Electrochemical nitrate reduction to high-value ammonia on two-dimensional molybdenum carbide nanosheets for nitrate-containing wastewater upcycling

被引:16
|
作者
Zhu, Donglin [1 ]
Li, Guoguang [1 ]
Yan, Xu [2 ]
Geng, Chunxia [4 ]
Gao, Li [3 ]
机构
[1] Nanjing Univ, Sch Environm, Nanjing 210023, Peoples R China
[2] Huizhou Innovat Res Inst Next Generat Ind Internet, Huizhou 516006, Peoples R China
[3] Victoria Univ, Inst Sustainable Ind & Liveable Cities, POB 14428, Melbourne, Vic 8001, Australia
[4] Beijing Water Planning Inst, Beijing 100089, Peoples R China
关键词
Nitrate wastewater upcycling; Electrochemical nitrate reduction; Ammonia electrosynthesis; Electrocatalysis; Molybdenum carbide; ELECTROCATALYTIC REDUCTION; NANOPARTICLES; FUNDAMENTALS; NITROGEN; DESIGN;
D O I
10.1016/j.scitotenv.2023.163145
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Electrochemical conversion of nitrate wastewater into high-value ammonia fertilizer has attracted extensive attention in wastewater treatment and resource recovery, but presents great challenges due to complicated reaction pathways and competing side reactions. Herein, we report a feasible method for the successful fabrication of Mo2C nanosheets (Mo2C NSs) as electrocatalyst for the electroreduction of nitrate to ammonia. Compared to Mo2C nanoparticles, the Mo2C NSs exhibited superior activity and selectivity in NH3 electrosynthesis with an NH3 yield rate of 25.2 m.h(-1).-mg(-1) fraction and transmission electron microscopy characterization verifted the controllable conversion of 2D MoO2 NSs into 2D Mo2C NSs. In situ spectroscopic studies and on-line differential electrochemical mass spectrometry revealed the proposed reaction pathway of NO3- to NH3 conversion, *NO3- *NO2- *NO *NOH *NH2OH *NH3. Den-sity functional theory calculations further verified the effective N-end NOH pathway with the conversion of *NH2OH to *NH2 as the rate-determining step requiring a low energy barrier of 0.58 eV. Importantly, the key hydrogenation of *NO to form *NOH species underwent a lower energy barrier of 0.39 eV compared with the formation of *ONH species (1.06 eV). cat. at -0.4 V and a Faradaic efficiency of 81.4 % at -0.3 V versus reversible hydrogen electrode. The X-ray dif-
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页数:8
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