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hal.structure.identifierFaculty of Materials Science
dc.contributor.authorMEZHUEV, E.M.
hal.structure.identifierDepartment of Chemistry
dc.contributor.authorAFANASOV, Mikhail I.
hal.structure.identifierFaculty of Materials Science
dc.contributor.authorLARIONOV, D.S.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorWATTIAUX, Alain
hal.structure.identifierPlateforme Aquitaine de Caractérisation des Matériaux [PLACAMAT]
dc.contributor.authorLABRUGÈRE, Christine
hal.structure.identifierDepartment of Chemistry
dc.contributor.authorFABRITCHNYI, Pavel B.
dc.date.issued2017-10
dc.identifier.issn0036-0236
dc.description.abstractEnThe influence of Ca2+ doped into the holmium sublattice on the magnetically active surrounding of Sn4+ ions located in the chromium sublattice of Ho1–xCaxCr0.997Sn0.003O3 (x = 0, 0.003, and 0.1) compounds was studied by 119Sn Mössbauer spectroscopy. At concentrations [Ca] = [Sn] = 0.3 mol %, an increase was observed in the spectral contribution of Sn4+ sites, having the full number of nearest-neighbor Cr3+cations (n = 6), where they perceived a magnetic field H(Sn)4.2 K = 82 kOe, compared to the contribution of the relevant sites in the undoped chromite (x = 0). This observation was interpreted as resulting from a reduced probability of appearance of Cr3+ vacancies in the nearest surrounding of heterovalent Sn4+ ions. For x = 0.1, on the contrary, the 119Sn spectrum revealed a reduced contribution from the Sn4+ sites with n = 6. This evolution is shown not to be due neither to the appearance of Cr4+ nor Cr6+ ions in the nearest neighborhood of Sn4+ in the chromium sublattice to balance the charge deficiency of the Ca2+ ions doped into the holmium sublattice. This allowed us to suggest that the observed effect was due to the onset of Sn4+ segregations in the structure of Ho0.9Ca0.1Cr0.997Sn0.003O3, which contained a far greater amount of Ca2+ ions whose charge deficiency was balanced mostly by Cr4+ formation. Studies of samples that were prepared under a hydrogen atmosphere revealed the reduction of Sn4+ to the oxidation state +2, with the concomitant stabilization of the formed Sn2+ ions on crystallite surfaces on sites having low coordination numbers.
dc.language.isoen
dc.publisherMAIK Nauka/Interperiodica
dc.title.enElectronic state and local surrounding of 119Sn in calcium-substituted holmium orthochromites
dc.typeArticle de revue
dc.identifier.doi10.1134/S0036023617100126
dc.subject.halChimie/Matériaux
bordeaux.journalRussian Journal of Inorganic Chemistry / Zhurnal Neorganicheskoi Khimii
bordeaux.page1384-1389
bordeaux.volume62
bordeaux.issue10
bordeaux.peerReviewedoui
hal.identifierhal-01676296
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01676296v1
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