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Autores principales: Kroll, Thomas, Doyle, Margaret, Halavanau, Aliaksei, Linker, Thomas M., Everts, Joshua, Michine, Yurina, Fuller, Franklin D., Weninger, Clemens, Alonso-Mori, Roberto, Pellegrini, Claudio, Benediktovich, Andrei, Yabashi, Makina, Inoue, Ichiro, Inubushi, Yuichi, Osaka, Taito, Hara, Toru, Yamada, Jumpei, Kern, Jan, Yano, Junko, Yachandra, Vittal K., Rohringer, Nina, Yoneda, Hitoki, Bergmann, Uwe
Formato: Preprint
Publicado: 2025
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Acceso en línea:https://arxiv.org/abs/2503.03993
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author Kroll, Thomas
Doyle, Margaret
Halavanau, Aliaksei
Linker, Thomas M.
Everts, Joshua
Michine, Yurina
Fuller, Franklin D.
Weninger, Clemens
Alonso-Mori, Roberto
Pellegrini, Claudio
Benediktovich, Andrei
Yabashi, Makina
Inoue, Ichiro
Inubushi, Yuichi
Osaka, Taito
Hara, Toru
Yamada, Jumpei
Kern, Jan
Yano, Junko
Yachandra, Vittal K.
Rohringer, Nina
Yoneda, Hitoki
Bergmann, Uwe
author_facet Kroll, Thomas
Doyle, Margaret
Halavanau, Aliaksei
Linker, Thomas M.
Everts, Joshua
Michine, Yurina
Fuller, Franklin D.
Weninger, Clemens
Alonso-Mori, Roberto
Pellegrini, Claudio
Benediktovich, Andrei
Yabashi, Makina
Inoue, Ichiro
Inubushi, Yuichi
Osaka, Taito
Hara, Toru
Yamada, Jumpei
Kern, Jan
Yano, Junko
Yachandra, Vittal K.
Rohringer, Nina
Yoneda, Hitoki
Bergmann, Uwe
contents We report the successful resolution of the multiplet structure of the Kα1 x-ray emission in manganese (Mn) complexes through seeded stimulated X-ray emission spectroscopy (seeded S-XES). By employing a femtosecond pump pulse above the Mn K edge to generate simultaneous 1s core-holes, and a second-color tunable seed pulse to initiate the stimulated emission process, we were able to enhance individual lines within the Kα1 emission. This approach allows to resolve the fine multiplet features that are obscured by the life-time broadening in conventional Mn Kα XES. The work builds on our previous observation that S-XES from Mn(II) and Mn(VII) complexes pumped at high intensities can exhibit stimulated emission without sacrificing the chemical sensitivity to oxidation states. This technique opens the door to controlled high-resolution electronic structure spectroscopy in transition metal complexes beyond core hole life time broadening with potential applications in catalysis, inorganic chemistry, and materials science.
format Preprint
id arxiv_https___arxiv_org_abs_2503_03993
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Observation of Multiplet Lines in Seeded Stimulated Mn Kα1 X-ray Emission
Kroll, Thomas
Doyle, Margaret
Halavanau, Aliaksei
Linker, Thomas M.
Everts, Joshua
Michine, Yurina
Fuller, Franklin D.
Weninger, Clemens
Alonso-Mori, Roberto
Pellegrini, Claudio
Benediktovich, Andrei
Yabashi, Makina
Inoue, Ichiro
Inubushi, Yuichi
Osaka, Taito
Hara, Toru
Yamada, Jumpei
Kern, Jan
Yano, Junko
Yachandra, Vittal K.
Rohringer, Nina
Yoneda, Hitoki
Bergmann, Uwe
Chemical Physics
Materials Science
We report the successful resolution of the multiplet structure of the Kα1 x-ray emission in manganese (Mn) complexes through seeded stimulated X-ray emission spectroscopy (seeded S-XES). By employing a femtosecond pump pulse above the Mn K edge to generate simultaneous 1s core-holes, and a second-color tunable seed pulse to initiate the stimulated emission process, we were able to enhance individual lines within the Kα1 emission. This approach allows to resolve the fine multiplet features that are obscured by the life-time broadening in conventional Mn Kα XES. The work builds on our previous observation that S-XES from Mn(II) and Mn(VII) complexes pumped at high intensities can exhibit stimulated emission without sacrificing the chemical sensitivity to oxidation states. This technique opens the door to controlled high-resolution electronic structure spectroscopy in transition metal complexes beyond core hole life time broadening with potential applications in catalysis, inorganic chemistry, and materials science.
title Observation of Multiplet Lines in Seeded Stimulated Mn Kα1 X-ray Emission
topic Chemical Physics
Materials Science
url https://arxiv.org/abs/2503.03993