Second-harmonic generation provides insight into the screening response of the liquid water interface

26 June 2023, Version 5
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

We use second harmonic generation (SHG), molecular dynamics simulation, and theoretical modeling to study the response of the neat liquid water-air interface to changes in the potential of an external electrode positioned near the liquid, but out of direct contact. We observe a parabolic dependence of second harmonic intensity on applied potential. Based on standard theory, we associate this dependence with the response of the diffuse layer water molecules to changes in interfacial potential profile. Taking the literature value for this response leads to the unexpected conclusion that the electric fields within the diffuse layer are opposite in sign from those originating from the electrodes. This conclusion implies that the traditional continuum-based models of interfacial screening lack the complexity necessary to properly describe the potential profile of the liquid water-vapor interface. Effects such as overscreening in the topmost interfacial layer and extended correlations in the interfacial hydrogen bonding network may play a role in governing the response of the water interface to external fields.

Keywords

external electric field
Second Harmonic Generation Hyperpolarizability Applied
sum Frequency Generation Vibrational Spectroscopy
Air-water interface
Dipole moment
MD simulation

Supplementary materials

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Title
Second-harmonic generation provides insight into the screening response of the liquid water interface
Description
We use second harmonic generation (SHG) spectroscopy, molecular dynamics simulation, and theoretical modeling to study the response of the neat liquid water-air interface to changes in the potential of an external electrode positioned near the liquid, but out of direct contact. We observe a parabolic dependence of second harmonic intensity on the applied potential. Taking the literature value for this response leads to the unexpected conclusion that the electric fields within the diffuse layer are opposite in sign from those originating from the electrodes. This conclusion implies that the traditional continuum-based models of interfacial screening lacks the complexity necessary to properly describe the potential profile of the liquid water-vapor interface. Effects such as overscreening in the topmost interfacial layer and extended correlations in the interfacial hydrogen bonding network may play a role in governing the response of the water interface to external fields.
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