Enhancement of Photocatalytic Water Splitting Rate via Rayleigh Convection
- 1 Department of Energy Engineering and Science, Nagoya University, Nagoya, Japan
- 2 School of Chemical Engineering, Purdue University, West Lafayette, USA
- 3 Kitchen and Bathroom Technology Research Institute, LIXIL Corporation, Tokoname, Japan
- 4 Department of Energy Engineering and Science, Nagoya University, Nagoya, Japan
- 5 Department of Energy Engineering and Science, Nagoya University, Nagoya, Japan
- 6 Department of Energy Engineering and Science, Nagoya University, Nagoya, Japan
- 7 Department of Energy Engineering and Science, Nagoya University, Nagoya, Japan
- 8 Department of Energy Engineering and Science, Nagoya University, Nagoya, Japan
- 9 Department of Energy Engineering and Science, Nagoya University, Nagoya, Japan
- 10 Department of Energy Engineering and Science, Nagoya University, Nagoya, Japan
- 11 Department of Energy Engineering and Science, Nagoya University, Nagoya, Japan
Abstract
In order to enhance photocatalytic water splitting rates with Pt/TiO 2 powder, sufficient agitation of the biphasic medium is required to switch surficial reactions to volumetric reactions. Additionally, agitation is conducive to higher diffusion rates of the generated hydrogen and co-produced oxygen, hindering their ability to re-couple to water on Pt loaded to TiO 2 powder. In order to create agitation without consuming any electricity, a novel technique utilizing Rayleigh convection was applied, and its ability to enhance photocatalytic water splitting rates was evaluated. Higher Rayleigh convective flow rates resulted in higher photocatalytic water splitting rates. Utilization of Rayleigh convection approximately doubled the photocatalytic water splitting rates, despite relatively low convective flow velocities (obtained through simple thermo-hydrodynamic simulations). The rate enhancement achieved through Rayleigh convection is a result of its ability to disperse the ultrafine Pt/TiO 2 particles throughout the whole medium, leading to volumetric reactions.
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