A Sulfonate-Functionalized Viologen Enabling Neutral Cation Exchange, Aqueous Organic Redox Flow Batteries toward Renewable Energy Storage AITranslate
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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.
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DOI:https://doi.org/10.1021/acsenergylett.7b01302
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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.
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| GB/T 7714-2015 | [1] Camden DeBruler, Bo Hu, Jared Moss, et al. ACS Energy Letters, 2018(3). DOI:10.1021/acsenergylett.7b01302. |
| MLA | [1] Camden DeBruler, et al., ACS Energy Letters, no. 3, 2018, https://doi.org/10.1021/acsenergylett.7b01302. |
| APA | [1] Camden DeBruler, Bo Hu, Jared Moss, Jian Luo, & T. Leo Liu. (2018). ACS Energy Letters(3). https://doi.org/10.1021/acsenergylett.7b01302 |
| IEEE | [1] Camden DeBruler, Bo Hu, Jared Moss, Jian Luo, and T. Leo Liu, ACS Energy Letters, no. 3, 2018, doi: 10.1021/acsenergylett.7b01302. |
