Photocatalytic Properties of Nanostructured TiO2 (110) Single Crystal Surfaces
Lead Presenter: Lauren Moore
Additional Presenters: Timothy Luttrell
Faculty Advisor/Principal Investigator: Matthias Batzill, Ph.D.
Method of Presentation: Oral Presentation
Photocatalytic chemical reactions are actively explored for direct production of chemical fuels from sun light through electrolysis or for the clean-up of organic pollutants through photocatalysis. Titanium dioxide is a prototypical photocatalyst which has been studied extensively. However, there are still unanswered questions regarding the relationship between its surface morphology and photocatalytic properties. In this study, we used ion beam-assisted surface nanopatterning and UV-catalysis to investigate the dependence of photoreactivity on surface nanostructures. Energetic argon gas ions were used to induce self-formation of nanopatterns on TiO2 surfaces and the structure formation was characterized by atomic force microscopy. The influence of the surface structure on the photochemical properties was assessed through photocatalytic degradation of methyl orange in aqueous solution with a flat sample and a nanopatterned sample of TiO2, respectively. The resulting absorbance spectrums were then compared. Through this experiment and analysis of results, we were able to show through grazing-incidence sputtering and UV-catalysis that there was a significant increase in the photoreactivity of the sputtered sample vs. the flattened sample. Further research will subsequently be performed with additional data points and increasing flux. Particular areas to be explored are UV-catalysis on atomically flat TiO2 and UV-catalysis on samples with nanostructures along different crystallographic directions.