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Communication: The electronic structure of matter probed with a single femtosecond hard x-ray pulse
Physical, biological, and chemical transformations are initiated by changes in the electronic configuration of the species involved. These electronic changes occur on the timescales of attoseconds (10(−18) s) to femtoseconds (10(−15) s) and drive all subsequent electronic reorganization as the syste...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Crystallographic Association
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4711597/ https://www.ncbi.nlm.nih.gov/pubmed/26798772 http://dx.doi.org/10.1063/1.4868260 |
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author | Szlachetko, J. Milne, C. J. Hoszowska, J. Dousse, J.-Cl. Błachucki, W. Sà, J. Kayser, Y. Messerschmidt, M. Abela, R. Boutet, S. David, C. Williams, G. Pajek, M. Patterson, B. D. Smolentsev, G. van Bokhoven, J. A. Nachtegaal, M. |
author_facet | Szlachetko, J. Milne, C. J. Hoszowska, J. Dousse, J.-Cl. Błachucki, W. Sà, J. Kayser, Y. Messerschmidt, M. Abela, R. Boutet, S. David, C. Williams, G. Pajek, M. Patterson, B. D. Smolentsev, G. van Bokhoven, J. A. Nachtegaal, M. |
author_sort | Szlachetko, J. |
collection | PubMed |
description | Physical, biological, and chemical transformations are initiated by changes in the electronic configuration of the species involved. These electronic changes occur on the timescales of attoseconds (10(−18) s) to femtoseconds (10(−15) s) and drive all subsequent electronic reorganization as the system moves to a new equilibrium or quasi-equilibrium state. The ability to detect the dynamics of these electronic changes is crucial for understanding the potential energy surfaces upon which chemical and biological reactions take place. Here, we report on the determination of the electronic structure of matter using a single self-seeded femtosecond x-ray pulse from the Linac Coherent Light Source hard x-ray free electron laser. By measuring the high energy resolution off-resonant spectrum (HEROS), we were able to obtain information about the electronic density of states with a single femtosecond x-ray pulse. We show that the unoccupied electronic states of the scattering atom may be determined on a shot-to-shot basis and that the measured spectral shape is independent of the large intensity fluctuations of the incoming x-ray beam. Moreover, we demonstrate the chemical sensitivity and single-shot capability and limitations of HEROS, which enables the technique to track the electronic structural dynamics in matter on femtosecond time scales, making it an ideal probe technique for time-resolved X-ray experiments. |
format | Online Article Text |
id | pubmed-4711597 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Crystallographic Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-47115972016-01-21 Communication: The electronic structure of matter probed with a single femtosecond hard x-ray pulse Szlachetko, J. Milne, C. J. Hoszowska, J. Dousse, J.-Cl. Błachucki, W. Sà, J. Kayser, Y. Messerschmidt, M. Abela, R. Boutet, S. David, C. Williams, G. Pajek, M. Patterson, B. D. Smolentsev, G. van Bokhoven, J. A. Nachtegaal, M. Struct Dyn Communications Physical, biological, and chemical transformations are initiated by changes in the electronic configuration of the species involved. These electronic changes occur on the timescales of attoseconds (10(−18) s) to femtoseconds (10(−15) s) and drive all subsequent electronic reorganization as the system moves to a new equilibrium or quasi-equilibrium state. The ability to detect the dynamics of these electronic changes is crucial for understanding the potential energy surfaces upon which chemical and biological reactions take place. Here, we report on the determination of the electronic structure of matter using a single self-seeded femtosecond x-ray pulse from the Linac Coherent Light Source hard x-ray free electron laser. By measuring the high energy resolution off-resonant spectrum (HEROS), we were able to obtain information about the electronic density of states with a single femtosecond x-ray pulse. We show that the unoccupied electronic states of the scattering atom may be determined on a shot-to-shot basis and that the measured spectral shape is independent of the large intensity fluctuations of the incoming x-ray beam. Moreover, we demonstrate the chemical sensitivity and single-shot capability and limitations of HEROS, which enables the technique to track the electronic structural dynamics in matter on femtosecond time scales, making it an ideal probe technique for time-resolved X-ray experiments. American Crystallographic Association 2014-03-17 /pmc/articles/PMC4711597/ /pubmed/26798772 http://dx.doi.org/10.1063/1.4868260 Text en © 2014 Author(s). 2329-7778/2014/1(2)/021101/8 All article content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 Unported License. |
spellingShingle | Communications Szlachetko, J. Milne, C. J. Hoszowska, J. Dousse, J.-Cl. Błachucki, W. Sà, J. Kayser, Y. Messerschmidt, M. Abela, R. Boutet, S. David, C. Williams, G. Pajek, M. Patterson, B. D. Smolentsev, G. van Bokhoven, J. A. Nachtegaal, M. Communication: The electronic structure of matter probed with a single femtosecond hard x-ray pulse |
title | Communication: The electronic structure of matter probed with a single
femtosecond hard x-ray pulse |
title_full | Communication: The electronic structure of matter probed with a single
femtosecond hard x-ray pulse |
title_fullStr | Communication: The electronic structure of matter probed with a single
femtosecond hard x-ray pulse |
title_full_unstemmed | Communication: The electronic structure of matter probed with a single
femtosecond hard x-ray pulse |
title_short | Communication: The electronic structure of matter probed with a single
femtosecond hard x-ray pulse |
title_sort | communication: the electronic structure of matter probed with a single
femtosecond hard x-ray pulse |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4711597/ https://www.ncbi.nlm.nih.gov/pubmed/26798772 http://dx.doi.org/10.1063/1.4868260 |
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