Triplet-triplet upconversion enhanced by spin-orbit coupling in organic light-emitting diodes

被引:138
作者
Ieuji, Ryota [1 ,2 ,3 ]
Goushi, Kenichi [1 ,2 ,3 ,4 ]
Adachi, Chihaya [1 ,2 ,3 ,4 ]
机构
[1] Kyushu Univ, Dept Appl Chem, Nishi Ku, 744 Motooka, Fukuoka, Fukuoka 8190395, Japan
[2] Kyushu Univ, Ctr Organ Photon & Elect Res OPERA, Nishi Ku, 744 Motooka, Fukuoka, Fukuoka 8190395, Japan
[3] Kyushu Univ, Adachi Mol Exciton Engn Project, Japan Sci & Technol Agcy JST, Exploratory Res Adv Technol ERATO,Nishi Ku, 744 Motooka, Fukuoka, Fukuoka 8190395, Japan
[4] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Nishi Ku, 744 Motooka, Fukuoka, Fukuoka 8190395, Japan
基金
日本科学技术振兴机构;
关键词
ACTIVATED DELAYED FLUORESCENCE; SINGLET; PHOSPHORESCENCE; EFFICIENCY; MECHANISM; EMISSION; EXCITONS; STATES;
D O I
10.1038/s41467-019-13044-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Triplet-triplet upconversion, in which two triplet excitons are converted to one singlet exciton, is a well-known approach to exceed the limit of electroluminescence quantum efficiency in conventional fluorescence-based organic light-emitting diodes. Considering the spin multiplicity of triplet pairs, upconversion efficiency is usually limited to 20%. Although this limit can be exceeded when the energy of a triplet pair is lower than that of a second triplet excited state, such as for rubrene, it is generally difficult to engineer the energy levels of higher triplet excited states. Here, we investigate the upconversion efficiency of a series of new anthracene derivatives with different substituents. Some of these derivatives show upconversion efficiencies close to 50% even though the calculated energy levels of the second triplet excited states are lower than twice the lowest triplet energy. A possible upconversion mechanism is proposed based on the molecular structures and quantum chemical calculations.
引用
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页数:10
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