Solution-processable iridium complexes for efficient orange-red and white organic light-emitting diodes

被引:66
作者
Wang, Renjie [1 ]
Liu, Di [2 ]
Zhang, Run [2 ]
Deng, Lijun [1 ]
Li, Jiuyan [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Dalian Univ Technol, Sch Chem, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTROLUMINESCENT DEVICES; IR(III) COMPLEXES; PHOTOPHYSICAL PROPERTIES; PHOSPHORESCENT OLEDS; QUANTUM EFFICIENCY; PERFORMANCE; EMISSION; ELECTROPHOSPHORESCENCE; BENZOTHIAZOLES; ARCHITECTURE;
D O I
10.1039/c1jm13846d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two homoleptic and heteroleptic cyclometalated iridium complexes containing the 2-phenylbenzothiozole derivative as the main ligand, 1 and 2, have been synthesized and characterized as efficient orange-red phosphors. Triarylamine was introduced as an important substituent into the 6-position of the benzothiazole ring to tune the photonic and electronic properties of these complexes. Different from most of small molecular iridium complexes, 1 and 2 are solution-processable and their neat films can be obtained by a spin-coating method. Furthermore, their homogeneously dispersed films in a small molecular matrix, 4,4'-N,N'-dicarbazolebiphenyl (CBP), were successfully prepared by solution method even with low doping levels. Organic light-emitting diodes (OLEDs) were fabricated by solution processing the emitting layer containing 1 and 2 as doped emitters in the CBP host. Efficient orange-red electroluminescence by using 5 wt% 2 as the dopant was realized with a maximum efficiency of 14.49 cd A(-1) (7.38 lm W-1 and 8.73%) and Commission Internationale de l'Eclairage (CIE) coordinates of (0.60, 0.40), which are among the highest luminance efficiency ever reported for partially solution-processed red and orange-red OLEDs so far. In addition, two-element white OLEDs were achieved with these orange-red phosphors and the traditional blue emitter by spin coating the emission layer. A maximum luminance efficiency of 8.97 cd A(-1) and CIE of (0.33, 0.35) were realized.
引用
收藏
页码:1411 / 1417
页数:7
相关论文
共 43 条
[1]   Nearly 100% internal phosphorescence efficiency in an organic light-emitting device [J].
Adachi, C ;
Baldo, MA ;
Thompson, ME ;
Forrest, SR .
JOURNAL OF APPLIED PHYSICS, 2001, 90 (10) :5048-5051
[2]   Very high-efficiency green organic light-emitting devices based on electrophosphorescence [J].
Baldo, MA ;
Lamansky, S ;
Burrows, PE ;
Thompson, ME ;
Forrest, SR .
APPLIED PHYSICS LETTERS, 1999, 75 (01) :4-6
[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]   Tris-cyclometalated iridium(III) complexes of carbazole(fluorenyl)pyridine ligands: Synthesis, redox and photophysical properties, and electrophosphoreseent light-emitting diodes [J].
Bettington, Sylvia ;
Tavasli, Mustafa ;
Bryce, Martin R. ;
Beeby, Andrew ;
Al-Attar, Hameed ;
Monkman, Andrew P. .
CHEMISTRY-A EUROPEAN JOURNAL, 2007, 13 (05) :1423-1431
[5]   Highly efficient red electrophosphorescence from a solution-processed zwitterionic cyclometalated iridium(III) complex [J].
Byun, Younghun ;
Lyu, Yi-Yeol ;
Das, Rupasree Ragini ;
Kwon, Ohyun ;
Lee, Tae-Woo ;
Park, Young Ja .
APPLIED PHYSICS LETTERS, 2007, 91 (21)
[6]   Highly efficient blue-emitting iridium(III) carbene complexes and phosphorescent OLEDs [J].
Chang, Chiung-Fang ;
Cheng, Yi-Ming ;
Chi, Yun ;
Chiu, Yuan-Chieh ;
Lin, Chao-Chen ;
Lee, Gene-Hsiang ;
Chou, Pi-Tai ;
Chen, Chung-Chia ;
Chang, Chih-Hao ;
Wu, Chung-Chih .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (24) :4542-4545
[7]   Highly efficient solution-processed red organic light-emitting diodes with long-side-chained triplet emitter [J].
Chao, Yu-Chiang ;
Huang, Sheng-Yang ;
Chen, Chun-Yu ;
Chang, Yu-Fan ;
Meng, Hsin-Fei ;
Yen, Feng-Wen ;
Lin, I-Feng ;
Zan, Hsiao-Wen ;
Horng, Sheng-Fu .
SYNTHETIC METALS, 2011, 161 (1-2) :148-152
[8]  
Cleave V, 1999, ADV MATER, V11, P285, DOI 10.1002/(SICI)1521-4095(199903)11:4<285::AID-ADMA285>3.0.CO
[9]  
2-N
[10]   Conversion of thiobenzamides to benzothiazoles via intramolecular cyclization of the aryl radical cation [J].
Downer-Riley, Nadale K. ;
Jackson, Yvette A. .
TETRAHEDRON, 2008, 64 (33) :7741-7744