When a charged membrane separates two salt solutions of different concentrations, a potential difference appears due to interfacial Donnan equilibrium and the diffusion junction. Here, we report a new mechanism for the generation of a membrane potential in polarizable conductive membranes via an induced surface charge. It results from an electric field generated by the diffusion of ions with different mobilities. For uncharged membranes, this effect strongly enhances the diffusion potential and makes it highly sensitive to the ion mobilities ratio, electrolyte concentration, and pore size. Theoretical predictions on the basis of the space-charge model extended to polarizable nanopores fully agree with experimental measurements in KCl and NaCl aqueous solutions.
We report a new mechanism for the generation of membrane potential in polarizable nanoporous membranes separating electrolytes with different concentrations. The electric field generated by diffusion of ions with different mobilities induces a non-uniform surface charge, which results in charge separation inside the nanopore. The corresponding Donnan potentials appear at the pore entrance and exit leading to a dramatic enhancement of membrane potential in comparison with an uncharged non-polarizable membrane. At high concentration contrast, the interaction between electric field and uncompensated charge at a low concentration side results in the development of electrokinetic vortices. The theoretical predictions are based on the Space-Charge model, which is extended to nanopores with polarizable conductive surface for the first time. This model is validated against full Navier-Stokes, Nernst-Planck, and Poisson equations, which are solved in a high aspect ratio nanopore connecting two reservoirs. The experimental measurements of membrane potential of dielectric and conductive membranes in KCl and NaCl aqueous solutions confirm the theoretical results. The membranes are prepared from Nafen nanofibers with 10 nm in diameter and modified by depositing a conductive carbon layer. It is shown theoretically that the enhancement effect becomes greater with decreasing the electrolyte concentration and pore radius. A high sensitivity of membrane potential to the ratio of ion diffusion coefficients is demonstrated. The described phenomenon may find applications in precise determination of ion mobilities, electrochemical and bio-sensing, as well as design of nanofluidic and bioelectronic devices.
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