Published online by Cambridge University Press: 28 December 2015
We recently demonstrated a sub-bandgap photoresponse with our wafer-scale Au/TiO2 metallic-semiconductor photonic crystals (MSPhC). The sub-bandgap energy with 590 nm peak could be absorbed in the form of hot electron and injected to TiO2, which provides 5.28 times more energy for photolysis than that of energy absorbed to flat TiO2. If the solar energy already absorbed above 700 nm could be injected to the catalyst, higher than 10 times improvement will be achieved, and above 20% solar to fuel efficiency will be feasible with the robust but inefficient TiO2 catalyst. In order to achieve photocurrent near and above 700 nm spectrum, we deposited gold nanorods on the surface of MSPhC to incur localized surface plasmon (LSP) modes absorption and subsequent injection to the TiO2 catalyst. We used electrophoretic deposition (EPD) method to deposit nanorods on the top, sidewall and bottom well surface of the photonic nanocavities. The deposition of nanorods was achieved reasonably uniform and sparse not to block the optical cavities of MSPhC. Flat gold surfaces were tested at 4 different suspension densities to get the optimum gold nanorods density. Under 10V applied electric field, positively charged gold nanorods at the concentration of 6.52×1013 #/mL could deposit MSPhC surface with the density of 230 #/µm2, which was reasonably uniform and sparse. Preliminary tests show an absorbance increase near 700 nm on flat device coated with gold nanorods. Photocurrent measurement is under way to demonstrate the enhanced hot electron transfer over full visible light and near-infrared solar spectrum.