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hal.structure.identifierInstitut für Anorganische und Analytische Chemie
dc.contributor.authorHERMES, Wilfried
hal.structure.identifierInstitut für Anorganische und Analytische Chemie
dc.contributor.authorRODEWALD, Ute Ch.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorCHEVALIER, Bernard
hal.structure.identifierInstitut für Anorganische und Analytische Chemie
dc.contributor.authorPÖTTGEN, Rainer
dc.date.issued2007
dc.identifier.issn1293-2558
dc.description.abstractEnCePtIn was synthesized from the elements via arc-melting and hydrogenated at 523 K and 4 MPa of hydrogen pressure leading to the hydride CePtInH0.7. The metal positions of both indides were refined from single crystal X-ray diffractometer data: ZrNiAl type, P̄62m, a = 765.3(2), c = 406.8(1) pm, wR2 = 0.0546, 276 F2 values and 14 variables for CePtIn and a = 770.6(1), c = 409.7(1) pm, wR2 = 0.0491, 354 F2 values and 14 variables for CePtInH0.7. Hydrogenation leads to an isotropic increase of the unit cell through filling of tetrahedral Ce3Pt sites. CePtInH0.7 decomposes under ambient condition within some weeks leaving the parent CePtIn structure. Magnetization measurements performed on the hydride reveal a trivalent state for the cerium but no magnetic ordering occurs above 2 K.
dc.language.isoen
dc.publisherElsevier
dc.subject.enCerium
dc.subject.enCrystal structure
dc.subject.enHydrogenation
dc.subject.enMagnetism
dc.title.enHydrogenation of the Kondo compound CePtIn
dc.typeArticle de revue
dc.identifier.doi10.1016/j.solidstatesciences.2007.06.015
dc.subject.halChimie/Matériaux
bordeaux.journalSolid State Sciences
bordeaux.page874-879
bordeaux.volume9
bordeaux.issue9
bordeaux.peerReviewedoui
hal.identifierhal-00181317
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00181317v1
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