Organic photostimulated luminescence associated with persistent spin-correlated radical pairs

被引:11
|
作者
Sakurai, Manabu [1 ]
Kabe, Ryota [2 ,3 ]
Fuki, Masaaki [4 ]
Lin, Zesen [2 ,3 ]
Jinnai, Kazuya [3 ,5 ]
Kobori, Yasuhiro [1 ,4 ]
Adachi, Chihaya [3 ,5 ,6 ]
Tachikawa, Takashi [1 ,4 ]
机构
[1] Kobe Univ, Grad Sch Sci, Dept Chem, Kobe, Hyogo, Japan
[2] Okinawa Inst Sci & Technol Grad Univ, Organ Optoelect Unit, Onna, Okinawa, Japan
[3] Kyushu Univ, JST, ERATO ADACHI Mol Exciton Engn Project, Fukuoka, Japan
[4] Kobe Univ, Mol Photosci Res Ctr, Kobe, Hyogo, Japan
[5] Kyushu Univ, Ctr Organ Photon & Elect Res OPERA, Fukuoka, Japan
[6] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Fukuoka, Japan
基金
日本科学技术振兴机构;
关键词
UP-CONVERSION; CRYSTALLINE RUBRENE; CHARGE-CARRIERS; MANIPULATION; ELECTROLUMINESCENCE; SPINTRONICS; PENTACENE;
D O I
10.1038/s43246-021-00178-3
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Materials that display photostimulated luminescence are attractive for multiple applications. Here, photostimulated luminescence is demonstrated in an all-organic blend film, in which a dopant molecule functions as both an electron trap and a light emitter. Photostimulated luminescence allows energy or data to be stored and released using electromagnetic waves as both the input and output, and has attracted considerable interest in the fields of biomedical and information technologies. However, this phenomenon is mostly limited to solid inorganic materials. Here, we report photostimulated luminescence from purely organic blend films, composed of electron donor, acceptor, and trap/emitter molecules. Charges in the films are accumulated as radical ions by ultraviolet light irradiation and then extracted by near-infrared light irradiation. Even after storage in the dark for one week they produce visible light with good repeatability, color tunability, and are responsive to weak external magnetic fields. These findings might broadly impact existing applications and provide new prospects for innovative flexible devices.
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页数:7
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