Efficient donor-σ-acceptor emitters with strengthened intramolecular charge-transfer and their use for high-efficiency organic light-emitting diodes

Thermally-activated delayed fluorescence (TADF) materials have emerged as next-generation emitters for organic light-emitting diodes (OLEDs). The donor-sigma-acceptor molecule is a promising paradigm for developing TADF, but its radiative decay rate (kr,s) and photoluminescent efficiency (& Fcy;PL) require large improvements, due to weak intramolecular charge-transfer (CT). Here, efficient donor-sigma-acceptor emitters (1-3) with strengthened intramolecular CT are developed by directly linking the donor and acceptor with a short alkyl chain. 9,9dimethyl-9,10-dihydroacridine and 2,4,6-triphenyl-1,3,5-triazine are employed as the donor and acceptor, respectively, and -CH2- (for 1),-CH2CH2- (for 2) and-CH2CH2CH2- (for 3) are employed as the sigma-linkers. The chemical structures of 1-3 have been verified by X-ray crystallography. In dilute solution and lightly doped films, emitters 1-3 show considerably strong intramolecular CT, due to the sigma-pi hyperconjugation between the donor/ acceptor and the alkyl sigma-linker. In the 20 wt.% doped films, emitters 1-3 show green-blue TADF with combined intra- and inter-molecular CT, with high & Fcy;PL kr,s and reverse intersystem crossing rates up to 0.91, 8.5 x 106 s- 1 and 2.6 x 106 s- 1, respectively. OLEDs based on emitters 1-3 show green-blue emission with high external quantum efficiencies (EQEs) over 20 %. A hyperfluorescent OLED with emitter 3 as the sensitizer and a typical multiple resonance emitter (DtBuCzB) as the terminal emitter shows narrowband blue-green emission with a high EQE of 28.1 %.