In Situ Synthesis of AIEgen-based Porous Organic Polymer Films by Interfacial Amino-yne Click Polymerization for Efficient Light-Harvesting

被引:11
|
作者
Song, Bo [1 ,2 ]
Zhang, Liang [1 ,2 ]
Sun, Jianwei [1 ,2 ]
Lam, Jacky W. Y. [1 ,2 ]
Tang, Ben Zhong [1 ,2 ,3 ]
机构
[1] Hong Kong Univ Sci & Technol, Hong Kong Branch Chinese Natl Engn Res Ctr Tissue, Dept Chem, Clear Water Bay, Hong Kong 999077, Peoples R China
[2] HongKong Univ Sci & Technol Clear Water Bay, Guangdong HongKong Macau Joint Lab Optoelect & Mag, Clear Water Bay, Kowloon, Guangdong, Peoples R China
[3] Chinese Univ Hong Kong, Shenzhen Inst Aggregate Sci & Technol, Sch Sci & Engn, Shenzhen 518172, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Aggregation-Induced Emission; Light-Harvesting; Luminescence; POP Films; FRAMEWORKS; CRYSTALLINE; NANOSHEETS; CHEMISTRY; POWERFUL; TRIAZINE; LINKAGE; PORES; TOOL;
D O I
10.1002/anie.202302543
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We developed a catalyst-free, atom-economical interfacial amino-yne click polymerization to in situ synthesize new aggregation-induced emission luminogen (AIEgen)-based free-standing porous organic polymer films at room temperature. The crystalline properties of POP films were confirmed by powder X-ray diffraction and high-resolution transmission electron microscopy. The good porosity of these POP films was proved by their N-2 uptake experiments. The thickness of POP films can be easily regulated from 16 nm to approximate to 1 mu m by adjusting monomer concentration. More importantly, these AIEgen-based POP films show bright luminescence with high absolute photoluminescent quantum yields up to 37.8 % and good chemical and thermal stability. The AIEgen-based POP film can encapsulate an organic dye (e.g., Nile red) to further form an artificial light-harvesting system with a large red-shift (Delta lambda=141 nm), highly efficient energy-transfer ability (phi(ET)=91 %), and high antenna effect (11.3).
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页数:9
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