微型多孔材料
共价键
多孔性
材料科学
化学工程
疏水效应
多孔介质
成核
化学物理
纳米技术
分子
聚合物
化学
有机化学
复合材料
工程类
作者
Ke Tian Tan,Shanshan Tao,Ning Huang,Donglin Jiang
标识
DOI:10.1038/s41467-021-27128-4
摘要
Progress over the past decades in water confinement has generated a variety of polymers and porous materials. However, most studies are based on a preconception that small hydrophobic pores eventually repulse water molecules, which precludes the exploration of hydrophobic microporous materials for water confinement. Here, we demonstrate water confinement across hydrophobic microporous channels in crystalline covalent organic frameworks. The frameworks are designed to constitute dense, aligned and one-dimensional polygonal channels that are open and accessible to water molecules. The hydrophobic microporous frameworks achieve full occupation of pores by water via synergistic nucleation and capillary condensation and deliver quick water exchange at low pressures. Water confinement experiments with large-pore frameworks pinpoint thresholds of pore size where confinement becomes dominated by high uptake pressure and large exchange hysteresis. Our results reveal a platform based on microporous hydrophobic covalent organic frameworks for water confinement.
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