Synergetic effect of MoS-RGO doping to enhance the photocatalytic performance of ZnO nanoparticles
New Journal of Chemistry, ISSN: 1369-9261, Vol: 40, Issue: 6, Page: 5185-5197
2016
- 128Citations
- 71Captures
- 1Mentions
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Article Description
The sunlight driven photocatalytic activity of semiconductor based nanostructures has attracted widespread attention in recent years for environmental remediation and energy applications. Numerous good semiconductors, including ZnO, have wide bandgaps and are active only under ultraviolet light, which comprises only 5% of sunlight. Several strategies, such as noble metal doping, non-metal doping, etc., have been adapted to make ZnO heterostructures active in the visible light region. One other strategy is to dope ZnO with narrow bandgap semiconductors like MoS. In addition, co-doping with graphene as a support material can enhance pollutant adsorption and can aid in electron transport, thereby leading to pollutant degradation. In this work, we report our investigations on the synergetic role played by MoS-RGO doping to enhance the photocatalytic activity of ZnO nanoparticles, and especially to utilize both the UV and visible light regions of the solar spectrum. The ZnO-MoS-RGO heterostructures, having different levels of doping, were prepared by a facile hydrothermal method and were characterized thoroughly using different spectroscopy and microscopy techniques. The photocatalytic performance was evaluated by studying the degradation of methylene blue, a model dye pollutant, and carbendazim, a colorless hazardous fungicide, under natural sunlight irradiation. The results reveal that doping of ZnO nanoparticles with 1 wt% MoS-RGO was optimal and possessed the highest photocatalytic activity among all the investigated samples. A possible mechanism is proposed and discussed in detail.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84974574011&origin=inward; http://dx.doi.org/10.1039/c5nj03595c; http://xlink.rsc.org/?DOI=C5NJ03595C; http://pubs.rsc.org/en/content/articlepdf/2016/NJ/C5NJ03595C; https://xlink.rsc.org/?DOI=C5NJ03595C; https://dx.doi.org/10.1039/c5nj03595c; https://pubs.rsc.org/en/content/articlelanding/2016/nj/c5nj03595c
Royal Society of Chemistry (RSC)
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