4.5 Article

Effect of cation on diffusion coefficient of ionic liquids at onion-like carbon electrodes

Journal

JOURNAL OF PHYSICS-CONDENSED MATTER
Volume 26, Issue 28, Pages -

Publisher

IOP PUBLISHING LTD
DOI: 10.1088/0953-8984/26/28/284104

Keywords

ionic liquids; onion-like carbons; electrochemical capacitor; solid electrolyte interphase; diffusion coefficient

Funding

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

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While most supercapacitors are limited in their performance by the stability of the electrolyte, using neat ionic liquids (ILs) as the electrolyte can expand the voltage window and temperature range of operation. In this study, ILs with bis(trifluoromethylsulfonyl) imide (Tf2N) as the anion were investigated as the electrolyte in onion-like carbon-based electrochemical capacitors. To probe the influence of cations on the electrochemical performance of supercapacitors, three different cations were used: 1-ethyl-3-methylimidazolium, 1-hexyl-3-methylimidazolium and 1,6-bis(3-methylimidazolium-1-yl). A series of electrochemical characterization tests was performed using cyclic voltammetry (CV), galvanostatic cycling and electrochemical impedance spectroscopy (EIS). Diffusion coefficients were measured using EIS and correlated with quasielastic neutron scattering and molecular dynamics simulation. These three techniques were used in parallel to confirm a consistent trend between the three ILs. It was found that the IL with the smaller sized cation had a larger diffusion coefficient, leading to a higher capacitance at faster charge-discharge rates. Furthermore, the IL electrolyte performance was correlated with increasing temperature, which limited the voltage stability window and led to the formation of a solid electrolyte interphase on the carbon electrode surface, evident in both the CV and EIS experiments.

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