Low-temperature CO oxidation over supported Pt, Pd catalysts: Particular role of FeOx support for oxygen supply during reactions

被引:291
|
作者
Liu, Lequan [1 ,2 ]
Zhou, Feng [1 ]
Wang, Liguo [1 ]
Qi, Xiujuan [1 ]
Shi, Feng [1 ]
Deng, Youquan [1 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, Ctr Green Chem & Catalysis, Lanzhou 730000, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
关键词
CO oxidation; Pt catalyst; Pd catalyst; Kinetic measurements; Strong metal-support interaction (SMSI) effect; Oxygen vacancy; H-2-O-2; titration; Time-resolved CO titration; PD-RH/CEO2-AL2O3 3-WAY CATALYST; CARBON-MONOXIDE; OXIDE CATALYSTS; METAL-CATALYSTS; SURFACE-AREA; GOLD; PLATINUM; MECHANISM; HYDROGEN; PT/GAMMA-AL2O3;
D O I
10.1016/j.jcat.2010.05.022
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of FeOx- and Al2O3-supported Pt, Pd catalysts (0.23-2.1%) were prepared in this study. Pt/FeOx exhibited high CO oxidation activity with turnover frequency of 151 x 10(-3) s(-1) (1% CO balanced with air, atmospheric pressure, 27 degrees C). A systematical study of FeOx- and Al2O3-supported Pt, Pd catalysts by means of X-ray photoelectron spectroscopy, X-ray diffraction, high-resolution transmission electron microscopy, temperature-programmed reduction, H-2-O-2 titration, and time-resolved CO titration is reported. From 7% to 39% of Fe3+ was reduced to Fe2+ over Fe(OH)(x)-supported Pd and Pt catalysts, accompanied by Pd, Pt hydrogenation and hydroxyl loss, and a large amount of oxygen vacancies were proposed to be produced. Results of H-2-O-2 titration and time-resolved CO titration showed that a large amount of oxygen adsorbed onto FeOx support in the presence of Pt, Pd. This made CO oxidations over Pt/FeOx, Pd/FeOx proceed over two adjacent but different active sites (Pt, Pd for CO and FeOx for oxygen) with low apparent activation energies (30-34 kJ/mol), which accounted for their high activity in low-temperature CO oxidation. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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