Single-pulse phase-contrast imaging at free-electron lasers in the hard X-ray regime

Author:

Hagemann JohannesORCID,Vassholz MalteORCID,Hoeppe Hannes,Osterhoff MarkusORCID,Rosselló Juan M.ORCID,Mettin RobertORCID,Seiboth FrankORCID,Schropp AndreasORCID,Möller Johannes,Hallmann JörgORCID,Kim Chan,Scholz MarkusORCID,Boesenberg Ulrike,Schaffer Robert,Zozulya AlexeyORCID,Lu Wei,Shayduk Roman,Madsen AndersORCID,Schroer Christian G.ORCID,Salditt TimORCID

Abstract

X-ray free-electron lasers (XFELs) have opened up unprecedented opportunities for time-resolved nano-scale imaging with X-rays. Near-field propagation-based imaging, and in particular near-field holography (NFH) in its high-resolution implementation in cone-beam geometry, can offer full-field views of a specimen's dynamics captured by single XFEL pulses. To exploit this capability, for example in optical-pump/X-ray-probe imaging schemes, the stochastic nature of the self-amplified spontaneous emission pulses, i.e. the dynamics of the beam itself, presents a major challenge. In this work, a concept is presented to address the fluctuating illumination wavefronts by sampling the configuration space of SASE pulses before an actual recording, followed by a principal component analysis. This scheme is implemented at the MID (Materials Imaging and Dynamics) instrument of the European XFEL and time-resolved NFH is performed using aberration-corrected nano-focusing compound refractive lenses. Specifically, the dynamics of a micro-fluidic water-jet, which is commonly used as sample delivery system at XFELs, is imaged. The jet exhibits rich dynamics of droplet formation in the break-up regime. Moreover, pump–probe imaging is demonstrated using an infrared pulsed laser to induce cavitation and explosion of the jet.

Funder

Bundesministerium für Bildung und Forschung

Max Planck School of Photonics

Publisher

International Union of Crystallography (IUCr)

Subject

Instrumentation,Nuclear and High Energy Physics,Radiation

Reference71 articles.

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2. X-Ray Holographic Imaging of Hydrated Biological Cells in Solution

3. Single Particle X-ray Diffractive Imaging

4. Diffraction enhanced x-ray imaging

5. Diffraction before destruction

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