催化作用
X射线光电子能谱
掺杂剂
微晶
铈
氧化态
无机化学
吸附
金属
共沉淀
材料科学
拉曼光谱
打赌理论
化学
化学工程
兴奋剂
物理化学
冶金
有机化学
工程类
物理
光学
光电子学
作者
Putla Sudarsanam,Baithy Mallesham,Padigapati S. Reddy,Dennis Großmann,Wolfgang Grünert,Benjaram M. Reddy
标识
DOI:10.1016/j.apcatb.2013.08.035
摘要
The present investigation was undertaken to know the influence of different dopants on the physicochemical properties and catalytic behavior of nano-Au/CeO2 catalyst for CO oxidation. Accordingly, various metal ions namely, Fe3+, La3+ and Zr4+ were incorporated into the ceria lattice by a facile coprecipitation approach using ultra-high dilute aqueous solutions. An anion adsorption method was used to prepare the Au/doped-CeO2 catalysts in the absence of any base, reducing and protective agents. The physicochemical characterization was performed by XRD, BET surface area, ICP-AES, TG-DTA, FT-IR, TEM, UV–vis DRS, Raman, XPS and TPD techniques. Doped CeO2 exhibited smaller crystallite size, higher BET surface area and larger amount of oxygen vacancies than the pure CeO2. These remarkable properties showed a beneficial effect toward gold particle size as confirmed by XRD and TEM studies. XPS results revealed that Au is present in the metallic state and Ce in both +3 and +4 oxidation states. Incorporation of Zr into the Au/CeO2 resulted in high CO oxidation activity attributed to the presence of more Ce3+ ions and oxygen vacancies. In contrast, the La-incorporation caused an opposite effect due to the presence of carbonate species on the surface of Au/CeO2–La2O3 catalyst, which blocked the active sites essential for CO oxidation. It was shown that accumulation of carbonate species strongly depends on the acid–base properties of the supports. The catalytic performance of Au catalysts is highly dependent on the nature of the support.
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