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hal.structure.identifierUniversidad de Cantabria [Santander] = University of Cantabria [Spain] = Université de Cantabrie [Espagne] [UC / UniCan]
dc.contributor.authorSANZ-ORTIZ, Marta N.
hal.structure.identifierUniversidad de Cantabria [Santander] = University of Cantabria [Spain] = Université de Cantabrie [Espagne] [UC / UniCan]
dc.contributor.authorRODRÍGUEZ, Fernando
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDEMAZEAU, Gérard
dc.date.issued2008
dc.identifier.issn0895-7959
dc.description.abstractEnThis work investigates the electronic structure of CoF3 by optical absorption and its relationship with the ground-state spin and the Jahn-Teller (JT) effect exhibited by Co3+(d6) in octahedral coordination (CoF6)3-. The results are compared with other Co3+ fluorides and oxides, where Co3+ is high spin (HS) and low spin (LS), respectively. In CoF3 we detect an absorption band with a doublet structure at 1.89eV (657nm) and 1.45eV (855nm) at 2.5GPa, which is associated with the T e JT effect on the 5T2 HS ground state. Absorption measurements under pressure have been carried out around the HS-LS (5T2 1A1) spin crossover transition in the 0-20 GPa range. We show that the JT effect is stable in a wide pressure range. No sign of intermediate spin (3T1, 2 states) is observed in the explored pressure range.
dc.language.isoen
dc.publisherTaylor & Francis
dc.subject.enCobalt
dc.subject.enCoF3
dc.subject.enIntermediate spin
dc.subject.enJahn-Teller effect
dc.subject.enSpin crossover
dc.title.enSpin transition in Co3+ by optical absorption and time-resolved spectroscopy under pressure: An appraisal of the different spin states
dc.typeArticle de revue
dc.identifier.doi10.1080/08957950802552119
dc.subject.halChimie/Chimie inorganique
dc.subject.halChimie/Chimie théorique et/ou physique
bordeaux.journalHigh Pressure Research
bordeaux.page571-576
bordeaux.volume28
bordeaux.issue4
bordeaux.peerReviewedoui
hal.identifierhal-00352991
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00352991v1
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