Inversion of the electric field at the electrified liquid-liquid interface

The thermodynamics of the general system of two immiscible electrolytes in the presence of an electric field depends strongly on the distribution of ions near the liquid interface. Here, we calculate the corresponding electrostatic potential difference, excess surface tension, and differential capacity via Monte Carlo simulations, which include ion correlations and polarization effects, and via a modified nonlinear Poisson-Boltzmann theory. Macroscopically, we find good agreement between our results and experimental data without needing any fitting parameter. At higher salt concentrations, charge overcompensation in the lower-permittivity region is observed, which results in a local inversion of the electric field accompanied by charge inversion near the interface. We find that these interesting phenomena are mainly driven by the excluded-volume effects associated with large organic ions in the oil phase, although polarization effects and between-layer ion correlations have a significant impact in the adsorption of ions close to the liquid interface. In addition, our Monte Carlo simulations predict that the differential capacity is maximal at the point of zero charge, in contrast with the classical Poisson-Boltzmann theory results. © 2012 American Chemical Society.

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