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二氧化铈负载金催化剂的结构与一氧化碳氧化活性之间的关系。

Relationship between structure and CO oxidation activity of ceria-supported gold catalysts.

作者信息

Venezia Anna Maria, Pantaleo Giuseppe, Longo Alessandro, Di Carlo Gabriella, Casaletto Maria Pia, Liotta F Leonarda, Deganello Giulio

机构信息

Istituto per lo Studio dei Materiali Nanostrutturati, CNR, Via Ugo La Malfa 155, 90146 Palermo, Italy.

出版信息

J Phys Chem B. 2005 Feb 24;109(7):2821-7. doi: 10.1021/jp045928i.

Abstract

Gold catalysts supported on cerium oxide were prepared by solvated metal atom dispersion (SMAD), by deposition-precipitation (DP), and by coprecipitation (CP) methods and were characterized by X-ray diffraction (XRD), temperature programmed reduction (TPR), and X-ray photoelectron spectroscopy (XPS). The catalytic activity was tested in the CO oxidation reaction. The structural and surface analyses evidenced the presence of a modified ceria phase in the case of the DP sample and the presence of pure ceria and gold metal crystallites in the case of the SMAD and CP samples. The DP sample, after a mild treatment in air at 393 K, exhibited only ionic gold, and it was very active below 273 K. By comparing the activities of the different catalysts, it is suggested that the presence of small gold particles, as obtained by the SMAD technique, is not the main requisite for the achievement of the highest CO conversion. The strong interaction between ionic gold and ceria, by enhancing the ceria surface oxygen reducibility, may determine the particularly high activity.

摘要

通过溶剂化金属原子分散法(SMAD)、沉积沉淀法(DP)和共沉淀法(CP)制备了负载在氧化铈上的金催化剂,并通过X射线衍射(XRD)、程序升温还原(TPR)和X射线光电子能谱(XPS)对其进行了表征。在CO氧化反应中测试了催化活性。结构和表面分析表明,DP样品中存在改性氧化铈相,而SMAD和CP样品中存在纯氧化铈和金金属微晶。DP样品在393 K的空气中进行温和处理后,仅显示离子态金,并且在273 K以下非常活跃。通过比较不同催化剂的活性,表明通过SMAD技术获得的小金颗粒的存在不是实现最高CO转化率的主要必要条件。离子态金与氧化铈之间的强相互作用通过提高氧化铈表面氧的还原能力,可能决定了其特别高的活性。

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