Efficient CO Oxidation using Co3O4-CeO2 Nanoparticles Supported on Resin-Based Spherical Activated Carbon with Controllable Oxygen Species

被引:1
作者
Chen, Zhiwei [1 ]
Liu, Yiqi [1 ]
Wang, Jitong [1 ,2 ]
Ling, Licheng [1 ]
Qiao, Wenming [1 ]
机构
[1] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[2] Guangxi Univ, Guangxi Key Lab Petrochem Resource Proc & Proc Int, Sch Chem & Chem Engn, Nanning 530004, Peoples R China
来源
CHEMISTRYSELECT | 2024年 / 9卷 / 12期
基金
中国国家自然科学基金;
关键词
Activated carbon; Cobalt; Cerium; Carbon monoxide; Oxygen species; Oxygen vacancies; VOLATILE ORGANIC-COMPOUNDS; PREFERENTIAL OXIDATION; CATALYTIC-OXIDATION; TEMPERATURE; PERFORMANCE; ADSORPTION; OXIDE; VACANCIES; MONOXIDE; DESIGN;
D O I
10.1002/slct.202400306
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The oxygen vacancies and surface oxygen species play pivotal roles in CO catalytic oxidation. In this study, Co3O4-CeO2 supported on resin based spherical activated carbon was fabricated and the effect of CeO2 on surface oxygen species was demonstrated through controlling various Ce contents. When Ce content was optimal (n(Co) : n(Ce)=9), the maximum surface adsorbed oxygen content (60.3 %) is displayed and the catalyst achieved good CO conversion (T-100=110 degree celsius), water resistance and robust stability. DFT simulation calculation confirmed that the energy barriers of two transition states significantly decreased to 0.60 eV and 0.37 eV, respectively, with the addition of CeO2. The results indicate that the presence of CeO2 is conducive to the increasement of surface adsorbed oxygen content and optimal Co/Ce ratio is the most favorable for the CO oxidation. It is attributed to the visible decline of the energy barrier between oxygen vacancies and gas-phase oxygen at the Co3O4-CeO2 interface, and the process of oxygen vacancies replenishment could be more prone to occur at the interface. This study may provide a protocol for further improving surface species on supporting catalysts.
引用
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页数:12
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