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Differential capacitance of the double layer at the electrode/ionic liquids interface

Lockett, Vera, Horne, Mike, Sedev, Rossen, Rodopoulos, Theo, Ralston, John·2010·Physical Chemistry Chemical Physics

Abstract

The differential capacitance of the electrical double layer at glassy carbon, platinum and gold electrodes immersed in various ionic liquids was measured using impedance spectroscopy. We discuss the influence of temperature, the composition of the ionic liquids and the electrode material on the differential capacitance/potential curves. For different systems these curves have various overall shapes, but all include several extremes and a common minimum near the open circuit potential. We attribute this minimum to the potential of zero charge (PZC). Significantly, the differential capacitance generally decreases if the applied potential is large and moving away from the PZC. This is attributed to lattice saturation [A. A. Kornyshev, J. Phys. Chem. B, 2007, 111, 5545] effects which result in a thicker double layer. The differential capacitance of the double layer grows and specific adsorption diminishes with increasing temperature. Specific adsorption of both cations and anions influences the shapes of curves close to the PZC. The general shape of differential capacitance/potential does not depend strongly on the identity of the electrode material.

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Metadata

Authors
Lockett, V., Horne, M., Sedev, R., Rodopoulos, T., & Ralston, J.
Venue
Physical Chemistry Chemical Physics
Published
2010
Volume
12
Issue
39
Pages
12499
ISSN
  • 1463-9076 (ISSN-L)
  • 1463-9084
OpenAlex
W1995574399
Cited by
344
References
2
FWCI
7.71
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Differential capacitance of the double layer at the electrode/ionic liquids interface. https://app.cochat.ai/papers/10.1039/c0cp00170h
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Lockett, V., Horne, M., Sedev, R., Rodopoulos, T., & Ralston, J. (2010). Differential capacitance of the double layer at the electrode/ionic liquids interface. Physical Chemistry Chemical Physics. https://doi.org/10.1039/c0cp00170h

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