Abstract
Ion transport near interfaces is a fundamental phenomenon of importance in electrochemical, biological, and colloidal systems. In particular, electric double layers in highly confined spaces have implications for ion transport in nanoporous energy storage materials. By exploiting redox cycling amplification in lithographically fabricated thin-layer electrochemical cells comprising two platinum electrodes separated by a distance of 150–450 nm, we observed current enhancement during cyclic voltammetry of the hexaamineruthenium(III) chloride redox couple (Ru(NH3)63/2+) at low supporting electrolyte concentrations, resulting from ion enrichment of Ru(NH3)63/2+ in the electrical double layers and an enhanced ion migration contribution to mass transport. The steady-state redox cycling was shown to decrease to predominately diffusion controlled level with increasing supporting electrolyte concentration. Through independent biasing of the potential on the individual Pt electrodes, the voltammetric transport limit...
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