Impact of Asymmetric Microstructure on Ion Transport in Ti3C2Tx Membranes

被引:0
|
作者
Ventura-Martinez, Kimberly [1 ,4 ]
Zhu, Yaguang [1 ]
Booth, Austin [1 ,2 ]
Hatzell, Kelsey B. [1 ,3 ]
机构
[1] Andlinger Center for Energy and the Environment, Princeton,NJ,08540, United States
[2] Department of Chemical and Biological Engineering, Princeton University, Princeton,NJ,08540, United States
[3] Department of Mechanical and Aerospace Engineering, Princeton University, Princeton,NJ,08540, United States
[4] Department of Chemistry, Princeton University, Princeton,NJ,08540, United States
基金
美国国家科学基金会;
关键词
Membrane structures - Mesopores - Microfiltration - Micropores - Microstructural evolution - Nafion membranes - Water filtration;
D O I
10.1021/acs.nanolett.4c03080
中图分类号
学科分类号
摘要
Consolidation or densification of low-dimensional MXene materials into membranes can result in the formation of asymmetric membrane structures. Nanostructural (short-range) and microstructural (long-range) heterogeneity can influence mass transport and separation mechanisms. Short-range structural dynamics include the presence of water confined between the 2D layers, while long-range structural properties include the formation of defects, micropores, and mesopores. Herein, it is demonstrated that structural heterogeneity in Ti3C2Tx membranes fabricated via vacuum-assisted filtration significantly affects ion transport. Higher ion permeabilities are achieved when the dense bottom side of the membrane, rather than the porous top side, faces the feed solution. Characterization of the membrane reveals distinct differences in flake alignment, surface roughness, and porosity across the membrane. The directional dependence on permeability suggests that one region of the membrane experiences stronger internal concentration polarization, potentially suppressing permeability through the porous side of the membrane. © 2024 American Chemical Society.
引用
收藏
页码:13551 / 13557
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