Nonresonant inelastic x-ray scattering involving excitonic excitations: the examples of NiO and CoO
In a recent publication Larson et al. reported remarkably clear d−d excitations for NiO and CoO with x-ray scattering. Here we present an accurate quantitative description based on a local many body approach, beyond local density approximation + Hubbard U approximations. The magnitude of →q determin...
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
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21 December 2007
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| In: |
Physical review letters
Year: 2007, Jahrgang: 99, Heft: 25, Pages: 257401 |
| ISSN: | 1079-7114 |
| DOI: | 10.1103/PhysRevLett.99.257401 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1103/PhysRevLett.99.257401 Verlag, Volltext: https://link.aps.org/doi/10.1103/PhysRevLett.99.257401 
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| Verfasserangaben: | M.W. Haverkort, A. Tanaka, L.H. Tjeng, and G.A. Sawatzky |
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| 245 | 1 | 0 | |a Nonresonant inelastic x-ray scattering involving excitonic excitations |b the examples of NiO and CoO |c M.W. Haverkort, A. Tanaka, L.H. Tjeng, and G.A. Sawatzky |
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| 520 | |a In a recent publication Larson et al. reported remarkably clear d−d excitations for NiO and CoO with x-ray scattering. Here we present an accurate quantitative description based on a local many body approach, beyond local density approximation + Hubbard U approximations. The magnitude of →q determines which of the allowed multipoles contributes most to the spectra. The direction of →q with respect to the crystal can be used as an equivalent to polarization similar to electron energy loss spectroscopy, allowing for a determination of the local symmetry of the initial and final states. This method is more generally applicable and could be a powerful tool for the study of local distortions and symmetries in transition metal and rare earth compounds. | ||
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