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Improved CO Oxidation Activity of 3DOM Pr-Doped Ceria Catalysts: Something Other Than an Ordered Macroporous Structure

机译:改进的3DOM Pr掺杂二氧化铈催化剂的CO氧化活性:有序的大孔结构以外的东西

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摘要

It is demonstrated that the synthesis procedure for preparing three-dimensionally ordered macroporous (3DOM) Pr-doped ceria catalysts using a polymethylmethacrylate (PMMA) template not only affects the porous structure, but also the chemistry of the ceria surface. The PMMA template does not affect the crystalline features (type of phases, crystallite size, and cell parameter) of Pr-doped ceria, Ce and Pr location into the particles, and the bulk reduction of the Ce-Pr mixed oxide catalysts. On the contrary, the utilization of the PMMA template improves both the porosity and surface redox properties. 3DOM Ce-Pr mixed oxide catalysts combine micro, meso, and macropores, the most area being in the macropore range, while a reference unshaped catalyst presents poor porosity in all ranges. However, the catalyzed CO oxidation rates do not correlate with the surface area of the catalysts (neither micro nor meso/macro). The Ce-Pr-3DOM catalyst also presents improved surface reducibility with regards to the counterpart reference material prepared without the template, and improved redox behavior under reaction conditions; that is, it has a higher area and this area is reduced and reoxidized more easily. X-ray photoelectron spectroscopy analysis evidences that this is mainly attributed to praseodymium cations, which accomplish redox cycles more easily than cerium cations.
机译:结果表明,使用聚甲基丙烯酸甲酯(PMMA)模板制备三维有序大孔(3DOM)Pr掺杂二氧化铈催化剂的合成过程不仅影响多孔结构,而且影响二氧化铈表面的化学性质。 PMMA模板不影响掺Pr的二氧化铈的晶体特征(相类型,微晶尺寸和晶胞参数),Ce和Pr在颗粒中的位置以及Ce-Pr混合氧化物催化剂的体积减少。相反,利用PMMA模板可以改善孔隙率和表面氧化还原性能。 3DOM Ce-Pr混合氧化物催化剂结合了微孔,中孔和大孔,最大面积在大孔范围内,而参比不定形催化剂在所有范围内均具有较差的孔隙率。然而,催化的CO氧化速率与催化剂的表面积不相关(微或中/微)。 Ce-Pr-3DOM催化剂相对于没有模板制备的相应参考材料还具有改善的表面还原性,并在反应条件下具有改善的氧化还原性能。也就是说,它具有更大的面积,并且该面积更容易被还原和再氧化。 X射线光电子能谱分析表明,这主要归因于阳离子,,阳离子比铈阳离子更容易完成氧化还原循环。

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