3D Flower-Like Zinc Cobaltite for Electrocatalytic Reduction of Nitrate to Ammonia under Ambient Conditions

被引:35
|
作者
Huang, Pingping [1 ]
Fan, Tingting [1 ]
Ma, Xintao [1 ]
Zhang, Jiguang [1 ]
Zhang, Yanping [1 ]
Chen, Zhou [2 ]
Yi, Xiaodong [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Coll Mat, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
Ambient conditions; Ammonia synthesis; Electrochemistry; Nitrate reduction; Water treatment; STORAGE; COPPER; ELECTROREDUCTION; CHALLENGES; REMOVAL; WATER;
D O I
10.1002/cssc.202102049
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nitrate (NO3-) as a common pollutant of groundwater causes drinking water safety problems and seriously endangers people's health. Electrochemical reduction of nitrate to ammonia under ambient condition is a green and significant route to reduce the concentration of NO3- and produce ammonia (NH3), known as a complement to the Haber-Bosch reaction. Currently, noble-metal electrocatalysts are often used in electrochemical reduction of NO3-, but high cost and scarcity limited their application. Herein, three-dimensional (3D) flower-like zinc cobaltite (ZnCo2O4) electrocatalyst was developed to convert nitrate into ammonia at room temperature. The NH3 yield rate could reach up to around 2100 mu g mg(-1) h(-1) at a potential of -0.6 V vs. reversible hydrogen electrode (RHE), which was around 2.0 times higher than that of pristine Co3O4. In addition, the NH3 faradaic efficiency of ZnCo2O4 electrocatalyst could reach around 95.4 % at potential of -0.4 V vs. RHE with good structural and morphological stability, which surpassed most reported non-noble metal-based electrocatalysts. Further studies concluded that the improved activity of electrocatalytic NO3- reduction was ascribed to the existence of abundant active sites and the charge transfer from Co atoms to Zn atoms after Zn doping. Importantly, this work opens a new path for the development of Co-based materials as electrocatalysts for reducing nitrate to ammonia.
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页数:9
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