TAP reactor studies of the oxidizing capability of CO2 on a Au/CeO2 catalyst - A first step toward identifying a redox mechanism in the Reverse Water-Gas Shift reaction

被引:100
作者
Wang, L. C. [1 ]
Khazaneh, M. Tahvildar [1 ]
Widmann, D. [1 ]
Behm, R. J. [1 ]
机构
[1] Univ Ulm, Inst Surface Chem & Catalysis, D-89069 Ulm, Germany
关键词
Reverse Water-Gas Shift (RWGS) reaction; Oxygen storage capacity (OSC); CO oxidation; CO2; reduction; Au/CeO2; catalyst; Temporal analysis of products (TAP); IN-SITU DRIFTS; PT/CEO2; CATALYST; OXYGEN-STORAGE; INFRARED-SPECTROSCOPY; ACTIVE OXYGEN; STEADY-STATE; OXIDATION; CERIA; AU/TIO2; CEO2;
D O I
10.1016/j.jcat.2013.02.021
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
As a first step toward elucidating the mechanism of the Reverse Water-Gas Shift (RWGS) reaction on a supported Au/CeO2 catalyst, in particular the role of the redox mechanism, we have investigated the ability and activity of CO2 for re-oxidizing a pre-reduced Au/CeO2 catalyst surface by quantitative temporal analysis of products (TAP) measurements. It is demonstrated that a surface-reduced Au/CeO2 catalyst can be (partially) re-oxidized by exposure to CO2 pulses and that the surface oxygen deposited this way can be reactively removed again. The probability for oxygen deposition from CO2, however, is significantly lower than that from O-2. Both the low reaction probability and the temperature dependence of oxygen deposition from CO2 point to an activated step. Implications of these results for the mechanism of the RWGS reaction are discussed. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:20 / 30
页数:11
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