Ion Selective Membranes

A. Razmjou, Matthias Wessling, Vicki Chen
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Our current understanding of ion transport based on electric double-layer overlapping, the dehydration of ions, ionic affinity difference, one-surface-charge-governed ion transport and higher mobility of target ions within nanochannels and membranes are not sufficient to explain new findings. Recent reports[3] identified that other contributory factors must be considered during ISM design such as Zig-Zag transport (twosurface-charge-governed transport because of spontaneous symmetry breaking of charge), different ionic velocity gradient (acceleration and deceleration behaviour of ions as a function of nanochannel dimensions, functional groups and asymmetry in morphology and chemistry), the effect of ice-like arrangements of water molecules on ion selectivity within the asymmetric nanoconfined areas, hydrated ion trapping phenomena, internal concentration polarization and accumulation of ions, orbital involvements of atoms of the nanoconfined areas, and gradual dehydration of ions within the asymmetric nanoconfined areas. The special section of ion-selective membranes covers both fundamental and practical topics that reflect the growing importance of the field over the years. To begin, Amiri et al. (2001308) reviewed recent reports on the design and development of ISMs to control proton transport within Vanadium Redox Flow Batteries (VRFB). A variety of modification strategies were reviewed and an attempt was made to introduce a design platform for future work. Jovanović et al. (2001136) reviewed recent advances in the performance of separators in Li–S batteries and proposed guidelines for measurements with respect to key properties. Ion-exchange membranes (IEMs) are categorized as one of the traditional types of ISMs. Shehzad et al. (2001171) reviewed systematically four types IEMs: self-assembled nanochannels, solid-state nanostructures, artificial surface structures, and fillers-integrated nanostructures. Although mixed matrix membranes have been extensively used for gas separation and water purification, their application for ion separation is yet to be fully explored. The new family of 2D materials called MXenes have attracted significant attention within the membrane community. In a comprehensive review, Mozafari et al. (2001189) reviewed the current status and prospects of ion-selective MXene-Based Membranes. Zhikao et al. (2000862) reviewed the potential of 2D material-based thin-film nanocomposite membranes for ion A. Razmjou Centre for Technology in Water and Wastewater University of Technology Sydney Sydney, NSW, Australia A. Razmjou, V. Chen UNESCO Centre for Membrane Science and Technology School of Chemical Engineering University of New South Wales Sydney, NSW 2052, Australia E-mail: amirr@unsw.edu.au M. Wessling RWTH Aachen University Chemical Process Engineering Forckenbeckstrasse 51, 52074 Aachen, Germany M. Wessling DWI–Leibniz Institute for Interactive Materials Forckenbeckstrasse 50, 52074 Aachen, Germany V. Chen School of Chemical Engineering University of Queensland Queensland 4072, Australia The ORCID identification number(s) for the author(s) of this article can be found under https://doi.org/10.1002/admt.202100930. Ion-selective membranes (ISMs) have recently gained significant attention as their functions have become more vital in many environmental and biomedical applications. ISMs play a critical role in the clean energy future and the battery industry. Rapid growth in renewable energy demand resulted in a significant increase in the price of energy-critical elements such as Lithium and rare earth elements. ISMs can be used to directly extract the elements from readily available resources such as seawater and underground brines without compromising the environment. They can also be used for numerous biomedical applications such as nanobiosensors and point-of-care testing. Although ISMs are highly demanded, their commercial implementation has encountered several limitations such as the trade-off between selectivity and permeability, long-term stability, and low throughput for example. This is mainly due to the lack of ability to observe and manipulate ion movement at the atomic scale, limited understanding of ion transport mechanisms, and insufficient knowledge about transport-controlling effects and contributing factors. To make a high-performance ion-selective membrane, its inner ionic topology (ionic domain size, domain spacing, and domain properties), as well as its surface chemistry (functional groups and surface charge) must be carefully designed with regards to environmental conditions (ionic strength and pH) and ion transport driving force (applied pressure or potential). However, tailoring the key internal and external design para meters can only enhance the ion selectivity to a certain level which usually does not meet industry requirements. Recent findings in the literature, inspired by biological ion","PeriodicalId":7200,"journal":{"name":"Advanced Materials & Technologies","volume":"9 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials & Technologies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/admt.202100930","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

Abstract

DOI: 10.1002/admt.202100930 filters, revealed that a boost in ion selectivity can be achieved by engineering the ionic topology into an ionic nanochannel by adding an asymmetric element into both “chemistry” and “morphology” of the membranes.[1,2] This can be achieved by building an asymmetrical factor in membrane building blocks or during assembly. There is a need for research on how to assemble at scale ion-selective nanochannels into defect-free membrane-like morphologies with high packing density and long-term stability. Achieving this technological development will allow conversion to viable materials manufacturing and novel ion sensing systems or extraction processes. Our current understanding of ion transport based on electric double-layer overlapping, the dehydration of ions, ionic affinity difference, one-surface-charge-governed ion transport and higher mobility of target ions within nanochannels and membranes are not sufficient to explain new findings. Recent reports[3] identified that other contributory factors must be considered during ISM design such as Zig-Zag transport (twosurface-charge-governed transport because of spontaneous symmetry breaking of charge), different ionic velocity gradient (acceleration and deceleration behaviour of ions as a function of nanochannel dimensions, functional groups and asymmetry in morphology and chemistry), the effect of ice-like arrangements of water molecules on ion selectivity within the asymmetric nanoconfined areas, hydrated ion trapping phenomena, internal concentration polarization and accumulation of ions, orbital involvements of atoms of the nanoconfined areas, and gradual dehydration of ions within the asymmetric nanoconfined areas. The special section of ion-selective membranes covers both fundamental and practical topics that reflect the growing importance of the field over the years. To begin, Amiri et al. (2001308) reviewed recent reports on the design and development of ISMs to control proton transport within Vanadium Redox Flow Batteries (VRFB). A variety of modification strategies were reviewed and an attempt was made to introduce a design platform for future work. Jovanović et al. (2001136) reviewed recent advances in the performance of separators in Li–S batteries and proposed guidelines for measurements with respect to key properties. Ion-exchange membranes (IEMs) are categorized as one of the traditional types of ISMs. Shehzad et al. (2001171) reviewed systematically four types IEMs: self-assembled nanochannels, solid-state nanostructures, artificial surface structures, and fillers-integrated nanostructures. Although mixed matrix membranes have been extensively used for gas separation and water purification, their application for ion separation is yet to be fully explored. The new family of 2D materials called MXenes have attracted significant attention within the membrane community. In a comprehensive review, Mozafari et al. (2001189) reviewed the current status and prospects of ion-selective MXene-Based Membranes. Zhikao et al. (2000862) reviewed the potential of 2D material-based thin-film nanocomposite membranes for ion A. Razmjou Centre for Technology in Water and Wastewater University of Technology Sydney Sydney, NSW, Australia A. Razmjou, V. Chen UNESCO Centre for Membrane Science and Technology School of Chemical Engineering University of New South Wales Sydney, NSW 2052, Australia E-mail: amirr@unsw.edu.au M. Wessling RWTH Aachen University Chemical Process Engineering Forckenbeckstrasse 51, 52074 Aachen, Germany M. Wessling DWI–Leibniz Institute for Interactive Materials Forckenbeckstrasse 50, 52074 Aachen, Germany V. Chen School of Chemical Engineering University of Queensland Queensland 4072, Australia The ORCID identification number(s) for the author(s) of this article can be found under https://doi.org/10.1002/admt.202100930. Ion-selective membranes (ISMs) have recently gained significant attention as their functions have become more vital in many environmental and biomedical applications. ISMs play a critical role in the clean energy future and the battery industry. Rapid growth in renewable energy demand resulted in a significant increase in the price of energy-critical elements such as Lithium and rare earth elements. ISMs can be used to directly extract the elements from readily available resources such as seawater and underground brines without compromising the environment. They can also be used for numerous biomedical applications such as nanobiosensors and point-of-care testing. Although ISMs are highly demanded, their commercial implementation has encountered several limitations such as the trade-off between selectivity and permeability, long-term stability, and low throughput for example. This is mainly due to the lack of ability to observe and manipulate ion movement at the atomic scale, limited understanding of ion transport mechanisms, and insufficient knowledge about transport-controlling effects and contributing factors. To make a high-performance ion-selective membrane, its inner ionic topology (ionic domain size, domain spacing, and domain properties), as well as its surface chemistry (functional groups and surface charge) must be carefully designed with regards to environmental conditions (ionic strength and pH) and ion transport driving force (applied pressure or potential). However, tailoring the key internal and external design para meters can only enhance the ion selectivity to a certain level which usually does not meet industry requirements. Recent findings in the literature, inspired by biological ion
离子选择膜
DOI: 10.1002 / admt。研究表明,通过在膜的“化学”和“形态”中添加不对称元素,将离子拓扑结构设计成离子纳米通道,可以提高离子选择性。[1,2]这可以通过在膜构建块中或在组装过程中构建不对称因子来实现。如何将离子选择纳米通道组装成无缺陷、高堆积密度和长期稳定性的膜状结构,是目前研究的热点。实现这一技术发展将允许转化为可行的材料制造和新型离子传感系统或提取工艺。我们目前对基于双电层重叠、离子脱水、离子亲和差异、单表面电荷控制的离子传输以及纳米通道和膜内目标离子的高迁移率的离子传输的理解不足以解释新的发现。最近的报告[3]指出,在ISM设计过程中必须考虑其他因素,如z形传输(由于电荷的自发对称性破缺而导致的双表面电荷控制的传输)、不同的离子速度梯度(离子的加速和减速行为作为纳米通道尺寸、官能团和形态和化学上的不对称性的函数)、研究了水分子的冰状排列对不对称纳米限制区内离子选择性的影响、水合离子捕获现象、离子的内部浓度极化和积累、纳米限制区内原子的轨道参与以及不对称纳米限制区内离子的逐渐脱水。离子选择膜的特殊部分涵盖了反映多年来该领域日益重要的基础和实用主题。首先,Amiri等人(2001308)回顾了最近关于控制钒氧化还原液流电池(VRFB)内质子传输的ISMs设计和开发的报告。回顾了各种修改策略,并尝试为今后的工作引入一个设计平台。jovanoviki等人(2001136)回顾了锂硫电池中隔膜性能的最新进展,并提出了有关关键性能的测量指南。离子交换膜(IEMs)是一种传统的离子交换膜。Shehzad等人(2001171)系统地回顾了四种类型的纳米材料:自组装纳米通道、固态纳米结构、人工表面结构和填料集成纳米结构。虽然混合基质膜已广泛用于气体分离和水净化,但其在离子分离方面的应用尚未得到充分的探索。新的二维材料家族被称为MXenes,在膜界引起了极大的关注。Mozafari等人(2001189)对离子选择性mxene基膜的现状和前景进行了综述。Zhikao et al.(2000862)综述了二维材料基薄膜纳米复合膜用于离子的潜力A. Razmjou水与废水技术中心悉尼科技大学悉尼,新南威尔士州,澳大利亚A. Razmjou, V. Chen联合国教科文组织膜科学与技术中心化学工程学院新南威尔士大学悉尼,新南威尔士州2052,澳大利亚amirr@unsw.edu.au M. Wessling德国亚琛工业大学化学过程工程Forckenbeckstrasse 51,52074德国亚琛M. Wessling dwi -莱布尼茨相互作用材料研究所Forckenbeckstrasse 50,52074德国亚琛V. Chen化学工程学院澳大利亚昆士兰州4072本文作者的ORCID识别号码可在https://doi.org/10.1002/admt.202100930找到。离子选择膜(ISMs)由于其功能在许多环境和生物医学应用中变得越来越重要,近年来引起了人们的极大关注。ISMs在清洁能源的未来和电池行业中发挥着关键作用。可再生能源需求的快速增长导致锂和稀土等能源关键元素的价格大幅上涨。ISMs可用于直接从现成的资源(如海水和地下盐水)中提取元素,而不会损害环境。它们还可用于许多生物医学应用,如纳米生物传感器和即时检测。尽管对ISMs的需求很高,但它们的商业实现遇到了一些限制,例如在选择性和渗透性、长期稳定性和低吞吐量之间的权衡。 这主要是由于缺乏在原子尺度上观察和操纵离子运动的能力,对离子传输机制的理解有限,以及对传输控制效应和影响因素的认识不足。为了制造高性能的离子选择膜,必须根据环境条件(离子强度和pH值)和离子传输驱动力(施加压力或电位)仔细设计其内部离子拓扑结构(离子畴大小、畴间距和畴性质)以及表面化学性质(官能团和表面电荷)。然而,裁剪关键的内外设计参数只能将离子选择性提高到一定程度,通常不能满足工业要求。最近在文献中的发现,受到了生物离子的启发
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