judicious emitter engineering, a synergy between different charge transfer excited states, can be achieved, providing an avenue to achieve highly efficient solution‐processed OLEDs.