纳米花
催化作用
氨
复合数
电化学
串联
硝酸盐
化学
氨生产
选择性
X射线光电子能谱
无机化学
阴极
化学工程
选择性催化还原
电子转移
选择性还原
塔菲尔方程
基质(水族馆)
镍
亚硝酸盐
产量(工程)
铜
电催化剂
钴
羟胺
热液循环
吸附
作者
Shuangshuang Mao,Yunqing Zhu,Gaigai Dong,Tian Wang,Fan Pan,Kejing Zhang,Shanshan Yu
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-10-08
卷期号:41 (41): 28170-28179
被引量:1
标识
DOI:10.1021/acs.langmuir.5c04125
摘要
Electrocatalytic nitrate reduction (eNO3RR) has gained widespread application as a green and efficient technique for ammonia synthesis. However, the accumulation of nitrite (NO2-) during the electrochemical reduction process significantly hampers the efficiency of converting nitrate (NO3-) into ammonia (NH3). In this study, a Cu-MOF/Co-MOF@NF composite catalyst was developed on a nickel foam substrate using a hydrothermal method. The catalyst is composed of interconnected Cu-MOF@NF and Co-MOF@NF nanosheets, forming a flower-like nanostructure. X-ray photoelectron spectroscopy (XPS) reveals there is an electronic transfer between copper (Cu) and cobalt (Co) sites at the interface of Cu-MOF/Co-MOF@NF, thereby accelerating both the adsorption and reduction of NO3- at Cu sites and enhancing selective conversion to NH3 at Co sites. At a potential of - 0.5 V vs RHE, the Cu-MOF/Co-MOF@NF exhibits a NO3- conversion to NH3 that surpasses those of the Cu-MOF@NF and Co-MOF@NF by 8.5 and 39.6%, respectively, achieving NH3 selectivity and yield of 93.3% and 318.5 μg·h-1·cm-2. In addition, Cu-MOF/Co-MOF@NF possesses exceptional catalytic activity and durability. Electron Paramagnetic Resonance (EPR) experiments reveal a significant amount of *H generated at the cathode interface. In-situ differential electrochemical mass spectrometry (DEMS) detection shows that the reduction pathway for NO3- over the Cu-MOF/Co-MOF@NF is as follows: *NO3- → *NO2- → *NO → *N → *NH → *NH2 → *NH3.
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