Quinoxaline-based thermally activated delayed fluorescence emitters for highly efficient organic light-emitting diodes†
Abstract
Thermally activated delayed fluorescence (TADF) materials are regarded as the most promising next-generation emitters in organic light-emitting diodes (OLEDs). In this work, three TADF compounds were designed and synthesized based on 1,2,3,4-tetrahydrophenazine as acceptor and 9,9-dimethyl-9,10-dihydroacridine (DMAC-TTPZ), phenoxazine (PXZ-TTPZ), and phenothiazine (PTZ-TTPZ) as donors. Wherein, cyclohexane was introduced to the acceptor segment to improve solubility and weaken the conjugate degree to realize blue-shifted emission. Due to the twisted conformation, the frontier molecular orbital (FMO) overlap was largely minimized, resulting in small singlet-triplet energy splitting (ΔEST) of 0.15, 0.09, and 0.07 eV for DMAC-TTPZ, PXZ-TTPZ, and PTZ-TTPZ, respectively. Taking these compounds as emitters for OLEDs, maximum brightness, power efficiency (PE), and external quantum efficiency (EQE) of up to 36 480 cd m−2, 41.0 lm W−1, and 15.3% were achieved, demonstrating their potential in OLEDs.