共 51 条
Polymer-supported graphene-TiO2 doped with nonmetallic elements with enhanced photocatalytic reaction under visible light
被引:19
作者:
Wu, Yuanwang
[1
]
Mu, Haiyan
[1
]
Cao, Xuejun
[1
]
He, Xiao
[2
]
机构:
[1] East China Univ Sci & Technol, Dept Bioengn, State Key Lab Bioreactor Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China
[2] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Engn Res Ctr Mol Therapeut & New Drug De, Shanghai 200062, Peoples R China
关键词:
ELECTRONIC-STRUCTURE;
TIO2;
NANOPARTICLES;
OPTICAL-PROPERTIES;
PERFORMANCE;
COCATALYST;
ANATASE;
NANOCOMPOSITES;
STABILITY;
REDUCTION;
DIOXIDE;
D O I:
10.1007/s10853-019-04100-8
中图分类号:
T [工业技术];
学科分类号:
08 ;
摘要:
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 TiO2 in the visible light. The nonmetallic elements (C, N, F, P and S) were doped with TiO2 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 TiO2 and graphene without precious metals.
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页码:1577 / 1591
页数:15
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