Quantum electrodynamics (QED), the quantum field theory that describes the interaction between light and matter, is commonly regarded as the best-tested quantum theory in modern physics. However, this claim is mostly based on extremely precise studies performed in the domain of relatively low field strengths and light atoms and ions 1 – 6 . In the realm of very strong electromagnetic fields such as in the heaviest highly charged ions (with nuclear charge Z ≫ 1), QED calculations enter a qualitatively different, non-perturbative regime. Yet, the corresponding experimental studies are very challenging, and theoretical predictions are only partially tested. Here we present an experiment sensitive to higher-order QED effects and electron–electron interactions in the high- Z regime. This is achieved by using a multi-reference method based on Doppler-tuned X-ray emission from stored relativistic uranium ions with different charge states. The energy of the 1 s 1/2 2 p 3/2 J = 2 → 1 s 1/2 2 s 1/2 J = 1 intrashell transition in the heaviest two-electron ion (U 90+ ) is obtained with an accuracy of 37 ppm. Furthermore, a comparison of uranium ions with different numbers of bound electrons enables us to disentangle and to test separately the one-electron higher-order QED effects and the bound electron–electron interaction terms without the uncertainty related to the nuclear radius. Moreover, our experimental result can discriminate between several state-of-the-art theoretical approaches and provides an important benchmark for calculations in the strong-field domain.

We report here on results of systematic experimental-theoretical investigation of high-order harmonic gen-eration (HHG) in layers of CdSe semiconductor quantum dots of different sizes and a reference bulk CdSe thin film. We observe a strong decrease in the efficiency, up to complete suppression of HHG with energies of quanta above the band gap for the smallest dots, whereas the intensity of below band gap harmonics remains weakly affected by the dot size. In addition, it is observed that the suppression of the above gap harmonics is enhanced with increasing the driving wavelength. These systematic investigations allow us to develop a simple physical picture explaining the observed suppression of the highest harmonics: the discretization of electronic energy levels seems to be not the predominant contribution to the observed suppression but rather the confined dot size itself, causing field-driven electrons to scatter off the dot's walls. The reduction in the dot size below the classical electron oscillatory radius and the corresponding scattering limits the maximum acceleration by the laser field. Moreover, this scattering leads to a chaotization of motion, causing dephasing and a loss of coherence, therefore suppressing the efficiency of the emission of highest-order harmonics. Our results demon-strate a regime of intense laser-nanoscale solid interaction, intermediate between the bulk and single-molecule response, and are crucial for nanophotonic platforms aiming at control over high-order harmonic properties and efficiency.

We present a here a non-parametric analysis of x-ray spectra for experiment E125 performed at GSI-FAIR in Darmstadt. This experiment measured intra-shell transitions of highly charged uranium with a twin-arm Bragg spectrometer equipped with x-rays CCDs. The method consists in slicing the CCD image and calculating the centroids of the lines, then adjusting the slice size in order to remove background. Due to the low count rate, we reveal the limitations of this method which provides an accuracy of only a few pixels, far from the sub-pixel requirement.

We report here on the results of comparative experimental measurements of laser energy absorption in a bulk and different morphology nanowire arrays interacting with relativistically intense, ultra-high temporal contrast femtosecond laser pulses. We compare polished, flat bulk samples with vertically and randomly oriented nanowires made of ZnO semiconductor material. The optical absorption of the 45° incident laser pulses of ∼40 fs duration with a central wavelength of 400 nm at intensities above 1019Wcm2 was determined using an integrating Ulbricht sphere. We demonstrate an almost twofold enhancement of absorption in both nanowire morphologies with an average of (79.6±1.9)% in comparison to the flat bulk sample of (45.8±1.9)%. The observed substantially enhanced absorption in nanowire arrays is also confirmed by high-resolution x-ray emission spectroscopy. The spectral analysis of the K-shell x-ray emission lines revealed that the He-like resonance line emission from highly ionized Zn (Zn28+) is only present in the case of nanowire arrays, whereas, for the flat bulk samples, only neutral and low charge states were observed. Our numerical simulations, based on radiative-collisional kinetic code FLYCHK, well reproduce the measured He-like emission spectrum and suggest that high charge state observed in nanowire arrays is due to substantially higher plasma temperature. Our results, which were measured for the first time with femtosecond laser pulses, can be used to benchmark theoretical models and numerical codes for the relativistic interaction of ultrashort laser pulses with nanowires.

We report on the realization of an extremely sensitive x-ray polarization microscope, allowing to detect tiniest polarization changes of 1 in 100 billion (10 −11 ) with a μ m-size focused beam. The extreme degree of polarization purity places the most stringent requirements on the orientation of the polarizer and analyzer crystals as well as the composition and the form fidelity of the lenses, which must not exhibit any birefringence. The results show that these requirements are currently only met by polymer lenses. Highly sensitive scanning x-ray polarization microscopy thus is established as a new method. It can provide new insights in a wide range of applications ranging from quantum electrodynamics and quantum optics to x-ray spectroscopy, materials research, and laser physics.

In this work, the first proof of the principal of an in situ diagnostics of the heavy-ion beam intensity distribution in irradiation of solid targets is proposed. In this scheme, x-ray fluorescence that occurs in the interaction of heavy-ions with target atoms is used for imaging purposes. The x-ray conversion to optical radiation and a transport-system was developed, and its first test was performed in experiments at the Universal Linear Accelerator in Darmstadt, Germany. The Au-beam intensity distribution on thin foils and Cu-mesh targets was imaged using multiple x-ray pinholes (polychromatic imaging) and 2D monochromatic imaging of Cu Kα radiation by using a toroidally bent silicon crystal. The presented results are of importance for application in experiments on the investigation of the equation of states of high energy density matter using high intensity GeV/u heavy-ion beams of ≥1010 particles/100 ns.

Dichroism is one of the most important optical effects in both the visible and the X-ray range. Besides absorption, scattering can also contribute to dichroism. This paper demonstrates that, based on the example of polyimide, materials can show tiny dichroism even far from electronic resonances due to scattering. Although the effect is small, it can lead to a measurable polarization change and might have influence on highly sensitive polarimetric experiments.

We introduce a setup to measure high-resolution inelastic x-ray scattering at the High Energy Density scientific instrument at the European X-Ray Free-Electron Laser (XFEL). The setup uses the Si (533) reflection in a channel-cut monochromator and three spherical diced analyzer crystals in near-backscattering geometry to reach a high spectral resolution. An energy resolution of 44 meV is demonstrated for the experimental setup, close to the theoretically achievable minimum resolution. The analyzer crystals and detector are mounted on a curved-rail system, allowing quick and reliable changes in scattering angle without breaking vacuum. The entire setup is designed for operation at 10 Hz, the same repetition rate as the high-power lasers available at the instrument and the fundamental repetition rate of the European XFEL. Among other measurements, it is envisioned that this setup will allow studies of the dynamics of highly transient laser generated states of matter.

We present a method to determine the bulk temperature of a single crystal diamond sample at an X-Ray free electron laser using inelastic X-ray scattering. The experiment was performed at the high energy density instrument at the European XFEL GmbH, Germany. The technique, based on inelastic X-ray scattering and the principle of detailed balance, was demonstrated to give accurate temperature measurements, within 8% for both room temperature diamond and heated diamond to 500 K. Here, the temperature was increased in a controlled way using a resistive heater to test theoretical predictions of the scaling of the signal with temperature. The method was tested by validating the energy of the phonon modes with previous measurements made at room temperature using inelastic X-ray scattering and neutron scattering techniques. This technique could be used to determine the bulk temperature in transient systems with a temporal resolution of 50 fs and for which accurate measurements of thermodynamic properties are vital to build accurate equation of state and transport models.

This work demonstrates efficient micro-lensing of laseraccelerated proton beams by transient electromagnetic (EM) fields in coil targets. In an all-optical principle, hig intensity ps-laser pulses are used to charge solid density t argets and induce EM target-discharges [1]. The strong transient EM-fields are guided by the target geometry. Such EM-mode propagation along wire targets [2] has already been used for the guiding of a proton beam [3]. Our collaboration aims at a more easily tunable energy-selective collimation and focusing with independent discharge and particle source targets: A sub-mm coil shaped part of the discharge target’s rod produces lensing effects. Protons with in an energy range of approximately ±2MeV, with energies up to12MeV, are focused over cm-scale distances.

Damage formation is investigated in GaAs implanted with 1 MeV Si ions to ion fluences from 3 x 10(12) to 5 x 10(15) cm(-2) at room temperature. Under the conditions applied, amorphization of the implanted layers does not occur. The weakly damaged layers are studied by applying different experimental techniques including Rutherford backscattering spectrometry in channeling configuration, x-ray diffraction, in situ curvature measurement, optical subgap spectroscopy, and transmission electron microscopy. The results are evaluated and quantitatively connected with each other. Damage formation is described as a function of the ion fluence using a common defect evolution model. Point defects and defect clusters have to be taken into account in the ion fluence range of main interest up to 2 x 10(15) cm(-2). Point defects contribute by a factor of about 8 more to both perpendicular strain and in-plane stress than defect clusters. When the concentration of point defects or the induced strain reaches a critical value, defect clusters form, which ensures that no further increase of perpendicular strain occurs. This reveals a clear driving force for cluster formation. The microstructure of the defect clusters cannot be determined from the results. As3Ga2 interstitial clusters are supposed. A remarkable decrease of the shear modulus of the implanted layers below the value of pristine GaAs by approximate to -35% is observed. Surprisingly, the change of shear modulus already sets in at a very low damage level of a few percent.

Accurate spectroscopy of highly charged high-Z ions in a storage ring is demonstrated to be feasible by the use of specially adapted crystal optics. The method has been applied for the measurement of the 1s Lamb shift in hydrogen-like gold (Au 78+) in a storage ring through spectroscopy of the Lyman x rays. This measurement represents the first result obtained for a high-Z element using high-resolution wavelength-dispersive spectroscopy in the hard x-ray regime, paving the way for sensitivity to higher-order QED effects.

We present experimental evidence of ultra-high energy density plasma states with the keV bulk electron temperatures and near-solid electron densities generated during the interaction of high contrast, relativistically intense laser pulses with planar metallic foils. Experiments were carried out with the Ti:Sapphire laser system where a picosecond pre-pulse was strongly reduced by the conversion of the fundamental laser frequency into 2ω. A complex diagnostics setup was used for evaluation of the electron energy distribution in a wide energy range. The bulk electron temperature and density have been measured using x-ray spectroscopy tools; the temperature of supra-thermal electrons traversing the target was determined from measured bremsstrahlung spectra; run-away electrons were detected using magnet spectrometers. Analysis of the bremsstrahlung spectra and results on measurements of the run-away electrons showed a suppression of the hot electron production in the case of the high laser contrast. Characteristic x-ray radiation has been used for evaluation of the bulk electron temperature and density. The measured Ti line radiation was simulated both in steady-state and transient approaches using the code FLYCHK that accounts for the atomic multi-level population kinetics. The best agreement between the measured and the synthetic spectrum of Ti was achieved at 1.8 keV electron temperature and 2 × 1023 cm−3 electron density. By application of Ti-foils covered with nm-thin Fe-layers, we have demonstrated that the thickness of the created keV hot dense plasma does not exceed 150 nm. Results of the pilot hydro-dynamic simulations that are based on a wide-range two-temperature Equation of States, wide-range description of all transport and optical properties, ionization, electron, and radiative heating, plasma expansion, and Maxwell equations (with a wide-range permittivity) for description of the laser absorption are in excellent agreement with experimental results. According to these simulations, the generation of keV-hot bulk electrons is caused by the collisional mechanism of the laser pulse absorption in plasmas with a near solid step-like electron density profile. The laser energy, first deposited into the nm-thin skin-layer, is then transported into 150 nm depth by the electron heat conductivity. This scenario is opposite to the volumetric character of the energy deposition produced by supra-thermal electrons.

We present an experimental study of X-ray generation from nanostructured ZnO targets. Samples of different morphology ranging from nanowires to polished surfaces are irradiated by relativistically intense femtosecond laser pulses. X-ray emission of plasma is generated by 45 fs 130 mJ laser pulses at 400 nm with picosecond temporal contrast better than 10(-9) interacting with an array of ZnO nanowires. The measured spectra indicate the existence of highly ionized states of Zn (up to He-like Zn). The obtained flux of similar to 10(10) photons per laser shot at the neutral Zn K-alpha energies around 8.65 keV and at the Zn He-alpha energies around 9 keV is almost 3 times higher for nanostructured targets compared to the reference polished sample and implies 10(-4) conversion efficiency from the laser energy to the total energy of the emitted X-ray photons.

An analysis of an electron spectrometer used to characterize fast electrons generated by ultraintense (10^{20}Wcm^{-2}) laser interaction with a preformed plasma of scale length measured by shadowgraphy is presented. The effects of fringing magnetic fields on the electron spectral measurements and the accuracy of density scale-length measurements are evaluated. 2D EPOCH PIC code simulations are found to be in agreement with measurements of the electron energy spectra showing that laser filamentation in plasma preformed by a prepulse is important with longer plasma scale lengths (>8 μm).

The linear polarization of the characteristic lines L alpha(1) (3d(5/2) -> 2p(3/2)) and L alpha(2) (3d(3/2) -> 2p(3/2)), following inner-shell photoionization of neutral tungsten, is analyzed both experimentally and theoretically. In the experiment, a tungsten target is photoionized by the primary emission of an x-ray tube with incident photon energies in the range of 10.2-30 keV. The sigma and pi components of the emitted fluorescence are measured by using a spectropolarimeter, based on x-ray diffraction at Bragg angles close to 45 degrees. The degree of linear polarization of the L alpha(1) and L alpha(2) lines is determined to be +(1.6 +/- 0.5)% and -(7 +/- 2)%, respectively. In addition, this degree of polarization is calculated within the framework of the density-matrix theory as a function of the incident photon energy. These calculations are in good agreement with the experimental results and show only a weak dependence of the degree of polarization on the energy of the incident photoionizing photon.

We report on the first observation of high-n hollow ions (ions having no electrons in the K or L shells) produced in Si targets via pumping by ultra-intense x-ray radiation produced in intense laser-plasma interactions reaching the radiation dominant kinetics regime (RDKR). The existence of these new types of hollow ions in high-energy density plasma has been found via observation of highly resolved x-ray emission spectra of silicon plasma. This has been confirmed by plasma kinetics calculations, underscoring the ability of powerful radiation sources to fully strip electrons from the innermost shells of light atoms. Hollow-ions spectral diagnostics provide a unique opportunity to characterize powerful x-ray radiation of laboratory and astrophysical plasmas. With the use of this technique we provide evidence for the existence of the RDKR via observation of asymmetry in the observed radiation of hollow ions from the front and rear sides of the target. Copyright (C) EPLA, 2016