共价键
材料科学
吸附
共价有机骨架
离子
纳米技术
选择性
比表面积
化学工程
拓扑(电路)
表面改性
多孔性
有机化学
化学
复合材料
催化作用
工程类
组合数学
数学
作者
Minghao Liu,Hui‐Yuan Kong,Shuai Bi,Xuesong Ding,George Z. Chen,Jun He,Qing Xu,Bao‐Hang Han,Gaofeng Zeng
标识
DOI:10.1002/adfm.202302637
摘要
Abstract The 3D covalent organic frameworks (COFs) have attracted considerable attention owing to their unique structural characteristics. However, most of 3D COFs have interpenetration phenomena, which will result in decreased surface area and porosities, and thus limited their applications in molecular/gas capture. Developing 3D COFs with non‐fold interpenetration is challenging but significant because of the existence of non‐covalent interactions between the adjacent nets. Herein, a new 3D COF (BMTA‐TFPM‐COF) with dia topology and non‐fold interpenetration for Au ion capture is first demonstrated. The constructed COF exhibits a high Brunauer–Emmett–Teller surface area of 1924 m 2 g −1 , with the pore volume of 1.85 cm 3 g −1 . The high surface area and abundant cavities as well as the abundant exposed CN linkages due to the non‐interpenetration enable to absorb Au 3+ with high capacity (570.18 mg g −1 ), selectivity (99.5%), and efficiency (68.3% adsorption of maximum capacity in 5 min). This work provides a new strategy to design 3D COFs for ion capture.
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