催化作用
电化学
X射线吸收光谱法
X射线光电子能谱
活动站点
拉曼光谱
价(化学)
材料科学
电催化剂
纳米技术
化学
化学工程
电极
吸收光谱法
物理化学
有机化学
光学
物理
工程类
量子力学
作者
Zhijiao Ji,Wei Yuan,Shenghao Zhao,Tianqi Wang,Sundus Umer,Shuaishuai Ding,Jiawei Liu,Jia Liu,Yanli Zhao,Wenping Hu
出处
期刊:Chem catalysis
[Elsevier]
日期:2023-01-20
卷期号:3 (2): 100501-100501
被引量:12
标识
DOI:10.1016/j.checat.2022.100501
摘要
The reconstruction of metastable materials in the electrocatalytic process brings difficulties to the determination of the relationship of structure to activity, but it also brings hope for new active structures of catalysts. Grasping the reconstruction rule of the metastable materials and further constructing the local supermetastable active structure artificially are essential for clarifying the nature of catalysis and breaking the bottleneck of catalytic activity. Herein, we used a hierarchical structural CoMoO4/Ni(OH)2 as a precursor to construct a local supermetastable active structure CoOOH(Mo)/NiOOH via an electrochemical reconstruction strategy. Based on in situ electrochemical XAS and Raman spectroscopy, combined with XPS and DFT calculations, the reconstruction process and the mechanism of electrocatalytic urea oxidation were explored in detail. The improved electrocatalytic activity, stability, and selectivity of CoOOH(Mo)/NiOOH can be attributed to the synergy between Ni(III), Co(III), and high-valence Mo. This research paves the way for the rational design and synthesis of catalysts to achieve energy conversion.
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