Enhanced visible light photoelectrocatalytic degradation of o-chloronitrobenzene through surface plasmonic Au nanoparticles and g-C3N4 co-modified TiO2 nanotube arrays photoanode

被引:35
作者
Xin, Shuaishuai [1 ,3 ]
Ma, Xiaoming [1 ]
Lu, Jinren [2 ]
Zhang, Guangshan [3 ]
Huo, Siyue [1 ]
Gao, Mengchun [1 ]
Xu, Peng [4 ]
Liu, Wenjie [1 ]
Fu, Wenxian [1 ]
机构
[1] Ocean Univ China, Minist Educ, Key Lab Marine Environm & Ecol, Qingdao 266100, Peoples R China
[2] Ocean Univ China, Coll Chem & Chem Engn, Qingdao 266100, Peoples R China
[3] Qingdao Agr Univ, Coll Resources & Environm, Qingdao Engn Res Ctr Rural Environm, Qingdao 266109, Peoples R China
[4] Harbin Inst Technol, Sch Environm, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2023年 / 323卷
基金
中国国家自然科学基金;
关键词
o-Chloronitrobenzene; Photoelectrocatalytic degradation; TiO2 nanotube arrays; Graphitic carbon nitride; Au nanoparticles; P-CHLORONITROBENZENE; REDUCTION; PHOTOCATALYST; PERFORMANCE; POLLUTANTS; MECHANISM; KINETICS; LAYER;
D O I
10.1016/j.apcatb.2022.122174
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
Chloronitrobenzenes are typical refractory aromatic halogenated nitroaromatic and high-toxic contaminants. The reduction process of chloronitrobenzenes cannot realize their mineralization, and the existence of chlorine group is detrimental to degradation through single chemical oxidation technology. Herein, the Au nanoparticles and graphitic carbon nitride co-modified TiO2 nanotube arrays (Au/g-C3N4/TNAs) photoanodes were fabricated to degrade o-chloronitrobenzene (o-CNB) target pollutant in photoelectrocatalytic (PEC) system. The Au/g-C3N4/ TNAs fabricated with 0.20 mM HAuCl(4)0.4 H2O (Au/g-C3N4/TNAs-0.20) had more superior optical and photo -electrochemical properties than other fabricated photoanodes. Au/g-C3N4/TNAs-0.20 photoanode increased dechlorination efficiency through reduction process, which was beneficial to o-CNB degradation and TOC removal. The coexistence of anions and humic acid inhibited the PEC degradation of o-CNB. The photogenerated electron, center dot O-2(-), hole and center dot OH participated in o-CNB degradation in PEC system. The degradation pathway of o- CNB was inferred through GC-MS spectra and DFT calculation. The acute toxicity and bioaccumulation factor of o-CNB were effectively reduced by PEC degradation.
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页数:14
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