We conduct molecular dynamics simulations
to study the effects
of cation–ligand interactions on salt permeation in ligand-functionalized
polymer membranes. Our results indicate that salt partitioning into
the membrane increases while the salt diffusivity decreases with enhancement
in the cation–ligand interaction strength. Moreover, the increase
in partitioning dominates the decline in salt diffusivity, leading
to a net enhancement in salt permeation at higher cation–ligand
interaction strengths. Equimolar binary mixed salt systems (having
a common anion) generally exhibit much more selective partitioning
of salts into the membrane as compared to their single salt counterparts.
However, single salt systems exhibit much higher ratio of salt diffusivities
than their mixed salt analogues. The permselectivity data closely
resemble the trends in selective partitioning for both single and
mixed salt systems, indicating that salt diffusivity selectivity plays
a weaker role than salt partitioning selectivity in dictating the
selective permeation of salts across the membrane.