Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/1803
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dc.contributor.authorHany, Saraen_US
dc.contributor.authorSkaf, Miraen_US
dc.contributor.authorAouad, Sameren_US
dc.contributor.authorGennequin, Cédricen_US
dc.contributor.authorLabaki, Madonaen_US
dc.contributor.authorAbi Aad, Edmonden_US
dc.contributor.authorAbouKais, Antoineen_US
dc.date.accessioned2020-12-23T09:00:13Z-
dc.date.available2020-12-23T09:00:13Z-
dc.date.issued2018-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/1803-
dc.description.abstractThree different types of Ag2+ ions ("a", "b", and "c") have been identified and examined by electron paramagnetic resonance (EPR) on 10% wt Ag/CeO2 prepared by impregnation method. One of them, Ag2+(b), behaves differently than the two others, Ag2+(a) and Ag2+(c), under redox atmospheres. The fact that, in reducing conditions (vacuum, propylene, hydrogen, and carbon black), Ag2+(a) and Ag2+(c) species were more easily reduced than Ag2+(b) ones, could not explain the catalytic performance and stability of this latter species compared to the first ones in the reaction of total oxidation of propylene. The EPR technique evidenced that Ag2+(b) species form, upon propene oxidation, a cluster. This cluster is composed of two parallel electron spins (dimer) and three nuclear spins (trimer). It seems that before propylene oxidation, Ag2+(b) clusters were ferromagnetic. This ferromagnetic character of Ag2+(b) species may explain their better catalytic performance, in propylene oxidation, than those of Ag2+(a) and Ag2+(c) ones.en_US
dc.language.isoengen_US
dc.subjectEPRen_US
dc.subjectRedox propertiesen_US
dc.subjectAg2+speciesen_US
dc.subjectDimeren_US
dc.subjectTrimeren_US
dc.subjectCatalytic activityen_US
dc.titleCorrelation between the size and the magnetic properties of Ag2+ clusters loaded on ceria surface and their catalytic performance in the total oxidation of propylene. EPR studyen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.chemphys.2018.01.001-
dc.contributor.affiliationDepartment of Chemistryen_US
dc.description.volume502en_US
dc.description.startpage1en_US
dc.description.endpage5en_US
dc.date.catalogued2019-09-19-
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=https://doi.org/10.1016/j.chemphys.2018.01.001en_US
dc.identifier.OlibID207728-
dc.relation.ispartoftextJournal of chemical physicsen_US
dc.provenance.recordsourceOliben_US
crisitem.author.parentorgFaculty of Arts and Sciences-
Appears in Collections:Department of Chemistry
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