# Effective dielectric constant of water at the interface with charged C$_{60}$ fullerenes

## TL;DR

This study uses molecular dynamics simulations to determine the dielectric constant of water at the interface with charged C60 fullerenes, revealing structural transitions and dielectric variations influenced by charge and temperature.

## Contribution

It introduces a computational approach to directly measure interface susceptibility and dielectric constants from simulation data for water interacting with fullerenes.

## Key findings

- Dielectric constants range from 10 to 22 depending on conditions.
- Hydration water undergoes a structural crossover with solute charge.
- Interface dielectric constant exhibits a spike at the structural transition.

## Abstract

Dipolar susceptibility of interfacial water and the corresponding interface dielectric constant were calculated from numerical molecular dynamics simulations for neutral and charged states of buckminsterfullerene C$_{60}$. Dielectric constants in the range 10--22, depending on temperature and solute charge, were found. The hydration water undergoes a structural crossover as a function of the solute charge. Its main signatures include the release of dangling O-H bonds pointing toward the solute and the change in the preferential orientations of hydration water from those characterizing hydrophobic to charged substrates. The interface dielectric constant marks the structural transition with a spike. The computational formalism adopted here provides direct access to interface susceptibility from configurations produced by computer simulations. The required property is the cross-correlation between the radial projection of the dipole moment of the solvation shell and the electrostatic potential of the solvent inside the solute.