Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2024Impact of sulfur addition on the structure and dynamics of Ni–Nb alloy melts1citations
  • 2024Impact of sulfur addition on the structure and dynamics of Ni–Nb alloy melts1citations
  • 2023Directly observing atomic-scale relaxations of a glass forming liquid using femtosecond X-ray photon correlation spectroscopy1citations

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Meyer, Andreas
2 / 18 shared
Ruschel, Lucas Matthias
1 / 4 shared
Dippel, Ann-Christin
2 / 29 shared
Khademorezaian, Saba
2 / 2 shared
Grund, Nicolai
2 / 2 shared
Busch, Ralf
2 / 44 shared
Kreuzer, Lucas P.
2 / 22 shared
Voigt, Hendrik
2 / 6 shared
Yang, Fan
3 / 31 shared
Blankenburg, Malte
2 / 26 shared
Banerjee, Soham
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Holland-Moritz, Dirk
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Divinski, Sergiy
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Wilde, Gerhard
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Neuber, Nico
2 / 24 shared
Ruschel, Lucas M.
1 / 4 shared
Wilden, Johanna
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Co-Authors (by relevance)

  • Meyer, Andreas
  • Ruschel, Lucas Matthias
  • Dippel, Ann-Christin
  • Khademorezaian, Saba
  • Grund, Nicolai
  • Busch, Ralf
  • Kreuzer, Lucas P.
  • Voigt, Hendrik
  • Yang, Fan
  • Blankenburg, Malte
  • Banerjee, Soham
  • Holland-Moritz, Dirk
  • Divinski, Sergiy
  • Wilde, Gerhard
  • Neuber, Nico
  • Ruschel, Lucas M.
  • Wilden, Johanna
OrganizationsLocationPeople

document

Directly observing atomic-scale relaxations of a glass forming liquid using femtosecond X-ray photon correlation spectroscopy

  • Sun, Peihao
  • Vila-Comamala, Joan
  • Wei, Shuai
  • Sokolowski-Tinten, Klaus
  • Makareviciute, Arune
  • Yang, Fan
  • Coleman, Garrett
  • David, Christian
  • Esposito, Vincent
  • Embs, Jan Peter
  • Li, Haoyuan
  • Zhu, Diling
  • Song, Sanghoon
  • Fuoss, Paul
  • Ruta, Beatrice
  • Mo, Mianzhen
  • Wang, Nan
  • Mamyrbayev, Talgat
  • Hastings, Jerome
  • Moesgaard, Jens
  • Lucas, Pierre
  • Cornet, Antoine
  • Fujita, Tomoki
  • Albert, Thies J.
  • Chen, Ying
  • Sato, Takahiro
  • Amini, Narges
  • Sun, Yanwen
Abstract

Glass forming liquids exhibit structural relaxation behaviors, reflecting underlying atomic rearrangements on a wide range of timescales. These behaviors play a crucial role in determining many material properties. However, the relaxation processes on the atomic scale are not well understood due to the experimental difficulties in directly characterizing the evolving correlations of atomic order in disordered systems. Here, taking the model system Ge15Te85, we demonstrate an experimental approach that probes the relaxation dynamics by scattering the coherent X-ray pulses with femtosecond duration produced by X-ray free electron lasers (XFELs). By collecting the summed speckle patterns from two rapidly successive, nearly identical X-ray pulses generated using a split-delay system, we can extract the contrast decay of speckle patterns originating from sample dynamics and observe the full decorrelation of local order on the sub-picosecond timescale. This provides the direct atomic-level evidence of fragile liquid behavior of Ge15Te85. Our results demonstrate the strategy for XFEL-based X-ray photon correlation spectroscopy (XPCS), attaining femtosecond temporal and atomic-scale spatial resolutions. This twelve orders of magnitude extension from the millisecond regime of synchrotron-based XPCS opens a new avenue of experimental studies of relaxation dynamics in liquids, glasses, and other highly disordered systems.

Topics
  • glass
  • glass
  • forming
  • spectroscopy