On the sensitivity of hard X-ray spectroscopies to the chemical state of Br

Amelie Bordage, Mátyás Imre Pápai, Norbert S. Sas, Jakub Szlachetko, Maarten Nachtegaal, Gyoergy Vanko

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

The sensitivity of the 1s X-ray emission and high-energy-resolution fluorescence-detected X-ray absorption spectroscopies (XES and HERFD-XAS) to resolve the variations in the chemical state (electronic structure and local coordination) of Br has been investigated for a selected set of compounds including NaBrO3, NH4Br and C2H4Br2 (1,2-dibromoethane). For the Br K-edge XAS, employing the HERFD mode significantly increases the energy resolution, which demonstrates that with a crystal spectrometer used as a detector the absorption technique becomes a more powerful analytical tool. In the case of XES, the experimental results as well as the density functional theory (DFT) modeling both show that the chemical sensitivity of the main 1s diagram emission lines (Kα1,2) and Kβ1,3) is rather limited. However, the valence-to-core (Kβ2) region of XES displays significant shape and intensity variations, as expected for transitions having the same final states as those of photoemission spectroscopy. The spectra are in good agreement with the molecular orbital description delivered by DFT calculations. Calculations for an extended series of Br compounds confirm that valence-to-core XES can serve as a probe for chemical analysis, and, being a hard X-ray photon-in/photon-out technique, it is particularly well-suited for in situ investigations of molecular transformations, even on the ultrafast time scales down to femtosecond time resolution.
Original languageEnglish
JournalPhysical Chemistry Chemical Physics
Volume15
Issue number26
Pages (from-to)11088-11098
Number of pages11
ISSN1463-9076
DOIs
Publication statusPublished - 2013
Externally publishedYes

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