亚硝酸盐
催化作用
氨
法拉第效率
氨生产
电化学
产量(工程)
化学
氢
无机化学
可逆氢电极
化学工程
材料科学
电极
纳米技术
物理化学
冶金
工作电极
硝酸盐
有机化学
工程类
作者
Guilai Wen,Jie Liang,Qian Liu,Tingshuai Li,Xuguang An,Fang Zhang,Abdulmohsen Ali Alshehri,Khalid Ahmed Alzahrani,Yonglan Luo,Qingquan Kong,Xuping Sun
出处
期刊:Nano Research
[Springer Nature]
日期:2021-06-09
卷期号:15 (2): 972-977
被引量:114
标识
DOI:10.1007/s12274-021-3583-9
摘要
Industrial-scale ammonia (NH3) production mainly relies on the energy-intensive and environmentally unfriendly Haber-Bosch process. Such issue can be avoided by electrocatalytic N2 reduction which however suffers from limited current efficiency and NH3 yield. Herein, we demonstrate ambient NH3 production via electrochemical nitrite (NO2−) reduction catalyzed by a CoP nanoarray on titanium mesh (CoP NA/TM). When tested in 0.1 M PBS (pH = 7) containing 500 ppm NO2−, such CoP NA/TM is capable of affording a large NH3 yield of 2,260.7 ± 51.5 µg·h−1·cm−2 and a high Faradaic efficiency of 90.0 ± 2.3% at −0.2 V vs. a reversible hydrogen electrode. Density functional theory calculations reveal that the potential-determining step for NO2− reduction over CoP (112) is *NO2 → *NO2H.
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