Strong Metal-Support Interactions between Nickel and Iron Oxide during CO2 Hydrogenation

被引:51
|
作者
Yuan, Xiaohan [1 ]
Pu, Tiancheng [1 ]
Gu, Mengwei [1 ]
Zhu, Minghui [1 ]
Xu, Jing [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
来源
ACS CATALYSIS | 2021年 / 11卷 / 19期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
strong metal-support interaction; CO2; hydrogenation; nickel-iron catalyst; CO; CH4; GAS SHIFT REACTION; NI-FE CATALYSTS; METHANOL SYNTHESIS; CARBON-DIOXIDE; METHANATION; SELECTIVITY; ACTIVATION; OXIDATION; SIZE;
D O I
10.1021/acscatal.1c03936
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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, H-2-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.
引用
收藏
页码:11966 / 11972
页数:7
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