Construction of surface active centers on the mesoporous Co/CeO2-δcatalysts for CO2 hydrogenation

被引:4
|
作者
Zhou, Guilin [1 ,2 ]
Zhao, Shan [1 ]
Xie, Fengqiong [1 ]
Chen, Shuang [2 ]
Xie, Hongmei [1 ]
机构
[1] Chongqing Technol & Business Univ, Dept Chem Engn, Key Lab Catalysis Sci & Technol, Chongqing Educ Commiss, Chongqing 400067, Peoples R China
[2] Minist Educ, Engn Res Ctr Waste Oil Recovery Technol & Equipmen, Chongqing 400067, Peoples R China
关键词
MesoporousCo/CeO(2-delta)catalyst; Active center; Oxygen vacancy; Interface structure; CO2 catalytic hydrogenation; GAS SHIFT REACTION; CARBON-DIOXIDE; SUPPORT INTERACTIONS; CATALYSTS; REDUCTION; COBALT; WATER; PERFORMANCE; METHANATION; ACTIVATION;
D O I
10.1016/j.ijhydene.2023.04.107
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The surface active centers, which include metal Co, surface oxygen vacancies, and Co-0 CeO2- delta interface structures, can be constructed on the mesoporous Co/CeO2- delta catalysts by wet impregnation method. And the surface active centers can be regulated by the Co species dosage. The interaction between the metal Co and CeO2- delta can promote surface oxygen vacancies and Co-0-CeO2- delta interface structures to be formed and be conducive to inhibit the aggregation and sintering of Co species in high temperature environment. The prepared Co/CeO(2- delta)catalysts have better catalytic performances for CO2 hydrogenation than the single component Co and CeO2- delta catalysts, which can be attributed to the synergistic effect between Co-0 active centers, surface oxygen vacancies, and Co-0-CeO(2- delta)interface structures. Therefore, the Co/CeO2- delta catalysts have strong adsorption and activation ability for reactant CO2 and H-2 molecules to improve the CO2 hydrogenation activity. At atmospheric pressure and 400 degrees C, the CO2 conversion and CH4 selectivity on the Co/CeO2- delta catalyst with Co loading of 12% could reach 59.7% and 95.7%, respectively, and maintained good stability in 9 cycles for CO2 hydrogenation reaction.
引用
收藏
页码:28980 / 28997
页数:18
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