Interaction between two polyelectrolytes in monovalent aqueous salt solutions

We use the recently developed soft-potential-enhanced Poisson-Boltzmann (SPB) theory to study the interaction between two parallel polyelectrolytes (PEs) in monovalent ionic solutions in the weak-coupling regime. The SPB theory is fitted to ion distributions from coarse-grained molecular dynamics (MD) simulations and benchmarked against all-atom MD modelling for poly(diallyldimethylammonium) (PDADMA). We show that the SPB theory is able to accurately capture the interactions between two PEs at distances beyond the PE radius. For PDADMA positional correlations between the charged groups lead to locally asymmetric PE charge and ion distributions. This gives rise to small deviations from the SPB prediction that appear as short-range oscillations in the potential of mean force. Our results suggest that the SPB theory can be an efficient way to model interactions in chemically specific complex PE systems.

Automated summary

We use the SPB theory to study the interaction between two parallel polyelectrolytes in monovalent ionic solutions. The theory accurately captures the interactions beyond the PE radius and accounts for positional correlations between charged groups. The results suggest that the SPB theory is an efficient way to model interactions in chemically specific complex PE systems.