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Solution-processed white organic light-emitting diode based on a single-emitting small molecule
被引:15
|作者:
Liu, Leijing
[1
]
Chen, Feipeng
[1
]
Xu, Bin
[1
]
Dong, Yujie
[1
]
Zhao, Zujin
[2
]
Tian, Wenjing
[1
]
Ping, Lu
[2
]
机构:
[1] Jilin Univ, State Key Lab Supramol Struct & Mat, Changchun 130012, Peoples R China
[2] Zhejiang Univ, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China
关键词:
White organic light-emitting diode;
Single-emitting component;
Electroluminescence;
Excimer;
Electromer;
COMPONENT;
EFFICIENT;
EXCIMER;
DEVICES;
D O I:
10.1016/j.synthmet.2010.07.017
中图分类号:
T [工业技术];
学科分类号:
08 ;
摘要:
A pure-white organic light-emitting diode (WOLED) with a simple device architecture of indium tin oxide (ITO)/poly-(3,4-ethylenedioxythiophene):poly-(styrenesuphonic acid) (PEDOT:PSS)/L-Z-390/1,3,5-tri(N-phenylbenzimidazol-2-yl)benzene (TPBi)/LiF/Al was realized by using a single small molecule 3,3'-(2,7-Dis((9-(2,3,5,6-tetrafluoroPhenyl)-9H-carbazol-3-yl)ethynyl)-9H-fluorene-9,9-diyl)bis(9-heptyl-9H-carbazole) (L-Z-390) as the light-emitting material. The WOLED exhibited efficient white emission with a turn-on voltage of 6V, a maximum luminous efficiency of 3.6 cd/A at 6V, a maximum luminous of 204 cd/m(2) at 13V and Commission Internationale de l'Eclairage (CIE) coordinates of (0.33, 0.34). The device performance characteristics are among the best ever reported for solution-processed WOLEDs with a single-emitting small molecule. The white light comes from the combination of the blue emission originating from the excimer of L-Z-390 and the long-wavelength orange emission originating from the electromer of L-Z-390 under a high electric field. The double-layer device based on 3,3'-(2,7-Dis((9-(2,3,5,6-tetrafiuoroPhenyl)9H-carbazol-3-yl)ethynyl)-9H-fluorene-9,9-diyl)bis(9-(2,3,5,6-tetrafluorophenyl)-9H-carbazole)(L-Z-398), the other molecule with two more electron-withdrawing 2,3,5,6-tetrafluorophenyl units than L-Z-390, shows green EL under the high voltages. That L-Z-398 cannot form electromer under a high voltage may be because the L-Z-398 cannot stably form L-Z-398(+) component and L-Z-398(-) component simultaneously due to the too strong electron-withdrawing ability of the four 2,3,5,6-tetrafluorophenyl units connected to each carbazole. (c) 2010 Elsevier B.V. All rights reserved.
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页码:1968 / 1972
页数:5
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