scholarly journals Size Dependence of Low-Temperature Catalytic Activity of CO Oxidation Driven by Platinum Clusters Directly Bound to Silicon Substrate Surface

2015 ◽  
Vol 119 (20) ◽  
pp. 11217-11223 ◽  
Author(s):  
Hisato Yasumatsu ◽  
Nobuyuki Fukui
Catalysts ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 724 ◽  
Author(s):  
Yan Cui ◽  
Leilei Xu ◽  
Mindong Chen ◽  
Chufei Lv ◽  
Xinbo Lian ◽  
...  

CuO-based catalysts are usually used for CO oxidation owing to their low cost and excellent catalytic activities. In this study, a series of metal oxide (La2O3, Fe2O3, PrO2, Sm2O3, and MnO2)-doped CuO-based catalysts with mesoporous Ce0.8Zr0.2O2 support were simply prepared by the incipient impregnation method and used directly as catalysts for CO catalytic oxidation. These mesoporous catalysts were systematically characterized by X-ray powder diffraction (XRD), N2 physisorption, transmission electron microscopy (TEM), energy-dispersed spectroscopy (EDS) mapping, X-ray photoelectron spectroscopy (XPS), and H2 temperature programmed reduction (H2-TPR). It was found that the CuO and the dopants were highly dispersed among the mesoporous framework via the incipient impregnation method, and the strong metal framework interaction had been formed. The effects of the types of the dopants and the loading amounts of the dopants on the low-temperature catalytic performances were carefully studied. It was concluded that doped transition metal oxides could regulate the oxygen mobility and reduction ability of catalysts, further improving the catalytic activity. It was also found that the high dispersion of rare earth metal oxides (PrO2, Sm2O3) was able to prevent the thermal sintering and aggregation of CuO-based catalysts during the process of calcination. In addition, their presence also evidently improved the reducibility and significantly reduced the particle size of the CuO active sites for CO oxidation. The results demonstrated that the 15CuO-3Fe2O3/M-Ce80Zr20 catalyst with 3 wt. % of Fe2O3 showed the best low-temperature catalytic activity toward CO oxidation. Overall, the present Fe2O3-doped CuO-based catalysts with mesoporous nanocrystalline Ce0.8Zr0.2O2 solid solution as support were considered a promising series of catalysts for low-temperature CO oxidation.


2019 ◽  
Vol 129 ◽  
pp. 105729 ◽  
Author(s):  
Zhiwen Li ◽  
Huan Wang ◽  
Weiwei Zhao ◽  
Xin Xu ◽  
Quan Jin ◽  
...  

2017 ◽  
Vol 41 (22) ◽  
pp. 13418-13424 ◽  
Author(s):  
Lu Zhang ◽  
Li Zhang ◽  
Guancheng Xu ◽  
Chi Zhang ◽  
Xin Li ◽  
...  

The excellent CO catalytic activity and stability of CeO2@Co3O4 composite were ascribed to the synergistic interactions between Co3O4 and CeO2.


RSC Advances ◽  
2018 ◽  
Vol 8 (35) ◽  
pp. 19499-19511 ◽  
Author(s):  
Abdallah F. Zedan ◽  
Assem T. Mohamed ◽  
M. Samy El-Shall ◽  
Siham Y. AlQaradawi ◽  
Amina S. AlJaber

Copper oxide (CuO) nanoparticles of tailored reducibility could be used as inexpensive, efficient and durable catalysts for CO oxidation at low temperature.


2018 ◽  
Vol 54 (79) ◽  
pp. 11168-11171 ◽  
Author(s):  
Zhimin Jia ◽  
Fei Huang ◽  
Jiangyong Diao ◽  
Jiayun Zhang ◽  
Jia Wang ◽  
...  

Platinum nanoparticles (Pt NPs) immobilized on a N-doped graphene@Al2O3 hybrid support (Al2O3@CNx) were synthesized and exhibit superior catalytic activity for low temperature CO oxidation, due to a strong metal–support interaction between Pt NPs and the N-doped.


2013 ◽  
Vol 4 ◽  
pp. 111-128 ◽  
Author(s):  
Lu-Cun Wang ◽  
Yi Zhong ◽  
Haijun Jin ◽  
Daniel Widmann ◽  
Jörg Weissmüller ◽  
...  

The catalytic properties of nanostructured Au and their physical origin were investigated by using the low-temperature CO oxidation as a test reaction. In order to distinguish between structural effects (structure–activity correlations) and bimetallic/bifunctional effects, unsupported nanoporous gold (NPG) samples prepared from different Au alloys (AuAg, AuCu) by selective leaching of a less noble metal (Ag, Cu) were employed, whose structure (surface area, ligament size) as well as their residual amount of the second metal were systematically varied by applying different potentials for dealloying. The structural and chemical properties before and after 1000 min reaction were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The catalytic behavior was evaluated by kinetic measurements in a conventional microreactor and by dynamic measurements in a temporal analysis of products (TAP) reactor. The data reveal a clear influence of the surface contents of residual Ag and Cu species on both O2 activation and catalytic activity, while correlations between activity and structural parameters such as surface area or ligament/crystallite size are less evident. Consequences for the mechanistic understanding and the role of the nanostructure in these NPG catalysts are discussed.


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