Design of Highly Photofunctional Porous Polymer Films with Controlled Thickness and Prominent Microporosity

被引:152
作者
Gu, Cheng [1 ]
Huang, Ning [1 ]
Wu, Yang [1 ]
Xu, Hong [1 ]
Jiang, Donglin [1 ]
机构
[1] Natl Inst Nat Sci, Dept Mat Mol Sci, Inst Mol Sci, Okazaki, Aichi 4448787, Japan
关键词
aggregation-induced emission; luminescence; porous polymers; sensors; thin films; METAL-ORGANIC FRAMEWORKS; GAS-STORAGE; EFFICIENT; FLUORESCENCE; CARBAZOLE; NETWORKS; EMISSION;
D O I
10.1002/anie.201504786
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Porous organic polymers allow the integration of various pi-units into robust porous pi-networks, but they are usually synthesized as unprocessable solids with poor light-emitting performance as a result of aggregation-related excitation dissipation. Herein, we report a general strategy for the synthesis of highly emissive photofunctional porous polymer films on the basis of a complementary scheme for the structural design of aggregation-induced-emissive pi-systems. We developed a high-throughput and facile method for the direct synthesis of large-area porous thin films at the liquid-electrode interface. The approach enables the preparation of microporous films within only a few seconds or minutes and allows precise control over their thickness with sub-nanometer precision. By virtue of rapid photoinduced electron transfer, the thin films can detect explosives with enhanced sensitivity to low parts-per-million levels in a selective manner.
引用
收藏
页码:11540 / 11544
页数:5
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