甲烷化
催化作用
镍
金属
化学
化学工程
材料科学
替代天然气
合成气
有机化学
工程类
作者
Liang Shen,Jing Xu,Minghui Zhu,Yi‐Fan Han
出处
期刊:ACS Catalysis
日期:2020-11-25
卷期号:10 (24): 14581-14591
被引量:172
标识
DOI:10.1021/acscatal.0c03471
摘要
The carbon dioxide (CO2) methanation reaction not only provides a solution for mitigating the excessive carbon dioxide emissions but also can potentially be employed for the storage and transportation of low-grade energies. A supported nickel-based catalyst is the most promising candidate for the CO2 methanation reaction. Additionally, understanding the role of the support is essential for the rational design of nickel-based CO2 methanation catalysts. Herein, we elaborated on the effect of the support on the catalyst structure, CO2 adsorption, CO2 activation, methanation mechanism, and deactivation process. Future directions are suggested to elucidate the fundamental aspects of this catalytic system, including the formation mechanism of preferentially exposed facets, the nature of strong metal–support interactions, the balance between support reducibility and basicity, and the CO2 methanation pathways over nickel-based catalysts with various supports.
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