Shi Yi-Zhong, Wang Kai, Li Xing, Dai Gao-Le, Liu Wei, Ke Ke, Zhang Ming, Tao Si-Lu, Zheng Cai-Jun, Ou Xue-Mei, Zhang Xiao-Hong
Institute of Functional Nano & Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou, Jiangsu, 215123, P. R. China.
School of Optoelectronic Science and Engineering, University of Electronic Science and Technology of China (UESTC), Chengdu, 610054, P. R. China.
Angew Chem Int Ed Engl. 2018 Jul 20;57(30):9480-9484. doi: 10.1002/anie.201804483. Epub 2018 Jul 4.
A novel molecular model of connecting electron-donating (D) and electron-withdrawing (A) moieties via a space-enough and conjugation-forbidden linkage (D-Spacer-A) is proposed to develop efficient non-doped thermally activated delayed fluorescence (TADF) emitters. 10-(4-(4-(4,6-diphenyl-1,3,5-triazin-2-yl) phenoxy) phenyl)-9,9-dimethyl-9,10-dihydroacridine (DMAC-o-TRZ) was designed and synthesized accordingly. As expected, it exhibits local excited properties in single-molecule state as D-Spacer-A molecular backbone strongly suppress the intramolecular charge-transfer (CT) transition. And intermolecular CT transition acted as the vital radiation channel for neat DMAC-o-TRZ film. As in return, the non-doped device exhibits a remarkable maximum external quantum efficiency (EQE) of 14.7 %. These results prove the feasibility of D-Spacer-A molecules to develop intermolecular CT transition TADF emitters for efficient non-doped OLEDs.
本文提出了一种新型分子模型,即通过具有足够空间和共轭禁阻的连接基团(D-间隔基-A)连接供电子(D)和吸电子(A)部分,以开发高效的非掺杂热激活延迟荧光(TADF)发光体。据此设计并合成了10-(4-(4-(4,6-二苯基-1,3,5-三嗪-2-基)苯氧基)苯基)-9,9-二甲基-9,10-二氢吖啶(DMAC-o-TRZ)。正如预期的那样,由于D-间隔基-A分子主链强烈抑制分子内电荷转移(CT)跃迁,它在单分子状态下表现出局部激发特性。分子间CT跃迁是纯DMAC-o-TRZ薄膜的重要辐射通道。作为回报,非掺杂器件表现出14.7%的显著最大外量子效率(EQE)。这些结果证明了D-间隔基-A分子用于开发用于高效非掺杂有机发光二极管的分子间CT跃迁TADF发光体的可行性。