Linker aggregation engineering of TADF materials to tune carrierbalance for highly efficient organic LEDs with long operationallifetime

Thermally activated delayedfluorescence(TADF)molecules are regarded as promis-ing materials for realizing high-performance organic light-emitting diodes(OLEDs).The connecting groups between donor(D)and acceptor(A)units in D–A type TADF molecules could affect the charge transfer and luminescence performance of TADF materials in aggregated states.In this work,we design and synthesize four TADF molecules using planar and twisted linkers to connect the aza-azulene donor(D)and triazine acceptor(A).Compared with planar linkers,the twisted ones(Az-NP-T and Az-NN-T)can enhance A–A aggregation interaction between adjacent molecules to balance hole and electron density.As a result,highly efficient and stable deep-red top-emission OLEDs with a high electroluminescence efficiency of 57.3%and an impressive long operational lifetime(LT_(95)∼30,000 h,initial luminance of 1000 cd m^(-2))are obtained.This study provides a new strategy for designing more effi-cient and stable electroluminescent devices through linker aggregation engineering in donor–acceptor molecules.