Chemical Resources Laboratory, Tokyo Institute of Technology, 4259 Nagatsuta Midori-ku, Yokohama 226-8503 (Japan).
Angew Chem Int Ed Engl. 2015 May 4;54(19):5677-82. doi: 10.1002/anie.201500203. Epub 2015 Mar 5.
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).
最近,热致延迟荧光(TADF)材料作为有机发光二极管(OLED)的有效发射器受到了越来越多的关注。然而,它们中的大多数通常被用作主体材料中的掺杂剂。在本报告中,报道了具有三苯基-s-三嗪核的咔唑树状大分子,这是首例可溶液加工的、非掺杂的、高分子量的 TADF 材料。这些树状大分子是通过一种新的简便合成方法得到的,其中使用叔丁基二甲基硅基作为保护基团。所有树状大分子在甲苯中均表现出 TADF。温度依赖性荧光寿命的测量表明,旋涂的纯膜也表现出具有中等量子产率的 TADF。将这些树状大分子作为旋涂发射层的 OLED 器件的外量子效率高达 3.4%,这表明该器件正在收集三重态激子。这一结果表明,由于其极化的电子结构(具有 HOMO-LUMO 分离),带有受体的咔唑树状大分子是潜在的 TADF 材料。