Photoluminescence (PL) represents a sensitive tool for probing molecular adsorption and surface reactions in photocatalytic materials. Titanium dioxide (TiO2) is one of the most widely used photocatalysis, and clarifying its basic PL mechanism can give important information. However, differently from other electronic and surface processes, the actual PL mechanisms of TiO2 are not extensively studied. In this work, we address the topic by focusing our investigation on which are the different states that trigger the PL activity and on identifying the specific recombination pathways acting in the two stable TiO2 polymorphs (rutile and anatase). On the basis of our experimental results on PL emission, PL excitation, and oxygen-induced and photoinduced PL modifications, we sketch an interpretative scheme for both the polymorphs. Excitation-resolved PL and recombination quenching caused by molecular oxygen evidence distinct contributions to anatase PL, originating from different kinds of hole-trapping and electron-trapping defects that we ascribe to surface and subsurface oxygen vacancies, respectively. Two possible mechanisms are discussed for rutile PL, involving self-trapped holes located at oxygen atoms or trapped electrons occupying midgap states positioned below the Fermi level. We argue that the validity of the former mechanism would imply that self-trapped holes are efficiently formed far from the rutile surface, while the latter mechanism seems more plausible although the very nature of the involved midgap electron state still has to be clarified.

In this work we demonstrate hyperbranched nanostructures, grown by pulsed laser deposition, composed of one-dimensional anatase single crystals assembled in arrays of high aspect ratio hierarchical mesostructures. The proposed growth mechanism relies on a two-step process: self-assembly from the gas phase of amorphous TiO2 clusters in a forest of tree-shaped hierarchical mesostructures with high aspect ratio; oriented crystallization of the branches upon thermal treatment. Structural and morphological characteristics can be optimized to achieve both high specific surface area for optimal dye uptake and broadband light scattering thanks to the microscopic feature size. Solid-state dye sensitized solar cells fabricated with arrays of hyperbranched TiO2 nanostructures on FTO-glass sensitized with D102 dye showed a significant 66% increase in efficiency with respect to a reference mesoporous photoanode and reached a maximum efficiency of 3.96% (among the highest reported for this system). This result was achieved mainly thanks to an increase in photogenerated current directly resulting from improved light harvesting efficiency of the hierarchical photoanode. The proposed photoanode overcomes typical limitations of 1D TiO2 nanostructures applied to ss-DSC and emerges as a promising foundation for next-generation high-efficiency solid-state devices comprosed of dyes, polymers, or quantum dots as sensitizers.