Carbazole Dendrimers as Solution-Processable Thermally Activated Delayed-Fluorescence Materials

被引:278
作者
Albrecht, Ken [1 ]
Matsuoka, Kenichi [2 ]
Fujita, Katsuhiko [2 ]
Yamamoto, Kimihisa [1 ]
机构
[1] Tokyo Inst Technol, Chem Resources Lab, Midori Ku, Yokohama, Kanagawa 2268503, Japan
[2] Kyushu Univ, Inst Mat Chem & Engn, Kasuga, Fukuoka 8168580, Japan
关键词
carbazoles; dendrimers; electroluminescence; fluorescence; LIGHT-EMITTING-DIODES; ORGANIC ELECTROLUMINESCENT DEVICES; ELECTRON-TRANSPORT MATERIALS; SOLAR-CELLS; IRIDIUM DENDRIMERS; CHARGE-TRANSPORT; HOST MATERIALS; DENDRONS; OLEDS; ELECTROPHOSPHORESCENCE;
D O I
10.1002/anie.201500203
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently, thermally activated delayed fluorescence (TADF) materials have received increasing attention as effective emitters for organic light-emitting diodes (OLEDs). However, most of them are usually employed as dopants in a host material. In this report, carbazole dendrimers with a triphenyl-s-triazine core are reported, which are the first solution-processable, non-doped, high-molecular-weight TADF materials. The dendrimers were obtained by a new and facile synthetic route using the tert-butyldimethylsilyl moiety as a protecting group. All dendrimers showed TADF in toluene. Measurements of the temperature-dependent luminescence lifetime revealed that spin-coated neat films also showed TADF with moderate quantum yields. OLED devices incorporating these dendrimers as spin-coated emitting layers gave external quantum efficiencies of up to a 3.4%, which suggests that this device is harvesting triplet excitons. This result indicates that carbazole dendrimers with attached acceptors are potential TADF materials owing to their polarized electronic structure (with HOMO-LUMO separation).
引用
收藏
页码:5677 / 5682
页数:6
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