催化作用
硝基苯
苯乙炔
氢溢流
光化学
化学
无机化学
价(化学)
吸附
金属
X射线光电子能谱
氢
物理化学
有机化学
化学工程
工程类
作者
Yanfu Ma,Banlan Chi,Wei Liu,Lina Cao,Yue Lin,Xiaohui Zhang,Xuxu Ye,Shiqiang Wei,Junling Lu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2019-07-31
卷期号:9 (9): 8404-8412
被引量:117
标识
DOI:10.1021/acscatal.9b01536
摘要
Atomically dispersed metal atoms on supports, so-called single-atom catalysts (SACs), have recently attracted extensive attention in the catalysis field. It has been found that besides the primary metal atom, the proximial atoms also contribute to the catalytic activity significantly. Here, we show that tailoring of the local coordination environment of Pt1 single atoms on CeO2 using phosphorus gives rise to an activity enhancement up to a 10 times higher than Pt1/CeO2 SAC in hydrogenation of styrene, cyclohexene, phenylacetylene, and nitrobenzene. X-ray absorption, photoelectron, and infrared spectroscopies showed that the Pt1 single atoms modulated by phosphorus have a higher valence state. Infrared spectroscopy and temperature-programmed reduction further unveiled that significantly stronger adsorption of reactant and facilitated hydrogen spillover on phosphorus-doped CeO2 both play important roles for the dramatic activity enhancement. These findings point out an avenue to design an advanced SACs with high activity.
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