TY - JOUR
T1 - Molecularly Selective Polymer Interfaces for Electrochemical Separations
AU - Kim, Nayeong
AU - Oh, Wangsuk
AU - Knust, Kyle N.
AU - Zazyki Galetto, Fábio
AU - Su, Xiao
N1 - This material is based upon work supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences Separations Science program under award number DE-SC0021409. X.S. is grateful for funding from the National Science Foundation (NSF) under NSF CBET (grant no. 1942971). N.K. is grateful for fellowship funding from TechnipFMC and the Parr Fellowship from UIUC.
PY - 2023/11/28
Y1 - 2023/11/28
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85178108006&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85178108006&partnerID=8YFLogxK
U2 - 10.1021/acs.langmuir.3c02389
DO - 10.1021/acs.langmuir.3c02389
M3 - Review article
C2 - 37955994
AN - SCOPUS:85178108006
SN - 0743-7463
VL - 39
SP - 16685
EP - 16700
JO - Langmuir
JF - Langmuir
IS - 47
ER -