With its unique electronic and optical properties, graphene is proposed to functionalize and tailor titania photocatalysts for improved reactivity. The two major solution-based pathways for producing graphene, oxidation-reduction and solvent exfoliation, result in nanoplatelets with different defect densities. Herein, we show that nanocomposites based on the less defective solvent-exfoliated graphene exhibit a significantly larger enhancement in CO(2) photoreduction, especially under visible light. This counterintuitive result is attributed to their superior electrical mobility, which facilitates the diffusion of photoexcited electrons to reactive sites.

Using the electron paramagnetic resonance technique, we have elucidated the multiple roles of water and carbonates in the overall photocatalytic reduction of carbon dioxide to methane over titania nanoparticles. The formation of H atoms (reduction product) and (•)OH radicals (oxidation product) from water, and CO(3)(-) radical anions (oxidation product) from carbonates, was detected in CO(2)-saturated titania aqueous dispersion under UV illumination. Additionally, methoxyl, (•)OCH(3), and methyl, (•)CH(3), radicals were identified as reaction intermediates. The two-electron, one-proton reaction proposed as an initial step in the reduction of CO(2) on the surface of TiO(2) is supported by the results of first-principles calculations.

Due to their unique optoelectronic structure and large specific surface area, carbon nanomaterials have been integrated with titania to enhance photocatalysis. In particular, recent work has shown that nanocomposite photocatalytic performance can be improved by minimizing the covalent defect density of the carbon component. Herein, carbon nanotube-titania nanosheet and graphene-titania nanosheet composites with low carbon defect densities are compared to investigate the role of carbon nanomaterial dimensionality on photocatalytic response. The resulting 2D-2D graphene-titania nanosheet composites yield superior electronic coupling compared to 1D-2D carbon nanotube-titania nanosheet composites, leading to greater enhancement factors for CO2 photoreduction under ultraviolet irradiation. On the other hand, 1D carbon nanotubes are shown to be more effective titania photosensitizers, leading to greater photoactivity enhancement factors under visible illumination. Overall, this work suggests that carbon nanomaterial dimensionality is a key factor in determining the spectral response and reaction specificity of carbon-titania nanosheet composite photocatalysts.

Titania nanotubes having diameters 8 to 12 nm and lengths of 50-300 nm were prepared using a hydrothermal method. Further, the titania nanotubes were calcined over the temperature range 200-800 °C in order to enhance their photocatalytic properties by altering their morphology. The calcined titania nanotubes were characterized by using X-ray diffraction and surface area analysis and their morphological features were studied by scanning and transmission electron microscopy. Nanotubes calcined at 400 °C showed the maximum extent of photocatalyitc reduction of carbon dioxide to methane, whereas samples calcined at 600 °C produced maximum photocatalytic oxidation of acetaldehyde. Electron paramagnetic resonance (EPR) spectroscopy was used to interrogate the effects of nanotube structure on the charge separation and trapping as a function of calcination temperature. EPR results indicated that undercoordinated titania sites are associated with maximum CO 2 reduction occurring in nanotubes calcined at 400 °C. Despite the collapse of the nantube structure to form nanorods and the concomitant loss of surface area, the enhanced charge separation associated with increased crystallinity promoted high rates of oxidation of acetaldehyde in titania materials calcined at 600 °C. These results illustrate that calcination temperature allows us to tune the morphological and surface features of the titania nanostructures for particular photocatalytic reactions.

An understanding of the adsorption of CO 2 , the first step in its photoreduction, is necessary for a full understanding of the photoreduction process. As such, the reactive adsorption of CO 2 on oxidized, reduced, and platinized TiO 2 nanotubes (Ti-NTs) was studied using infrared spectroscopy. The Ti-NTs were characterized with TEM and XRD, and XPS was used to determine the oxidation state as a function of oxidation, reduction, and platinization. The XPS data demonstrate that upon oxidation, surface O atoms become more electronegative, producing sites that can be characterized as strong Lewis bases, and the corresponding Ti becomes more electropositive producing sites that can be characterized as strong Lewis acids. Reduction of the Ti-NTs produces Ti 3+ species, a very weak Lewis acid, along with a splitting of the Ti 4+ peak, representing two sites, which correlate with O sites with a corresponding change in oxidation state. Ti 3+ is not observed on reduction of the platinized Ti-NTs, presumably because Pt acts as an electron sink. Exposure of the treated Ti-NTs to CO 2 leads to the formation of differing amounts of bidentate and monodentate carbonates, as well as bicarbonates, where the preference for formation of a given species is rationalized in terms of surface Lewis acidity and or Lewis basicity and the availability of hydrogen. Our data suggest that one source of hydrogen is water that remains adsorbed to the Ti-NTs even after heating to 350 °C and that reduced platinized NTs can activate H 2 . Carboxylates, which involve CO 2 − moieties and are similar to what would be expected for adsorbed CO 2 − , a postulated intermediate in CO 2 photoreduction, are also observed but only on the reduced Ti-NTs, which is the only surface on which Ti 3+ /O vacancy formation is observed.