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Antoine Sarracini

Publications and source records attributed to Antoine Sarracini.

3 recordsLinked to original sources

High-Power Polarization-Controlled Attosecond-Scale Soft X-ray Pulses

We demonstrate a versatile platform for high-power attosecond soft X-ray pulse generation with polarization and photon energy control at the SwissFEL free-electron laser. An isolated high-current spike embedded within a long electron-beam pedestal emits soft X-ray pulses with single-spike spectra and multi-electronvolt bandwidths in the tunable magnetic fields of Apple-X undulators. Demonstrated pulse parameters include a photon energy range of 450--1070 eV, circular as well as linear polarization, and pulse energies from tens to above hundred microjoules. By tuning the longitudinal slice-dependent transverse electron beam orbit we can rapidly switch between attosecond and few femtosecond pulse length. By exploiting magnetic chicanes in the undulator line we can produce two-colour pulse pairs with tunable delay or increase the pulse energy beyond 200~\textmu J through multi-stage amplification schemes. High-resolution longitudinal phase-space measurements and start-to-end simulations in addition to spectral measurements provide consistent evidence for attosecond-scale pulse durations. This unique combination of high pulse energy and polarization control of attosecond-scale soft X-ray pulses enables the element-specific investigations of spin and chiral dynamics on the natural time scale of electron motion.

physics.acc-ph

Dichography: Two-frame Ultrafast Imaging from a Single Diffraction Pattern

We experimentally demonstrate that pairs of time-delayed ultrabright and ultrashort X-ray pulses of two different colors, delivered by modern X-ray Free Electron Lasers, can provide two time-delayed snapshots of a sample. We introduce Dichography, a method that algorithmically separates the diffraction signals overlapping on the detector and independently retrieves the two images of the specimen. We employ Dichography to reconstruct two views of individual xenon-doped helium nanodroplets with 20 nm spatial resolution. The consistency of structures observed in both images at delays up to 750 fs provides evidence that, under these illumination conditions, significant structural damage only occurs at longer timescales. We further validate the method by imaging pairs of silver nanoparticles intercepted by the same light pulse. Dichography enables a new class of experiments across physics, chemistry, and materials science, making a significant step toward the original promise of X-ray free-electron lasers to capture ultrafast movies of nanomatter.

physics.optics

Coherent all X-ray four wave mixing at core shell resonances

Nonlinear wave mixing in the X-ray range can provide valuable insights into the structural and electron dynamics of atomic and molecular systems on ultrafast time scales, with state- and site-selectivity and atomic resolution. This promising experimental toolbox was so far limited by requiring at least one near-visible laser, thus preventing core-shell two-dimensional X-ray spectroscopy. In this work, we demonstrate the generation of background-free all-X-ray four-wave mixing (XFWM) signals from a dilute gaseous sample (Ne). The measured and simulated two-dimensional spectral maps ($ω_{\text{in}},ω_{\text{out}}$) show multiple contributions involving the coherent response from core electrons. Notably, two-color resonant XFWM signals, essential for generalized multi-color schemes that allow to locally probe the electronic excitation of matter, are observed in neutral Ne. Moreover, stimulated Ne$^+$ emission in each of the propagating X-ray pulses leads to an increase of the temporal coherence in a narrow-bandwidth, which results in the coherent mixing of three X-ray lasers. Preliminary X-ray excitation experiments making use of multi-color time-delayed X-ray pulses demonstrate temporal resolution capability and show a time dependency consistent with a signal dominated by resonant XFWM processes. This first all-X-ray four-wave-mixing approach represents a major breakthrough towards multidimensional X-ray correlation spectroscopy and the general application of nonlinear all-X-ray wave-mixing.

physics.optics