Non‐Doped Blue AIEgen‐Based OLED with EQE Approaching 10.3 %

Author:

Han Pengbo1,Lin Chengwei1,Xia Erhan1,Cheng Jiawei1,Xia Qing1,Yang Dezhi1,Qin Anjun1ORCID,Ma Dongge1,Tang Ben Zhong234

Affiliation:

1. State Key Laboratory of Luminescent Materials and Devices Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates Center for Aggregation-Induced Emission South China University of Technology Guangzhou 510640 China

2. Center for Aggregation-Induced Emission AIE Institute South China University of Technology Guangzhou 510640 China

3. School of Science and Engineering Shenzhen Institute of Aggregate Science and Technology The Chinese University of Hong Kong, Shenzhen (CUHK-Shenzhen) Guangdong 518172 China

4. Hong Kong Branch of Chinese National Engineering Research Centre for Tissue Restoration and Reconstruction The Hong Kong University of Science & Technology Kowloon 999077 Hong Kong China

Abstract

AbstractAggregation‐induced emission (AIE) luminogens (AIEgens) are attractive for the construction of non‐doped blue organic light‐emitting diodes (OLEDs) owning to their high emission efficiency in the film state. However, the large internal inversion rate (kIC(Tn)) between high‐lying triplet levels (Tn) and Tn‐1 causes a huge loss of triplet excitons, resulting in dissatisfied device performance of these AIEgens‐based non‐doped OLEDs. Herein, we designed and synthesized a blue luminogen of DPDPB‐AC by fusing an AIEgen of TPB‐AC and a DMPPP, which feature hot exciton and triplet‐triplet annihilation (TTA) up‐conversion process, respectively. DPDPB‐AC successfully inherits the AIE feature and excellent horizontal dipole orientation of TPB‐AC. Furthermore, it owes smaller kIC(Tn) than TPB‐AC. When DPDPB‐AC was applied in OLED as non‐doped emitting layer, an outstanding external quantum efficiency of 10.3 % and an exceptional brightness of 69311 cd m−2 were achieved. The transient electroluminescent measurements and steady‐state dynamic analysis confirm that both TTA and hot exciton processes contribute to such excellent device performance. This work provides a new insight into the design of efficient organic fluorophores by managing high‐lying triplet excitons.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Innovation and Technology Commission

Postdoctoral Research Foundation of China

Guangzhou Municipal Science and Technology Bureau

Publisher

Wiley

Subject

General Chemistry,Catalysis

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