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dc.contributor.authorAlbers, Christian-
dc.contributor.authorSakrowski, Robin-
dc.contributor.authorThiering, Nicola-
dc.contributor.authorLibon, Lélia-
dc.contributor.authorSpiekermann, Georg-
dc.contributor.authorKaa, Johannes M.-
dc.contributor.authorGretarsson, Hlynur-
dc.contributor.authorSundermann, Martin-
dc.contributor.authorTolan, Metin-
dc.contributor.authorWilke, Max-
dc.contributor.authorSternemann, Christian-
dc.date.accessioned2024-07-08T12:33:49Z-
dc.date.available2024-07-08T12:33:49Z-
dc.date.issued2023-04-04-
dc.identifier.urihttp://hdl.handle.net/2003/42585-
dc.identifier.urihttp://dx.doi.org/10.17877/DE290R-24420-
dc.description.abstractX-ray spectroscopy of iron-bearing compounds under high pressure and high temperature is an important tool to understand geological processes in the deep Earth. However, the sample environment using a diamond anvil cell complicates spectroscopic measurements and leads to long data acquisition times. We present a setup for resonant and non-resonant X-ray emission spectroscopy and showcase its capabilities for in situ studies at high pressure and high temperature. Spin-state imaging of laser-heated FeCO3 at 75 GPa via Kβ1,3 emission spectroscopy demonstrates the great potential of this setup with measurement times within seconds for robust spin-state analysis results. The results of Kβ1,3 emission spectroscopy of cold-compressed Fe2O3 reveal a two-step spin transition with the ζ-phase between 57 GPa and 64 GPa, having iron in different spin states at the different iron sites. The phase transition via ζ- to Θ-phase causes a delocalization of the electronic states, which is supported by 1s2p resonant X-ray emission spectroscopy.en
dc.language.isoende
dc.relation.ispartofseriesJournal of analytical atomic spectrometry;38(5)-
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/-
dc.subject.ddc530-
dc.titleHigh-efficiency X-ray emission spectroscopy of cold-compressed Fe2O3 and laser-heated pressurized FeCO3 using a von Hámos spectrometeren
dc.typeTextde
dc.type.publicationtypeArticlede
dcterms.accessRightsopen access-
eldorado.secondarypublicationtruede
eldorado.secondarypublication.primaryidentifierhttps://doi.org/10.1039/D3JA00014Ade
eldorado.secondarypublication.primarycitationJ. Anal. At. Spectrom., 2023,38, 1097-1107de
Appears in Collections:Experimentelle Physik I

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