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Few-femtosecond time resolution in optically pumped hard X-ray scattering at a free-electron laser

  • Eleanor Weckwerth
  • , Maria Trinidad Castro Duran
  • , Ian Gabalski
  • , Felix Allum
  • , Matthew Bain
  • , Surjendu Bhattacharyya
  • , Christian Brahms
  • , Logan Brenner
  • , Mathew A. Britton
  • , Andrés Moreno Carrascosa
  • , Chuan Cheng
  • , Xinxin Cheng
  • , Stuart W. Crane
  • , Alexandra Fraser
  • , Aaron M. Ghrist
  • , Ching-Chi Hang
  • , Andrew J. Howard
  • , Lisa Huang
  • , Ramesh Jarupula
  • , Brian Kaufman
  • Adam Kirrander, Eirik M. Liane, Yusong Liu, Haoran Ma, Michael P. Minitti, Sandra Mous, Nicole S. Muir, Alex Narkiewicz-Jodko, Joseph S. Robinson, David J. Romano, Mats Simmermacher, Jacob Stamm, Blanca Teodoro, John C. Travers, Jonathan Tsao, Peter M. Weber, Haowei Wu, Ruaridh Forbes, Haiwang Yong, Philip H. Bucksbaum, Mengning Liang, Kirk A. Larsen

Research output: Contribution to journalLetterpeer-review

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Abstract

Capturing chemical dynamics in real time is a central goal of ultrafast science, necessitating measurements fast enough to track atomic motion on few-femtosecond timescales with high precision. We present time-resolved hard X-ray scattering that meets these criteria by combining 7 fs full-width at half maximum (FWHM) near-infrared laser pulses with sub10 fs FWHM hard X-ray pulses from a free-electron laser. Using heavy water’s electronic response to strong-field ionization as a benchmark, we achieve a sub-8 fs FWHM instrument response function. These optical pump X-ray probe measurements enable direct observation of chemical dynamics with angstrom spatial and few-fs temporal resolution.
Original languageEnglish
Pages (from-to)863-866
Number of pages4
JournalOptica
Volume13
Issue number5
Early online date4 May 2026
DOIs
Publication statusPublished - 20 May 2026

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