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Morphology-controlled synthesis of cage-bell Pd@CeO2 structured nanoparticle aggregates as catalysts for the low-temperature oxidation of CO

机译:形态学控制的笼形钟形Pd @ CeO2结构纳米颗粒聚集体作为CO低温氧化的催化剂

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摘要

A facile generic strategy of combining template assisted and solvothermal alcoholysis is employed to prepare cage-bell Pd@CeO2 nanoparticle aggregates as catalysts for the low-temperature oxidation of CO. The synthetic parameters are regulated to control the size of the as-prepared CeO2 mesospheres. The activities of Pd@CeO2 catalysts are higher than that of Pd supported on Al2O3, and the activity of 1 wt% Pd@CeO2 can be further improved and its T_(90) is 2 °C. The intrinsic cage-bell nature as well as high porosity of the unique nanostructures of the CeO2 support contributes greatly to the formation of large numbers of surface oxygen vacancies on Pd@CeO2 catalysts, and thus it exhibits superior catalytic activity. This method is simple, low cost, mass-productive, and can also be used to prepare other advanced functional materials.
机译:结合模板辅助和溶剂热醇解的简便通用策略,制备了笼形的钟形Pd @ CeO2纳米粒子聚集体,作为CO低温氧化的催化剂。调节合成参数以控制制备的CeO2中层微球的大小。 Pd @ CeO2催化剂的活性高于负载在Al2O3上的Pd,可以进一步提高1 wt%Pd @ CeO2的活性,其T_(90)为2°C。 CeO2载体独特的纳米结构的固有的笼钟性质以及高孔隙度极大地促进了Pd @ CeO2催化剂上大量表面氧空位的形成,因此具有优越的催化活性。该方法简单,成本低,可大量生产,也可用于制备其他高级功能材料。

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