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The size and valence state effect of Pt on photocatalytic H2 evolution over platinized TiO2 photocatalyst
Photocatalytic hydrogen production from water or organic compounds is a promising way to resolve our energy crisis and environmental problems in the near future. Over the past decades, many photocatalysts have been developed for solar water splitting. However, most of these photocatalysts require co...
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Published in: | International journal of hydrogen energy 2014-01, Vol.39 (3), p.1237-1242 |
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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: | Photocatalytic hydrogen production from water or organic compounds is a promising way to resolve our energy crisis and environmental problems in the near future. Over the past decades, many photocatalysts have been developed for solar water splitting. However, most of these photocatalysts require cocatalyst to facilitate H2 evolution reaction and noble metals as key cocatalysts are widely used. Consequently, the condition of noble metal cocatalyst including the size and valence state etc plays the key role in such photocatalytic system. Here, the size and valence state effect of Pt on photocatalytic H2 evolution over platinized TiO2 photocatalyst were studied for the first time. Surprisingly, it was found that Pt particle size does not affect the photoreaction rate with the size range of several nanometers in this work, while it is mainly depended on the valence state of Pt particles. Typically, TOFs of TiO2 photodeposited with 0.1–0.2 wt% Pt can exceed 3000 h−1.
•Size and valence state effect of Pt on photocatalysis was studied.•Pt particle size could cease to be determiner for photoreactivity.•Photocatalytic activity mainly depended on the valence state of Pt cocatalyst.•TOFs of TiO2 loaded with 0.1–0.2 wt% Pt with oxidized state can exceed 3000 h−1. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2013.11.041 |