偶氮苯
膜
共价键
光致变色
紫外线
异构化
紫外线
纳米技术
光异构化
共价有机骨架
材料科学
光电开关
溶剂
光化学
分子开关
选择性
智能材料
化学工程
化学
分子
聚合物
光电子学
有机化学
催化作用
复合材料
工程类
生物化学
作者
Jiangtao Liu,Shaofei Wang,Tiefan Huang,Priyanka Manchanda,Edy Abou-Hamad,Suzana Pereira Nunes
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2020-08-21
卷期号:6 (34)
被引量:58
标识
DOI:10.1126/sciadv.abb3188
摘要
Development of the new-generation membranes for tunable molecular separation requires materials with abilities beyond strict separation. Stimuli response could remotely adjust the membrane selectivity. Azobenzene derivatives can be photo-switched between trans and cis isomers under ultraviolet or visible light. Here, the azobenzenes were implanted as light switches to bridge the flexible cyclen building blocks. The smart covalent organic network membranes fold and unfold as origami that can be photo-switched between on-state (large) and off-state (small) pores. The cis membranes with off state under ultraviolet (UV) light have higher dye rejection than trans membranes with on-state channels. By controlling the trans-to-cis azobenzene isomerization via UV/Vis light, the pore size can be remotely controlled at the molecular level and the solvent permeance and dye rejection can be dynamically tuned.
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