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Updated: Aug 6, 2025

Multiscale Sampling of a Heterogeneous Water/Metal Catalyst Interface using Density Functional Theory and Force-Field Molecular Dynamics
Published on: April 12, 2019
Dynamic Equilibrium at the HCOOH-Saturated TiO2(110)-Water Interface
Fernanda Brandalise Nunes1, Nicolò Comini2,3, J Trey Diulus2,3
1Department of Chemistry, University of Zürich, CH-8057 Zürich, Switzerland.
Abstract:
Carboxylic acids bind to titanium dioxide (TiO2) dissociatively, forming surface superstructures that give rise to a (2 × 1) pattern detected by low-energy electron diffraction. Exposing this system to water, however, leads to a loss of the highly ordered surface structure. The formate-covered surface was investigated by a combination of diffraction and spectroscopy techniques, together with static and dynamic ab initio simulations, with the conclusion that a dynamic equilibrium exists between adsorbed formic acid and water molecules. This equilibrium process is an important factor for obtaining a better understanding of controlling the self-cleaning properties of TiO2, because the formic acid monolayer is responsible for the amphiphilic character of the surface.
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