Silicon dioxide, organic monolayers covalently attached to silicon and gold are used as biosensor substrates and anchoring platforms for hybrid, tethered and supported lipid membranes used in membrane-protein studies. Electrical impedance spectroscopy (EIS) studies of gold in contact with potassium chloride electrolytes of concentrations ranging from I mM to 300 mM, characterized the gold-electrolyte interface as principally a Stern layer 20-30 angstrom thick and conductivity many orders of magnitude less than that of the bulk electrolyte. EIS studies of SiO2-electrolyte system that were similar to studies of a tetradecane-electrolyte system are presented herein that reveal an interface comprised of at least two interfacial layers and extending some 10(5) angstrom into the electrolyte. The average conductivity and thickness values for the layer in contact with the SiO2 surface (similar to 10(-6) S m(-1) and similar to 28 angstrom, respectively) were of the order of magnitude expected for the Gouy-Chapman layer but the dependency of the thickness on concentration did not reflect the expected dependency of the Debye length over the full range of concentrations. The average values for the next layer (similar to 10(-3) S m(-1) and similar to 10(5) angstrom) exhibited a dependency on concentration similar to that expected for the bulk electrolyte. The theoretical derivations of ionic partitioning arising from the Born (dielectric) energy distributions in both the SiO2 and gold interfaces were generally consistent with the respective EIS studies and revealed that partitioning in the SiO2 interface mimicked that in bio-membranous interfaces. The dielectric characterizations suggest that; ionic partitioning in biomimetic interfaces play a role in long-ranging sequestration of organic molecules, the extensiveness of these interfaces contributes to differences in the lipid densities of bilayers formed on biomimetic substrates, and chloride ions have a greater affinity than the smaller potassium ions for gold substrates. (C) 2013 Elsevier Ltd. All rights reserved.