MoSe2 with Ultra-Fine Pt Decoration for Efficient Photodegradation
Transition metal dichalcogenides are widely studied for their photocatalytic ability due to the adjustable bandgap, high carrier mobility and possibility of foreign-element doping. In this work, multilayer molybdenum diselenide (MoSe2) was decorated with ultra-fine Pt nanoparticles through the mild...
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Veröffentlicht in: | Applied sciences 2024-05, Vol.14 (9), p.3592 |
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Zusammenfassung: | Transition metal dichalcogenides are widely studied for their photocatalytic ability due to the adjustable bandgap, high carrier mobility and possibility of foreign-element doping. In this work, multilayer molybdenum diselenide (MoSe2) was decorated with ultra-fine Pt nanoparticles through the mild hydrothermal method. MoSe2-Pt nanocomposites were synthesized and showed good structural and chemical stabilities. The incorporation of Pt nanoparticles provides plenty of active sites for MoSe2. The dominant Pt particle sizes are 1.8 nm, 1.8 nm, and 1.9 nm for the three synthesized samples, respectively. The mean crystal sizes of Pt (111) were calculated from X-ray diffraction patterns and we found that they were in accordance with the particle sizes. Both the particle sizes and mean crystal sizes are related to the synthesis conditions. X-ray photoelectron spectroscopy (XPS) characterizations revealed the formation of Se–Pt bonding. The relative contents of Pt–Se bonding were also calculated from XPS results, and they show the same trends as the optical absorption properties. Combining the XPS and optical absorption results, the effects of Se–Pt bonding during the photo-related process could be further confirmed. By degrading methylene blue (MB) under visible light, the synthesized nanocomposites proved promising for application in real-case degradation of organic pollutants. The sample synthesized with a moderate content of MoSe2 exhibited the best photodegradation efficiency, which could be explained by the maximum Pt-Se contents. Based on the experimental findings, we proposed a possible photodegradation mechanism. |
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ISSN: | 2076-3417 2076-3417 |
DOI: | 10.3390/app14093592 |