4.6 Article

Mixed Ionic Liquid Improves Electrolyte Dynamics in Supercapacitors

期刊

JOURNAL OF PHYSICAL CHEMISTRY C
卷 122, 期 19, 页码 10476-10481

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.8b02521

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  1. Fluid Interface Reactions, Structures and Transport (FIRST) Center, an Energy Frontier Research Center - U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences
  2. Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy
  3. U.S. DOE
  4. Office of Science of the U.S. Department of Energy [DE-AC02-05CH11231]

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Well-tailored mixtures of distinct ionic liquids can act as optimal electrolytes that extend the operating electrochemical window and improve charge storage density in supercapacitors. Here, we explore two room-temperature ionic liquids, 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EmimTFSI) and 1-ethyl-3-methylimidazolium tetrafluoroborate (EmimBF4). We study their electric double-layer behavior in the neat state and as binary mixtures on the external surfaces of onion-like carbon electrodes using quasielastic neutron scattering (QENS) and classical density functional theory techniques. Computational results reveal that a mixture with 4:1 EmimTFSI/EmimBF(4) volume ratio displaces the larger [TESI-] anions with smaller [BF4-] ions, leading to an excess adsorption of [Emim(+)] cations near the electrode surface. These findings are corroborated by the manifestation of nonuniform ion diffusivity change, complementing the description of structural modifications with changing composition, from QENS measurements. Molecular-level understanding of ion packing near electrodes provides insight for design of ionic liquid formulations that enhance the performance of electrochemical energy storage devices.

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