Issue 46, 2020

A hydrogen-bonding structure in self-formed nanodroplets of water adsorbed on amorphous silica revealed via surface-selective vibrational spectroscopy

Abstract

Water adsorption onto a material surface is known to change macroscopic surface properties such as wettability and friction coefficient. While the role of the adsorbed water has been discussed for a long time, the interfacial structure of the adsorbed water has not been fully recognized in many cases. In this study, the hydration structure of water adsorbed on a vapor/silica interface at room temperature was studied via heterodyne-detected vibrational sum-frequency generation spectroscopy. The vibrational spectra of the interfacial molecules obtained here were different from those estimated via conventional sum-frequency generation spectroscopy. Interestingly, our results suggest that, at low humidity, the adsorbed water on silica forms nanodroplets instead of a uniform film. Because no silanol group was found to be hydrogen-bonding free, it was concluded that water molecules gather around the silanol group to form strongly hydrogen-bonded droplets. At high humidity, while the adsorbed water partially behaves like a bulk liquid, deprotonation of the silanol was not observed, unlike the case of silica surfaces in contact with bulk liquid water.

Graphical abstract: A hydrogen-bonding structure in self-formed nanodroplets of water adsorbed on amorphous silica revealed via surface-selective vibrational spectroscopy

Supplementary files

Article information

Article type
Paper
Submitted
15 Jun 2020
Accepted
19 Sep 2020
First published
23 Sep 2020
This article is Open Access
Creative Commons BY license

Phys. Chem. Chem. Phys., 2020,22, 27031-27036

A hydrogen-bonding structure in self-formed nanodroplets of water adsorbed on amorphous silica revealed via surface-selective vibrational spectroscopy

S. Urashima, T. Uchida and H. Yui, Phys. Chem. Chem. Phys., 2020, 22, 27031 DOI: 10.1039/D0CP03207G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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