Constructing S-scheme Au/g-C3N4/BiVO4 heterojunction with peroxymonosulfate-enhanced photocatalytic activity and mechanism insight

被引:4
|
作者
Mu, Feihu [1 ]
Huang, Jin [1 ]
Xu, Shengpan [1 ]
Wang, Ruiqing [1 ]
Chu, Xiaozhong [1 ]
Cheng, Zhipeng [1 ]
Guo, Xujing [2 ]
Zhao, Wei [3 ]
Dai, Benlin [1 ]
Zhu, Wenshuai [4 ]
机构
[1] Huaiyin Normal Univ, Sch Chem & Chem Engn, Jiangsu Key Lab Chem Low Dimens Mat, Huaian 223300, Peoples R China
[2] Chengdu Univ Informat Technol, Coll Resources & Environm, Chengdu 610225, Peoples R China
[3] Changshu Inst Technol, Sch Mat Engn, Changshu 215500, Peoples R China
[4] China Univ Petr, State Key Lab Heavy Oil Proc, Coll Chem Engn & Environm, Beijing 102249, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; S-scheme; DOM; PMS; LIGHT; EFFICIENT; HETEROSTRUCTURES; REDUCTION; DEGRADATION; COMPOSITE; OXIDATION; G-C3N4;
D O I
10.1016/j.colsurfa.2024.134320
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
Dissolved organic matter (DOM) in black-odorous water can cause excessive growth of plants and algae, leading to deterioration of water quality. Herein, an S-scheme Au/g-C3N4/BiVO4 heterojunction was constructed using a three-step method for DOM degradation in real black-odorous water in the presence of peroxymonosulfate (PMS). 4Au/g-C3N4/BiVO4/PMS exhibited highly efficient photocatalytic performance, and the DOM removal rate could reach 92.9 %, which was 19.1 and 9.9 times higher than that of g-C3N4/PMS and BiVO4/PMS, respectively. The changes of fluorescence components in DOM were detected using synchronous fluorescence spectra and two-dimensional correlated spectroscopy analysis, and the toxicity of catalytically treated black odorous water was evaluated by growth inhibition of Escherichia coli . A reasonable S -scheme mechanism was suggested by theoretical calculations and photoelectrochemical tests. The S -scheme mechanism and the syner- gistic effect of photocatalysis and hybrid advanced oxidation process (HAOP) increased the catalytic activity of Au/g-C 3 N 4 /BiVO 4 /PMS.
引用
收藏
页数:14
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