author_facet Błachucki, W.
Kayser, Y.
Czapla-Masztafiak, J.
Guo, M.
Juranić, P.
Kavčič, M.
Källman, E.
Knopp, G.
Lundberg, M.
Milne, C.
Rehanek, J.
Sá, J.
Szlachetko, J.
Błachucki, W.
Kayser, Y.
Czapla-Masztafiak, J.
Guo, M.
Juranić, P.
Kavčič, M.
Källman, E.
Knopp, G.
Lundberg, M.
Milne, C.
Rehanek, J.
Sá, J.
Szlachetko, J.
author Błachucki, W.
Kayser, Y.
Czapla-Masztafiak, J.
Guo, M.
Juranić, P.
Kavčič, M.
Källman, E.
Knopp, G.
Lundberg, M.
Milne, C.
Rehanek, J.
Sá, J.
Szlachetko, J.
spellingShingle Błachucki, W.
Kayser, Y.
Czapla-Masztafiak, J.
Guo, M.
Juranić, P.
Kavčič, M.
Källman, E.
Knopp, G.
Lundberg, M.
Milne, C.
Rehanek, J.
Sá, J.
Szlachetko, J.
Structural Dynamics
Inception of electronic damage of matter by photon-driven post-ionization mechanisms
Spectroscopy
Condensed Matter Physics
Instrumentation
Radiation
author_sort błachucki, w.
spelling Błachucki, W. Kayser, Y. Czapla-Masztafiak, J. Guo, M. Juranić, P. Kavčič, M. Källman, E. Knopp, G. Lundberg, M. Milne, C. Rehanek, J. Sá, J. Szlachetko, J. 2329-7778 AIP Publishing Spectroscopy Condensed Matter Physics Instrumentation Radiation http://dx.doi.org/10.1063/1.5090332 <jats:p>“Probe-before-destroy” methodology permitted diffraction and imaging measurements of intact specimens using ultrabright but highly destructive X-ray free-electron laser (XFEL) pulses. The methodology takes advantage of XFEL pulses ultrashort duration to outrun the destructive nature of the X-rays. Atomic movement, generally on the order of &amp;gt;50 fs, regulates the maximum pulse duration for intact specimen measurements. In this contribution, we report the electronic structure damage of a molecule with ultrashort X-ray pulses under preservation of the atoms' positions. A detailed investigation of the X-ray induced processes revealed that X-ray absorption events in the solvent produce a significant number of solvated electrons within attosecond and femtosecond timescales that are capable of coulombic interactions with the probed molecules. The presented findings show a strong influence on the experimental spectra coming from ionization of the probed atoms' surroundings leading to electronic structure modification much faster than direct absorption of photons. This work calls for consideration of this phenomenon in cases focused on samples embedded in, e.g., solutions or in matrices, which in fact concerns most of the experimental studies.</jats:p> Inception of electronic damage of matter by photon-driven post-ionization mechanisms Structural Dynamics
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title Inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_unstemmed Inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_full Inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_fullStr Inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_full_unstemmed Inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_short Inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_sort inception of electronic damage of matter by photon-driven post-ionization mechanisms
topic Spectroscopy
Condensed Matter Physics
Instrumentation
Radiation
url http://dx.doi.org/10.1063/1.5090332
publishDate 2019
physical
description <jats:p>“Probe-before-destroy” methodology permitted diffraction and imaging measurements of intact specimens using ultrabright but highly destructive X-ray free-electron laser (XFEL) pulses. The methodology takes advantage of XFEL pulses ultrashort duration to outrun the destructive nature of the X-rays. Atomic movement, generally on the order of &amp;gt;50 fs, regulates the maximum pulse duration for intact specimen measurements. In this contribution, we report the electronic structure damage of a molecule with ultrashort X-ray pulses under preservation of the atoms' positions. A detailed investigation of the X-ray induced processes revealed that X-ray absorption events in the solvent produce a significant number of solvated electrons within attosecond and femtosecond timescales that are capable of coulombic interactions with the probed molecules. The presented findings show a strong influence on the experimental spectra coming from ionization of the probed atoms' surroundings leading to electronic structure modification much faster than direct absorption of photons. This work calls for consideration of this phenomenon in cases focused on samples embedded in, e.g., solutions or in matrices, which in fact concerns most of the experimental studies.</jats:p>
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author Błachucki, W., Kayser, Y., Czapla-Masztafiak, J., Guo, M., Juranić, P., Kavčič, M., Källman, E., Knopp, G., Lundberg, M., Milne, C., Rehanek, J., Sá, J., Szlachetko, J.
author_facet Błachucki, W., Kayser, Y., Czapla-Masztafiak, J., Guo, M., Juranić, P., Kavčič, M., Källman, E., Knopp, G., Lundberg, M., Milne, C., Rehanek, J., Sá, J., Szlachetko, J., Błachucki, W., Kayser, Y., Czapla-Masztafiak, J., Guo, M., Juranić, P., Kavčič, M., Källman, E., Knopp, G., Lundberg, M., Milne, C., Rehanek, J., Sá, J., Szlachetko, J.
author_sort błachucki, w.
container_issue 2
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container_title Structural Dynamics
container_volume 6
description <jats:p>“Probe-before-destroy” methodology permitted diffraction and imaging measurements of intact specimens using ultrabright but highly destructive X-ray free-electron laser (XFEL) pulses. The methodology takes advantage of XFEL pulses ultrashort duration to outrun the destructive nature of the X-rays. Atomic movement, generally on the order of &amp;gt;50 fs, regulates the maximum pulse duration for intact specimen measurements. In this contribution, we report the electronic structure damage of a molecule with ultrashort X-ray pulses under preservation of the atoms' positions. A detailed investigation of the X-ray induced processes revealed that X-ray absorption events in the solvent produce a significant number of solvated electrons within attosecond and femtosecond timescales that are capable of coulombic interactions with the probed molecules. The presented findings show a strong influence on the experimental spectra coming from ionization of the probed atoms' surroundings leading to electronic structure modification much faster than direct absorption of photons. This work calls for consideration of this phenomenon in cases focused on samples embedded in, e.g., solutions or in matrices, which in fact concerns most of the experimental studies.</jats:p>
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spelling Błachucki, W. Kayser, Y. Czapla-Masztafiak, J. Guo, M. Juranić, P. Kavčič, M. Källman, E. Knopp, G. Lundberg, M. Milne, C. Rehanek, J. Sá, J. Szlachetko, J. 2329-7778 AIP Publishing Spectroscopy Condensed Matter Physics Instrumentation Radiation http://dx.doi.org/10.1063/1.5090332 <jats:p>“Probe-before-destroy” methodology permitted diffraction and imaging measurements of intact specimens using ultrabright but highly destructive X-ray free-electron laser (XFEL) pulses. The methodology takes advantage of XFEL pulses ultrashort duration to outrun the destructive nature of the X-rays. Atomic movement, generally on the order of &amp;gt;50 fs, regulates the maximum pulse duration for intact specimen measurements. In this contribution, we report the electronic structure damage of a molecule with ultrashort X-ray pulses under preservation of the atoms' positions. A detailed investigation of the X-ray induced processes revealed that X-ray absorption events in the solvent produce a significant number of solvated electrons within attosecond and femtosecond timescales that are capable of coulombic interactions with the probed molecules. The presented findings show a strong influence on the experimental spectra coming from ionization of the probed atoms' surroundings leading to electronic structure modification much faster than direct absorption of photons. This work calls for consideration of this phenomenon in cases focused on samples embedded in, e.g., solutions or in matrices, which in fact concerns most of the experimental studies.</jats:p> Inception of electronic damage of matter by photon-driven post-ionization mechanisms Structural Dynamics
spellingShingle Błachucki, W., Kayser, Y., Czapla-Masztafiak, J., Guo, M., Juranić, P., Kavčič, M., Källman, E., Knopp, G., Lundberg, M., Milne, C., Rehanek, J., Sá, J., Szlachetko, J., Structural Dynamics, Inception of electronic damage of matter by photon-driven post-ionization mechanisms, Spectroscopy, Condensed Matter Physics, Instrumentation, Radiation
title Inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_full Inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_fullStr Inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_full_unstemmed Inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_short Inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_sort inception of electronic damage of matter by photon-driven post-ionization mechanisms
title_unstemmed Inception of electronic damage of matter by photon-driven post-ionization mechanisms
topic Spectroscopy, Condensed Matter Physics, Instrumentation, Radiation
url http://dx.doi.org/10.1063/1.5090332