Ion correlations drive charge overscreening and heterogeneous nucleation at solid-aqueous electrolyte interfaces

Classical electrical double layer (EDL) models are foundational to the representation of atomistic structure and reactivity at charged interfaces. An important limitation to these models is their dependence on a mean-field approximation that is strictly valid for dilute aqueous solutions. Theoretical efforts to overcome this limitation are severely impeded by the lack of visualization of the structure over a wide range of ion concentration. Here, we report the salinity-dependent evolution of EDL structure at negatively charged mica-water interfaces, revealing transition from the Langmuir-type charge compensation in dilute salt solutions to nonclassical charge overscreening in highly concentrated solutions. The EDL structure in this overcharging regime is characterized by the development of both lateral positional correlation between adsorbed ions and vertical layering of alternating cations and anions reminiscent of the structures of strongly correlated ionic liquids. These EDL ions can spontaneously grow into nanocrystalline nuclei of ionic compounds at threshold ion concentrations that are significantly lower than the bulk solubility limit. These results shed light on the impact of ion cooperativity that drives heterogeneous nonclassical behaviors of the EDL in highsalinity conditions.

Automated summary

Classical electrical double layer (EDL) models are crucial for representing atomistic structure and reactivity at charged interfaces, but in highly concentrated salt solutions, nonclassical charge overscreening occurs due to ion cooperativity, leading to the development of ionic compounds at significantly lower ion concentrations than the bulk solubility limit.