Camden DeBruler,Bo Hu,Jared Moss,Jian Luo,Tianbiao Liu
出处
期刊:ACS energy letters [American Chemical Society] 日期:2018-02-13卷期号:3 (3): 663-668被引量:245
标识
DOI:10.1021/acsenergylett.7b01302
摘要
Redox flow batteries using synthetically tunable and resource abundant organic molecules have gained increasing attention for large-scale energy storage. Herein we report a sulfonate-functionalized viologen molecule, 1,1′-bis(3-sulfonatopropyl)-4,4′-bipyridinium, (SPr)2V, as an anolyte in neutral aqueous organic redox flow batteries (AORFBs) functioning through a cation charge-transfer mechanism. Demonstrated (SPr)2V/KI AORFBs manifested high current performance from 40 to 100 mA/cm2 with up to 71% energy efficiency. In extended cycling studies, the (SPr)2V/KI redox flow battery delivered stable cycling performance at 60 mA/cm2, up to 67% energy efficiency, and 99.99% capacity retention per cycle. Density functional theory modeling of the electrostatic charge surface of (SPr)2V and its charged state, [(SPr)2V]–1, suggests charge repulsion and size exclusion enable their compatibility with a cation exchange membrane. The present findings expand the battery design of neutral viologen AORFBs and represent an attractive RFB technology for sustainable and benign renewable energy storage.