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Enhanced hydrogen production from water via a photo-catalyzed reaction using chalcogenide d-element nanoparticles induced by UV light
Hydrogen has the potential to meet the requirements as a clean non-fossil fuel in the future. The photocatalytic production of H 2 through water splitting has been demonstrated and enormous efforts have been published. The present work is an attempt to enhance the production of H 2 during water spli...
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Published in: | Nanoscale 2013-10, Vol.5 (2), p.9994-9999 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Hydrogen has the potential to meet the requirements as a clean non-fossil fuel in the future. The photocatalytic production of H
2
through water splitting has been demonstrated and enormous efforts have been published. The present work is an attempt to enhance the production of H
2
during water splitting using synthesized nanoparticles based on chalcogenide d-element semiconductors
via
a photochemical reaction under UV-light in the presence of methanol as a hole-scavenger. In general, the enhanced activity of a semiconductor is most likely due to the effective charge separation of photo generated electrons and holes in the semiconductors. Hence, the utilization of different semiconductors in combination can consequently provide better hydrogen production. Accordingly in this research work, two different semiconductors, with different concentrations, either used individually or combined together were introduced. They in turn produced a high concentration of H
2
as detected and measured using gas chromatography. Herein, data revealed that the nano-structured semiconductors prepared through this work are a promising candidate in the production of an enhanced H
2
flux under visible UV radiation.
Selecting an interesting combination of ZnO-CdS produced at least a five times enhanced hydrogen production than the highest result given in the literature. |
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ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/c3nr02640j |