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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorMATAR, Samir F.
hal.structure.identifierInstitut für Anorganische und Analytische Chemie
dc.contributor.authorPÖTTGEN, Rainer
dc.date.issued2015
dc.identifier.issn1293-2558
dc.description.abstractEnThe electronic and magnetic structures and the properties of chemical bonding in isopointal CeMgSn and CePdSn (both phases belong to the family of TiNiSi related intermetallics, space group Pnma) and CeMgPb belonging to the family of CeScSi intermetallics, space group I4/mmm, have been investigated within the density functional theory (DFT). The charge analyses indicate negatively charged tin and lead leading to assign the compounds as stannides and plumbides, as also illustrated by the mapping of the electron localization function ELF. Calculations within spin-degenerate non-magnetic spin-polarized ferro- (SP-F) and SP-antiferromagnetic configurations led to assign a major role of Ce 4f states in the onset of ordered moments within SP-AF ground states from energy differences. Chemical bonding analyses from crystal orbital overlap populations revealed the strongest interactions for Ce–Sn in CeMgSn, Ce–Pb in CeMgPb, and Ce–Pd in CePdSn.
dc.language.isoen
dc.publisherElsevier
dc.subject.enStannides
dc.subject.enPlumbides
dc.subject.enCerium intermetallics
dc.subject.enChemical bonding
dc.title.enChemical bonding in equiatomic cerium intermetallics – The case of CeMgSn, CePdSn, and CeMgPb
dc.typeArticle de revue
dc.identifier.doi10.1016/j.solidstatesciences.2015.07.008
dc.subject.halChimie/Matériaux
bordeaux.journalSolid State Sciences
bordeaux.page205-211
bordeaux.volume48
bordeaux.peerReviewedoui
hal.identifierhal-01218872
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01218872v1
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