Achieving efficient and stable electrochemical nitrate removal by in-situ reconstruction of Cu2O/Cu electroactive nanocatalysts on Cu foam

被引:115
|
作者
Zhou, Jianjun [1 ]
Pan, Fan [1 ]
Yao, Qiaofeng [3 ]
Zhu, Yunqing [1 ]
Ma, Hongrui [1 ]
Niu, Junfeng [1 ,2 ]
Xie, Jianping [3 ]
机构
[1] Shaanxi Univ Sci & Technol, Sch Environm Sci & Engn, Xian 710021, Peoples R China
[2] Dongguan Univ Technol, Sch Environm & Civil Engn, Dongguan 523808, Peoples R China
[3] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 117585, Singapore
基金
中国国家自然科学基金;
关键词
Electrochemical nitrate reduction; Cu2O/Cu; Atomic hydrogen; Electrocatalytic denitrification; Nitrogen pollution control; ELECTROCATALYTIC REDUCTION; EVOLUTION REACTION; WATER-TREATMENT; OXIDE; FUNDAMENTALS; SURFACES; KINETICS; CATHODE; AMMONIA;
D O I
10.1016/j.apcatb.2022.121811
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
Efficient and stable electrocatalysts are essential for electrochemical denitrification of nitrate contamination in water. Herein, a cost-effective Cu2O/Cu NRs/CF cathode bearing abundant Cu active sites and electron-rich Cu2O sites with good atomic H* provision performance is reported to exhibit rapid nitrate reduction kinetics (0.04815 min(-1)) and no nitrite accumulation. Benefiting from the enhanced mass transfer and sufficient H* provision, the rapid adsorption of *NO3, fast reduction of *NO2 to *NO, and highly selective *NO to *NOH transformation played critical roles in the electrochemical nitrate reduction process. Although ammonia was the main final nitrate reduction product, the electrocatalytic system we designed could effectively oxidize ammonia into N-2 with the assistance of simultaneous electrochlorination, finally achieving 96.81% of N-2 selectivity. Significantly, the long-term stability and low energy consumption to treat actual nitrate-contaminated wastewater make the Cu2O/Cu NRs/CF electrode promising for practical applications.
引用
收藏
页数:14
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