Efficient Deep‐Blue Organic Light‐Emitting Diodes Employing Doublet Sensitization

Author:

Sun Yu‐Fu1234,Chen Xu‐Lin12,Zhang Dong‐Hai12,Huo Peihao5,Liu Zhiwei5,Zhou Liang6,Lin Fu‐Lin12,Lu Can‐Zhong1234ORCID

Affiliation:

1. State Key Laboratory of Structural Chemistry Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences Fuzhou Fujian 350002 China

2. Xiamen Key Laboratory of Rare Earth Photoelectric Functional Materials Xiamen Institute of Rare Earth Materials Haixi Institutes Chinese Academy of Sciences Xiamen Fujian 361021 China

3. Ganjiang Innovation Academy Chinese Academy of Sciences Ganzhou 341119 China

4. School of Rare Earths University of Science and Technology of China Hefei 230026 China

5. Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Rare Earth Materials Chemistry and Applications, Beijing Engineering Technology Research Centre of Active Display, College of Chemistry and Molecular Engineering Peking University Beijing 100871 China

6. State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun 130022 China

Abstract

AbstractFast and efficient exciton utilization is a crucial solution and highly desirable for achieving high‐performance blue organic light‐emitting diodes (OLEDs). However, the rate and efficiency of exciton utilization in traditional OLEDs, which employ fully closed‐shell materials as emitters, are inevitably limited by spin statistical limitations and transition prohibition. Herein, a new sensitization strategy, namely doublet‐sensitized fluorescence (DSF), is proposed to realize high‐performance deep‐blue electroluminescence. In the DSF‐OLED, a doublet‐emitting cerium(III) complex, Ce‐2, is utilized as sensitizer for multi‐resonance thermally activated delayed fluorescence emitter ν‐DABNA. Experimental results reveal that holes and electrons predominantly recombine on Ce‐2 to form doublet excitons, which subsequently transfer energy to the singlet state of ν‐DABNA via exceptionally fast (over 108 s−1) and efficient (≈100%) Förster resonance energy transfer for deep‐blue emission. Due to the circumvention of spin‐flip in the DSF mechanism, near‐unit exciton utilization efficiency and remarkably short exciton residence time of 1.36 µs are achieved in the proof‐of‐concept deep‐blue DSF‐OLED, which achieves a Commission Internationale de l'Eclairage coordinate of (0.13, 0.14), a high external quantum efficiency of 30.0%, and small efficiency roll‐off of 14.7% at a luminance of 1000 cd m−2. The DSF device exhibits significantly improved operational stability compared with unsensitized reference device.

Funder

Fujian Science and Technology Innovation Laboratory for Optoelectronic Information of China

National Natural Science Foundation of China

Publisher

Wiley

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