Motivation on Intramolecular Through-Space Charge Transfer for the Realization of Thermally Activated Delayed Fluorescence (TADF)-Thermally Stimulated Delayed Phosphorescence (TSDP) in C∧C∧N Gold(III) Complexes and Their Applications in Organic Light-Emitting Devices

被引:0
|
作者
Li, Panpan [1 ,2 ,3 ]
Chen, Ziyong [1 ,2 ]
Leung, Ming-Yi [1 ,2 ,3 ]
Lai, Shiu-Lun [1 ,2 ]
Cheng, Shun-Cheung [4 ]
Kwok, Wing-Kei [1 ,2 ,3 ]
Ko, Chi-Chiu [4 ]
Chan, Mei-Yee [1 ,2 ,3 ]
Yam, Vivian Wing-Wah [1 ,2 ,3 ]
机构
[1] Univ Hong Kong, Inst Mol Funct Mat, Hong Kong, Peoples R China
[2] Univ Hong Kong, Dept Chem, Hong Kong, Peoples R China
[3] Hong Kong Quantum AI Lab Ltd, Hong Kong, Peoples R China
[4] City Univ Hong Kong, Dept Chem, Hong Kong, Peoples R China
关键词
EMISSION; EFFICIENCY; EMITTERS; DESIGN; LIGAND; TADF;
D O I
10.1021/jacs.5c00121
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thermally activated delayed fluorescence (TADF) and the very recently established thermally stimulated delayed phosphorescence (TSDP) are two promising approaches for enhancing the performance of organic light-emitting devices (OLEDs). Here, we have developed a new class of through-space charge transfer (TSCT) carbazolylgold(III) (CCN)-C-boolean AND-N-boolean AND complexes with unique TADF-TSDP properties by introducing a rigid arylamine on the carbazolyl auxiliary ligand. The highly twisted conformation between the (CCN)-C-boolean AND-N-boolean AND and carbazolyl ligands induces strong through-bond ligand-to-ligand charge transfer (TB-LLCT) character in their lowest singlet and triplet excited states, with small singlet-triplet energy gaps for efficient TADF. Moreover, the close spatial proximity between the cyclometalating ligand and the lateral arylamine enables appreciable intramolecular through-space electronic coupling that allows the generation of relatively low-lying triplet through-space ligand-to-ligand charge transfer ((TS)-T-3-LLCT) excited states. The TADF-TSDP properties are verified by temperature-dependent emission, lifetimes, and ultrafast transient absorption studies. Interestingly, through better alignment with extended planarity and the strengthening of the electron-donating ability of the lateral arylamine, the enhanced through-space electronic coupling can effectively perturb the energies of (TBCT)-T-3, (TSCT)-T-3, and intraligand ((IL)-I-3) excited states and thus manipulates the TSDP efficiency. Orange-emitting vacuum-deposited OLEDs made with these gold(III) complexes demonstrate respectable maximum external quantum efficiencies of >10% and long operational half-lifetimes of up to 65,314 h at a luminance of 100 cd m(-2). This work not only demonstrates the realization of interesting TADF-TSDP and TSCT properties in the gold(III) (CCN)-C-boolean AND-N-boolean AND cyclometalated system but also enriches the diversity of molecular design for high-performance TSDP and TSCT emitters.
引用
收藏
页码:12092 / 12104
页数:13
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