期刊
JOULE
卷 3, 期 10, 页码 2381-2389出版社
CELL PRESS
DOI: 10.1016/j.joule.2019.07.007
关键词
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资金
- Agency for Science, Technology, and Research (A*STAR, Singapore)
- SERC Career Development Award
- Cyber Physiochemical Interface Programmatic
- Thousand Talent Program
- Zhejiang University Education Foundation Global Partnership Fund
- Engineering and Physical Sciences Research Council (EPSRC) [EP/M005143/1]
- EPSRC [EP/M005143/1] Funding Source: UKRI
The integration of organic light-emitting diodes (OLEDs) into modern electronics has affirmed their role in next-generation display technologies, presenting advantages in energy efficiency, flexibility, large-area fabrication, and low-cost solution processability. Maintaining high luminance and color purity in OLEDs is an important goal, particularly for high-efficiency devices utilizing triplet excitons. Here, we report solution-processed dual-dopant polymer LEDs, in which highly efficient electroluminescence occurs via an intermolecular energy transfer from carbenemetal-amides (CMAs) (which exhibit rapid singlet-triplet interconversion) to a fluorescent rubrene derivative. This design enables solution-processed OLEDs with external quantum efficiencies of >20% (corresponding to near 100% internal quantum efficiencies) and a peak luminance of 75,000 cd m(-2). We show that the emission originates from the singlet state of the rubrene derivative. Ultrafast optical measurements indicate that the inter-fluorophore energy transfer occurs within 0.3 ps, at an efficiency of >96%. Such devices preserve the relatively narrow emission bandwidth of conventional fluorophores for color purity, showing potential in energy-efficient printable electronics.
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