Light Amplification in Molecules Exhibiting Thermally Activated Delayed Fluorescence

被引:88
作者
Nakanotani, Hajime [1 ,2 ,3 ]
Furukawa, Taro [1 ]
Hosokai, Takuya [2 ,4 ]
Hatakeyama, Takuji [5 ]
Adachi, Chihaya [1 ,2 ,3 ]
机构
[1] Kyushu Univ, Ctr Organ Photon & Elect Res OPERA, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
[2] Kyushu Univ, Ctr Organ Photon & Elect Res OPERA, Adachi Mol Exciton Engn Project, JST,ERATO, 744 Motooka, Fukuoka 8190395, Japan
[3] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
[4] Natl Inst Adv Ind Sci & Technol, Natl Metrol Inst Japan, Tsukuba Cent 2,1-1-1 Umezono, Tsukuba, Ibaraki 3058568, Japan
[5] Kansei Gakuin Univ, Sch Sci & Technol, Dept Chem, 2-1 Gakuen, Sanda, Hyogo 6691337, Japan
基金
日本科学技术振兴机构;
关键词
amplified spontaneous emission; fluorescent dyes; organic lasers; thermally activated delayed fluorescence; SINGLET UP-CONVERSION; EMISSION; LASERS; ABSORPTION; FILM;
D O I
10.1002/adom.201700051
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
To reduce the threshold current density and move closer toward the realization of future current-injection organic semiconductor lasers, the harvesting of triplet excitons is anticipated because 75% excitons are directly formed as triplet excited states under electrical excitation according to spin statics. However, the observation of light amplification in pure phosphorescent or thermally activated delayed fluorescence (TADF) materials has nor yet been reported even under optical excitation. Herein, light amplification was observed in the TADF emitter 9-([1,1 '-biphenyl]-3-yl)-N, N, 5,11-tetraphenyl- 5,9-dihydro-5,9-diaza-13b-boranaphtho[3,2,1-de] anthracen-3-amine (DABNA-2). It is found that DABNA-2 possesses not only a large stimulated emission cross-section but also a favorable window for light amplification. These results indicate that TADF emitters can form a new category of laser dyes and are important candidates for the realization of an organic semiconductor laser.
引用
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页数:5
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共 23 条
[1]   Excitonic singlet-triplet ratio in a semiconducting organic thin film [J].
Baldo, MA ;
O'Brien, DF ;
Thompson, ME ;
Forrest, SR .
PHYSICAL REVIEW B, 1999, 60 (20) :14422-14428
[2]   Prospects for electrically pumped organic lasers [J].
Baldo, MA ;
Holmes, RJ ;
Forrest, SR .
PHYSICAL REVIEW B, 2002, 66 (03) :353211-3532116
[3]   Highly efficient phosphorescent emission from organic electroluminescent devices [J].
Baldo, MA ;
O'Brien, DF ;
You, Y ;
Shoustikov, A ;
Sibley, S ;
Thompson, ME ;
Forrest, SR .
NATURE, 1998, 395 (6698) :151-154
[4]   ABSORPTION AND EMISSION SPECTROSCOPIC INVESTIGATION OF CYANOVINYLDIETHYLANILINE DYE VAPORS [J].
DESHPANDE, AV ;
BEIDOUN, A ;
PENZKOFER, A ;
WAGENBLAST, G .
CHEMICAL PHYSICS, 1990, 142 (01) :123-131
[5]   The Importance of Vibronic Coupling for Efficient Reverse Intersystem Crossing in Thermally Activated Delayed Fluorescence Molecules [J].
Gibson, Jamie ;
Monkman, Andrew P. ;
Penfold, Thomas J. .
CHEMPHYSCHEM, 2016, 17 (19) :2956-2961
[6]   Ultrapure Blue Thermally Activated Delayed Fluorescence Molecules: Efficient HOMO-LUMO Separation by the Multiple Resonance Effect [J].
Hatakeyama, Takuji ;
Shiren, Kazushi ;
Nakajima, Kiichi ;
Nomura, Shintaro ;
Nakatsuka, Soichiro ;
Kinoshita, Keisuke ;
Ni, Jingping ;
Ono, Yohei ;
Ikuta, Toshiaki .
ADVANCED MATERIALS, 2016, 28 (14) :2777-2781
[7]  
Hirata S, 2015, NAT MATER, V14, P330, DOI [10.1038/nmat4154, 10.1038/NMAT4154]
[8]   Solvent Effect on Thermally Activated Delayed Fluorescence by 1,2,3,5-Tetrakis(carbazol-9-yl)-4,6-dicyanobenzene [J].
Ishimatsu, Ryoichi ;
Matsunami, Shigeyuki ;
Shizu, Katsuyuki ;
Adachi, Chihaya ;
Nakano, Koji ;
Imato, Toshihiko .
JOURNAL OF PHYSICAL CHEMISTRY A, 2013, 117 (27) :5607-5612
[9]   Ultrafast Relaxation as a Possible Limiting Factor of Electron Injection Efficiency in Black Dye Sensitized Nanocrystalline TiO2 Films [J].
Katoh, Ryuzi ;
Furube, Aidhiro ;
Fuke, Nobuhiro ;
Fukui, Atsushi ;
Koide, Naold .
JOURNAL OF PHYSICAL CHEMISTRY C, 2012, 116 (42) :22301-22306
[10]  
Kawamura M., 2010, SID Symp. Dig. Tech. Pap, V41, P560, DOI DOI 10.1889/1.3500528