Metal coordination complexes in nonaqueous redox flow batteries

被引:38
|
作者
Hogue, Ross W. [1 ]
Toghill, Kathryn E. [1 ]
机构
[1] Univ Lancaster, Dept Chem, Lancaster LA1 4YB, England
基金
英国工程与自然科学研究理事会;
关键词
Redox flow batteries; Coordination complexes; Transition metal complexes; Nonaqueous electrolytes; Energy storage; SUPPORTING ELECTROLYTES; NEXT-GENERATION; ENERGY-STORAGE; NI FOAM; SOLVENTS; PROGRESS; DESIGN; COBALT; CHALLENGES; CROSSOVER;
D O I
10.1016/j.coelec.2019.08.006
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
The ongoing search for new electroactive materials for next-generation redox flow batteries has within the last decade encompassed metal-ligand coordination chemistry. Here, we review the handful of metal coordination complexes proposed as redox flow battery electrolytes. We highlight examples with careful ligand design, driving research towards higher energy density storage materials. Metal coordination complexes designed to be highly soluble not only in the initial redox state but also in all charged states accessed during the battery cycle give particularly impressive performances. Optimisation of flow cell conditions for metal coordination complexes remains largely unexplored, with most complexes screened in nonideal H-cell experiments with little investigation into membrane and electrode materials.
引用
收藏
页码:37 / 45
页数:9
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