普鲁士蓝
化学
尿素
双金属片
催化作用
氧化态
无机化学
二价
镍
氧化还原
电化学
核化学
电极
有机化学
物理化学
作者
Xiaofang Liu,Jian‐Hua Zhang,Liujun Jin,Chun‐Chao Chen,Jinghui He,Qingfeng Xu,Jianmei Lu
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2023-02-15
卷期号:62 (8): 3637-3645
被引量:7
标识
DOI:10.1021/acs.inorgchem.2c04465
摘要
Urea degradation is one of the most crucial links in the natural nitrogen cycle. Exploring the real active species in the urea electro-oxidation process is of great significance for understanding the urea electro-oxidation mechanism and designing catalysts. A highly active and stable Prussian blue analogue catalyst (PBA@NiFe/NF) loaded on nickel foam was synthesized for electro-oxidation of urea. In situ Raman spectra revealed that Ni in PBA@NiFe/NF was able to maintain a stable divalent nickel (Ni(II)) state for up to 3.5 h during the initial urea oxidation process, which is rarely reported in previous research studies. In addition, with the participation of iron, the Ni-Fe bimetallic center significantly improves the electro-oxidation of urea. Our work provides a new idea for prolonging the Ni(II) activity in electrocatalytic oxidation of urea.
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