Abstract
Understanding the double layer at the
electrode-electrolyte interface is of fundamental importance to
electrochemistry, and also lays the basis for rational design of energy storage
and conversion technologies. The prevailing Gouy-Chapman-Stern (GCS) model and
its many derivatives invariably picture the double layer as a serial connection
of a compact layer and a diffuse layer. We unravel that these models based on
the serial connection tacitly prescribe a zero potential gradient at the
solution-side boundary. This assumption is generally invalid, resulting in an
incorrect expression for the double-layer impedance. Amendment of this deficiency
gives out a revised analytical expression for the double-layer impedance at the
potential of zero charge with new features. Specifically, the contribution of
the compact layer now shows frequency dispersion. The deviation between the
original and amended models is greater when the double layer is confined in narrower
space. This work changes our basic understanding of double layer model and its
impedance response.
Supplementary materials
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Supporting material V3
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