Anisotropic Water Structure at Charged Interfaces Studied by Depth Resolved Vibrational SFG/DFG Spectroscopy

TL;DR

This study introduces a novel depth-resolved vibrational spectroscopy technique to analyze the anisotropic water structure at charged interfaces, revealing detailed orientation profiles and hydrogen-bonding characteristics.

Contribution

The paper presents a new experimental method for directly correlating vibrational spectra with depth, enabling detailed analysis of water anisotropy at charged interfaces.

Findings

Identification of two distinct anisotropic regions with different molecular orientations.

Hydrogen-bond structure of water remains largely unchanged near charged surfaces.

Depth-resolved data allows full reconstruction of vibrational responses as a function of depth.

Abstract

The molecular water structure at charged aqueous interfaces is shaped by interfacial electric fields, which can induce significant anisotropy in the molecular orientations extending over nanometer-scale distances. Despite great relevance, very little is known about the details of this depth-dependent anisotropic water structure, mainly due to the lack of appropriate experimental techniques. Here, we present a depth-resolved study of the water anisotropy at the interface to insoluble charged surfactants using a newly developed technique which allows for directly correlating nonlinear vibrational spectra with depth information on the nanometer scale. We demonstrate that the obtained data allows for a full reconstruction of the nonlinear vibrational responses as function of depth. The results for the case of low salinity solutions show the presence of two pronounced regions within the interfacial anisotropy with largely deviating degrees of preferential molecular orientations. A spectral analysis of the depth-dependent vibrational responses furthermore reveals that the natural local hydrogen-bond structure of bulk water remains largely unperturbed throughout the interfacial region, including water in direct proximity of the surface charges. These findings significantly refine our understanding of the anisotropic water structure at the interface to hydrophilic charged surfactants and showcase the large potential of our depth-resolved spectroscopic technique.