Au nanoparticle modified three-dimensional network PVA/RGO/TiO2 composite for enhancing visible light photocatalytic performance

被引:45
|
作者
Zhang, Liang [1 ,2 ,3 ]
Qi, Haojie [2 ]
Zhao, Yuan [4 ]
Zhong, Lvling [1 ]
Zhang, Yujuan [1 ]
Wang, Yao [1 ]
Xue, Juanqin [1 ]
Li, Yue [5 ]
机构
[1] Xian Univ Architecture & Technol, Sch Chem & Chem Engn, Xian 710055, Shaanxi, Peoples R China
[2] Xian Univ Architecture & Technol, Sch Environm & Municipal Engn, Xian 710055, Shaanxi, Peoples R China
[3] Xian Univ Architecture & Technol, Shaanxi Prov Key Lab Gold & Resource, Xian 710055, Shaanxi, Peoples R China
[4] China Nucl Power Technol Res Inst Co Ltd, Reactor Engn & Safety Res Ctr, Shenzhen 518031, Peoples R China
[5] Xian Univ Architecture & Technol, Coll Mat Sci & Engn, Xian 710055, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalyst; TiO2; Au nanoparticle; Visible light; Rhodamine B; ORGANIC-DYES; DEGRADATION; TIO2; WATER; GRAPHENE; REMOVAL; WASTE; OPTIMIZATION; NANOFIBERS; NANOSHEETS;
D O I
10.1016/j.apsusc.2019.143855
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
To improve photocatalytic performance, a composite of gold nanoparticle-modified titanium dioxide/reduced graphene oxide/polyvinyl alcohol (PVA/RGO/TiO2/Au) was successfully synthesized via a mild, low-temperature wet chemical method and characterized by FTIR, XRD, SEM, TEM, XPS, UV-vis DRS, PL, BET, and BJH. The PVA/RGO/TiO2/Au composite had a uniform, hierarchically network structure with many pores, which showed great absorbance in the visible light range and effectively inhibited the recombination of photogenerated electron-hole pairs. The synthesized composite showed a high photocatalytic degradation activity for rhodamine B (RhB) under high pressure sodium lamp irradiation. The photocatalytic degradation activity was closely related to the catalyst concentration, the initial RhB concentration, the pH, and the H2O2 concentration. The composite remained at nearly 94% of the initial photocatalytic degradation activity after five cycles.
引用
收藏
页数:11
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