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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorMATAR, Samir F.
dc.date.issued2017
dc.identifier.issn2352-2143
dc.description.abstractEnIn the context of the need to recycle depleted uranium coming from nuclear waste, hydrogen absorption in uranium and mainly its alloys is an important solution. We here consider hydrogen insertion in UZr2 intermetallic leading to experimentally observed composition UZr2H6. Drastic changes are shown from density functional calculations to induce atom reordering within the metal substructures in the ground state. Particularly among different starting hypotheses for H sites, energy minimization is observed when the hydrogenated intermetallic undergoes metal substructures reordering with unmixed occupancy of Al (U) and B (Zr) sites in AlB2 type structure. Hydrogen is identified as covalently bonded within the plane of Zr metal, illustrated by anionic charged H−0.55 derived from Bader analysis of charge density. Hydrogen uptake leads to prevailing volume expansion effects versus chemical bonding ones, involving strong localization of uranium 5f states and increased magnetization versus the pristine intermetallic. Both the intermetallic and the ternary hydride are found ferromagnetic in the ground state.
dc.language.isoen
dc.publisherElsevier
dc.subject.enUranium intermetallics
dc.subject.enHydrides
dc.subject.enMagnetism
dc.subject.enDFT
dc.subject.enAIM
dc.subject.enASW
dc.subject.enPAW-GGA
dc.title.enFirst principles studies of hydrogen insertion effects on magnetic properties, bonding and structure reordering of UZr 2
dc.typeArticle de revue
dc.identifier.doi10.1016/j.cocom.2017.08.001
dc.subject.halChimie/Matériaux
bordeaux.journalComputational Condensed Matter
bordeaux.page19-24
bordeaux.volume12
bordeaux.peerReviewedoui
hal.identifierhal-01583743
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01583743v1
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