Host: The Japan Society of Vacuum and Surface Science
We have found that the photocatalytic methane reforming under water vapor is induced at room temperature on surfaces of metal-loaded Ga2O3 particulate photocatalysts. In this reaction, we also found that the reaction activity significantly depends on the pressure of methane and the amount of metal co-catalyst. However, detailed reaction mechanisms including the dynamics of photogenerated carriers and surface adsorbed species relevant to the redox reactions of methane have been unclear. To clarify the behavior of photo-excited carriers and the reaction intermediates on the surfaces of Ga2O3 photocatalysts, we conducted operand FT-IR spectroscopy under intensity modulation of UV light. Then, we succeeded in observing a clear correlation between the reaction activity and a broad mid-infrared band (1000-5000 cm-1) derived from the photo-generated electrons.