双金属片
催化作用
材料科学
X射线光电子能谱
原位
氢
纳米棒
吸附
无机化学
化学工程
金属
物理化学
纳米技术
化学
有机化学
工程类
冶金
作者
Jing Li,Yu Tang,Yuanyuan Ma,Zhiyun Zhang,Franklin Feng Tao,Yongquan Qu
标识
DOI:10.1021/acsami.8b15585
摘要
Identification of the chemical states of catalytic sites is critical for an atomic-level understanding of catalytic mechanisms. Herein, hydrogen thermal pretreatment of the Pt single atoms on porous nanorods of CeO2 (Pt1/PN-CeO2) induced the formation of isolated bimetallic PtCe sites as a new type of active center for CO oxidation. The evolutions of Pt1/PN-CeO2 catalysts during the hydrogen pretreatment and CO oxidation were examined by various in situ techniques including infrared, ambient-pressure X-ray photoelectron and X-ray absorption spectroscopy. The experimental results demonstrate that these bimetallic sites can be partially preserved or reoxidized into Pt–O–Ce with a low coordination number with oxygen under realistic conditions, leading to the appropriate CO adsorption and activating the efficient activity of Pt1/PN-CeO2 for CO oxidation at low temperature.
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