Modeling of electrochemical deionization across length scales: Recent accomplishments and new opportunities

被引:6
作者
Liu, Sizhe [1 ]
Do, Vu Quoc [1 ]
Smith, Kyle C. [1 ,2 ,3 ,4 ]
机构
[1] Univ Illinois, Dept Mech Sci & Engn, Urbana, IL 61801 USA
[2] Univ Illinois, Computat Sci & Engn Program, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
[4] Univ Illinois, Beckman Inst Adv Sci & Technol, Urbana, IL 61801 USA
基金
美国国家科学基金会;
关键词
Capacitive deionization; Faradaic deionization; Electrodialysis; Modeling; Multiscale; Intercalation; Desalination; Water; CAPACITIVE DEIONIZATION; ENERGY-CONSUMPTION; WATER DESALINATION; ELECTRODE MATERIAL; PERFORMANCE; GENERATION; REMOVAL;
D O I
10.1016/j.coelec.2020.05.003
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Theoretical models have recently been used to simulate deionization technology by capturing electrochemical processes at atomistic, electrode, and plant length scales in electrodialysis, capacitive deionization using electric double layers, and Faradaic deionization using intercalation materials and redox-active polymers. We review the salient features of such models, identifying their major accomplishments in quantifying energy consumption and ion removal, analyzing the feasibility of large-scale systems, and discovering new electrode materials and understanding their deionization mechanisms. After summarizing strengths and weaknesses of recent modeling strategies, we identify research directions to expand modeling capabilities that can be used to inform electrode material/microstructure design, to assign energy losses to electrode-scale mechanisms, to bridge length scales, and to capture Faradaic kinetic/diffusion processes.
引用
收藏
页码:72 / 79
页数:8
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