Influence of the core hole on K beta emission following photoionization or orbital electron capture: A comparison using MnO and (Fe2O3)-Fe-55

  • P Glatzel*
  • , U Bergmann
  • , FMF de Groot
  • , SP Cramer
  • *Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    Abstract

    The Mn K beta fluorescence emission in MnO after photoionization and in (Fe2O3)-Fe-55 after radioactive electron capture decay from the K shell have been measured using a crystal array spectrometer with an instrumental energy bandwidth of 0.7 eV (full width at half maximum). Both compounds have a 3d(5) valence electron configuration in the ionic approximation. It is found that the spectral features after K capture in (Fe2O3)-Fe-55 are shifted in emission energy and are sharper, compared to the spectra following photoionization in MnO, i.e., the spectra exhibit a dependence on the mode of excitation. Crystal-field multiplet calculations including ligand-to-metal charge transfer have been carried out for the 1 s intermediate states as well as for the 3p to 1 s (K beta) radiative transition. The populated I s intermediate states after photoionization are found to be spread over several eV. In comparison, only the lowest-lying Is intermediate states split by the weak (1s, 3d) exchange interaction are populated after K capture. It is proposed that the differences in population of the Is intermediate states together with a term-dependent final-state lifetime broadening can account for the changes in the spectral shapes due to the different modes of excitation.

    Original languageEnglish
    Article number045109
    Number of pages10
    JournalPhysical review. B, Condensed matter and materials physics
    Volume64
    Issue number4
    DOIs
    Publication statusPublished - 15 Jul 2001

    Keywords

    • RAY-FLUORESCENCE SPECTROSCOPY
    • CHARGE-TRANSFER SATELLITES
    • ABSORPTION-SPECTROSCOPY
    • PHOTOEMISSION SPECTRA
    • PHOTOELECTRON-SPECTRA
    • INTENSITY RATIOS
    • NICKEL COMPOUNDS
    • FE
    • EXCITATION
    • DIHALIDES

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