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Fe–Zn–Ti combined systems as photocatalysts for hydroxyl radicals production in sunlight
In this research, we focused on a photocatalyst for hydroxyl radicals (•OH) production in sunlight and proposed to extend TiO2 photocatalytic capacity to a visible range by combining it with oxides derived from metals such as iron and zinc. The systems were synthesized through the sol-gel method and...
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Published in: | International journal of hydrogen energy 2022-08, Vol.47 (74), p.31888-31902 |
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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: | In this research, we focused on a photocatalyst for hydroxyl radicals (•OH) production in sunlight and proposed to extend TiO2 photocatalytic capacity to a visible range by combining it with oxides derived from metals such as iron and zinc. The systems were synthesized through the sol-gel method and were characterized by TGA, FTIR-ATR, XRD, Raman, XPS, UV–Vis, and •OH quantification was carried out by disodium terephthalate hydroxylation reaction. Two key annealing temperatures of 400 and 800 °C, were detected by TGA studies. The iron-systems treated at 400 °C show the best balance between •OH production and less degradation effect attributed to staggering bands potentials of α–Fe2O3, ZnO, and anatase phases detected by XRD, making them a good option for partial oxidation. On the other hand, the 800 °C treated systems have the worst •OH production due to some phases with narrow bandgap promoting a fast charge carriers recombination.
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•Binary and ternary systems of Fe–Zn–Ti were obtained by the sol-gel method.•Iron-systems at 400 °C shows the best balance between.•OH production/degradation.•Iron-systems at 800 °C promotes a fast charge carriers recombination.•Iron-systems at 400 °C are a good option for partial oxidation processes.•Above 400 °C treatment, additional phases are formed and reduce catalytic yield. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2022.02.203 |