Chloride doping of Co4S3 via methanol solvothermal synthesis for enhanced electrocatalytic nitrate reduction to ammonia

被引:0
|
作者
Feng, Shuoshuo [1 ]
Rao, Xufeng [1 ]
Chen, Xiaoyu [1 ]
Ning, Fanghua [1 ]
Wang, Min [2 ]
Liu, Yuyu [1 ]
机构
[1] Shanghai Univ, Inst Sustainable Energy, Coll Sci, Shanghai 200444, Peoples R China
[2] Yancheng Inst Technol, Sch Chem & Chem Engn, Yancheng 224051, Peoples R China
关键词
Nitrate; Electrocatalytic reduction; Chloride doping; Co4S3; WATER;
D O I
10.1016/j.psep.2024.09.117
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The electrocatalytic reduction of nitrate offers an environmentally friendly means of eliminating hazardous nitrate from wastewater while simultaneously yielding ammonia, a vital fertilizer precursor. Given the importance of nitrate reduction for environmental remediation and the potential of electrochemical methods, the development of a highly efficient and selective electrocatalyst specifically for nitrate reduction to ammonia (NO3ER) is crucial. The Cl-doped Co4S3 (Cl-Co4S3) catalyst was successfully synthesized via a solvothermal method in methanol, aiming to enhance nitrate electroreduction. The incorporation of chlorine was found to modulate the local electronic environment around cobalt atoms, enhancing their reactivity and leading to exceptional catalytic performance for nitrate reduction, leading to exceptional catalytic performance. At an operating potential of -0.61 V vs. the reversible hydrogen electrode, Cl-Co4S3 exhibited remarkable Faradaic efficiency (97.64 +/- 2.03 %) and yield rate (0.652 +/- 0.012 mmol h(-1) cm(-2)) for ammonia production, surpassing the majority of reported electrocatalysts for NO3ER.
引用
收藏
页码:2026 / 2033
页数:8
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