Abstract
Rational design of composite catalysts with efficient charge separation and transfer and good light collection ability is of great significance to achieve high photoelectrochemical conversion efficiency. In this paper, a Co9S8/MoS2/Ni2P dual S-scheme heterojunction photocatalyst was successfully synthesized by a simple sulfidation and hydrothermal method. The optimized Co9S8/MoS2/Ni2P composite with hierarchical structure, large surface area and numerous reactive active sites showed a good photocatalytic hydrogen evolution rate of 5.69 mmol g−1 h−1, which is 2.28, 4.12 and 10.74 times higher than that of pure Co9S8, MoS2 and Ni2P, respectively. A combination of time-resolved photoluminescence (TRPL) spectroscopy, valence band XPS (VB-XPS), ultraviolet photoelectron spectroscopy (UPS), and density-functional theory (DFT) calculations confirms that the formation of the Co9S8/MoS2/Ni2P double S-scheme greatly facilitates charge migration and spatial separation, and improves the oxidation and reduction ability. This work will provide insights into the development of PBA-based dual S-scheme heterojunction catalysts for photocatalytic hydrogen evolution.
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