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New photocatalysts based on Cd0.3Zn0.7S and Ni(OH)2 for hydrogen production from ethanol aqueous solutions under visible light
[Display omitted] •The Cd0.3Zn0.7S photocatalysts modified by Ni(OH)2 were studied in details.•The highest value of the photocatalytic activity was 27 mmol H2 per hour per gram.•The apparent quantum efficiency was 91% in optimal conditions.•A kinetic model connecting the H2 production and the reagen...
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Published in: | Applied catalysis. A, General General, 2018-08, Vol.563, p.170-176 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•The Cd0.3Zn0.7S photocatalysts modified by Ni(OH)2 were studied in details.•The highest value of the photocatalytic activity was 27 mmol H2 per hour per gram.•The apparent quantum efficiency was 91% in optimal conditions.•A kinetic model connecting the H2 production and the reagent contents was proposed.
The Cd0.3Zn0.7S photocatalysts modified by nickel hydroxide were prepared and characterized by different experimental techniques including X-ray diffraction, UV–vis spectroscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. The obtained photocatalysts were tested in the photocatalytic hydrogen evolution from ethanol aqueous solutions under visible light irradiation (λ = 450 nm). The nickel-modified photocatalysts were found to be more active than the zinc-modified ones. The reasons of high activity of Ni-contained photocatalysts and their transformations during the photocatalytic hydrogen production were discussed. The dependences of hydrogen production rate on ethanol and NaOH concentrations were obtained, the highest value of the photocatalytic activity was 27 mmol h−1 g−1 for 1%Pt/10% Ni(OH)2/Cd0.3Zn0.7S (50% vol. ethanol, 1 M NaOH), apparent quantum efficiency exceeded 90%. A kinetic model describing the experimental data was proposed. |
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ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2018.07.002 |