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dc.contributor.authorJimenez-Mier, J.-
dc.contributor.authorOlalde-Velasco, P.-
dc.contributor.authorDe. La. Mora, P.-
dc.contributor.authorYang, W. -L.-
dc.contributor.authorDenlinger, J.-
dc.date.accessioned2022-04-07T05:44:32Z-
dc.date.available2022-04-07T05:44:32Z-
dc.date.issued2017-08-07-
dc.identifier.issn2321-8649-
dc.identifier.issn2321-9289-
dc.identifier.urihttp://dspace.chitkarauniversity.edu.in/xmlui/handle/123456789/337-
dc.description.abstractResonant inelastic x-ray scattering (RIXS) is used to study the electronic structure of NiF2, which is the most ionic of the nickel compounds. RIXS can be viewed as a coherent two-steps process involving the absorption and the emission of x-rays. The soft x-ray absorption spectrum (XAS) at the metal L2,3 edge indicate the importance of atomic multiplet effects. RIXS spectra at L2,3 contain clearly defined emission peaks corresponding to d-excited states of Ni2+ at energies few eV below the elastic emission, which is strongly suppressed. These results are confirmed by atomic multiplet calculations using the Kramers-Heisenberg formula for RIXS processes. For larger energy losses, the emission spectra have a broad charge-transfer peak that results from the decay of hybridized Ni(3d)-F(2p) valence states. This is confirmed by comparison of the absorption and emission spectra recorded at the nickel L and fluorine K edges with F p and Ni d partial density of states using LDA + U calculations.en_US
dc.language.isoenen_US
dc.relation.ispartofseries;CHAENG/2013/51628-
dc.subjectCore-level spectroscopiesen_US
dc.subjectRIXSen_US
dc.subjectNickel difluorideen_US
dc.subjectElectronic structureen_US
dc.titleAtomic Multiplet and Charge Transfer Effects in the Resonant Inelastic X-Ray Scattering (RIXS) Spectra at the Nickel L2,3 Edge of NiF2en_US
dc.typeArticleen_US
Appears in Collections:Vol. 5 No. 1 (2017)

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