Xu Rongming, Kang Yuan, Zhang Weiming, Pan Bingcai, Zhang Xiwang
State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, 210023, Nanjing, China.
Research Center for Environmental Nanotechnology (ReCENT), Nanjing University, 210023, Nanjing, China.
Nat Commun. 2023 Aug 15;14(1):4907. doi: 10.1038/s41467-023-40742-8.
Membranes with high ion permeability and selectivity are of considerable interest for sustainable water treatment, resource extraction and energy storage. Herein, inspired by K channel of streptomyces A (KcsA K), we have constructed cation sieving membranes using MXene nanosheets and Ethylenediaminetetraacetic acid (EDTA) molecules as building blocks. Numerous negatively charged oxygen atoms of EDTA molecules and 6.0 Å two-dimensional (2D) sub-nanochannel of MXene nanosheets enable biomimetic channel size, chemical groups and tunable charge density for the resulting membranes. The membranes show the capability to recognize monovalent/divalent cations, achieving excellent K/Mg selectivity of 121.2 using mixed salt solution as the feed, which outperforms other reported membranes under similar testing conditions and transcends the current upper limit. Characterization and simulations indicate that the cation recognition effect of EDTA and partial dehydration effects play critical roles in cations selective sieving and increasing the local charge density within the sub-nanochannel significantly improves cation selectivity. Our findings provide a theoretical basis for ions transport in sub-nanochannels and an alternative strategy for design ions separation membranes.
具有高离子渗透性和选择性的膜对于可持续水处理、资源提取和能量存储具有相当大的吸引力。在此,受链霉菌A的钾通道(KcsA K)启发,我们使用MXene纳米片和乙二胺四乙酸(EDTA)分子作为构建单元构建了阳离子筛分膜。EDTA分子大量带负电荷的氧原子以及MXene纳米片6.0 Å的二维(2D)亚纳米通道,为所得膜赋予了仿生通道尺寸、化学基团和可调电荷密度。这些膜表现出识别单价/二价阳离子的能力,以混合盐溶液为进料时,实现了121.2的优异钾/镁选择性,在类似测试条件下优于其他报道的膜,并且超越了当前的上限。表征和模拟表明,EDTA的阳离子识别效应和部分脱水效应在阳离子选择性筛分中起关键作用,并且显著提高亚纳米通道内的局部电荷密度可提高阳离子选择性。我们的发现为亚纳米通道中的离子传输提供了理论基础,并为设计离子分离膜提供了一种替代策略。