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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
hal.structure.identifierInstitut für Allgemeine, Anorganische und Theoretische Chemie
dc.contributor.authorHUPPERTZ, Hubert
dc.date.issued2012
dc.identifier.issn0966-9795
dc.description.abstractEnThe stannides LaPdSn (orthorhombic TiNiSi type, Pnma) and ErAgSn (hexagonal NdPtSb type, P63mc) both transform to ZrNiAl type (P--62m) high-pressure phases with different transition metal-tin ordering. The electronic structure and the chemical bonding of all four modifications have been studied by quantum theoretical DFT methodologies. Geometry optimizations are in good agreement with the experimentally determined structures. Strongest bonding interactions were observed for Pd-Sn (LaPdSn) and Er-Sn (ErAgSn). These findings result from different site occupancies and the chemical natures and electronegativities of the interacting species forming the prevailing chemical bonds in the NP/HP varieties of the two compounds.
dc.language.isoen
dc.publisherElsevier
dc.subject.enRare earth intermetallics
dc.subject.enElectronic structure of metals and alloys
dc.subject.enAb initio calculations
dc.subject.enElectronic structure
dc.subject.encalculations
dc.title.enDimorphic LaPdSn and ErAgSn - A first principles study
dc.typeArticle de revue
dc.identifier.doi10.1016/j.intermet.2011.08.018
dc.subject.halChimie/Matériaux
bordeaux.journalIntermetallics
bordeaux.page33-38
bordeaux.volume20
bordeaux.issue1
bordeaux.peerReviewedoui
hal.identifierhal-00649657
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00649657v1
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