化学
催化作用
非阻塞I/O
尿素
氧化还原
无机化学
氧化态
有机化学
作者
Xingyu Huang,Runze He,Shuli Wang,Yun Quan Yang,Ligang Feng
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-11-02
卷期号:61 (45): 18318-18324
被引量:45
标识
DOI:10.1021/acs.inorgchem.2c03498
摘要
The microenvironment tuning of Ni species, a promising non-precious catalyst, is significant in the energy and environmentally relevant urea electro-oxidation reaction (UOR). Herein, we found that the high-valent Ni species induced by the inactive MoO 2 in mixed nanocrystals of NiO/MoO 2 were effective for urea oxidation. The redox interaction of MoO 2 and NiO revealed by the spectroscopic analysis well supported the formation of high-valent Ni species and the changes in the surface chemical state. High catalytic activity and stability for urea oxidation were observed by a series of electrochemical measures compared to the counterpart catalysts of MoO 2 and NiO. The optimal NiO/MoO 2 hybrid catalyst showed a UOR activity of 73.1 mA cm –2 at 1.50 V, which was about 12-fold that of the NiO catalyst. In addition, largely improved catalytic kinetics and catalytic stability for UOR were also demonstrated. Because of the inactive activity of MoO 2 and the low performance of NiO, the largely improved preference can be affirmatively attributed to the efficient catalytic synergism of NiO/MoO 2 in the mixed nanocrystals. The current finding clarifies the catalytic promotion effect of the inactive Mo species on Ni-based catalysts for urea oxidation, which would be instructive for Ni/Mo-relevant catalyst development.
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