膜
配体(生物化学)
位阻效应
嵌入
聚合物
材料科学
纳米尺度
离子
化学工程
纳米技术
转化式学习
离子运输机
热稳定性
合成膜
化学稳定性
理论(学习稳定性)
图表
资源(消歧)
化学
路径(计算)
作者
Venkat Ganesan,Everett S. Zofchak
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2025-10-20
卷期号:14 (11): 1684-1693
标识
DOI:10.1021/acsmacrolett.5c00572
摘要
Selective ion separations are central to technologies spanning water purification, resource recovery, and clean energy. Conventional polymer membranes, which rely on steric hindrance or Donnan exclusion, struggle to discriminate between chemically similar ions in high-ionic-strength environments. Ligand-functionalized membranes offer a transformative strategy by embedding molecular recognition directly into polymer matrices, enabling selective complexation and transport. This Viewpoint highlights the structure-function relationships underlying ligand-mediated ion separation, emphasizing the interplay of dehydration penalties, ligand coordination, and nanoscale confinement. We discuss design principles, denticity, donor identity, rigidity, and spatial organization, alongside the permeability-selectivity trade-off, multicomponent effects, and stability challenges. Finally, we outline emerging strategies, from bioinspired ligands to computationally guided design, that chart a path toward next-generation membranes for precise and energy-efficient ion separations.
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