氧化剂
催化作用
化学
氧化还原
水煤气变换反应
氧气
反应机理
沉积(地质)
无机化学
化学工程
有机化学
沉积物
生物
工程类
古生物学
作者
Lu‐Cun Wang,M. Tahvildar Khazaneh,Daniel Widmann,R. Jürgen Behm
标识
DOI:10.1016/j.jcat.2013.02.021
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 O2. 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.
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