堆积
介孔材料
材料科学
复合数
复合材料
化学工程
热稳定性
多孔性
极限抗拉强度
氢键
纤维
催化作用
纳米技术
分子
化学
有机化学
工程类
作者
Kaikai Ma,Peng Li,John H. Xin,Yongwei Chen,Zhijie Chen,Subhadip Goswami,Xiaofeng Liu,Satoshi Kato,Haoyuan Chen,Xuan Zhang,Jiaquan Bai,Megan C. Wasson,Rodrigo R. Maldonado,Randall Q. Snurr,Omar K. Farha
标识
DOI:10.1016/j.xcrp.2020.100024
摘要
Creating crystalline porous materials with large pores is typically challenging due to undesired interpenetration, staggered stacking, or weakened framework stability. Here, we report a pore size expansion strategy by “shape-matching” intermolecular π-π stacking interactions in a series of two-dimensional (2D) hydrogen-bonded organic frameworks (HOFs), HOF-10x (x = 0,1,2), self-assembled from pyrene-based tectons with systematic elongation of π-conjugated molecular arms. This strategy successfully avoids interpenetration or staggered stacking and expands the pore size of HOF materials to access mesoporous HOF-102, which features a surface area of ∼2,500 m2/g and the largest pore volume (1.3 cm3/g) to date among all reported HOFs. More importantly, HOF-102 shows significantly enhanced thermal and chemical stability as evidenced by powder X-ray diffraction and N2 isotherms after treatments in challenging conditions. Such stability enables the easy fabrication of a HOF-102/fiber composite for the efficient photochemical detoxification of a mustard gas simulant.
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