Rational design of perfectly oriented thermally activated delayed fluorescence emitter for efficient red electroluminescence

Abstract

How to control the dipole orientation of organic emitters is a challenge in the field of organic light-emitting diodes (OLEDs). Herein, a linear thermally activated delayed fluorescence (TADF) molecule, PhNAI-PMSBA, bearing a 1,8-naphthalimide-acridine framework was designed by a double-site long-axis extension strategy to actively control the dipole orientation. The horizontal ratio of emitting dipole orientation of PhNAI-PMSBA reaches 95%, substantially higher than that of isotropic emitters (67%). This unique feature is associated with the intrinsically horizontal molecular orientation of PhNAI-PMSBA and the good agreement between its transition dipole moment direction and molecular long axis. The PhNAI-PMSBA-based OLED achieves an ultrahigh optical outcoupling efficiency of 43.2% and thus affords one of the highest red electroluminescence with an external quantum efficiency of 22.3% and the Commission International de l’Eclairage 1931 coordinates at around (0.60, 0.40).