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Sepiolite-Supported WS2 Nanosheets for Synergistically Promoting Photocatalytic Rhodamine B Degradation Bai, Jiaxuan; Cui, Kaibin; Xie, Xinlei; Fang, Baizeng; Wang, Fei
Abstract
Pristine tungsten disulfide (WS₂) nanosheets are extremely prone to agglomeration, leading to blocked active sites and the decrease of catalytic activity. In this work, highly dispersed WS₂ nanosheets were fabricated via a one-step in situ solvothermal method, using sepiolite nanofibers as a functional carrier. The ammonium tetrathiotungstate was adopted as W and S precursors, and N,N-dimethylformamide could provide a neutral reaction environment. The electron microscope analysis revealed that the WS₂ nanosheets were stacked compactly in the shape of irregular plates, while they were uniformly grown on the surface of sepiolite nanofibers . Meanwhile, the BET measurement confirmed that the as-prepared composite has a larger specific surface area and is more mesoporous than the pure WS₂. Due to the improved dispersion of WS₂ and the synergistic effect between WS₂ and the mesoporous sepiolite mineral which significantly facilitated the mass transport, the WS₂/sepiolite composite exhibited ca. 2.6 times the photocatalytic efficiency of the pure WS₂ for rhodamine B degradation. This work provides a potential method for low-cost batch preparation of high-quality 2D materials via assembling on natural materials. This approach aligns with recent research trends in enhancing the photocatalytic activity of WS₂ nanosheets. For instance, another study reported that WS₂/sepiolite composites exhibited about 7 times the specific surface area and 7.4 times the photocatalytic efficiency toward rhodamine B degradation compared to pure WS₂. The use of sepiolite as a support for growing highly-dispersed ultrathin WS₂ architecture has been shown to be superior to other minerals, enabling better dispersion of WS₂ nanosheets and synergetic effects.
Item Metadata
Title |
Sepiolite-Supported WS2 Nanosheets for Synergistically Promoting Photocatalytic Rhodamine B Degradation
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Creator | |
Publisher |
Multidisciplinary Digital Publishing Institute
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Date Issued |
2022-11-09
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Description |
Pristine tungsten disulfide (WS₂) nanosheets are extremely prone to agglomeration, leading to blocked active sites and the decrease of catalytic activity. In this work, highly dispersed WS₂ nanosheets were fabricated via a one-step in situ solvothermal method, using sepiolite nanofibers as a functional carrier. The ammonium tetrathiotungstate was adopted as W and S precursors, and N,N-dimethylformamide could provide a neutral reaction environment. The electron microscope analysis revealed that the WS₂ nanosheets were stacked compactly in the shape of irregular plates, while they were uniformly grown on the surface of sepiolite nanofibers
. Meanwhile, the BET measurement confirmed that the as-prepared composite has a larger specific surface area and is more mesoporous than the pure WS₂. Due to the improved dispersion of WS₂ and the synergistic effect between WS₂ and the mesoporous sepiolite mineral which significantly facilitated the mass transport, the WS₂/sepiolite composite exhibited ca. 2.6 times the photocatalytic efficiency of the pure WS₂ for rhodamine B degradation. This work provides a potential method for low-cost batch preparation of high-quality 2D materials via assembling on natural materials. This approach aligns with recent research trends in enhancing the photocatalytic activity of WS₂ nanosheets. For instance, another study reported that WS₂/sepiolite composites exhibited about 7 times the specific surface area and 7.4 times the photocatalytic efficiency toward rhodamine B degradation compared to pure WS₂. The use of sepiolite as a support for growing highly-dispersed ultrathin WS₂ architecture has been shown to be superior to other minerals, enabling better dispersion of WS₂ nanosheets and synergetic effects.
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Subject | |
Genre | |
Type | |
Language |
eng
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Date Available |
2025-01-20
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Provider |
Vancouver : University of British Columbia Library
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Rights |
CC BY 4.0
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DOI |
10.14288/1.0447782
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URI | |
Affiliation | |
Citation |
Catalysts 12 (11): 1400 (2022)
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Publisher DOI |
10.3390/catal12111400
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Peer Review Status |
Reviewed
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Scholarly Level |
Faculty; Researcher
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Rights URI | |
Aggregated Source Repository |
DSpace
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Item Media
Item Citations and Data
Rights
CC BY 4.0