Thermally Activated Delayed Near-Infrared Photoluminescence from Functionalized Lead-Free Nanocrystals

被引:34
|
作者
He, Shan [1 ,2 ]
Du, Jun [1 ,2 ]
Liang, Wenfei [1 ,2 ]
Zhang, Boyu [1 ,2 ,3 ]
Liang, Guijie [3 ]
Wu, Kaifeng [1 ,2 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Mol React Dynam, Dalian 116023, Liaoning, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Collaborat Innovat Ctr Chem Energy Mat iChEM, Dalian 116023, Liaoning, Peoples R China
[3] Hubei Univ Arts & Sci, Hubei Key Lab Low Dimens Optoelect Mat & Devices, Xiangyang 441053, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Energy Transfer; Lead-Free Nanocrystals; Near-Infrared Emission; Thermally-Activated Delayed Emission; Time-Resolved Spectroscopy; TRIPLET ENERGY-TRANSFER; CHARGE-TRANSFER DYNAMICS; LIGHT-EMITTING-DIODES; CDSE QUANTUM DOTS; ELECTRON TRANSFERS; LUMINESCENT; CONVERSION; TETRACENE; EMISSION; EXCITONS;
D O I
10.1002/anie.202217287
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As an analogue to thermally activated delayed fluorescence (TADF) of organic molecules, thermally activated delayed photoluminescence (TADPL) observed in molecule-functionalized semiconductor nanocrystals represents an exotic mechanism to harvest energy from dark molecular triplets and to obtain controllable, long-lived PL from nanocrystals. The reported TADPL systems have successfully covered the visible spectrum. However, TADF molecules already emit very efficiently in the visible, diminishing the technological impact of the less-efficient nanocrystal-molecule TADPL. Here we report bright, near-infrared TADPL in lead-free CuInSe2 nanocrystals functionalized with carboxylated tetracene ligands, which results from efficient triplet energy transfer from photoexcited nanocrystals to ligands, followed with thermally activated reverse energy transfer from ligand triplets back to nanocrystals. This strategy prolonged the nanocrystal exciton lifetime from 100 ns to 60 mu s at room temperature.
引用
收藏
页数:7
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