The photocatalytic degradation of methylene blue is a straightforward and cost-effective solution for water decontamination. Although many materials have been reported so far for this purpose, the proposed solutions inflicted high fabrication costs and low efficiencies. Here, we report on the synthesis of tetragonal (1T) and hexagonal (2H) mixed molybdenum disulfide (MoS) heterostructures for an improved photocatalytic degradation efficiency by means of a single-step chemical vapor deposition (CVD) technique. We demonstrate that the 1T-MoS/2H-MoS heterostructures exhibited a narrow bandgap ∼ 1.7 eV, and a very low reflectance (<5%) under visible-light, owing to their particular vertical micro-flower-like structure. We exfoliated the CVD-synthesised 1T-MoS/2H-MoS films to assess their photodegradation properties towards the standard methylene blue dye. Our results showed that the photo-degradation rate-constant of the 1T-MoS/2H-MoS heterostructures is much greater under UV excitation (i.e., 12.5 × 10 min) than under visible light illumination (i.e., 9.2 × 10 min). Our findings suggested that the intermixing of the conductive 1T-MoS with the semi-conducting 2H-MoS phases favors the photogeneration of electron-hole pairs. More importantly, it promotes a higher efficient charge transfer, which accelerates the methylene blue photodegradation process.
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http://dx.doi.org/10.1016/j.ultsonch.2023.106381 | DOI Listing |
Ultrason Sonochem
May 2023
Laboratory of Physics of Condensed Matter, University of Picardie Jules Verne, Scientific Pole, 33 rue Saint-Leu, 80039 Amiens Cedex 1, France. Electronic address:
The photocatalytic degradation of methylene blue is a straightforward and cost-effective solution for water decontamination. Although many materials have been reported so far for this purpose, the proposed solutions inflicted high fabrication costs and low efficiencies. Here, we report on the synthesis of tetragonal (1T) and hexagonal (2H) mixed molybdenum disulfide (MoS) heterostructures for an improved photocatalytic degradation efficiency by means of a single-step chemical vapor deposition (CVD) technique.
View Article and Find Full Text PDFSmall
May 2021
State Center for International Cooperation on Designer Low-Carbon and Environmental Materials (CDLCEM), School of Materials Science and Engineering, Zhengzhou University, 100 Kexue Avenue, Zhengzhou, 450001, China.
Accelerating the conversion of polysulfide to inhibit shutting effect is a promising approach to improve the performance of lithium-sulfur batteries. Herein, the hollow titanium nitride (TiN)/1T-MoS heterostructure nanospheres are designed with efficient electrocatalysis properties serving as a sulfur host, which is formed by in situ electrochemical intercalation from TiN/2H-MoS . Metallic, few-layered 1T-MoS nanosheets with abundant active sites decorated on TiN nanospheres enable fast electron transfer, high adsorption ability toward polysulfides, and favorable catalytic activity contributing to the conversion kinetics of polysulfides.
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August 2020
State Key Laboratory for Mechanical Behavior of Materials, Shaanxi International Research Center for Soft Matter, Xi'an Jiaotong University, Xi'an, 710049, China.
Metallic phase (1T) MoS has been regarded as an appealing material for hydrogen evolution reaction. In this work, a novel interface-induced strategy is reported to achieve stable and high-percentage 1T MoS through highly active 1T-MoS /CoS hetero-nanostructure. Herein, a large number of heterointerfaces can be obtained by interlinked 1T-MoS and CoS nanosheets in situ grown from the molybdate cobalt oxide nanorod under moderate conditions.
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