Molecularly Selective Polymer Interfaces for Electrochemical Separations

被引:11
|
作者
Kim, Nayeong [1 ]
Oh, Wangsuk [1 ]
Knust, Kyle N. [2 ]
Galetto, Fabio Zazyki [3 ]
Su, Xiao [1 ]
机构
[1] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[2] Millikin Univ, Dept Chem, Decatur, IL 62522 USA
[3] Univ Fed Santa Catarina UFSC, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
基金
美国国家科学基金会;
关键词
ION-EXCHANGE MEMBRANES; CAPACITIVE DEIONIZATION; CONCENTRATION POLARIZATION; NEUTRON REFLECTIVITY; BLOCK-COPOLYMERS; CHARGE-TRANSPORT; REDOX; REMOVAL; FILMS; WATER;
D O I
10.1021/acs.langmuir.3c02389
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The molecular design of polymer interfaces has been key for advancing electrochemical separation processes. Precise control of molecular interactions at electrochemical interfaces has enabled the removal or recovery of charged species with enhanced selectivity, capacity, and stability. In this Perspective, we provide an overview of recent developments in polymer interfaces applied to liquid-phase electrochemical separations, with a focus on their role as electrosorbents as well as membranes in electrodialysis systems. In particular, we delve into both the single-site and macromolecular design of redox polymers and their use in heterogeneous electrochemical separation platforms. We highlight the significance of incorporating both redox-active and non-redox-active moieties to tune binding toward ever more challenging separations, including structurally similar species and even isomers. Furthermore, we discuss recent advances in the development of selective ion-exchange membranes for electrodialysis and the critical need to control the physicochemical properties of the polymer. Finally, we share perspectives on the challenges and opportunities in electrochemical separations, ranging from the need for a comprehensive understanding of binding mechanisms to the continued innovation of electrochemical architectures for polymer electrodes.
引用
收藏
页码:16685 / 16700
页数:16
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