A Novel Strategy toward Thermally Activated Delayed Fluorescence from a Locally Excited State

It is well-known that thermally activated delayed fluorescence (TADF) is always generated from charge-transfer (CT) excited states in donor-acceptor (D-A) systems, which limits its application owing to a slow radiative process and a small stimulated emission cross section. Herein, a design strategy is proposed for realizing TADF from a locally excited (LE) state without a typical donor-acceptor type structure through controlling the intersystem crossing(ISC) and reverse intersystem crossing (RISC) processes between the lowest excited singlet with LE character and higher triplet states. Using this strategy, a boron difluoride derivative is theoretically predicted and experimentally synthesized to exhibit locally excited TADF (LE-TADF) with a fairly large radiative rate of 1.12x108s-1, extremely fast RISC rate of 5.09x1010s-1, and a large stimulated emission cross section of 4.35x10-17cm2, making this a promising organic amplified spontaneous emission (ASE) material. This work might open a new avenue to extend TADF materials, especially TADF laser emitters.

Automated summary

This study proposes a new design strategy to achieve thermally activated delayed fluorescence (TADF) without a typical donor-acceptor structure by controlling the processes between different excited states. Theoretical predictions and experimental synthesis show that a boron difluoride derivative synthesized using this strategy exhibits high radiative rate, fast reverse intersystem crossing rate, and large stimulated emission cross section, making it a promising material for organic amplified spontaneous emission (ASE).