Maria Krikunova

Single-shot timing measurement of extreme-ultraviolet free-electron laser pulses

Arrival time fluctuations of extreme-ultraviolet (EUV) pulses from the free-electron laser in Hamburg (FLASH) are measured single-pulse resolved at the experimental end-station. To this end, they are non-collinearly superimposed in space and time with visible femtosecond laser pulses on a GaAs substrate. The EUV irradiation induces changes of the reflectivity for the visible pulse. The temporal delay between the two light pulses is directly encoded in the spatial position of the reflectivity change which is captured with a CCD camera. For each single shot, the relative EUV/visible arrival-time can be measured with about 40 fs rms accuracy. The method constitutes a novel route for an improvement of future pump–probe experiments at short-wavelength free-electron lasers (FELs) by a pulse-wise correction with simultaneously measured arrival times of individual EUV pulses.

AMO science at the FLASH and European XFEL free-electron laser facilities

Present performance and future development of the free-electron lasers (FELs) in Hamburg—FLASH for the extreme ultraviolet and the European XFEL for the soft and hard x-ray regimes—are presented. As an illustration of the unprecedented characteristics of these sources a few recent examples of experiments performed in the area of atomic, molecular and optical (AMO) physics are described. The results highlight in particular the available high photon intensities, the short pulse durations and the coherence of the FEL beam. Nonlinear processes involving for the first time inner-shell electrons, time-resolved experiments on the few femtosecond timescales, and imaging experiments on small particles have been the focus of these studies, demonstrating the unique potential of short-wavelength FELs and pointing to numerous exciting future opportunities.

SH3P7/mAbp1 deficiency leads to tissue and behavioral abnormalities and impaired vesicle transport

The intracellular adaptor protein SH3P7 is the mammalian ortholog of yeast actin‐binding protein 1 and thus alternatively named as mAbp1 (or HIP55). Structural properties, biochemical analysis of its interaction partners and siRNA studies implicated mAbp1 as an accessory protein in clathrin‐mediated endocytosis (CME). Here, we describe the generation and characterization of mice deficient for SH3P7/mAbp1 owing to targeted gene disruption in embryonic stem cells. Mutant animals are viable and fertile without obvious deficits during the first weeks of life. Abnormal structure and function of organs including the spleen, heart, and lung is observed at about 3 months of age in both heterozygous and homozygous mouse mutants. A moderate reduction of both receptor‐mediated and synaptic endocytosis is observed in embryonic fibroblasts and in synapses of hippocampal neurons, respectively. Recycling of synaptic vesicles in hippocampal boutons is severely impaired and delayed four‐fold. The presynaptic defect of SH3P7/mAbp1 mouse mutants is associated with their constricted physical capabilities and disturbed neuromotoric behaviour. Our data reveal a nonredundant role of SH3P7/mAbp1 in CME and places its function downstream of vesicle fission.

A modular end-station for atomic, molecular, and cluster science at the low density matter beamline of FERMI@Elettra

The low density matter end-station at the new seeded free electron laser FERMI@Elettra is a versatile instrument for the study of atoms, molecules and clusters by means of electron and ion spectroscopies. Beams of atoms, molecules and helium droplets as well as clusters of atoms, molecules and metals can be produced by three different pulsed valves. The atomic and molecular beams may be seeded, and the clusters and droplets may be pure, or doped with other atoms and molecules. The electrons and ions produced by the ionization and fragmentation of the samples by the intense light of FERMI can be analysed by the available spectrometers, to give mass spectra and energy as well as angular distributions of charged particles. The design of the detector allows simultaneous detection of electrons and ions using velocity map imaging and time-of-flight techniques respectively. The instruments have a high energy/mass resolution and large solid-angle collection efficiency. We describe the current status of the apparatus and illustrate the potential for future experiments.

Time-resolved ion spectrometry on xenon with the jitter-compensated soft x-ray pulses of a free-electron laser

Atomic inner-shell relaxation dynamics were measured at the free-electron laser in Hamburg, FLASH, delivering 92 eV pulses. The decay of 4d core holes created in xenon was followed by detection of ion charge states after illumination with delayed 400 nm laser pulses. A timing jitter of the order of several hundred femtoseconds between laser- and accelerator-pulses was compensated for by a simultaneous delay measurement in a single-shot x-ray/laser cross-correlator. After sorting of the tagged spectra according to the measured delays, a temporal resolution equivalent to the pulse duration of the optical laser could be established. While results on ion charge states up to Xe4+ are compatible with a previous study using a high-harmonic soft x-ray source, a new relaxation pathway is opened by the nonlinear excitation of xenon atoms in the intense free-electron laser light field, leading to the formation of Xe5+.

Ionization dynamics in expanding clusters studied by XUV pump?probe spectroscopy

The expansion and disintegration dynamics of xenon clusters initiated by the ionization with femtosecond soft x-ray extreme ultraviolet (XUV) pulses were studied with pump–probe spectroscopy using the autocorrelator setup of the Free-Electron LASer in Hamburg (FLASH) facility. The ionization by the first XUV pulse of 92 eV photon energy (8 × 10 12 Wc m −2 ) leads to the generation of a large number of quasi-free electrons trapped by the space charge of the cluster ions. A temporally delayed, more intense probe (4 × 10 13 Wc m −2 ) pulse substantially increases a population of nanoplasma electrons providing a way of probing plasma states in the expanding cluster by tracing the average charge of fragment ions. The results of the study reveal a timescale for cluster expansion and disintegration, which depends essentially on the initial cluster size. The average charge state of fragment ions, and thus the cluster plasma changes significantly on a timescale of 1–3 ps. (Some figures may appear in colour only in the online journal)

Ultrafast photofragmentation dynamics of molecular iodine driven with timed XUV and near-infrared light pulses.

Photofragmentation dynamics of molecular iodine was studied as a response to the joint illumination with femtosecond 800 nm near-infrared and 13 nm extreme ultraviolet (XUV) pulses delivered by the free-electron laser facility FLASH. The interaction of the molecular target with two light pulses of different wavelengths but comparable pulse energy elucidates a complex intertwined electronic and nuclear dynamics. To follow distinct pathways out of a multitude of reaction channels, the recoil of created ionic fragments is analyzed. The delayed XUV pulse provides a way of following molecular photodissociation of I(2) with a characteristic time-constant of (55 ± 10) fs after the laser-induced formation of antibonding states. A preceding XUV pulse, on the other hand, preferably creates a 4d(-1) inner-shell vacancy followed by the fast Auger cascade with a revealed characteristic time constant τ(A2)=(23±11) fs for the second Auger decay transition. Some fraction of molecular cationic states undergoes subsequent Coulomb explosion, and the evolution of the launched molecular wave packet on the repulsive Coulomb potential was accessed by the laser-induced postionization. A further unexpected photofragmentation channel, which relies on the collective action of XUV and laser fields, is attributed to a laser-promoted charge transfer transition in the exploding molecule.

Time-to-space mapping in a gas medium for the temporal characterization of vacuum-ultraviolet pulses

The authors introduce a method for cross correlating vacuum-ultraviolet with near-infrared femtosecond light pulses in a perpendicular geometry. Photoelectrons generated in an atomic gas by laser-assisted photoionization are used to create a two-dimensional image of the cross-correlation volume, thereby mapping time onto a space coordinate. Thus, information about pulse duration and relative timing between the pulses can be obtained without the need to scan an optical delay line. First tests using vacuum-ultraviolet pulses from the free-electron laser at the Deutsches Elektronen Synchrotron set an upper limit for their temporal jitter with respect to external optical laser pulses.

Recombination dynamics of clusters in intense extreme-ultraviolet and near-infrared fields

We investigate electron-ion recombination processes in clusters exposed to intense extreme-ultraviolet (XUV) or near-infrared (NIR) pulses. Using the technique of reionization of excited atoms from recombination (REAR), recently introduced in Schutte et al (2014 Phys. Rev. Lett. 112 253401), a large population of excited atoms, which are formed in the nanoplasma during cluster expansion, is identified under both ionization conditions. For intense XUV ionization of clusters, we find that the significance of recombination increases for increasing cluster sizes. In addition, larger fragments are strongly affected by recombination as well, as shown for the case of dimers. We demonstrate that for mixed Ar–Xe clusters exposed to intense NIR pulses, excited atoms and ions are preferentially formed in the Xe core. As a result of electron-ion recombination, higher charge states of Xe are efficiently suppressed, leading to an overall reduced expansion speed of the cluster core in comparison to the shell.

AP‐1 Membrane–Cytoplasm Recycling Regulated by μ1A‐Adaptin

The adaptor protein complex AP‐1 mediates vesicular protein sorting between the trans Golgi network and endosomes. AP‐1 recycles between membranes and the cytoplasm together with clathrin during transport vesicle formation and vesicle uncoating. AP‐1 recycles independent of clathrin, indicating binding to unproductive membrane domains and premature termination of vesicle budding. Membrane recruitment requires ADP ribosylation factor‐1‐GTP, a transmembrane protein containing an AP‐1‐binding motif and phosphatidyl‐inositol phosphate (PI‐4‐P). Little is known about the regulation of AP‐1 membrane–cytoplasm recycling. We identified the N‐terminal domain of μ1A‐adaptin as being involved in the regulation of AP‐1 membrane–cytoplasm recycling by constructing chimeras of μ1A and its homologue μ2. The AP‐1* complex containing this μ2–μ1A chimera had slowed down recycling kinetics, resulting in missorting of mannose 6‐phosphate receptors. The N‐terminal domain is only accessible from the cytoplasmic AP‐1 surface. None of the proteins known to influence AP‐1 membrane recycling bound to this μ1A domain, indicating the regulation of AP‐1 membrane–cytoplasm recycling by an yet unidentified cytoplasmic protein.