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Polymer-supported graphene–TiO2 doped with nonmetallic elements with enhanced photocatalytic reaction under visible light
Exploiting photocatalysts with environmental friendliness, noble-metal-free and high efficiency is a great challenge for photocatalytic hydrogen evolution under visible light. In this work, we had successfully loaded anatase titanium dioxide with a special graphene structure [the reduced graphene ox...
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Published in: | Journal of materials science 2020-02, Vol.55 (4), p.1577-1591 |
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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: | Exploiting photocatalysts with environmental friendliness, noble-metal-free and high efficiency is a great challenge for photocatalytic hydrogen evolution under visible light. In this work, we had successfully loaded anatase titanium dioxide with a special graphene structure [the reduced graphene oxide loaded on amine-functionalized poly (styrene/glycidyl methacrylate) (rGO/PSGM) microspheres. This special structure could greatly improve the catalytic performance of TiO
2
in the visible light. The nonmetallic elements (C, N, F, P and S) were doped with TiO
2
to further improve the performance of the composite photocatalysts in the visible-light region. After the first-principles density functional theory calculation, the calculated results of the density of states and dielectric function showed that the doped N element has the highest optical absorption capacity. We had proved this through experimental synthesis. Under the full-wavelength illumination, the degradation rate was 20 times higher than that of physically mixed sample; under the visible light, the
k
value of the degradation rate was 0.0046 min
−1
while physically mixed sample had almost no reaction within 5 h. Our study provides a promising approach to achieving efficient photocatalytic reaction under visible light based on TiO
2
and graphene without precious metals. |
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ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-019-04100-8 |