A low-valent cobalt oxide co-catalyst to boost photocatalytic water oxidation via enhanced hole-capturing ability

Co-catalysts have been widely studied to improve photocatalytic water oxidation efficiency, and the precise control of their oxidation states and minimizing particle sizes can optimize the practical performance. In this work, ultrafine cobalt oxide (CoOx) co-catalysts with specific Co valence states have been successfully synthesized, which are anchored on a tantalum oxynitride (TaON) host photocatalyst via a photochemical metal-organic deposition method. Photoelectrochemical and photoluminescence analyses prove that the Co2+ dominant CoOx co-catalyst is favorable for charge separation and transportation because of its excellent hole-capturing properties, consequently enhancing the photocatalytic water oxidation performance. The resultant TaON with the Co2+ dominant CoOx co-catalyst exhibits an outstanding O-2 production rate up to 6.10 +/- 0.17 mmol h(-1) g(-1) and possesses an excellent apparent quantum efficiency of 21.2% at 420 nm, which are among the best values of water-oxidation photocatalysts.

Automated summary

The study successfully synthesized ultrafine cobalt oxide co-catalysts with specific oxidation states, which significantly enhance photocatalytic water oxidation performance by optimizing charge separation and transportation. The TaON photocatalyst with CoOx co-catalysts exhibited outstanding O-2 production rate and high quantum efficiency.