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Breaking resolution limits in ultrafast X-ray diffractive imaging

Project description

Novel efficient far-field imaging for nanoscale studies

Nanoscale processes have been an important scientific interest in a number of fields ranging from biology to chemistry and more. A better understanding of their workings could offer a wider variety of advantages. Unfortunately, no far-field imaging technique is capable of efficiently studying nanoscale functions, with either their temporal or spatial resolutions being inadequate for study. The EU-funded HIGH-Q project will develop a novel far-field imaging technique utilising X-ray free-electron laser pulses, ultrafast coherent diffractive imaging, ultrafast X-ray and reconstruction algorithms that will allow for efficient study of nanoscale processes. This project will allow for great scientific pushes in the studies of photochemistry, material and catalysis sciences, among others.

Objective

Our ability to observe processes and study function at the nanoscale is hindered by the compromise between temporal and spatial resolutions inherent to the majority of far-field imaging techniques. This limits our perspective on a wide range of non-equilibrium processes at the nanoscale such as chemical/catalytic reactions, ultrafast phase-transitions and biological processes at room temperature in native phase. Intense and spatially coherent femtosecond-short X-ray flashes from free-electron laser (XFEL) sources can combine high spatial and temporal resolutions through 'diffraction-before-destruction' coherent diffractive imaging (CDI) of individual nano-specimens within a single exposure. XFEL CDI studies have found surprising variety of morphologies in soot, unknown metastable shapes of metal nanoparticles and exotic states of water, which are otherwise inaccessible. PI and colleagues applied this technique to follow an ultrafast irreversible laser-superheating process with few nanometers spatial and 100 femtosecond temporal resolutions at the single nanoparticle level.

Despite significant efforts, the spatial resolution of single XFEL CDI images of non-periodic specimen could not be improved beyond few nanometers. This proposal will overcome this limit by exploiting previously little explored phenomena which arise when specimen are exposed to newly available intense 500 attosecond to few femtosecond short FEL pulses. All matter exposed to intense X-rays is photo-ionised. When XFEL pulses are comparable or shorter than subsequent relaxation processes, non-linear effects such as transient resonances and resonant stimulated emission increase the brightness of images by several orders of magnitudes and significantly improve the spatial resolution. In combination with sparsity based reconstruction algorithms this proposal will push ultrafast CDI towards the single macromolecule limit and open novel avenues for photochemistry, catalysis, and material studies.

Host institution

UNIVERSITY OF HAMBURG
Net EU contribution
€ 1 500 000,00
Address
MITTELWEG 177
20148 Hamburg
Germany

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Region
Hamburg Hamburg Hamburg
Activity type
Higher or Secondary Education Establishments
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Total cost
€ 1 500 000,00

Beneficiaries (1)