Solid-state NMR of active sites in TiO2 photocatalysis: a critical review

Abstract

Titanium dioxide (TiO2) is one of the optimal semiconductor metal oxide photocatalysts with a wide range of application fields, such as heterogeneous catalysis, energy science, and environmental science. Solid-state nuclear magnetic resonance (NMR) spectroscopy is a powerful tool for characterizing both structure and dynamics at an atomic-molecular level in heterogeneous catalysts. In this review, we first provide a brief discussion on the progress in investigating the structures of titanium and oxygen in bulk and on the surface of TiO2 by using various solid-state NMR techniques. Advances in the understanding of electronic structure and properties of TiO2 with distinct surface features, including various crystal facets and heteroatomic adsorption by chemical probe-assisted NMR techniques, are secondly presented. The solid-state NMR characterization of heteroatom active sites (such as 13C, 15N, 11B, 27Al) and their function in TiO2 photocatalysts is described in detail. Finally, a critical discourse assesses the current limitations and prospects of solid-state NMR in its application to the optimization and design of advanced TiO2 photocatalysts.