Gold-Iron Oxide Catalyst for CO Oxidation: Effect of Support Structure

Gold-Iron Oxide Catalyst for CO Oxidation: Effect of Support Structure
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金铁氧化物催化剂用于 CO 氧化:支撑结构的影响

DOI:
10.3390/catal6030037
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发表时间:
2016-03-01
期刊:
影响因子:
3.9
通讯作者:
Si, Rui
Si, Rui
中科院分区:
化学3区
文献类型:
--
作者:
Cui, Hui-Zhen;Guo, Yu;Si, Rui

文献摘要

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相似文献

金-铁氧化物(Au/FeOx)是一种高活性的CO氧化催化剂,也是研究金催化化学的典型体系。在这项工作中,两种不同类型的氧化铁载体,即,羟基化氧化铁(Fe_OH)和脱水氧化铁(Fe_O)已被用于通过沉积-沉淀(DP)法沉积金。通过选择沉淀pH值为6.7-11.2(Fe_OH)或改变煅烧温度为200 - 600 °C(Fe_O)来调节氧化铁的结构。然后,lwt. %的Au催化剂在这些氧化铁载体上的低温CO氧化反应进行了测量。新鲜样品和使用过的样品都通过多种技术进行了表征,包括透射电子显微镜(TEM)和高分辨率TEM(HRTEM),X射线衍射(XRD),X射线光电子能谱(XPS),X射线吸收近边结构(XANES)和氢气程序升温还原(H2-TPR)。研究表明,铁氧化物载体的表面性质以及金属-载体间的相互作用对Au/FeOx催化剂的CO氧化性能起着至关重要的作用。
Gold-iron oxide (Au/FeOx) is one of the highly active catalysts for CO oxidation, and is also a typical system for the study of the chemistry of gold catalysis. In this work, two different types of iron oxide supports, i.e., hydroxylated (Fe_OH) and dehydrated iron oxide (Fe_O), have been used for the deposition of gold via a deposition-precipitation (DP) method. The structure of iron oxide has been tuned by either selecting precipitated pH of 6.7–11.2 for Fe_OH or changing calcination temperature of from 200 to 600 °C for Fe_O. Then, 1 wt. % Au catalysts on these iron oxide supports were measured for low-temperature CO oxidation reaction. Both fresh and used samples have been characterized by multiple techniques including transmission electron microscopy (TEM) and high-resolution TEM (HRTEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), X-ray absorption near edge structure (XANES) and temperature-programmed reduction by hydrogen (H2-TPR). It has been demonstrated that the surface properties of the iron oxide support, as well as the metal-support interaction, plays crucial roles on the performance of Au/FeOx catalysts in CO oxidation.