Tetrabenzo[a,c]phenazine Backbone for Highly Efficient Orange-Red Thermally Activated Delayed Fluorescence with Completely Horizontal Molecular Orientation

Abstract

Three thermally activated delayed fluorescence (TADF) molecules, namely PQ1, PQ2, and PQ3, are composed of electron-accepting (A) tetrabenzo[a,c]phenazine (TBPZ) and electron-donating (D) phenoxazine (PXZ) units are designed and characterized. The combined effects of planar acceptor manipulation and high steric hindrance between D and A units endow high molecular rigidity that suppresses nonradiative decay of the excitons with improved photoluminescence quantum yields (PLQYs). Particularly, the well-aligned excited states involving a singlet and a triplet charge-transfer excited states and a localized excited triplet state in PQ3 enhances the reverse intersystem crossing rate constant (k_RISC ) with a short delay lifetime (τ_d ). The orange-red OLED based on PQ3 displays a maximum external EL quantum efficiency (EQE) of 27.4 % with a well-suppressed EL efficiency roll-off owing to a completely horizontal orientation of the transition dipole moment in the film state.

Keywords: horizontal orientation; organic light-emitting diodes; reverse intersystem crossing; suppressed efficiency roll-off; thermally activated delayed fluorescence.