三联烯
共价键
拓扑(电路)
氢气储存
吸附
甲烷
网络拓扑
多孔性
材料科学
共价有机骨架
联苯
纳米技术
化学
氢
计算机科学
有机化学
复合材料
组合数学
操作系统
数学
作者
Zonglong Li,Li Sheng,Chou-Hung Hsueh,Xiaolin Wang,Hao Cui,Hongqiang Gao,Yanzhou Wu,Jianlong Wang,Yaping Tang,Hong Xu,Xiangming He
标识
DOI:10.1021/acs.chemmater.1c03156
摘要
Three-dimensional (3D) covalent organic frameworks (COFs) are a new type of crystalline organic porous material, which have great application potential in various fields due to their complex pore structures and fully exposed active sites. The synthesis of 3D COFs with novel topologies is still challenging on account of limited secondary building units. Herein, we report a 3D COF with hea topology, which has never been reported before, utilizing a D3h-symmetric precursor [2,3,6,7,14,15-hexakis(4-formylphenyl)triptycene (HFPTP)] and [tetrakis(4-amino biphenyl)methane (TABPM)]. 3D-hea-COFs display permanent porosity and a Brunauer–Emmett–Teller surface area of 1804.0 m2 g–1. Owing to the huge internal free volume of triptycene, 3D-hea-COFs show good adsorption performance for H2, CO2, and CH4. Moreover, theoretical calculation reveals that both triptycene and tetraphenylmethane units contribute to enhance hydrogen storage capacity. The novel topology in this work expands the family of 3D COFs and provides new possibilities for designing efficient gas storage materials.
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