Highly Efficient Luminescence from a Red Thermally Activated Delayed Fluorescence Emitter with Flexible Conformation of Ancillary Groups

Author:

Jin Yu‐Xin1,Chen Zi‐Qi1,Zhang Kai2,Yang Chen‐Zong1,Pan Ze‐Hui1,Ding Lei3,Sun Yan‐Qiu3,Wang Chuan‐Kui2,Fung Man‐Keung1,Fan Jian14ORCID

Affiliation:

1. Institute of Functional Nano & Soft Materials (FUNSOM) Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices Soochow University Suzhou, Jiangsu 215123 China

2. Shandong Province Key Laboratory of Medical Physics and Image Processing Technology School of Physics and Electronics Shandong Normal University 250014 Jinan China

3. School of Chemistry and Life Sciences Suzhou University of Science and Technology Suzhou, Jiangsu 215009 China

4. State Key Laboratory of Structural Chemistry Fujian Institute of Research on Structure of Matter Chinese Academy of Sciences Fuzhou, Fujian 35002 China

Abstract

AbstractRobust scaffolds were typically applied in thermally activated delayed fluorescence (TADF) molecules to suppress the non‐radiative decay, trigger the fast spin‐flipping, and enhance the light out‐coupling efficiency. Herein, we disclosed for the first time the positive effect of flexible conformation of ancillary groups on the photophysical properties of TADF emitter. The red TADF emitter Ph‐TPA with flexible conformation demonstrated small excited‐state structural distortion and low reorganization energy compared to the counterpart Mc‐TPA with a rigid macrocycle. Consequently, Ph‐TPA showed an excellent photoluminescent quantum yield (PLQY) of 92 % and a state‐of‐the‐art external quantum efficiency (EQE) of 30.6 % at 630 nm. This work could deepen our understanding of structure‐property relationships of organic luminophores and help us to rationalize the design of efficient TADF materials.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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