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Thermally stable and highly active Pt/CeO2@SiO2 catalysts with a porous/hollow structure

机译:热稳定、高活性Pt / CeO2@SiO2用多孔催化剂/空心结构

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摘要

The encapsulation of noble metal nanoparticles (NPs) into SiO2 has been widely demonstrated to be a good strategy to prevent NPs from sintering at high temperature. However, in most cases, the protective dense, thick SiO2 shell may retard the diffusion of reactant and product molecules, thus inhibiting the catalytic activity. And the size of encapsulated noble metal NPs is always big (1 nm). Most importantly, their integration with active metal oxides (e.g. CeO2) and the creation of porous/hollow structure surrounded by SiO2 are still rarely reported at present. Herein, we propose an efficient way to acquire thermally stable and highly active Pt/CeO2@SiO2 catalysts with a porous/hollow structure. The synthetic procedure starts with co-encapsulation of Pt NPs and Ce-Cu bimetal oxide into SiO2 using a microemulsion method, followed by selective etching of CuO with dilute acid. Thanks to the ultra-small size of Pt NPs (1 nm), the synergistic effect between Pt and CeO2, the beneficial porous/hollow structure for reactant and product molecule diffusion, and the effective protection by the SiO2 shell, the catalyst exhibits high catalytic activity and remarkable durability toward CO oxidation.
机译:贵金属纳米粒子的封装(NPs)二氧化硅已被广泛证实是一个很好的策略,防止NPs烧结在高温度。保护密集,厚二氧化硅壳可能延迟反应物和产物分子的扩散,因此催化活性的抑制能力。封装的贵金属NPs总是大(在1海里)。与活性金属氧化物(如CeO2)建立多孔/空心结构包围二氧化硅目前还很少报道。在此,我们提出一个有效的方式获取热稳定、高活性Pt / CeO2@SiO2用多孔催化剂/空心结构。合成过程始于co-encapsulationPt NPs和Ce-Cu双金属氧化物为二氧化矽微乳液法,其次是有选择性的措和稀酸的腐蚀。超小尺寸的Pt NPs (& 1海里),Pt, CeO2之间的协同效应有益的多孔为反应物/空心结构和产品的分子扩散,有效二氧化硅壳保护的催化剂表现出较高的催化活性和显著耐久性对CO氧化。

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