Visualizing the strong field–induced molecular breakup of C <sub>60</sub> via x-ray diffraction

Laser-driven dynamics in polyatomic molecules poses a complex many-body problem. Understanding intense light-matter interaction is crucial for steering intramolecular quantum dynamical processes. Here, we record time-resolved x-ray diffraction images of [Formula: see text] molecules during and after their interaction with intense near-infrared fields, giving direct access to structural changes of the molecules and their fragmentation in real time. Tuning the intensity of the excitation pulses, we uncover a transition from a weak-field regime of excited but stable molecules to a high-field regime dominated by Coulomb explosion. In the transition region, the molecules expand by up to 50% of their initial size within just 140 fs, with major fragmentation only setting in afterward. This work demonstrates that x-ray diffractive imaging is capable of retrieving time-resolved structural information of large molecules reshaped by intense laser fields. Laser-driven fragmentation is a first step toward observing molecular processes modified by laser fields of increasing intensity.

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Publication Details

Journal
Science Advances
Published
2025-11-21
DOI
https://doi.org/10.1126/sciadv.adz1900
Primary Topic
Laser-Matter Interactions and Applications
Type
article
Field-Weighted Citation Impact
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article

Visualizing the strong field–induced molecular breakup of C 60 via x-ray diffraction

Arnaud Rouzée, Simone Techert, Yu Hang Lai, Daniel Rolles et al.
Science Advances
Laser-Matter Interactions and Applications
article

Visualizing the strong field–induced molecular breakup of C 60 via x-ray diffraction

Arnaud Rouzée, Simone Techert, Yu Hang Lai, Daniel Rolles, Thomas Möller, Florian Trost, Katharina Kubiček, Jochen Küpper, Kirsten Schnorr, Ulf Saalmann, Marc J. J. Vrakking, Yuta Ito, Sven Augustin, Ryan Coffee, Jan M. Rost, F. Remacle, Thomas Pfeifer, T. Osipov, Severin Meister, Ruth A. Livingstone, Yoshiaki Kumagai, Kaz Nakahara, G. Carini, Christoph Bostedt, N. Berrah, Hannes Lindenblatt, Louis F. DiMauro, Kiyoshi Ueda, Ilme Schlichting, Philip Hart, Gaurav Pandey, Manuel Cardosa-Gutierrez, C. P. Schulz, Razib Obaid, D. Ray, Julian Zimmermann, R. Moshammer, André Al Haddad, Georg Schmid, R. Schmidt, Cosmin I. Blaga, J. Ullrich, Koji Motomura
article en

Abstract

Laser-driven dynamics in polyatomic molecules poses a complex many-body problem. Understanding intense light-matter interaction is crucial for steering intramolecular quantum dynamical processes. Here, we record time-resolved x-ray diffraction images of [Formula: see text] molecules during and after their interaction with intense near-infrared fields, giving direct access to structural changes of the molecules and their fragmentation in real time. Tuning the intensity of the excitation pulses, we uncover a transition from a weak-field regime of excited but stable molecules to a high-field regime dominated by Coulomb explosion. In the transition region, the molecules expand by up to 50% of their initial size within just 140 fs, with major fragmentation only setting in afterward. This work demonstrates that x-ray diffractive imaging is capable of retrieving time-resolved structural information of large molecules reshaped by intense laser fields. Laser-driven fragmentation is a first step toward observing molecular processes modified by laser fields of increasing intensity.

Science AdvancesVol. 11(47)
Argonne National Laboratory (US), Physikalisch-Technische Bundesanstalt (DE), University of Connecticut (US), University of Liège (BE), Universität Hamburg (DE), Kansas State University (US), Brookhaven National Laboratory (US), Tohoku University (JP), Board of the Swiss Federal Institutes of Technology (CH), Deutsches Elektronen-Synchrotron DESY (DE), SLAC National Accelerator Laboratory (US), Paul Scherrer Institute (CH), ETH Zurich (CH), Max Planck Institute for Medical Research (DE), Max Planck Institute for the Physics of Complex Systems (DE), Max Planck Institute for Biophysical Chemistry (DE), Max-Born-Institute for Nonlinear Optics and Short Pulse Spectroscopy (DE), Center for Free-Electron Laser Science (DE), Max Planck Institute for Nuclear Physics (DE), Technische Universität Berlin (DE), École Polytechnique Fédérale de Lausanne (CH), The Ohio State University (US), Technische Universität Dresden (DE)
Openalex Percentile: Top 72%
Laser-Matter Interactions and Applications
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