Precise Functionalization of a Multiple-Resonance Framework: Constructing Narrowband Organic Electroluminescent Materials with External Quantum Efficiency over 40.

Abstract

It is of important strategic significance to develop high-efficiency narrowband organic electroluminescent materials that can be employed to fabricate ultrahigh-definition displays with wide color gamut. This topic implies a great challenge to molecular design and synthesis, especially for the development of universality, diversity, scalability, and robustness of molecular architectonics. In this work, a synthetic methodology is demonstrated for functionalizing brominated BN-containing multiple-resonance (MR) frameworks with multifarious functional groups, such as donors, acceptors, and moieties without obvious push-pull electron properties. The m-DPAcP-BNCz-based organic light-emitting diode (OLED) exhibits green emission with a full-width at half-maximum (FWHM) of 28 nm and a maximum external quantum efficiency (EQE) of 40.6%. The outstanding performance of m-DPAcP-BNCz is attributed to the perfect integration of the inherent advantages of the MR framework and the donor-acceptor configuration, which can not only achieve bathochromic shift and narrowband emission, but also obtain high photoluminescence (PL) quantum yield (Φ_PL ) and horizontal emitting dipole orientation ratio (Θ_// ). This straightforward and efficient approach provides insightful guidance for the construction and enrichment of more high-efficiency narrowband emitters.