Tuning electronic levels in photoactive hydroxylated titania nanosystems: combining the ligand dipole effect and quantum confinement.

Reducing the size of titania (TiO2) to the nanoscale promotes the photoactive anatase phase for use in a range of applications from industrial catalysis to environment remediation. The nanoscale dimensions of these systems affect the magnitude of the electronic energy gap by quantum confinement. Upon interaction with aqueous environments or water vapour, the surfaces of these systems will also be hydroxylated to some degree. In turn, this affects the electronic energy levels due to the cumulative electrostatic effect of the dipolar hydroxyl (-OH) ligands (i.e. the ligand dipole effect). Using accurate density functional calculations, we investigate the combined effects of quantum confinement and the hydration-induced ligand dipole effect on a set of realistic titania nanosystems over a wide range of hydroxylation. Our detailed investigation reveals that, contrary to previous models, the ligand dipole effect does not-linearly depend on the ligand coverage due to the formation of inter-ligand OH⋯OH hydrogen bonds. To account for the resulting effects, we propose a refined model, which describes the ligand dipole effect more accurately in our systems. We show that both hydroxylation (by the ligand dipole effect) and size (by quantum confinement) have significant but distinct impacts on the electronic energy levels in nanotitania. As an example, we discuss how variations in these effects can be used to tune the highest unoccupied energy level in nanotitania for enhancing the efficiency of the hydrogen evolution reaction. Overall, we show that any specific energy shift can be achieved by a range of different combinations of nanosystem size and degree of hydroxylation, thus providing options for energy-level tuning while also allowing consideration of practical constraints (e.g. synthetic limitations, operating conditions) for photochemical applications.

Crystal properties without crystallinity? Influence of surface hydroxylation on the structure and properties of small TiO2 nanoparticles.

Titania (TiO2) nanoparticles (NPs) are widely employed in applications that take advantage of their photochemical properties (e.g. pollutant degradation, photocatalysis). Here, we study the interrelation between crystallinity, surface hydroxylation and electronic structure in titania NPs with 1.4-2.3 nm diameters using all electron density functional theory-based calculations. We show how the distribution of local coordination environments of the atoms in thermally annealed quasi-spherical non-crystalline NPs converge to those in correspondingly sized faceted crystalline anatase NPs upon increasing hydroxylation. When highly hydroxylated, annealed NPs also possess electronic energy gaps with very similar energies and band edge orbital characters to those of the crystalline anatase NPs. We refer to the crystallite-mimicking non-crystalline annealed NPs as "crystalikes". Small stable crystalike NPs could allow for photochemical applications of titania in the size range where crystalline anatase NPs tend to become thermodynamically unfavoured (<3-5 nm). Our work implies the anatase crystal structure may not be as essential as previously assumed for TiO2 NP applications and generally suggests that crystalikes could be possible in other nanomaterials.