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Towards ultrafast dynamics with split-pulse X-ray photon correlation spectroscopy at free electron laser sources

One of the important challenges in condensed matter science is to understand ultrafast, atomic-scale fluctuations that dictate dynamic processes in equilibrium and non-equilibrium materials. Here, we report an important step towards reaching that goal by using a state-of-the-art perfect crystal base...

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Autores principales: Roseker, W., Hruszkewycz, S. O., Lehmkühler, F., Walther, M., Schulte-Schrepping, H., Lee, S., Osaka, T., Strüder, L., Hartmann, R., Sikorski, M., Song, S., Robert, A., Fuoss, P. H., Sutton, M., Stephenson, G. B., Grübel, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923200/
https://www.ncbi.nlm.nih.gov/pubmed/29703980
http://dx.doi.org/10.1038/s41467-018-04178-9
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author Roseker, W.
Hruszkewycz, S. O.
Lehmkühler, F.
Walther, M.
Schulte-Schrepping, H.
Lee, S.
Osaka, T.
Strüder, L.
Hartmann, R.
Sikorski, M.
Song, S.
Robert, A.
Fuoss, P. H.
Sutton, M.
Stephenson, G. B.
Grübel, G.
author_facet Roseker, W.
Hruszkewycz, S. O.
Lehmkühler, F.
Walther, M.
Schulte-Schrepping, H.
Lee, S.
Osaka, T.
Strüder, L.
Hartmann, R.
Sikorski, M.
Song, S.
Robert, A.
Fuoss, P. H.
Sutton, M.
Stephenson, G. B.
Grübel, G.
author_sort Roseker, W.
collection PubMed
description One of the important challenges in condensed matter science is to understand ultrafast, atomic-scale fluctuations that dictate dynamic processes in equilibrium and non-equilibrium materials. Here, we report an important step towards reaching that goal by using a state-of-the-art perfect crystal based split-and-delay system, capable of splitting individual X-ray pulses and introducing femtosecond to nanosecond time delays. We show the results of an ultrafast hard X-ray photon correlation spectroscopy experiment at LCLS where split X-ray pulses were used to measure the dynamics of gold nanoparticles suspended in hexane. We show how reliable speckle contrast values can be extracted even from very low intensity free electron laser (FEL) speckle patterns by applying maximum likelihood fitting, thus demonstrating the potential of a split-and-delay approach for dynamics measurements at FEL sources. This will enable the characterization of equilibrium and, importantly also reversible non-equilibrium processes in atomically disordered materials.
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spelling pubmed-59232002018-04-30 Towards ultrafast dynamics with split-pulse X-ray photon correlation spectroscopy at free electron laser sources Roseker, W. Hruszkewycz, S. O. Lehmkühler, F. Walther, M. Schulte-Schrepping, H. Lee, S. Osaka, T. Strüder, L. Hartmann, R. Sikorski, M. Song, S. Robert, A. Fuoss, P. H. Sutton, M. Stephenson, G. B. Grübel, G. Nat Commun Article One of the important challenges in condensed matter science is to understand ultrafast, atomic-scale fluctuations that dictate dynamic processes in equilibrium and non-equilibrium materials. Here, we report an important step towards reaching that goal by using a state-of-the-art perfect crystal based split-and-delay system, capable of splitting individual X-ray pulses and introducing femtosecond to nanosecond time delays. We show the results of an ultrafast hard X-ray photon correlation spectroscopy experiment at LCLS where split X-ray pulses were used to measure the dynamics of gold nanoparticles suspended in hexane. We show how reliable speckle contrast values can be extracted even from very low intensity free electron laser (FEL) speckle patterns by applying maximum likelihood fitting, thus demonstrating the potential of a split-and-delay approach for dynamics measurements at FEL sources. This will enable the characterization of equilibrium and, importantly also reversible non-equilibrium processes in atomically disordered materials. Nature Publishing Group UK 2018-04-27 /pmc/articles/PMC5923200/ /pubmed/29703980 http://dx.doi.org/10.1038/s41467-018-04178-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Roseker, W.
Hruszkewycz, S. O.
Lehmkühler, F.
Walther, M.
Schulte-Schrepping, H.
Lee, S.
Osaka, T.
Strüder, L.
Hartmann, R.
Sikorski, M.
Song, S.
Robert, A.
Fuoss, P. H.
Sutton, M.
Stephenson, G. B.
Grübel, G.
Towards ultrafast dynamics with split-pulse X-ray photon correlation spectroscopy at free electron laser sources
title Towards ultrafast dynamics with split-pulse X-ray photon correlation spectroscopy at free electron laser sources
title_full Towards ultrafast dynamics with split-pulse X-ray photon correlation spectroscopy at free electron laser sources
title_fullStr Towards ultrafast dynamics with split-pulse X-ray photon correlation spectroscopy at free electron laser sources
title_full_unstemmed Towards ultrafast dynamics with split-pulse X-ray photon correlation spectroscopy at free electron laser sources
title_short Towards ultrafast dynamics with split-pulse X-ray photon correlation spectroscopy at free electron laser sources
title_sort towards ultrafast dynamics with split-pulse x-ray photon correlation spectroscopy at free electron laser sources
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923200/
https://www.ncbi.nlm.nih.gov/pubmed/29703980
http://dx.doi.org/10.1038/s41467-018-04178-9
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