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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorMATAR, Samir F.
hal.structure.identifierFaculté des Sciences et de Génie Informatique
dc.contributor.authorAL ALAM, Adel F.
hal.structure.identifierFaculté des Sciences et de Génie Informatique
dc.contributor.authorOUAÏNI, Naïm
dc.date.issued2013
dc.identifier.issn0932-0776
dc.description.abstractEnFor equiatomic MgNi which can be hydrogenated up to the composition MgNiH1.6 at an absorption/desorption temperature of 200 °C, the effects of hydrogen absorption are approached with the model structures MgNiH, MgNiH2 and MgNiH3. From full geometry optimization and calculated cohesive energies obtained within DFT, the MgNiH2 composition close to the experimental limit is identified as most stable. Charge density analysis shows an increasingly covalent character of hydrogen: MgNiH (H−0.67) → MgNiH2 (H−0.63) → MgNiH3 (H−0.55). While Mg-Ni bonding prevails in MgNi and hydrogenated model phases, extra itinerant low-energy Ni states appear when hydrogen is introduced signaling Ni-H bonding which prevails over Mg-H as evidenced from total energy calculations and chemical bonding analyses.
dc.language.isoen
dc.publisherVerlag der Zeitschrift Fuer Naturforschung
dc.subject.enHydrogen
dc.subject.enEquiatomic MgNi
dc.subject.enIono-covalent character
dc.subject.enBader charge
dc.subject.enChemical bonding
dc.title.enHydrogen insertion effects on the electronic structure of equiatomic MgNi traced by ab initio calculations
dc.typeArticle de revue
dc.identifier.doi10.5560/ZNB.2013-2282
dc.subject.halChimie/Matériaux
bordeaux.journalZeitschrift fur Naturforschung B
bordeaux.page44-50
bordeaux.volume68
bordeaux.issue1
bordeaux.peerReviewedoui
hal.identifierhal-00776491
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00776491v1
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