Journal
JOURNAL OF ENVIRONMENTAL SCIENCES
Volume 65, Issue -, Pages 347-355Publisher
SCIENCE PRESS
DOI: 10.1016/j.jes.2017.07.004
Keywords
CdS; MoS2; Sulfur sources; One-step hydrothermal method; Photocatalytic degradation
Categories
Funding
- National Natural Science Foundation of China [51478431]
- Science and Technology Planning Project from the Science and Technology Department in Zhejiang Province [2014C33028]
- Xinmiao Talent Project of Zhejiang Province [2016R408074]
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CdS/MoS2, an extremely efficient photocatalyst, has been extensively used in hydrogen photoproduction and pollutant degradation. CdS/MoS2 can be synthesized by a facile one-step hydrothermal process. However, the effect of the sulfur source on the synthesis of CdS/MoS2 via one-step hydrothermal methods has seldom been investigated. We report herein a series of one-step hydrothermal preparations of CdS/MoS2 using three different sulfur sources: thioacetamide, L-cysteine, and thiourea. The results revealed that the sulfur source strongly affected the crystallization, morphology, elemental composition and ultraviolet (UV)-visible-light-absorption ability of the CdS/MoS2. Among the investigated sulfur sources, thioacetamide provided the highest visible-light absorption ability for CdS/MoS2, with the smallest average particle size and largest surface area, resulting in the highest efficiency in Methylene Blue (MB) degradation. The photocatalytic activity of CdS/MoS2 synthesized from the three sulfur sources can be arranged in the following order: thioacetamide > L-cysteine > thiourea. The reaction rate constants (k) for thioacetamide, L-cysteine, and thiourea were estimated to be 0.0197, 0.0140, and 0.0084 min(-1), respectively. However, thioacetamide may be limited in practical application in terms of its price and toxicity, while L-cysteine is relatively economical, less toxic and exhibited good photocatalytic degradation performance toward MB. (c) 2017 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
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