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A facile synthesis of Ag@PdAg core-shell architecture for efficient purification of ethene feedstock

机译:AG @ PDAG核心壳架构的容易合成,用于高效纯化乙烯原料

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Precise control of elemental configurations within multimetallic nanoparticles could enable access to functional nanomaterials with significant performance benefits. Here, we present a one-pot synthesis of supported Ag@PdAg core-shell catalyst with an ordered PdAg alloy shell and an Ag core. Both the relative reduction potential and ratio of metal precursors are essential for this synthesis strategy. The distinguished properties of Ag@PdAg, particularly the electronic structure, indicates the existence of electron modification not only between Pd and Ag on PdAg shell, but between Ag core and alloy shell. The Ag@PdAg catalyst displays 97% ethene yield in the partial hydrogenation of acetylene, which is 2.0 and 8.1 times that of over PdAg alloy and pure Pd catalysts, and this is the most selective catalyst reported to data under industrial evaluation conditions. Moreover, this core-shell structure exhibits preferable stability with comparison to PdAg alloy catalyst. The facile synthesis of core-shell architecture with alloy shell structure provides a new platform for efficient catalytic transfer of chemical resource. (C) 2018 Elsevier Inc. All rights reserved.
机译:多金属纳米颗粒内的元素配置的精确控制可以通过具有显着性能效益的功能纳米材料进行进入。在这里,我们介绍了具有有序的PDAG合金壳和Ag核心的支持的AG @ PDAG核心 - 壳催化剂的单罐合成。金属前体的相对降低电位和比例均对于该合成策略至关重要。 AG @ PDAG,特别是电子结构的可分辨率表明,不仅在PDAG壳上的Pd和Ag之间存在电子改性,而是在Ag核心和合金壳之间。 AG @ PDAG催化剂在乙炔的部分氢化中显示97%乙烯产率,其为PDAG合金和纯Pd催化剂的2.0%和8.1倍,这是在工业评估条件下报告的最多选择性催化剂。此外,与PDAG合金催化剂相比,该芯壳结构表现出优选的稳定性。具有合金壳结构的核心壳结构的容易合成为化学资源有效催化转移提供了一种新的平台。 (c)2018年Elsevier Inc.保留所有权利。

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