Abstract
Aqueous electrolytes are very effective for supercapacitor applications but their narrow electrochemical potential window (∼1 V) and associated limited energy currently limits their use. Here, we demonstrate a new strategy to enlarge the potential window by designing an artificial interface ( ai ). An effective ai was achieved via a mixture of siloxanes doped with an ionic liquid, 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMI TFSI). Indeed, the as-deposited ai on the carbon-based electrode hinders the electron charge transfer but not the ionic charge transfer, making the ai ionic conductive. As a result, a cell voltage of about 1.8 V was obtained in aqueous electrolyte-EMI HSO 4 1 mol l −1 in water. Used as a membrane, the ai was found to be ionically specific to EMI + ; the proton transference number being close to zero. These results show the strategy of developing an ai at the electrode/electrolyte interface could represent a new path for aqueous-based carbon-carbon supercapacitors to reach higher cell voltages, providing both higher specific energy and power.
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CITATION STYLE
Olarte, M., Menu, M.-J., Simon, P., Gressier, M., & Taberna, P.-L. (2021). An Artificial Interface for High Cell Voltage Aqueous-Based Electrochemical Capacitors. Journal of The Electrochemical Society, 168(7), 070520. https://doi.org/10.1149/1945-7111/ac10f5
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