Visible-light-driven photocatalytic hydrogen production coupled with selective oxidation of benzyl alcohol over CdS@MoS2 heterostructures

• Published in: Science China materials 2020-11, Vol.63 (11), p.2239-2250
• Main Authors: Li, Peixian, Zhao, Hui, Yan, Xuyan, Yang, Xue, Li, Jingjun, Gao, Shuiying, Cao, Rong
• Format: Article
• Language: English
• Subjects: Alcohol; Benzaldehyde; Benzyl alcohol; Charge transfer; Chemistry and Materials Science; Chemistry/Food Science; Dehydrogenation; Dyes; Electrochemical impedance spectroscopy; Electron microscopy; Fine chemicals; Heterojunctions; Heterostructures; Holes (electron deficiencies); Hydrogen; Hydrogen production; Image transmission; Materials Science; Microscopy; Molybdenum disulfide; N-type semiconductors; Nanorods; Noble metals; Oxidation; P-n junctions; Photocatalysis; Photoelectric effect; Photoelectric emission; Photoluminescence; Separation; Substrates
• ISSN: 2095-8226; 2199-4501
• DOI: 10.1007/s40843-020-1448-2

Photocatalytic hydrogen production coupled with selective oxidation of organic substrates to produce high-value-added fine chemicals has drawn increasing attention. Herein, we report a noble metal-free photocatalyst for the highly efficient and simultaneous generation of hydrogen and the selective oxidation of benzyl alcohol into benzaldehyde over CdS@MoS 2 heterostructures under visible light. Without the need for a sacrificial agent, CdS@MoS 2 displayed an excellent hydrogen production rate of 4233 µmol g −1 h −1 with 0.3 mmol benzyl alcohol, which is approximately 53 times higher than that of bare CdS nanorods (80 µmol g −1 h −1 ). The reaction system was highly selective for the oxidation of benzyl alcohol into benzaldehyde. When the amount of benzyl alcohol increased to 1.0 mmol, the hydrogen production reached 9033 µmol g −1 h −1 . Scanning electron microscopy and transmission electron microscopy images revealed that p-type MoS 2 sheets with a flower-like structure closely adhered to n-type semiconductor CdS nanorods through the formation of a p-n heterojunction. As a potential Z-scheme photocatalyst, the CdS@MoS 2 heterostructure effectively produces and separates electron-hole pairs under visible light. Thus, the electrons are used for reduction to generate hydrogen, and the holes oxidize benzyl alcohol into benzaldehyde. Moreover, a mechanism of photogenerated charge transfer and separation was proposed and verified by photoluminescence, electrochemical impedance spectroscopy, photocurrent and Mott-Schottky measurements. The results reveal that the CdS@MoS 2 heterojunctions have rapid and efficient charge separation and transfer, thereby greatly improving benzyl alcohol dehydrogenation. This work provides insight into the rational design of high-performance Z-scheme photocatalysts and the use of holes and electrons to obtain two valuable chemicals simultaneously.