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 language | English |
|---|---|
| Pages (from-to) | 863-866 |
| Number of pages | 4 |
| Journal | Optica |
| Volume | 13 |
| Issue number | 5 |
| Early online date | 4 May 2026 |
| DOIs | |
| Publication status | Published - 20 May 2026 |
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