催化作用
硝酸盐
吸附
废水
法拉第效率
碳纤维
无机化学
氨
X射线光电子能谱
化学
材料科学
电催化剂
化学工程
核化学
电化学
电极
有机化学
废物管理
复合数
物理化学
复合材料
工程类
作者
Yaling Chen,Song Shu,Jianjun Li
标识
DOI:10.1016/j.jtice.2024.105399
摘要
Electrocatalytic nitrate reduction reaction (ENRR) to recyclable ammonia has become a green treatment NO3– technology for wastewater. However, poor stability of Cu-based electrocatalysts hinders their application. In this study, three derived catalysts were prepared using Cu-BTC as a precursor at different temperatures: Cu@C-250, Cu@C-350, and Cu@C-450. The catalysts' activity was investigated through a series of nitrate reduction performance tests, and the reaction mechanism was explored through various characterization methods. The batch ENRR test revealed that Cu@C-350 exhibited the best performance in terms of NO3– removal rate (73.70 %) and faradaic efficiency for NH4+ (80.01 %) at –0.58 V vs. RHE. EIS and XPS analyses show that Cu+ accelerates electron transfer, reduce interfacial resistance, and interact with catalytic carriers to enhance the adsorption of NO3–. Additionally, the durability as an electrocatalyst is verified by consecutive cycling tests. Therefore, the use of roasted carbon material derivatives as electrocatalysts for the purification of nitrate-contaminated wastewater is a reliable strategy.
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