Confined Electrolytes Show Bulk Dynamics Modulated by Hydrodynamic Couplings with the Walls

We use numerical simulations at the mesoscopic scale, namely, multiparticle collision dynamics (MPCD), to investigate the properties of electrolyte solutions in a charged slit pore. The solution is described within the primitive model of electrolytes, where ions are charged hard spheres embedded in a dielectric medium. Hydrodynamic couplings between ions and with the charged walls are precisely accounted for by the MPCD algorithm. We show that the dynamic properties of ions in this situation strongly differ from the behavior at infinite dilution (ideal case), contrary to what is usually assumed in the usual Poisson-Nernst-Planck description of this kind of systems. As a consequence of confinement, the diffusion coefficients of ions unexpectedly increase with the average ionic density in the systems. This is due to a decrease of the proportion of ions that are slowed down by the wall. Moreover, nonequilibrium simulations are used to estimate the electrical conductivity of these confined electrolytes. We show that the simulation results can be accounted for quantitatively by combining bulk descriptions of the electrical conductivity of electrolytes with a simple description of the hydrodynamics of ions in a slit pore.