Co3O4-CeO2 Nanocomposites for Low-Temperature CO Oxidation

被引:19
|
作者
Yang, Jingxia [1 ,2 ]
Yigit, Nevzat [1 ]
Moller, Jury [1 ]
Rupprechter, Gunther [1 ]
机构
[1] Tech Univ Wien, Inst Mat Chem, Getreidemarkt 9-BC-01, A-1060 Vienna, Austria
[2] Shanghai Univ Engn Sci, Coll Chem & Chem Engn, Longteng Rd 333, Shanghai, Peoples R China
基金
奥地利科学基金会;
关键词
catalysis; CO oxidation; nanocomposites; solvothermal synthesis; SELECTIVE CATALYTIC-REDUCTION; METAL-SUPPORT INTERACTION; SURFACE OXYGEN VACANCIES; COBALT OXIDE; MIXED OXIDES; PREFERENTIAL OXIDATION; CARBON NANOTUBES; CEO2; NANOFLAKES; SOL-GEL; NAP-XPS;
D O I
10.1002/chem.202100927
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In an effort to combine the favorable catalytic properties of Co3O4 and CeO2, nanocomposites with different phase distribution and Co3O4 loading were prepared and employed for CO oxidation. Synthesizing Co3O4-modified CeO2 via three different sol-gel based routes, each with 10.4 wt % Co3O4 loading, yielded three different nanocomposite morphologies: CeO2-supported Co3O4 layers, intermixed oxides, and homogeneously dispersed Co. The reactivity of the resulting surface oxygen species towards CO were examined by temperature programmed reduction (CO-TPR) and flow reactor kinetic tests. The first morphology exhibited the best performance due to its active Co3O4 surface layer, reducing the light-off temperature of CeO2 by about 200 degrees C. In contrast, intermixed oxides and Co-doped CeO2 suffered from lower dispersion and organic residues, respectively. The performance of Co3O4-CeO2 nanocomposites was optimized by varying the Co3O4 loading, characterized by X-ray diffraction (XRD) and N-2 sorption (BET). The 16-65 wt % Co3O4-CeO2 catalysts approached the conversion of 1 wt % Pt/CeO2, rendering them interesting candidates for low-temperature CO oxidation.
引用
收藏
页码:16947 / 16955
页数:9
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