Organic Phosphorescence Lasing Based on a Thermally Activated Delayed Fluorescence Emitter

Organic phosphorescence materials provide an opportunity to use triplets for lasing. However, population inversion based on phosphorescence is hard to establish, owing to low luminescent quantum efficiency and intensive optical loss. By comparison, thermally activated delayed fluorescence emitters exhibit excellent optical gain with the aid of the reverse intersystem crossing (RISC) process. In this work, we designed a multifunctional gain material, not only serving as a thermally activated delayed fluorescence (TADF) emitter with excellent optical gain but also working as a phosphorescence source with high utilization of triplets. The lone pair of electrons in oxygen substitutions promotes a fast spin-flip and high delayed fluorescence quantum yield (Φ DF = 55%), enabling TADF amplified spontaneous emissions (ASE) of CH 2 Cl 2 solution. Single-crystalline nanowires of H-aggregates effectively lower triplet energy levels with high phosphorescence quantum yield (Φ P = 27%), demonstrating Fabry–Perot mode phosphorescence lasing at 630 nm.