Abstract
The activation of CO2 on ceria-based catalysts opens chemical routes to the use of CO2 as an oxidizing agent. Toward a better understanding of the underlying surface reactions, we have performed a model study on well-defined CeO2-x thin films on Cu(1 1 1) under ultra-high-vacuum conditions.
Resonant photoelectron spectroscopy is used as a highly sensitive tool to monitor changes in the oxidation state of cerium as a function of CO2 exposure and thermal treatment. It is shown that partial reoxidation of CeO2-x by CO2 occurs with high reaction probabilities (i) even at temperatures as low as room temperature, (ii) on pure CeO2-x in the complete absence of any noble metal co-catalysts, and (iii) in the absence of surface hydroxyl groups or water.
In contrast to previous studies on ceria powders, the findings clearly demonstrate the high activity of pure hydroxyl- and metal-free ceria surfaces for CO2 activation, even at low reaction temperatures.