Controlled fabrication and enhanced visible-light photocatalytic hydrogen production of Au@CdS/MIL-101 heterostructure

• Published in: Applied catalysis. B, Environmental Vol. 185; pp. 307 - 314
• Main Authors: Wang, Yajun, Zhang, Yunnuan, Jiang, Zhiqiang, Jiang, Guiyuan, Zhao, Zhen, Wu, Qiaohuan, Liu, Ying, Xu, Quan, Duan, Aijun, Xu, Chunming
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 15.05.2016
• Subjects: Au@CdS; CdS; MIL-101; MOFs; Photocatalytic hydrogen production; MIL-101; CdS; MOFs; Photocatalytic hydrogen production; Au@CdS
• ISSN: 0926-3373; 1873-3883
• DOI: 10.1016/j.apcatb.2015.12.020

[Display omitted] •A highly efficient Au@CdS/MIL-101 heterostructure was synthesized.•The Au@CdS/MIL-101 heterostructure presents a higher H2 evolution rate.•The H2 evolution rate of Au@CdS/MIL-101 is 2.6 times higher than that of pure CdS.•The enhanced performance is ascribed to MIL-101 and surface plasmon resonance of Au. A novel and highly efficient three-component Au@CdS/MIL-101 heterostructure was successfully synthesized. The MIL-101(Cr) with large surface area was introduced as a matrix for the well-dispersed growth of Au nanoparticles, and the CdS was selectively coated on the Au nanoparticles. Under visible light irradiation, the Au@CdS/MIL-101 heterostructure presents superior hydrogen evolution rate over the pure CdS, CdS/MIL-101 and Au/MIL-101 composites. The Au@CdS/MIL-101 heterostructure exhibits an unusual H2 production rate of 250μmolh−1/10mg, which is 2.6 times higher than that of pure CdS. The performance enhancement of Au@CdS/MIL-101 heterostructure can be attributed to the following reasons: (i) the large surface area of MIL-101(Cr) can effectively disperse the Au and CdS nanoparticles, resulting in more active adsorption sites and reaction centers. (ii) the strong surface plasmon resonance absorption of Au could accelerate the charge transfer and extend the light response spectrum of CdS. This three-component Au@CdS/MIL-101 heterostructure combining the large surface area of MOF and the surface plasmon resonance of Au into a single structure may provide a potential way to design highly efficient and solar-energy-harvesting photocatalysts.