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To overcome the limitation of photocatalysts with dual functionality of water oxidation and proton reduction, we proposed a novel bismuth-based Ba2BiV3O11 (BBVO) photocatalyst, which can simultaneously drive the proton reduction reaction under UV light and water oxidation reaction under visible light. After doping with sulfur through an in situ vulcanization strategy, the light absorption and charge separation efficiencies of the sulfur-doped BBVO were significantly improved, thus boosting its oxygen evolution activity (64 μmol h−1) by more than 16 times compared with independent BBVO. The experimental results demonstrate that BBVO can be employed as a very promising bismuth-based photocatalyst for solar energy conversion. [ABSTRACT FROM AUTHOR]

Here, we successfully prepared Ba2Bi3Ta2O11Cl via a simple one-step molten salt method and adjusted its crystal morphology and structure, based on which the O2-evolving activity was significantly improved. In addition, W doping promotes the charge separation efficiency, lowers the energy barrier for water oxidation reaction, and thus improves the activity. Finally, the optimized W-doped sample after molten salt treatment shows the best O2 production activity (55 μmol h−1) without loading any cocatalyst, which is 6 times higher than that of pristine Ba2Bi3Ta2O11Cl and 2 times higher than that of the undoped Ba2Bi3Ta2O11Cl treated with molten salt, respectively. [ABSTRACT FROM AUTHOR]

A pyrochlore-structural oxynitride Nd2Ta2O5N2 with a visible light absorption edge of ca. 620 nm was explored for photocatalytic water splitting. Dual functions of Nd2Ta2O5N2 were confirmed by proton reduction and water oxidation half-reactions through separately loading Pt or CoOx as a cocatalyst in the presence of the corresponding sacrificial reagent. Finally, the platinum modified sample (Pt/Nd2Ta2O5N2) was prepared and employed as the H2-evolving photocatalyst to fabricate an effective photocatalytic Z-scheme overall water splitting together with PtOx/WO3 as the O2-evolving photocatalyst and IO3−/I− as shuttle ions under visible light irradiation. [ABSTRACT FROM AUTHOR]