A novel luminophor and host polymer from fluorene-carbazole derivatives for preparing solution-processed non-doped blue and closed-white light devices

被引:9
作者
Sun, Jing [1 ,2 ]
Zhang, Tiaomei [1 ,2 ]
Liao, Xiaoqing [3 ]
Wang, Kexiang [1 ,2 ]
Hou, Minna [1 ,2 ]
Wu, Dongyu [1 ,2 ]
Miao, Yanqin [1 ,2 ]
Wang, Hua [1 ,2 ]
Xu, Bingshe [1 ,2 ]
机构
[1] Taiyuan Univ Technol, Minist Educ, Key Lab Interface Sci & Engn Adv Mat, Taiyuan 030024, Shanxi, Peoples R China
[2] Taiyuan Univ Technol, Res Ctr Adv Mat Sci & Technol, Taiyuan 030024, Shanxi, Peoples R China
[3] Chongqing Univ Arts & Sci, Res Inst New Mat & Technol, Coinnovat Ctr Micro Nano Optoelect Mat & Devices, Chongqing 402160, Peoples R China
关键词
Fluorene-carbazole derivatives; Blue luminophor; Host materials; Electroluminescent performance; EMITTING-DIODES PLEDS; ORGANIC ELECTRONICS; CONJUGATED POLYMER; DEEP-BLUE; POLYFLUORENE; GREEN; RED; PHOSPHORESCENCE; COMPLEX; OLEDS;
D O I
10.1016/j.tet.2018.01.028
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A novel blue light emitting polymer was designed and synthesized via alternative conjugated 9,9-dioctylfluorene and 9-(6-(9H-carbazol-9-yl)hexyl)-9H-carbazole, named PF2Cz. It exhibited high thermal stability, good film morphology and strong deep-blue emission peaks at 408 and 429 nm in film. The triplet energy level of PF2Cz (E-T = 2.30 eV) was also improved. Non-doped and doped devices were both prepared by solution process to characterize the electroluminescent (EL) properties of PF2Cz. In non doped devices, PF2Cz acted as blue emitter which exhibited a Commission Internation de L'Eclairage (CIE) coordinate of (0.164, 0.102) and a external quantum efficiency (EQE) values of 1.28%. Moreover, the doped phosphorescent devices utilized PF2Cz as host material obtained a closed-white light emission with a content of 1 dopant. All these results indicated that the fluorene-carbazole derivatives could be a promising molecular design strategy for the synthesis of blue light and host organic semiconductors. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1053 / 1058
页数:6
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