渗透
膜
选择性
化学工程
吸附
气体分离
材料科学
X射线光电子能谱
分子
基质(水族馆)
扩散
多孔性
纳米技术
化学
有机化学
催化作用
复合材料
工程类
地质学
物理
海洋学
热力学
生物化学
作者
Renhao Li,Xufang Fu,Guozhen Liu,Jiahui Li,Guangyuan Zhou,Gongping Liu,Wanqin Jin
标识
DOI:10.1016/j.memsci.2022.121097
摘要
MXene-based membranes with well-defined nanochannels are promising for gas separation. However, manipulating the interlayer structure to obtain high permeance and selectivity remains a great challenge. Herein, we report the construction of [email protected] membrane with significantly enhanced gas permeance and selectivity using room-temperature in situ synthesized [email protected] nanosheets as building blocks. Specifically, negatively charged MXene nanosheets can anchor Zr-metal ions from the surrounding through electrostatic interaction, and then coordinate with ligands at room temperature, yielding MOF-801 crystals with a particle size of approximately 20 nm uniformly grown on the MXene nanosheets. The membranes were then fabricated by vacuum filtration of the as-synthesized [email protected] nanosheets on the surface of porous organic substrate. The physicochemical properties of the as-synthesized [email protected] nanosheets and corresponding membranes were observed by XPS, AFM, SEM, IR, XRD, and gas adsorption analysis. Because the MOF-801 crystals can provide more transport channels for H2 molecules and exhibit high adsorption capacity for CO2 molecules to impede its diffusion, the resulting membranes display excellent gas separation performance with a H2 permeance of 2200 GPU and H2/CO2 selectivity of 26.6. Such a facile preparation method for [email protected] membranes could provide valuable insights into the development of advanced materials for molecular separation.
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