Novel carbazole/indole/thiazole-based host materials with high thermal stability for efficient phosphorescent organic light-emitting diodes

被引:14
|
作者
Jia, Bin [1 ]
Lian, Hong [2 ]
Chen, Zheng [2 ]
Chen, Yi [3 ]
Huang, Jinhai [3 ]
Dong, Qingchen [2 ]
机构
[1] Shanxi Med Univ, Sch Basic Med Sci, Taiyuan 030001, Shanxi, Peoples R China
[2] Taiyuan Univ Technol, Res Ctr Adv Mat Sci & Technol, MOE Key Lab Interface Sci & Engn Adv Mat, 79 Yingze West St, Taiyuan 030024, Shanxi, Peoples R China
[3] Shanghai Taoe Chem Technol Co Ltd, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Thiazole derivatives; Carbazole derivatives; Indole derivatives; Host materials; Phosphorescent organic light-emitting diodes; BIPOLAR HOST; IRIDIUM(III) COMPLEXES; ELECTROLUMINESCENT DEVICES; BLUE; OLEDS; GREEN; TRIAZINE; PERFORMANCES; EMITTERS; VOLTAGE;
D O I
10.1016/j.dyepig.2017.08.051
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two host materials TIC1 (N-linked carbazole) and TIC2 (C-3-linked carbazole) via changing the substitution position of carbazole, indole and thiazole moieties are reported. Their structural and physical properties were fully characterized. The thermal analysis demonstrated that both TIC1 and TIC2 are thermally stable. The triplet energy levels of TIC1 and TIC2 were determined to be 2.54 and 2.58 eV, respectively. Green and blue OLEDs with TIC1 and TIC2 acting as host materials were fabricated to investigate their performances in PHOLED. Both green and blue PHOLEDs based on TIC2 show the best performance with the maximum current efficiency and maximum power efficiency of 60.0 cd/A and 48.0 lm/W (for green), 18.4 cd/A and 15.2 Im/W (for blue), respectively. The characteristic measurements of OLED devices reveal that both TIC1 and TIC2 are promising host materials for practical application. By comparing with the commercial host material of 4,4 '-bis(carbazol-9-yl)biphenyl (CBP) and N,N-dicarbazoyl-3,5-benzene (mCP), the power efficiency of green and blue PHOLED was enhanced by 553% and 245%, respectively. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:552 / 559
页数:8
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