Thermally Activated Upconversion with Metal-Free Sensitizers Enabling Exceptional Anti-Stokes Shift and Anti-counterfeiting Application

被引:24
|
作者
Yin, Wenxia [1 ,2 ]
Yu, Tianjun [1 ]
Chen, Jinping [1 ]
Hu, Rui [3 ]
Yang, Guoqiang [2 ,3 ]
Zeng, Yi [1 ,2 ]
Li, Yi [1 ,2 ]
机构
[1] Chinese Acad Sci, Tech Inst Phys & Chem, Key Lab Photochem Convers & Optoelect Mat, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Inst Chem, Key Lab Photochem, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
upconversion; triplet-triplet annihilation; thermally activated sensitization; sensitizer; anti-Stokes shift; anti-counterfeit; SINGLET OXYGEN; ENERGY-TRANSFER; EFFICIENT; STATE; CELLS; DYES; IRRADIANCE; MOLECULES; BODIPY; DESIGN;
D O I
10.1021/acsami.1c19181
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Photochemical upconversion (UC) via triplet-triplet annihilation (TTA) has attracted considerable attention for its potential applications in solar energy conversion, photocatalysis, and bioimaging. Achieving a large antiStokes shift in photochemical UC is appealing but still a great challenge, especially for purely organic sensitizers. Here, we develop solid-state TTA UC systems with metal- and heavy atom-free dyes as the sensitizers, which sensitize the 9,10-diphenylanthracene acceptor through thermally activated triplet-triplet energy transfer. Solid-state UC emission with remarkable anti-Stokes shifts up to 1.10 eV is achieved owing to an evident enthalpy gain by the endothermic sensitization. The solid upconverter shows air-stable UC emission and potentials in dual-mode anti-counterfeiting and encryption applications. The present UC approach involving thermally activated sensitization enabled by purely organic dyes provides a versatile strategy to develop TTA UC materials with large anti-Stokes shift, air-tolerant emission, and environmental compatibility, which would have promising applications in information encryption, photochemical conversion, and bioimaging.
引用
收藏
页码:57481 / 57488
页数:8
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