Solid-state NMR study of adsorbed water molecules in covalent organic framework materials

被引:13
作者
Ma, Jiaqi [1 ,2 ]
Fu, Xiao-Bin [3 ]
Li, Yuquan [1 ,2 ]
Xia, Tian [1 ,2 ]
Pan, Likun [1 ,2 ]
Yao, Ye-Feng [1 ,2 ]
机构
[1] East China Normal Univ, Dept Phys, Sch Phys & Elect Sci, Shanghai 200062, Peoples R China
[2] East China Normal Univ, Shanghai Key Lab Magnet Resonance, Sch Phys & Elect Sci, Shanghai 200062, Peoples R China
[3] Chinese Acad Sci, Key Lab Interfacial Phys & Technol, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China
基金
中国国家自然科学基金;
关键词
Water adsorption; Covalent organic framework materials; Solid state NMR; Water molecule redistribution; Porous material; CRYSTALLINE; EFFICIENT; MEMBRANE; ACID;
D O I
10.1016/j.micromeso.2020.110287
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This study investigates the locations and interactions of adsorbed water molecules within a porous COF material, TpPa-1. The TpPa-1 samples include the as-synthesized powder samples and the samples first subjected to compression at high pressure and then ground into a powder form. The investigation applies a variety of advanced solid-state NMR techniques. The results indicate that the adsorbed water molecules in the as-synthesized and compressed samples can exist in different locations and bonding states. Here, the adsorbed water molecules in the as-synthesized samples are found to be mainly located in the pore spaces and interact only loosely with the chemical groups of the material. In contrast, a proportion of the water molecules in the compressed samples enter into the interstices between the layers and interact with the amino groups and the carbonyl groups of the material. The relocation of the water molecules in the compressed samples provides a plausible explanation for the molecular origin of the water adsorption capability of TpPa-1. In addition, the revealed weak interactions between the water molecules and the chemical groups of TpPa-1 are correlated with the molecular origin of the high water permeance.
引用
收藏
页数:6
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