双金属片
催化作用
镍
金属
纳米颗粒
X射线光电子能谱
材料科学
原位
化学
氧化铁
无机化学
氧化还原
过渡金属
化学工程
氧化物
纳米技术
冶金
有机化学
工程类
作者
Xiaohan Yuan,Tiancheng Pu,Mengwei Gu,Minghui Zhu,Jing Xu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2021-09-13
卷期号:11 (19): 11966-11972
被引量:55
标识
DOI:10.1021/acscatal.1c03936
摘要
Understanding the interaction of metal with metal oxides is essential for establishing the structure–activity relationship in heterogeneous catalysis. Herein, a series of nickel–iron-based bimetallic catalysts are systematically investigated to unveil the nature of active sites for the CO2 hydrogenation reaction. An environmental-sensitive strong metal–support interaction between Ni nanoparticles and iron oxides is revealed by a series of characterizations, including HR-TEM, H2-TPR, quasi in situ XPS, and time-resolved in situ DRIFTS. Iron oxides migrate and entirely cover the metallic Ni nanoparticles during the reaction, yielding a more active core–shell-type structure with much-improved reducibility. Such a reconstruction process is also indirectly monitored in a time-resolved manner by in situ DRIFTS and confirmed to complete within 30 min of the reaction.
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