Related Experiment Video
Updated: Sep 15, 2025

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Structure-Dependent Pyrene[4,5-d]imidazole-Based Deep Blue-Emitters with High-Performance OLEDs
Tao Jiang1, Jiayi Qin2, Jieyu Lin1
1Guangdong Provincial Key Laboratory of Functional Soft Condensed Matter, School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006, P. R. China.
None:
Hybridized local and charge-transfer (HLCT) excited-state emitters have garnered significant attention due to their ability to efficiently utilize triplet excitons. Pyreno[4,5-d]imidazole (PyI) is considered an outstanding building block for constructing HLCT blue emitters. To understand the influence of the substituent position, the electronic effect, and the steric effect of the PyI substituents on the optical behavior and the electronic transition in the excited state, herein, a set of L-shaped and V-shaped PyI-based blue emitters has been designed and synthesized. The L-shaped compounds exhibit HLCT-dominated characteristics, which demonstrate better electroluminescence properties, while the V-shaped compounds are primarily LE-dominated with a relatively narrower full width at half-maximum (FWHM, <60 nm) in their EL spectra. The L-shaped PyI-based HLCT blue emitters achieve a maximum brightness (Lmax) of 11060 cd m-2 and maximum external quantum efficiency (ηext) of 4.77% in the OLED devices, with significantly reduced efficiency roll-off. Thus, this work provides detailed examples demonstrating how the substitution positions on the PyI core can significantly influence the emission behavior and OLED properties of HLCT materials. Moreover, this work offers a valuable synthetic strategy for the preparation of high-performance HLCT materials that can efficiently harness triplet excitons in OLED devices.

