Towards Efficient Blue Delayed-Fluorescence Molecules by Modulating Torsion Angle Between Electron Donor and Acceptor

Abstract

Constructing blue thermally activated delayed-fluorescence materials for high-performance organic light-emitting diodes (OLEDs) remains challenging due to the intrinsically strong intramolecular charge transfer nature of the nearly orthogonal connection of electron donor (D) and acceptor (A), which results in long-wavelength emission. Herein, an effective delayed-fluorescence design strategy of modulating D–A torsion angles is proposed and efficient sky-blue, pure-blue, and deep-blue delayed-fluorescence molecules consisting of a xanthenone acceptor and carbazole-based donors are created by decreasing the torsion angles. They exhibit strong delayed fluorescence with high photoluminescence quantum yields of 85–94% in doped films, and their delayed-fluorescence lifetimes are elongated from 1.0 to 27.6 μs as the torsion angles decrease. These molecules can function as excellent emitters in OLEDs, providing efficient electroluminescence peaking at 442 nm (CIEx,y = 0.15, 0.08), 462 nm (CIEx,y = 0.15, 0.18), and 482 nm (CIEx,y = 0.17, 0.30) with state-of-the-art external quantum efficiencies of up to 22.2%, 33.7%, and 32.1%, respectively, demonstrating the proposed molecular design for efficient blue delayed-fluorescence molecules is successful and promising.