†Electronic supplementary information (ESI) available: Histograms of length and thickness of the platelets; perpendicular component of dielectric function; thickness dependence of perpendicular component of loss function; VEEL spectra of edge-on platelet along c-axis; VEEL spectra of face-on and edge platelets stacks.
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AbstractAnatase titania nanoplatelets predominantly exposing {001} facets have been reported to have enhanced catalytically properties in comparison to bulk anatase. To understand their unusual behaviour, it is essential to fully characterize their electronic and optical properties at the nanometer scale. One way of accessing these fundamental properties is to study the dielectric function. Valence electron energy-loss spectroscopy (EELS) performed in the scanning transmission electron microscope (STEM) is the only analytical method that can probe the complex dielectric function with both high energy (< 100 meV) and high spatial (< 1 nm) resolution. By correlating experimental STEM-EELS data with simulations based on semiclassical dielectric theory, the dielectric response of thin (< 5 nm) anatase nanoplatelets was found to be largely dominated by characteristic (optical) surface modes, which are linked to surface plasmon modes of anatase. For platelets less than 10 nm thick, the frequency of these optical modes varies according to their thickness. This unique optical behaviour prompts the enhancement of light absorption in the ultraviolet regime. Finally, the effect of finite size on the dielectric signal is gradually lost by stacking consistently two or more platelets in a specific crystal orientation, and eventually suppressed for large stacks of platelets.