CeO2 supported low-loading Au as an enhanced catalyst for low temperature oxidation of carbon monoxide

被引:14
|
作者
Li, Lingling [1 ,2 ]
Liu, Yu [1 ,2 ]
Wang, Qishun [1 ,2 ]
Zhou, Xuan [1 ,2 ]
Li, Jian [1 ,2 ]
Song, Shuyan [1 ,2 ]
Zhang, Hongjie [1 ,2 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Jilin, Peoples R China
[2] Univ Sci & Technol China, Sch Appl Chem & Engn, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
PREFERENTIAL CO OXIDATION; NANOSIZED GOLD CATALYSTS; AU/CEO2; CATALYSTS; CERIA; NANOPARTICLES; SIZE; DEACTIVATION; ACTIVATION; NANOSCALE; MECHANISM;
D O I
10.1039/c9ce01301f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A CeO2-supported Au nanohybrid is regarded as a promising catalytic system for CO oxidation, but its unsatisfactory catalytic activity and high cost are still challenges for sustainable application. In this work, we have synthesized a series of low loading and high activity Au/CeO2 supported catalysts using a coprecipitation method. Au/CeO2 catalysts with a low Au content (0.2 wt%) showed extremely high activity for CO oxidation with 100% conversion of CO around 60 degrees C. The key to the success is that the unique oxygen-deficient structure of cerium oxide can capture gold to provide a strong synergistic effect between the metal and the support. The content of gold in their oxidation states (Au+1, Au+3) present in the catalyst is one of the important factors affecting the catalytic activity. Furthermore, all of the prepared catalysts present a high BET surface area of roughly 140 m(2) g(-1). This high specific surface area provides adequate adsorption sites for CO. Moreover, the low loading of Au is critical to reducing the cost of noble metal-based catalysts and making them practical for industrial applications.
引用
收藏
页码:7108 / 7113
页数:6
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