High-performance Ce doped three-dimensional ordered macroporous Co-based catalysts on CO oxidation

被引:8
|
作者
Zhou, Kun [1 ]
Hu, Miaomiao [1 ,3 ]
Zhao, Tingyi [1 ]
Shi, Qingzhao [2 ]
Feng, Jiaxin [1 ]
Ma, Xue [1 ]
Zhao, Mingqin [1 ]
Shao, Zhihui [1 ]
Cui, Bing [1 ]
机构
[1] Henan Agr Univ, Coll Tobacco Sci, Flavors & Fragrance Engn & Technol Res Ctr Henan P, Zhengzhou 450002, Peoples R China
[2] Zhengzhou Tobacco Res Inst CNTC, Key Lab Tobacco Flavor Basic Res CNTC, Zhengzhou 450000, Peoples R China
[3] Zhengzhou Univ, Sch Ecol & Environm, Zhengzhou 450001, Peoples R China
关键词
TOTAL-ENERGY CALCULATIONS; DIESEL SOOT; REDUCTION; COBALT; CERIA; NANOSHEETS; TIO2;
D O I
10.1039/d2cy01242a
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
A series of Co3O4 and CoxCe1Oy catalysts were successfully prepared by a colloidal crystal template method, and various characterization results confirmed the formation of a three-dimensional ordered microporous (3DOM) structure and Ce doping into the lattice of Co3O4. The catalytic activity of the prepared catalysts was measured on CO oxidation. Compared with a bulk catalyst, 3D-Co3O4 and 3D-CoxCe1Oy were more favorable for CO diffusion and had the advantage in terms of contact state with CO. In addition, XPS and d-band center results demonstrated that Ce doping regulated the valence states of Co ions and produced more Co3+ with stronger oxidation capacity, enhancing the intrinsic activity. Meanwhile, the DFT calculation of the adsorption energy for O-2 and CO showed that 3D-Co16Ce1Oy could easily utilize O-2 and adsorb CO preferentially. Under the synergistic promotion of the 3DOM structure and Ce doping, 3D-Co16Ce1Oy has the best catalytic activity performance (T-50 = 124.8 degrees C) and the lowest activation energy (E-a = 95.85 kJ mol(-1)). Besides, the stability test showed that the catalyst has good thermal stability. Therefore, the combined improvement in morphology and intrinsic activity has a bright prospect for the synthesis of high-performance CO oxidation catalysts.
引用
收藏
页码:2015 / 2025
页数:12
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