Structural diversity in transition metal-doped titanium oxo-alkoxy complexes: Potential sol-gel intermediates for doped titania nanoparticles and complex titanates

Abstract

AbstractSince the discovery of its photocatalytic properties, titanium dioxide has remained one of the most popular and widely used metal oxide photocatalysts. Its major drawback, however, lies in the narrow region (UV) of sunlight necessary to produce reactive oxygen species. This have been countered by sensitizing with organic dyes to red-shift the absorption spectrum but also with doping of other metals and non-metals. Volume doping or surface modification have demonstrated improved photocatalytic efficiency, mainly via red-shifted absorption by introduction of intermediate energy states between the valence band (VB) and conduction band (CB) and increased number of surface hydroxyl groups (which can form reactive hydroxyl radicals) from charge compensation, and in some cases by improved surface-adsorption of organic molecules. Doped titania and complex titanates have traditionally been produced via, for instance, co-precipitation of mixed metal salts or via solid-state synthesis. While these methods usually are simple, they offer limited control over size, shape, and phase composition. An alternative is the use of single-source precursors (SSPs), i.e., molecules already containing the desired metal ratio in a homogenous distribution. The last one or two decades have seen an increased number of reported transition metal-doped titanium oxo-alkoxides (TOA), particularly for the first-row transition metals as potential single-source precursors (SSP) for doped titania and complex titanates. This review aims at providing an overview of TM-doped TOAs, focusing on first and second row TM elements, with special emphasis on their synthesis, photochemical properties, and their applications as SSPs.