Impact of Cation-Ligand Interactions on the Permselectivity of Ligand- Functionalized Polymer Membranes in Single and Mixed Salt Systems

HS Sachar and ES Zofchak and N Marioni and ZD Zhang and S Kadulkar and TJ Duncan and BD Freeman and V Ganesan, MACROMOLECULES, 55, 4821-4831 (2022).

DOI: 10.1021/acs.macromol.2c00543

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.

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