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The research on photocatalytic oxygen evolution of Bi4Ti3O12 microsphere by different Ag-loading content
[Display omitted] •Ag/BTO nanocomposites were successfully synthesized by a simple solvothermal method.•The photocatalytic activity of BTO is obviously improved by the loading of Ag nanoparticles.•SPR effect enhances the absorption intensity of BTO in 400–700 nm region.•Ag/BTO reduces the energy bar...
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Published in: | Materials letters 2023-06, Vol.341, p.134219, Article 134219 |
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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]
•Ag/BTO nanocomposites were successfully synthesized by a simple solvothermal method.•The photocatalytic activity of BTO is obviously improved by the loading of Ag nanoparticles.•SPR effect enhances the absorption intensity of BTO in 400–700 nm region.•Ag/BTO reduces the energy barrier of the key step (O* → OOH*).•Schottky barrier facilitates the separation of photo-generated electrons-hole pairs.
The search of catalysts with high efficiency for photocatalytic oxygen evolution by water splitting has always attracted great attention of global scientists. In this study, Ag/Bi4Ti3O12 (Ag/BTO) nanocomposites with surface plasmon resonance (SPR) effect were synthesized by a solvothermal method. Compared with BTO, Ag/BTO narrowed the band gap, improved the absorption intensity in 400–700 nm region, increased the separation efficiency of photo-induced electron-hole pairs, reduced the energy barrier (from 2.18 to 1.39 eV) of the key step (O* → OOH*) from water splitting, and remarkably enhanced the photocatalytic water oxidation ability. The oxygen evolution rate of visible-light-driven 3-Ag/BTO with an appropriate silver content is 2623.51 μmol∙g−1∙h−1, which is 8.39 times higher than that of BTO without any sacrificial agent. Moreover, the excellent performance of 3-Ag/BTO is also obviously higher than that of most reported photocatalysts. |
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ISSN: | 0167-577X |
DOI: | 10.1016/j.matlet.2023.134219 |