Co3O4-CeO2 Nanocomposites for Low-Temperature CO Oxidation

被引:20
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
相关论文
共 76 条
[1]   Role of rubidium promotion on the nitrous oxide decomposition activity of nanocrystalline Co3O4-CeO2 catalyst [J].
Abu-Zied, Bahaa M. ;
Soliman, Soliman A. ;
Asiri, Abdullah M. .
APPLIED SURFACE SCIENCE, 2019, 479 :148-157
[2]  
[Anonymous], 2016, ANGEW CHEM, V128, P7581
[3]  
[Anonymous], 2008, ANGEW CHEM, V120, P2926
[4]  
[Anonymous], 2012, ANGEW CHEM, V124, P10185
[5]   Co3O4@PC derived from ZIF-67 as an efficient catalyst for the selective catalytic reduction of NOx with NH3 at low temperature [J].
Bai, Yarong ;
Dong, Junping ;
Hou, Yaqin ;
Guo, Yaoping ;
Liu, Yongjin ;
Li, Yulin ;
Han, Xiaojin ;
Huang, Zhanggen .
CHEMICAL ENGINEERING JOURNAL, 2019, 361 :703-712
[6]   Transient structural and catalytic behaviour of Pt-particles probed by operando spectroscopy during a realistic driving cycle [J].
Benzi, Federico ;
Sheppard, Thomas L. ;
Doronkin, Dmitry E. ;
Meira, Debora M. ;
Gaenzler, Andreas M. ;
Baier, Sina ;
Grunwaldt, Jan-Dierk .
CATALYSIS SCIENCE & TECHNOLOGY, 2017, 7 (18) :3999-4006
[7]   Promoting effect of CeO2 in combustion synthesized Pt/CeO2 catalyst for CO oxidation [J].
Bera, P ;
Gayen, A ;
Hegde, MS ;
Lalla, NP ;
Spadaro, L ;
Frusteri, F ;
Arena, F .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (25) :6122-6130
[8]   A New Type of Strong Metal-Support Interaction and the Production of H2 through the Transformation of Water on Pt/CeO2(111) and Pt/CeOx/TiO2(110) Catalysts [J].
Bruix, Albert ;
Rodriguez, Jose A. ;
Ramirez, Pedro J. ;
Senanayake, Sanjaya D. ;
Evans, Jaime ;
Park, Joon B. ;
Stacchiola, Dario ;
Liu, Ping ;
Hrbek, Jan ;
Illas, Francesc .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (21) :8968-8974
[9]   Control of Metal Nanocrystal Size Reveals Metal-Support Interface Role for Ceria Catalysts [J].
Cargnello, Matteo ;
Doan-Nguyen, Vicky V. T. ;
Gordon, Thomas R. ;
Diaz, Rosa E. ;
Stach, Eric A. ;
Gorte, Raymond J. ;
Fornasiero, Paolo ;
Murray, Christopher B. .
SCIENCE, 2013, 341 (6147) :771-773
[10]   Synthesis of uniform diameter single wall carbon nanotubes in Co-MCM-41: effects of CO pressure and reaction time [J].
Chen, Y ;
Ciuparu, D ;
Lim, S ;
Yang, YH ;
Haller, GL ;
Pfefferle, L .
JOURNAL OF CATALYSIS, 2004, 226 (02) :351-362