Supporting electrolytes contain inert dissolved salts to increase the conductivity, to change microenvironments near the electrodes and to assist in electrochemical reactions. This combined experimental and computational study examines the impact of supporting salts on the ion transport and related limited currents in electrochemical cells. A physical model that describes the multi-ion transport in liquid electrolytes and the resulting concentration gradients is presented. This model and its parameterization are evaluated by the measured limited current of the copper deposition in a CuSO electrolyte under a gradually increasing amount of NaSO that acts as a supporting salt. A computational sensibility analysis of the transport model reveals that the shared conductance between the ions lowers the limited currents with larger supporting salt concentrations. When the supporting salt supplies most of the conductance, the electric-field-driven transport of the electrochemically active ions becomes negligible so that the limited current drops to the diffusion-limited current that is described by Fick's first law. The transition from diluted supporting electrolyte to the case of ionic liquids is elucidated with the transport model, highlighting the different physical transport mechanisms in a non-conducting (polar) and a conducting (ionic) solvent.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9008042 | PMC |
http://dx.doi.org/10.1038/s41598-022-10183-2 | DOI Listing |
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