Issue 19, 2021

Anchoring Zn0.5Cd0.5S solid solution onto 2D porous Co–CoO nanosheets for highly improved photocatalytic H2 generation

Abstract

Co-Based cocatalysts have attracted considerable attention as potential alternatives for the noble metal (Pt) in photocatalytic water splitting. However, the two-dimensional (2D) porous-structured Co-based cocatalysts toward photocatalytic hydrogen (H2) production application are rarely reported. In this study, 2D porous Co–CoO (CC) nanosheets prepared by a facile annealing approach were employed as a support to anchor Zn0.5Cd0.5S (ZCS) solid solution toward visible-light-induced photocatalytic H2 production. The optimized 5CC/ZCS composite exhibits a high H2 generation rate of 8152 μmol h−1 g−1, which is approximately 46- and 10-fold that of pristine ZCS and 3% Pt/ZCS, respectively. Moreover, the Co–CoO/Zn0.5Cd0.5S (CC/ZCS) also processes long-term activity and superior stability during the photocatalytic H2-evolution reactions. The significant improvement in the photocatalytic water splitting of CC/ZCS is mainly derived from the intimate interface between CC nanosheets and ZCS nanoparticles. The 2D porous CC nanosheets serve as an efficient cocatalyst to promote photogenerated charge carrier separation, reduce reaction overpotential, and provide abundant reaction sites. This work paves a promising way to construct hybrid nanostructures based on porous Co-based nanosheets and metal sulfides for enhanced photo/electro-catalysis.

Graphical abstract: Anchoring Zn0.5Cd0.5S solid solution onto 2D porous Co–CoO nanosheets for highly improved photocatalytic H2 generation

Supplementary files

Article information

Article type
Research Article
Submitted
08 May 2021
Accepted
09 Aug 2021
First published
11 Aug 2021

Mater. Chem. Front., 2021,5, 7208-7215

Anchoring Zn0.5Cd0.5S solid solution onto 2D porous Co–CoO nanosheets for highly improved photocatalytic H2 generation

X. Gao, D. Zeng, Q. Zeng, Z. Xie, T. Fujita, X. Wang, G. He and Y. Wei, Mater. Chem. Front., 2021, 5, 7208 DOI: 10.1039/D1QM00669J

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