Direct Operando Identification of Reactive Electron Species Driving Photocatalytic Hydrogen Evolution on Metal-Loaded...

Performing operando spectroscopy under practical reaction conditions and extracting spectral components correlating with reaction activity are crucial in elucidating the reactive species in photocatalysis. However, the observation of weak signals corresponding to reactive photogenerated species is frequently hampered under reaction conditions owing to intense background signals originating from thermally induced species unrelated to the photoinduced reactions. Herein, by synchronizing the millisecond periodic excitations of photocatalysts with a Michelson interferometer used for FT-IR spectroscopy, we succeeded in significantly suppressing the signals derived from thermally excited electrons and observing the reactive photogenerated electrons contributing to the photocatalytic hydrogen evolution. This demonstration was achieved for metal-loaded oxide photocatalysts under steam methane reforming and water splitting conditions. Although it has long been conventionally believed that loaded metal cocatalysts function as sinks for reactive photogenerated electrons and active sites for reduction reactions, we found that the free electrons in the metal cocatalysts were not directly involved in the reduction reaction. Alternatively, the electrons shallowly trapped in the in-gap states of oxides contributed to enhancing the hydrogen evolution rate upon the loading of metal cocatalysts. We verified that the electron abundance in the in-gap states was clearly correlated to the reaction activity, suggesting that metal-induced semiconductor surface states formed in the periphery of the metal cocatalyst play key roles in the photocatalytic hydrogen evolution. Our microscopic insights shift a paradigm on the traditionally believed role of metal cocatalysts in photocatalysis and provide a fundamental basis for rational design of the metal/oxide interfaces as promising platforms for nonthermal hydrogen evolution.