Please use this identifier to cite or link to this item:
https://scholarhub.balamand.edu.lb/handle/uob/1961
Title: | EPR investigation of the nature of oxygen species present on the surface of gold impregnated cerium oxide | Authors: | Aboukaïs, Antoine Aouad, Samer Skaf, Mira Hany, Sara Labaki, Madona Cousin, Renaud Abi Aad, Edmond |
Affiliations: | Department of Chemistry | Keywords: | Electron paramagnetic resonance (EPR) Surface properties Oxides Adsorption |
Issue Date: | 2016 | Part of: | Journal of materials chemistry and physics | Volume: | 170 | Start page: | 285 | End page: | 293 | Abstract: | The electron paramagnetic resonance (EPR) spectroscopy was used to study the adsorption of air at room temperature on Au/CeO2 solids prepared by impregnating gold on cerium oxide. Two EPR signals, P and M, where then identified. The P signal having g//>g⊥, was mainly present on the EPR spectra recorded at room temperature and −196 °C for solids with low gold content (Au less than 1.25 wt.%). This signal was attributed to O2− species strongly attached to the CeO2 surface. The M signal with g⊥ > g// was only observed at −196 °C. Both P and M signals were obtained for solids with low gold content while M alone was present for solids with high gold content (2.5 wt.% and above). The M signal was also obtained even when air was adsorbed at −196 °C on the solids. 17O-enriched molecular oxygen adsorption allowed the identification of the M signal as being the result of O2− species. These species are weakly interacting with the surface of ceria containing Cl− ions probably present in CeOCl micro-phase. The O2− species responsible of the P signal are formed in solids containing gold nanoparticles and are efficient in the catalytic total oxidation of propylene. |
URI: | https://scholarhub.balamand.edu.lb/handle/uob/1961 | DOI: | 10.1016/j.matchemphys.2015.12.053 | Ezproxy URL: | Link to full text | Type: | Journal Article |
Appears in Collections: | Department of Chemistry |
Show full item record
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.