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Photocatalytic Degradation of Rhodamine B Dye and Hydrogen Evolution by Hydrothermally Synthesized NaBH4—Spiked ZnS Nanostructures
Frontiers in Chemistry, Volume: 10
Swansea University Authors: Michael Warwick , Daniel Raymond Jones , Charlie Dunnill
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Copyright © 2022 Amakali, Živković, Warwick, Jones, Dunnill, Daniel, Uahengo, Mitchell, Dzade and de Leeuw. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY)Download (4.44MB)
DOI (Published version): 10.3389/fchem.2022.835832
Metal sulphides, including zinc sulphide (ZnS), are semiconductor photocatalysts that have been investigated for the photocatalytic degradation of organic pollutants as well as their activity during the hydrogen evolution reaction and water splitting. However, devising ZnS photocatalysts with a high...
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Metal sulphides, including zinc sulphide (ZnS), are semiconductor photocatalysts that have been investigated for the photocatalytic degradation of organic pollutants as well as their activity during the hydrogen evolution reaction and water splitting. However, devising ZnS photocatalysts with a high overall quantum efficiency has been a challenge due to the rapid recombination rates of charge carriers. Various strategies, including the control of size and morphology of ZnS nanoparticles, have been proposed to overcome these drawbacks. In this work, ZnS samples with different morphologies were prepared from zinc and sulphur powders via a facile hydrothermal method by varying the amount of sodium borohydride used as a reducing agent. The structural properties of the ZnS nanoparticles were analysed by X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS) techniques. All-electron hybrid density functional theory calculations were employed to elucidate the effect of sulphur and zinc vacancies occurring in the bulk as well as (220) surface on the overall electronic properties and absorption of ZnS. Considerable differences in the defect level positions were observed between the bulk and surface of ZnS while the adsorption of NaBH4 was found to be highly favourable but without any significant effect on the band gap of ZnS. The photocatalytic activity of ZnS was evaluated for the degradation of rhodamine B dye under UV irradiation and hydrogen generation from water. The ZnS nanoparticles photo-catalytically degraded Rhodamine B dye effectively, with the sample containing 0.01 mol NaBH4 being the most efficient. The samples also showed activity for hydrogen evolution, but with less H2 produced compared to when untreated samples of ZnS were used. These findings suggest that ZnS nanoparticles are effective photocatalysts for the degradation of rhodamine B dyes as well as the hydrogen evolution, but rapid recombination of charge carriers remains a factor that needs future optimization.
ZnS, photocatalysis, rhodamine B degradation, NaBH4 adsorption, density functional theory, HSE06,defect states, sulphur vacancies
Faculty of Science and Engineering
This work was performed using the computational facilities of the Centre for High Performance Computing in Cape Town (CHPC) and the Dutch national e-infrastructure with the support of SURF
Cooperative. Via our membership of the UK’s HEC Materials Chemistry Consortium, which is funded by EPSRC (EP/R029431), this work used the ARCHER2 United Kingdom National Supercomputing Service (http://www.archer2.ac.uk). AŽ and NL acknowledge the NWO ECHO grant (712.018.005) for funding.