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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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