Understanding the detailed kinetics and mechanisms of water oxidation is crucial because water oxidation is the bottleneck reaction in overall water splitting. Here, we investigated photocatalytic water oxidation on NaTaO3-based photocatalysts. With in situ FT-IR spectroscopy, two new water oxidation intermediates with IR absorption peaks centered at 1058 and 935 cm-1 were observed and assigned to Ta(vi)O and Ta(O2) peroxo species, respectively. With H218O as the reactant and NaTa16O3 as the photocatalyst, both 16O18O and 18O2 were evolved continuously from overall water splitting as analyzed by mass spectroscopy (MS), demonstrating that the lattice O atoms in NaTaO3-based photocatalysts participate in the formation of O2 during the reaction. DFT results are consistent with the formation of TaO, 16O18O and 18O18O intermediates and products, while predicting that several water oxidation pathways are thermodynamically accessible for water oxidation on NaTaO3. Based on these observations, we propose a three-step two-site mechanism for photocatalytic water oxidation on NaTaO3-based photocatalysts in which lattice oxygen plays a key role. The elucidation of the present mechanism should help in broadly understanding water oxidation on semiconductor-based photocatalysts.
ASJC Scopus subject areas
- Renewable Energy, Sustainability and the Environment
- Materials Science(all)