Novel synthetic approaches and TWC catalytic performance of flower-like Pt/CeO2  

Novel synthetic approaches and TWC catalytic performance of flower-like Pt/CeO2

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作  者:Zongcheng ZHAN Xiaojun LIU Dongzhu MA Liyun SONG Jinzhou LI Hong HE Hongxing DAI 

机构地区:[1]Department of Chemistry and Chemical Engineering, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124, China

出  处:《Frontiers of Environmental Science & Engineering》2014年第4期483-495,共13页环境科学与工程前沿(英文)

基  金:The authors are grateful for the National Natural Science Foundation of China (Grant Nos. 20877006 and 20833011), National Industrial Project of Rare Earth and Rare Metal New Materials and the Project funding for Academic Human Resources Development in Institutions of Higher Learning under the Jurisdiction of Beijing Municipality (Nos. PHR201107104 and PHR200907105). We also thank Mining and Metallurgy Research Institute of Beijing for the TEM access.

摘  要:A novel Ultrasonic Assisted Membrane Reduction (UAMR)-hydrothermal method was used to prepare flower-like Pt/CeO2 catalysts. The texture, physical/chemical properties, and reducibility of the flower-like Pt/CeO2 catalysts were characterized by X-Ray Diffraction (XRD), Scanning Electron Microscope (SEM), Transmission Electron Microscope (TEM), N2 adsorption, and hydrogen temperature programmed reduction (HE-TPR) techniques. The catalytic performance of the catalysts for treating automobile emission was studied relative to samples prepared by the conventional wetness impregnation method. The Pt/CeO2 catalysts fabricated by this novel method showed high specific surface area and metal dispersion, excellent three-way catalytic activity, and good thermal stability. The strong interaction between the Pt nanoparticles and CeO2 improved the thermal stability. The Ce4+ ions were incorporated into the surfactant chains and the Pt nanoparticles were stabilized through an exchange reaction of the surface hydroxyl groups. The SEM results demonstrated that the Pt/CeO2 catalysts had a typical three-dimensional (3D) hierarchical porous struc- ture, which was favorable for surface reaction and enhanced the exposure degree of the Pt nanoparticles. In brief, the flower-like Pt/CeO2 catalysts prepared by UAMR-hydrothermal method exhibited a higher Pt metal dispersion, smaller particle size, better three-way catalytic activity, and improved thermal stability versus conven- tional materials.A novel Ultrasonic Assisted Membrane Reduction (UAMR)-hydrothermal method was used to prepare flower-like Pt/CeO2 catalysts. The texture, physical/chemical properties, and reducibility of the flower-like Pt/CeO2 catalysts were characterized by X-Ray Diffraction (XRD), Scanning Electron Microscope (SEM), Transmission Electron Microscope (TEM), N2 adsorption, and hydrogen temperature programmed reduction (HE-TPR) techniques. The catalytic performance of the catalysts for treating automobile emission was studied relative to samples prepared by the conventional wetness impregnation method. The Pt/CeO2 catalysts fabricated by this novel method showed high specific surface area and metal dispersion, excellent three-way catalytic activity, and good thermal stability. The strong interaction between the Pt nanoparticles and CeO2 improved the thermal stability. The Ce4+ ions were incorporated into the surfactant chains and the Pt nanoparticles were stabilized through an exchange reaction of the surface hydroxyl groups. The SEM results demonstrated that the Pt/CeO2 catalysts had a typical three-dimensional (3D) hierarchical porous struc- ture, which was favorable for surface reaction and enhanced the exposure degree of the Pt nanoparticles. In brief, the flower-like Pt/CeO2 catalysts prepared by UAMR-hydrothermal method exhibited a higher Pt metal dispersion, smaller particle size, better three-way catalytic activity, and improved thermal stability versus conven- tional materials.

关 键 词:Ultrasonic Assisted Membrane Reduction (UAMR) Pt nanoparticles three-way catalyst FLOWER-LIKE 

分 类 号:O643.36[理学—物理化学] U464.136[理学—化学]

 

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