Anomalous Ion Confinement Penalties and Giant Ion-Screening Effects in One-Dimensional Nanopores

Abstract

Nanoconfinement reduces the favorable hydration free energies of single ions, which is correlated with ion rejection and modified chemical reactivity in water-filled nanopores. Many factors contribute to the magnitude of the observed confinement effect. Here we use simple classical force fields and non-polarizable carbon nanotubes filled with water as minimal, "hydrogen atom"-like models to evaluate the single-ion intrinsic confinement hydration free energy penalty (Delta Delta G(hyd)). In tubes of radius R=7.5 Angstrom, we predict Delta Delta G(hyd)'s that are up to 7.8 kcal/mol, are much larger for Cl${}^{-}$ than the smaller Na+ ion, and contradict the canonical Born Equation for ion solvation. Adding a 1.0~M background electrolyte reduces Delta Delta G(hyd) for the Na${}^{+}$/Cl${}^{-}$ pair by an amount exceeding the Debye-Huckel estimate in unconfined media by almost an order of magnitude. We identify concentration-dependent ion-screening of confinement effects as a major, unheralded consequence of electrolytes in cylindrical nanopores.

arXiv comment18 pages, 5 figures. To appear in J. Phys. Chem. Lett

References in corpus (6)

• Anomalously low dielectric constant of confined water
• Ion Sizes and Finite-Size Corrections for Ionic-Solvation Free Energies
• Adsorption at Nanoconfined Solid-Water Interfaces
• Study of a water-graphene capacitor with molecular density functional theory
• Non-Reciprocal Interactions Induced by Water in Confinement
• Machine Learning Potential for Electrochemical Interfaces with Hybrid Representation of Dielectric Response