纳米棒
X射线光电子能谱
无机化学
氨
化学
法拉第效率
可逆氢电极
氢
吸附
材料科学
电化学
化学工程
纳米技术
物理化学
电极
有机化学
工程类
参比电极
作者
Yan Shi,Yumeng Li,Rujin Li,Xiaogang Zhao,Yanling Yu,Min Yang
标识
DOI:10.1016/j.cej.2023.147574
摘要
Electrocatalytic nitrate reduction to ammonia (ENRA) is crucial for environmental pollution treatment and sustainable energy development, but the complicated reduction mechanism of ENRA leads to limited ammonia selectivity and low Faradaic efficiency. In this work, Cu/Cu2O heterogeneous nanorods with oxygen vacancies were successfully obtained by creating Cu sites via the in-situ reconstruction of Cu2O nanorods. These oxygen vacancies can weaken the N-O bond. The Cu sites and heterogeneous interfaces were investigated using X-ray photoelectron spectroscopy Auger spectra and transmission electron microscopy. The active species trapping experiments and density functional theory (DFT) calculations demonstrated that the Cu sites promoted the reduction of NO3- to NO2- due to their strong adsorption of NO3-, and the sufficient atomic hydrogen originating from Cu2O facilitated the formation of a *NOH intermediate. In addition, abundant heterogeneous interfaces facilitated the reduction of N-containing intermediates by atomic hydrogen, leading to a high Faradaic efficiency of 84.93 % and ammonia yield of 4.58 mg/h/cm2 in neutral solution. Our findings will diversify the methodologies for constructing Cu/Cu2O electrocatalysts and provide new insight into the mechanism of ammonia synthesis from nitrate reduction.
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