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hal.structure.identifierDepartment of Science and Engineering of Oxide Materials and Nanomaterials
dc.contributor.authorSTAN, Cristina
hal.structure.identifierDepartment of Science and Engineering of Oxide Materials and Nanomaterials
dc.contributor.authorANDRONESCU, Ecaterina
hal.structure.identifierNational Institute of Advanced Industrial Science and Technology [AIST]
dc.contributor.authorASANO, Kohta
hal.structure.identifierNational Institute of Advanced Industrial Science and Technology [AIST]
dc.contributor.authorSAKAKI, Kouji
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorBOBET, Jean-Louis
dc.date.issued2008
dc.identifier.issn0360-3199
dc.description.abstractEnThe hydrogenation and dehydrogenation behaviours of the YNi3.5Al0.5Mg compound were studied by in situ X-ray diffraction under hydrogen pressure and at room temperature. The changes of (i) the lattice parameters, (ii) the crystallite size and (iii) the lattice strain during the sorption process (i.e. along the PC isotherms) were studied. These results indicate that the crystallite size decreases by a factor of 2. The micro deformations increase at first and then tend to almost zero at the end of the sorption cycle. This behaviour is explained in terms of co-existence of the metal (i.e. greek small letter alpha phase) and metal hydride (i.e. β phase) phases. The change in crystallinity is consistent with the hydrogen induced amorphisation process existing in a lot of AB2 compounds. No anisotropic effects can be highlighted on this pseudo-AB2 compounds in contrary with what could be observed in AB5 compounds.
dc.language.isoen
dc.publisherElsevier
dc.title.enIn situ X-ray diffraction under H2 of the pseudo-AB2 compounds: YNi3.5Al0.5Mg
dc.typeArticle de revue
dc.identifier.doi10.1016/j.ijhydene.2008.02.009
dc.subject.halChimie/Matériaux
bordeaux.journalInternational Journal of Hydrogen Energy
bordeaux.page2053-2058
bordeaux.volume33
bordeaux.issue8
bordeaux.peerReviewedoui
hal.identifierhal-00281311
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00281311v1
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