Efficient organic light-emitting device from exciplex emission between 4,4′ 4"-tris[3-methylphenyl(phenyl)amino] triphenylamine and 2,2′,2"-(1,3,5-benzenetriyl)tris[1-phenyl-1H-benzimidazole]

被引:32
|
作者
Chen, SF [1 ]
Wu, ZJ [1 ]
Zhao, Y [1 ]
Li, CN [1 ]
Hou, JY [1 ]
Liu, SY [1 ]
机构
[1] Jilin Univ, Natl Lab Optoelect, Changchun 130023, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1016/j.orgel.2005.03.005
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A new-type exciplex emission was obtained employing hole-transporting material 4,4,4"-tris[3-methylphenyl(phenyl)amino]triphenylamine (m-MTDATA) doped in the electron-transporting material 2,2,2"-(1,3,5-benzenetriyl)tris-[1-phenyl-1H-benzimidazole] (TPBI) with structures of ITO/m-MTDATA (45 nm)/NPB (5 nm)/ m-MTDATA:TPBI ((10 nm, molecular weight ratio were 3:1, 1:1 and 1:3)/TPBI (25 nm)/Alq(3) (15 nm)/LiF (0.5 nm)/ Al. For comparison, a device with exciplex emission generated at the interface between a hole-transporting material m-MTDATA and an electron-transporting material TPBI with a structure ITO/m-MTDATA (45 nm)/NPB (5 nm)/ m-MTDATA (5 nm)/TPBI (30 nm)/Alq3 (15 nm)/LiF (0.5 nm)/Al was also fabricated. The maximum efficiencies of the doped-devices reached 3.8 lm/W (at 4 V with a luminance of 145.7 cd/m(2)), 3.2 lm/W(at 4 V with a luminance of 132 cd/m(2)) and 4.6 lm/W (at 4 V with a luminance of 170.5 cd/m(2)) with different molecular weight ratio (MWR) 3:1, 1: 1 and 1:3, respectively, comparing to that of the none-doped device of 1.8 lm/W (at 4 V with a luminance of 49.6 cd/m(2)). At such a low voltage, exciplex emission was major for all the devices above. Only yellow emission was obtained in none-doped structure and the maximum luminance reached 2555 cd/m(2) at 12 V. Commission International de L'Eclairage coordinate (1931, CIE) in this structure changed from (0.397, 0.532) to (0.311, 0.413) with voltage from 4 to 16 V. In doped devices, a yellow emission was obtained at a low bias voltage and then turned into white emission with increasing of voltage for stronger blue emission from m-MTDATA due to the sufficient charge trapping from TPBI to m-MTDATA. The CIE coordinates were (0.406, 0.533), (0.409, 0.533) and (0.427, 0.536) at 4 V for MWR 3:1, 1:1 and 1:3, respectively. At 8, 8, 12 V, white emission were obtained with CIE coordinates (0.320, 0.400), (0.311, 0.384), (0.319, 0.401) for MWR 3:1, 1:1, 1:3 and turned into (0.264, 0.303), (0.246, 0.275), (0.302, 0.363) when voltage increased to 16 V. The maximum luminance was 3810 (at 14 V), 4210 (at 12 V) and 4583 cd/m(2) (at 12 V) for MWR 3:1, 1:1 and 1:3, respectively. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:111 / 117
页数:7
相关论文
共 50 条
  • [1] Organic field-effect transistors with a sandwich structure from inserting 2,2′,2"-(1,3,5-benzenetriyl)tris[1-phenyl-1H-benzimidazole] in the pentacene active layer
    Yu, Xinge
    Yu, Junsheng
    Zhou, Jianlin
    Huang, Wei
    Lin, Hui
    [J]. EUROPEAN PHYSICAL JOURNAL-APPLIED PHYSICS, 2013, 62 (02):
  • [2] Exciplex emission and decay of co-deposited 4,4′,4"-tris[3-methylphenyl (phenyl)amino] triphenylamine: tris-[3-(3-pyridyl)mesityl]borane organic light-emitting devices with different electron transporting layer thicknesses
    Huang, Qingyu
    Zhao, Suling
    Xu, Zheng
    Fan, Xing
    Shen, Chongyu
    Yang, Qianqian
    [J]. APPLIED PHYSICS LETTERS, 2014, 104 (16)
  • [3] Electrochemical and ferromagnetic couplings in 4,4′,4"-( 1,3,5-benzenetriyl)tris(phenoxyl) radical formation
    Nishide, H
    Doi, R
    Oyaizu, K
    Tsuchida, E
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (05): : 1680 - 1685
  • [4] Stable and highly bright white organic light-emitting diode based on 4,4′,4"-tris(N-3-methylphenyl-N-phenyl-amino)-triphenylamine
    Yang, Su-Hua
    Liu, Mine-Huang
    Su, Yan-Kuin
    [J]. JOURNAL OF APPLIED PHYSICS, 2006, 100 (08)
  • [5] 2-(4-Fluorophenyl)-1-phenyl-1H-benzimidazole
    Jayamoorthy, K.
    Rosepriya, S.
    Thiruvalluvar, A.
    Jayabharathi, J.
    Butcher, R. J.
    [J]. ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2012, 68 : O2708 - +
  • [6] 2-(4-Methoxyphenyl)-1-phenyl-1H-benzimidazole
    Mohandas, T.
    Jayamoorthy, K.
    Jayabharathi, J.
    Sakthivel, P.
    [J]. ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2013, 69 : O269 - +
  • [7] Photochromic reaction in a molecular glass as a novel host matrix:: the 4-dimethylaminoazobenzene-4,4′,4"-tris[3-methylphenyl(phenyl)amino]triphenylamine system
    Moriwaki, K
    Kusumoto, H
    Akamatsu, K
    Nakano, H
    Shirota, Y
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 1998, 8 (12) : 2671 - 2676
  • [8] Hole mobility enhancement of pentacene organic field-effect transistors using 4,4′,4"-tris[3-methylphenyl(phenyl)amino] triphenylamine as a hole injection interlayer
    Yu, Xinge
    Yu, Junsheng
    Zhou, Jianlin
    Huang, Jiang
    Jiang, Yadong
    [J]. APPLIED PHYSICS LETTERS, 2011, 99 (06)
  • [9] Photoinduced Surface-relief-grating Formation Using a Mixed Film of 4-[Bis(4-methylphenyl)amino]azobenzene and 4,4′,4"-Tris[3-methylphenyl(phenyl)amino]triphenylamine
    Nakano, Hideyuki
    [J]. CHEMISTRY LETTERS, 2011, 40 (05) : 473 - 475
  • [10] Organic electroluminescent devices using novel starburst molecules, 1,3,5-tris[4-(3-methylphenyl-phenylamino)phenyl]benzene and 4,4',4''-tris(3-methylphenylphenylamino)triphenylamine, as hole-transport materials
    Inada, H
    Yonemoto, Y
    Wakimoto, T
    Imai, K
    Shirota, Y
    [J]. MOLECULAR CRYSTALS AND LIQUID CRYSTALS SCIENCE AND TECHNOLOGY SECTION A-MOLECULAR CRYSTALS AND LIQUID CRYSTALS, 1996, 280 : 331 - 336