Multi-Mode Color-Tunable Long Persistent Luminescence in Single-Component Coordination Polymers

被引:0
|
作者
Wang, Zheng [1 ,2 ]
Zhu, Cheng-Yi [1 ]
Mo, Jun-Ting [1 ]
Xu, Xian-Yan [3 ]
Ruan, Jia [1 ]
Pan, Mei [1 ]
Su, Cheng-Yong [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem, Lehn Inst Funct Mat, MOE Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Peoples R China
[2] Shaanxi Univ Sci & Technol, Coll Chem & Chem Engn, Key Lab Chem Addit China Natl Light Ind, Xian 710021, Peoples R China
[3] Shaoguan Univ, Coll Chem & Civil Engn, Shaoguan 512005, Peoples R China
关键词
cadmium; color tuning; coordination polymers; halides; long persistent luminescence (LPL); ROOM-TEMPERATURE PHOSPHORESCENCE; ORGANIC PHOSPHORESCENCE; CARBON DOTS; SYNERGISM;
D O I
10.1002/anie.202012831
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Materials with tunable long persistent luminescence (LPL) properties have wide applications in security signs, anti-counterfeiting, data encrypting, and other fields. However, the majority of reported tunable LPL materials are pure organic molecules or polymers. Herein, a series of metal-organic coordination polymers displaying color-tunable LPL were synthesized by the self-assembly of HTzPTpy ligand with different cadmium halides (X=Cl, Br, and I). In the solid state, their LPL emission colors can be tuned by the time-evolution, as well as excitation and temperature variation, realizing multi-mode dynamic color tuning from green to yellow or green to red, and are the first such examples in single-component coordination polymer materials. Single-crystal X-ray diffraction analysis and theoretical calculations reveal that the modification of LPL is due to the balanced action from single molecule and aggregate triplet excited states caused by an external heavy-atom effect. The results show that the rational introduction of different halide anions into coordination polymers can realize multi-color LPL.
引用
收藏
页码:2526 / 2533
页数:8
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