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|Title:||Physicochemical characterization of Au/CeO2 solids. Part 2: the impregnation preparation method||Authors:||Aboukaïs, Antoine
Ayadi, Houda El
Abi Aad, Edmond
|Affiliations:||Department of Chemistry||Keywords:||Adsorption
|Issue Date:||2012||Part of:||Materials chemistry and physics||Volume:||137||Issue:||1||Start page:||42||End page:||47||Abstract:||
Au/CeO2 solids with different gold contents were prepared using the impregnation method. Electron microscopy (SEM and TEM) studies indicated the formation of both nanoparticles and large gold particles on the surface of the ceria support. SEM and XRD analyses revealed that the number and size of large particles increases with the gold content in the solid. The XPS technique showed that 90% of the total gold is in the metallic form Au0 while the remaining 10% were cationic gold species Au+. These latter were formed following calcination under dry air at 400 °C and are located in the proximity of the O2− and/or Cl− present on the support. These Au+ species are present at the edge of gold particles and they were reduced into metallic gold when the solid was vacuum treated (5–7.10−4 mbar) at 400 °C for 1 h. When air was adsorbed at room temperature on the latter vacuum treated solids, two EPR signals were obtained. The first one was assigned to O2− species whereas attributing the second signal was difficult and required a more detailed investigation that will be presented in a forthcoming work. Highlights ► Au/CeO2 solids prepared by the impregnation method present Au particles ranging from 5 nm up to 600 nm. ► The adsorption of air on Au/CeO2 to the formation of two different species. ► The adsorption of air at room temperature leads to the formation of O2−. ► The adsorption of air at room temperature leads to another species which is not obtained when pure oxygen is adsorbed. ► The Au/CeO2 solid is a potential candidate for DeNOx at room temperature.
|URI:||https://scholarhub.balamand.edu.lb/handle/uob/2397||DOI:||10.1016/j.matchemphys.2012.08.074||Ezproxy URL:||Link to full text||Type:||Journal Article|
|Appears in Collections:||Department of Chemistry|
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