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hal.structure.identifierDepartment of Science and Engineering of Oxide Materials and Nanomaterials
dc.contributor.authorSTAN, Cristina
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.identifierNational Institute of Advanced Industrial Science and Technology [AIST]
dc.contributor.authorAKIBA, Etsuo
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorCOUILLAUD, Samuel
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorBOBET, Jean-Louis
dc.date.issued2009
dc.identifier.issn0360-3199
dc.description.abstractEnThe hydrogenation behaviour of the Gd<sub>0.5</sub>Y<sub>0.5</sub>Ni<sub>3.75</sub>Al<sub>0.25</sub>Mg compound was studied by in situ X-ray diffraction under hydrogen pressure and at room temperature. The presence of gadolinium induce an exchange between the 4a (occupied by RE) and 4c sites (occupied by Mg). Nevertheless, only the Gd atoms are mixed by Mg atoms and no occurrence of Y/Mg mixing can be observed. The exchange is then directly correlated with the 4f electrons. Moreover, in the compounds without Gd (i.e. YNi<sub>3.75</sub>Al<sub>0.25</sub>Mg) no exchange was observed. The structure of the metal hydrides was carefully investigated by refining the in situ XRD patterns obtained under various H<sub>2</sub> pressures. It was concluded that the structure remains cubic during the sorption process with an increase of the cell volume close to 13%, in agreement with the maximum sorption capacity (i.e. 3H/formula unit). No variation of the exchange rate between the hydride and the initial intermetallic can be highlighted. The changes of both the crystallite size and lattice strains during the sorption process (i.e. along the PC isotherms) indicated that a decrease of the crystallinity is observed but no HIA process occurred.
dc.language.isoen
dc.publisherElsevier
dc.subject.enHydrogen sorption
dc.subject.enIn situ XRD
dc.subject.enLaves phases
dc.title.enIn situ XRD for pseudo Laves phases hydrides highlighting the remained cubic structure
dc.typeArticle de revue
dc.identifier.doi10.1016/j.ijhydene.2009.02.012
dc.subject.halChimie/Matériaux
bordeaux.journalInternational Journal of Hydrogen Energy
bordeaux.page3038-3043
bordeaux.volume34
bordeaux.issue7
bordeaux.peerReviewedoui
hal.identifierhal-00378358
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00378358v1
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=International%20Journal%20of%20Hydrogen%20Energy&amp;rft.date=2009&amp;rft.volume=34&amp;rft.issue=7&amp;rft.spage=3038-3043&amp;rft.epage=3038-3043&amp;rft.eissn=0360-3199&amp;rft.issn=0360-3199&amp;rft.au=STAN,%20Cristina&amp;ASANO,%20Kohta&amp;SAKAKI,%20Kouji&amp;AKIBA,%20Etsuo&amp;COUILLAUD,%20Samuel&amp;rft.genre=article


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