Quasiphase transition of a single-file water chain influenced by atomic charges in a water model using orientational-biased replica exchange Monte Carlo simulations

TL;DR

This study uses advanced simulations to investigate how atomic charges in water models influence the temperature-dependent quasiphase transition of single-file water chains confined in nanotubes, revealing charge-dependent structural and thermodynamic behaviors.

Contribution

It demonstrates how varying atomic charges in the SPC/E water model affect the structural phases and transition temperatures of confined water chains, providing new insights into electrostatic effects under nanoconfinement.

Findings

Higher atomic charges inhibit chain fragmentation and disorder.

Transition temperatures shift higher with increased charges.

Enhanced hydrogen bonding and dipole correlation length at elevated charges.

Abstract

The recently observed temperature-dependent quasiphase transition of the single-file water chain confined within a carbon nanotube in experiments has been validated by the simple lattice theory and molecular dynamics simulations. It has been pointed out that the atomic charges in water models are important, yet how the values will affect the structural details and thermodynamic properties of the quasiphase transition has not been fully revealed. In this work, we perform orientational-biased replica exchange Monte Carlo simulations in the canonical ensemble to explore the effect of atomic charges in the SPC/E water model on the quasiphase transition of a single-file water chain. Based on the atomic charge values reported in literature, three distinct quasiphases are reproduced, comprising a fully hydrogen-bonded water chain at lower temperatures, a more ordered dipolar orientation along the tube axis at intermediate temperatures, and a completely disordered structure at higher temperatures. Then by increasing the atomic charge values, we find that the fragmentation of the entire water chain into shorter water segments, the orientational ordering of water dipoles along the tube axis, and the transition towards complete disorder are all inhibited. Consequently, the transition temperatures between three quasiphases have been shifted to higher temperatures. The thermodynamic analysis demonstrates that the increased atomic charge values enhance the hydrogen bonding between neighbouring water molecules also the electrostatic attraction within the water chain, leading to a longer water dipole correlation length even at higher temperatures. These findings highlight the vital role of atomic charges in water models also the electrostatic interaction in regulating the orientational ordering of water molecules under nanoconfinement.