Understanding long-range opposite charge repulsion in multivalent salt solutions
Nikhil R. Agrawal, Carlo Carrao, Rui Wang

TL;DR
This study uses advanced theoretical modeling to explain the long-range repulsion between oppositely charged surfaces in multivalent salt solutions, revealing its dependence on ion correlations and salt concentration.
Contribution
It introduces a modified Gaussian Renormalized Fluctuation theory to quantitatively describe opposite-charge repulsion and its independence from overcharging phenomena.
Findings
Opposite-charge repulsion is long-ranged with nanometer scale.
Repulsion strength increases monotonically with salt concentration.
No causal link between repulsion and surface overcharging.
Abstract
The electrostatic correlations between ions profoundly influence the structure and forces within electrical double layers. Here, we apply the modified Gaussian Renormalized Fluctuation theory to investigate the counter-intuitive phenomenon of repulsion between two oppositely charged surfaces and discuss its relationship with overcharging. By accurately accounting for the effect of spatially varying ion-ion correlations, we capture these repulsive forces for divalent, trivalent as well as tetravalent ions, in quantitative agreement with reported simulation results. We show that the opposite-charge repulsion is long-ranged with an effective length scale of a few nanometers. The strength of opposite-charge repulsion increases monotonically with the multivalent salt concentration, in stark contrast with the non-monotonic salt concentration dependence of other ion correlation-driven…
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Taxonomy
TopicsChemical and Physical Properties in Aqueous Solutions · Membrane-based Ion Separation Techniques
