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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorCHEVALIER, Bernard
hal.structure.identifierInstitut für Anorganische Chemie
dc.contributor.authorSEBASTIAN, C. P.
hal.structure.identifierInstitut für Anorganische Chemie
dc.contributor.authorPÖTTGEN, Rainer
dc.date.created2006
dc.date.issued2006
dc.identifier.issn1293-2558
dc.description.abstractEnCeRhSn and CeIrSn were synthesized from the elements via arc-melting. A single crystal from the CeIrSn sample was investigated on the basis of X-ray diffractometer data: ZrNiAl type, P2m, a=743.8(2), c=407.58(7) pm, wR2=0.0308, 352 F2 values and 14 variable parameters. An important structural feature of CeIrSn are relatively short Cesingle bondIr distances (4×303 and 1×308 pm). Hydrogenation of these ternary stannides leads to the formation of the new hydrides CeRhSnH0.8 and CeIrSnH0.7 which adopt the same crystal symmetry as the original compounds but a larger unit cell volume after hydrogen insertion. Magnetization, electrical resistivity and thermoelectric power measurements reveal a change of the ground state of the cerium from intermediate valence to the nearly trivalent state induced by hydrogenation. Moreover, 119Sn Mössbauer spectroscopic data of CeRhSn, CeIrSn and their hydrides at 4.2 and 78 K indicate only one tin site. The isomer shifts are slightly larger for the hydrogenated samples suggesting a slightly higher s electron density at the tin nuclei of the hydrides.
dc.language.isoen
dc.publisherElsevier
dc.subject.enCerium
dc.subject.enHydrogenation
dc.subject.enCrystal structure
dc.subject.enMagnetism
dc.title.enHydrogenation of the intermediate valence ternary stannides CeRhSn and CeIrSn
dc.typeArticle de revue
dc.identifier.doi10.1016/j.solidstatesciences.2006.02.047
dc.subject.halChimie/Matériaux
bordeaux.journalSolid State Sciences
bordeaux.page1000-1008
bordeaux.volume8
bordeaux.issue8
bordeaux.peerReviewedoui
hal.identifierhal-00112519
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00112519v1
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