Designing CdS-Based Ternary Heterostructures Consisting of Co-Metal and CoOx Cocatalysts for Photocatalytic H2 Evolution under Visible Light.

Abstract

Heterostructure formation is an effective method used for designing photocatalysts that solve problems caused by photoexcited charge recombination phenomena associated with the photocatalytic water redox reaction. This work reports a new Co-metal-incorporated ternary heterostructured photocatalyst, CdS/CoOx/Co-metal, which enhanced charge separation to increase photocatalytic H2 evolution 30.5-fold in comparison to pure CdS under visible light. This work demonstrates for the first time the effect of the Co metal on photocatalytic H2 evolution using the CdS/CoOx/Co-metal ternary heterostructure. In the ternary heterostructure, Co metal and CoOx act as photogenerated electron- and hole-capturing cocatalysts, respectively. Results from photoelectrochemical studies along with photocatalytic H2 evolution data proved the enhancement of charge transfer and separation in the CdS/CoOx/Co-metal heterostructure due to the addition of Co metal and CoOx. Hence, the synergistic charge separation improvement achieved by the combination of CoOx and the Co metal with CdS produced a photocatalytic H2 evolution rate of 9.54 μmol/h, which is the highest reported H2 evolution rate for a CdS-based system under l sun solar irradiance (>420 nm) to the best of our knowledge.