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

• Published in: Journal of materials chemistry. A, Materials for energy and sustainability Vol. 9; no. 26; pp. 14786 - 14792
• Main Authors: Xiao, Shi Yang, Liu, Yuanwei, Wu, Xue Feng, Gan, Li Ting, Lin, Hao Yang, Zheng, Li Rong, Dai, Sheng, Liu, Peng Fei, Yang, Hua Gui
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 01.01.2021
• Subjects: Carbon dioxide; Catalysts; Cobalt; Cobalt oxides; Oxidation; Photocatalysis; Photocatalysts; Photochemicals; Photoluminescence; Photons; Quantum efficiency; Tantalum; Ultrafines; Valence
• ISSN: 2050-7488; 2050-7496
• DOI: 10.1039/D1TA01858B

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 (CoO x ) 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 Co 2+ dominant CoO x 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 Co 2+ dominant CoO x 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.