膜
选择性
化学
电渗析
渗透
废水
化学工程
氯化物
金属有机骨架
离子
能源消耗
材料科学
纳米技术
工作(物理)
适应性
污水处理
高能
纳滤
离子通道
脱水
能量转换
工业废水处理
作者
Suixin Zhang,Zongliang Wan,Xu Zhang,Guifeng Liang,Qinshan Zhu,Jin ran,Peng Cui,Cen‐Feng Fu,Peipei Zuo,Tongwen Xu
标识
DOI:10.1038/s41467-026-69947-3
摘要
Biological ion channels exemplify nature’s high-efficiency ion selectivity filters, yet replicating their functional architectures in synthetic membranes remains a fundamental challenge. Here, we report an ultramicroporous hydrogen-bonded organic framework membrane that structurally emulates the CLC chloride filter. Its channels exhibit size adaptability to anions and incorporate hydrogen-bond donors that provide “low-viscosity” compensatory interactions, thereby alleviating anion dehydration energy penalties. By leveraging differential dehydration and energy compensation between Cl− and larger anions such as SO42−, this bioinspired design achieves an exceptional Cl−/SO42− selectivity of over 400—several tens of times higher than those of existing counterparts—while maintaining a high Cl− permeation rate double that of the commercial Neosepta® ACS membrane, setting a new benchmark for advanced anion-sieving membranes. In electrodialysis (ED) for high-salinity wastewater valorization, our membrane enables higher NaCl product purity (99.62 wt% vs. 72.86 wt%) with 28.7% lower energy consumption than the Neosepta® ACS membrane. This work establishes a biomimetic design principle of biological anion channels that is potentially extendable to a wide range of selective and conductive membranes. Replicating the functional architecture of biological ion channels in synthetic membranes remains challenging. Here the authors design an ultramicroporous hydrogen-bonded organic framework membrane that structurally emulates the CLC chloride filter.
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