Asymmetric intramolecular charge transfer enables highly efficient red thermally activated delayed fluorescent emitters
Asymmetric intramolecular charge transfer enables highly efficient red thermally activated delayed fluorescent emitters
复制标题
不对称分子内电荷转移可实现高效的红色热激活延迟荧光发射器
DOI:
10.1016/j.cej.2022.141061
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发表时间:
2022
影响因子:
15.1
通讯作者:
Hui Xu
中科院分区:
文献类型:
--
作者:
Chao Qu;Huiqin Wang;Yi Man;Zhe Li;Peng Ma;Peng Chang;Xin Li;Chunmiao Han;Yudong Pang;Hui Xu
A feasible strategy of asymmetric donor–acceptor-second acceptor (D-A-A) structure is proposed for improving the photoluminecense (PL) and electroluminescence (EL) performance of red thermally activated delayed fluorescence (TADF) emitters. As a concept, four newly TADF emitters are designed and synthesized, D-A-A structureoTPAPO-DTPZandpTPAPO-DTPZand D-A-D typeoDTPA-DTPZandpDTPA-DTPZ, by using triphenylamine (TPA), dithieno[2,3-a:3′,2′-c]phenazine (DTPZ) and diphenylphosphine oxide (DPPO) groups as the donor, acceptor and second acceptor, respectively. It is demonstrated that abound intra- and inter-molecular Csingle bondH···O hydrogen bonds are forming between TPA donor and DPPO acceptor for the asymmetric compounds, which effectively promote the intra- and inter-molecular charge transfer. Moreover, the steric hindrance of DPPO group availably suppresses the concentration quenching. As a consequence, the asymmetric D-A-A structuredoTPAPO-DTPZandpTPAPO-DTPZexhibit relatively higher PL quantum yields and lower nonradiation rates, and thus better EL performance. In particular, device based onpTPAPO-DTPZachieves the maximum luminance of 19360 cd m−2and external quantum efficiency of 11.4 % at 632 nm, which are 2.3 and 1.5 times the values ofpDTPA-DTPZbased device.