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[1Fp09] Operando spectroscopic identification of reactive electron species for photocatalytic hydrogen evolution on metal-loaded oxide surfaces
Identification of reactive carriers on photocatalysts provides a firm framework for rational design of catalysts. Here, using operando IR spectroscopy under periodic modulation of excitation light intensity, we succeeded in identifying the reactive electrons for photocatalytic H2 evolution on Pt- or Pd-loaded Ga2O3 particulate catalysts exposed to methane gas and water vapor. We demonstrated that the only band intensity derived from electrons trapped at the in-gap state ~0.26 eV below the conduction band minimum of Ga2O3 changed in clear response to the enhancement of H2 formation rate among the several observed bands attributed to various electron species. This indicates that the trapped electrons in Ga2O3 directly contribute to H2 evolution instead of electrons in metal cocatalysts. Furthermore, capacity of the reactive electrons was drastically changed between Pt/Ga2O3 and Pd/Ga2O3, suggesting that these reactive states are localized at the periphery of metal cocatalysts.
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