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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorKIM, Seung-Joo
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDEMAZEAU, Gérard
hal.structure.identifierLomonosov Moscow State University [MSU]
dc.contributor.authorPRESNIAKOV, Igor A.
hal.structure.identifierInstituto de Ciencia de Materiales de Madrid [ICMM]
dc.contributor.authorALONSO, José A.
dc.date.issued2002
dc.identifier.issn0895-7959
dc.description.abstractEnAn evolution of local structure of Ni and chemical bonding, Ni(III)-O in perovskite lattice with strongly distorted structure is investigated with 57Fe Mössbauer spectroscopy. The Mössbauer spectra for 57Fe-doped TlNiO3 were resolved to two quadrupole doublets with different isomer shifts, which underlines a partial charge disproportionation phenomenon: 2Fe3+ -> Fe3+alpha +Fe3-alpha. This result supports the existence of two different crystallographic sites for Ni in the distorted perovskite lattice.
dc.language.isoen
dc.publisherTaylor & Francis
dc.subject.enTrivalent nickel
dc.subject.enPerovskite
dc.subject.enMössbauer spectroscopy
dc.subject.enCharge disproportionation
dc.title.enHigh oxygen pressures and the improvement of the Mn+ -- O chemical bond through the stabilization of the highest oxidation states (n+)
dc.typeArticle de revue
dc.identifier.doi10.1080/08957950212427
dc.subject.halChimie/Matériaux
dc.subject.halChimie/Chimie inorganique
bordeaux.journalHigh Pressure Research
bordeaux.page555-557
bordeaux.volume22
bordeaux.issue3-4
bordeaux.peerReviewedoui
hal.identifierhal-00715271
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00715271v1
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