钴
催化作用
氢溢流
材料科学
立方氧化锆
X射线光电子能谱
粒径
离解(化学)
化学工程
金属
无机化学
多相催化
化学
陶瓷
物理化学
冶金
有机化学
工程类
作者
Alexander Parastaev,Valery Muravev,Elisabet Huertas Osta,Arno J. F. van Hoof,Tobias F. Kimpel,Nikolay Kosinov,Emiel J. M. Hensen
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2020-05-11
卷期号:3 (6): 526-533
被引量:357
标识
DOI:10.1038/s41929-020-0459-4
摘要
Metal–support interactions have a strong impact on the performance of heterogeneous catalysts. Specific sites at the metal–support interface can give rise to unusual high reactivity, and there is a growing interest in optimizing not only the properties of metal particles but also the metal–support interface. Here, we demonstrate how varying the particle size of the support (ceria–zirconia) can be used to tune the metal–support interactions, resulting in a substantially enhanced CO2 hydrogenation rate. A combination of X-ray diffraction, X-ray absorption spectroscopy, near-ambient pressure X-ray photoelectron spectroscopy, transmission electron microscopy and infrared spectroscopy provides insight into the active sites at the interface between cobalt and ceria–zirconia involved in CO2 hydrogenation to CH4. Reverse oxygen spillover from the support during treatment in hydrogen results in the generation of oxygen vacancies. Stabilization of cobalt particles by ceria–zirconia particles of intermediate size leads to oxygen spillover to the support during the CO2 and CO dissociation steps, followed by further hydrogenation of the resulting intermediates on cobalt. Metal–support interactions can effectively modify the catalytic properties of heterogeneous composites. Here, the authors report the possibility of controlling the interaction between cobalt and a ceria–zirconia support by changing the particle size of the latter, resulting in a superior CO2 hydrogenation system.
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