Unraveling the atomic structure and dissociation of interfacial water on anatase TiO2 (101) under ambient conditions with solid-state NMR spectroscopy.

Abstract

Anatase TiO2 is a widely used component in photo- and electro-catalysts for water splitting, and the (101) facet of anatase TiO2 is the most commonly exposed surface. A detailed understanding of the behavior of H2O on this surface could provide fundamental insights into the catalytic mechanism. This, however, is challenging due to the complexity of the interfacial environments, the high mobility of interfacial H2O, and the interference from outer-layer H2O. Herein, we investigate the H2O/TiO2 interface using advanced solid-state NMR techniques. The atomic-level structures of surface O sites, OH groups, and adsorbed H2O have been revealed and the detailed interactions among them are identified on the (101) facet of anatase TiO2. By following the quantitative evolution of surface O and OH sites along with H2O loading, it is found that more than 40% of the adsorbed water spontaneously dissociated under ambient conditions on the TiO2 surface at a loading of 0.3 mmol H2O/g, due to the delicate interplay between water-surface and water-water interactions. Our study highlights the importance of understanding the atomic-level structures of H2O on the surface of TiO2 in catalytic reactions. Such knowledge can promote the design of more efficient catalytic systems for renewable energy production involving activation of water molecules.