Referierte Publikationen

The Dirac-Heisenberg-Wigner formalism is employed to investigate electron-positron pair production in cylindrically symmetric but otherwise spatially inhomogeneous, oscillating electric fields. The oscillation frequencies are hereby tuned to obtain multiphoton pair production in the nonperturbative threshold regime. An effective mass, as well as a trajectory-based semiclassical analysis, is introduced in order to interpret the numerical results for the distribution functions as well as for the particle yields and spectra. The results, including the asymptotic particle spectra, display clear signatures of ponderomotive forces.

We investigate the quantum interference induced shifts between energetically close states in highly charged ions, with the energy structure being observed by laser spectroscopy. In this work, we focus on hyperfine states of lithiumlike heavy-Z isotopes and quantify how much quantum interference changes the observed transition frequencies. The process of photon excitation and subsequent photon decay for the transition 2s→2p→2s is implemented with fully relativistic and full-multipole frameworks, which are relevant for such relativistic atomic systems. We consider the isotopes 207Pb79+ and 209Bi80+ due to experimental interest, as well as other examples of isotopes with lower Z, namely 141Pr56+ and 165Ho64+. We conclude that quantum interference can induce shifts up to 11% of the linewidth in the measurable resonances of the considered isotopes, if interference between resonances is neglected. The inclusion of relativity decreases the cross section by 35%, mainly due to the complete retardation form of the electric dipole multipole. However, the contribution of the next higher multipoles (e.g., magnetic quadrupole) to the cross section is negligible. This makes the contribution of relativity and higher-order multipoles to the quantum interference induced shifts a minor effect, even for heavy-Z elements.

The elastic Rayleigh scattering of twisted light and, in particular, the polarization (transfer) of the scattered photons have been analyzed within the framework of second-order perturbation theory and Dirac's relativistic equation. Special attention was paid hereby to the scattering on three different atomic targets: single atoms, a mesoscopic (small) target, and a macroscopic (large) target, which are all centered with regard to the beam axis. Detailed calculations of the polarization Stokes parameters were performed for C5+ ions and for twisted Bessel beams. It is shown that the polarization of scattered photons is sensitive to the size of an atomic target and to the helicity, the opening angle, and the projection of the total angular momentum of the incident Bessel beam. These computations indicate more that the Stokes parameters of the (Rayleigh) scattered twisted light may significantly differ from their behavior for an incident plane-wave radiation.

Abstract A comprehensive spatio-temporal characterization is presented describing the pump-induced wavefront aberrations in Yb3 + -doped YAG, CaF2, and fluorophosphate glass. Time-resolved interferometric measurements were performed to reveal the profiles of the total optical path differences (OPDs), which are described by the spatio-temporal superposition of thermal as well as electronic contributions, across the free aperture of the considered diode-pumped active materials. These contributions were individually determined by a COMSOL-based thermal profile model along with a detailed characterization of the electronic changes by measuring the single-pass gain and the spatial fluorescence profile. Due to the low quantum defect, the amplitude of the electronic component becomes comparable for all three materials and, in the case of Yb:CaF2, almost completely compensates the thermal component resulting from a pump pulse during the time frame of laser pulse amplification. Finally, all relevant material constants – such as the photoelastic constant and the polarizability difference – could be determined during this investigation, allowing the accurate modeling of the total pump-induced wavefront aberrations and subsequent optimization for laser systems worldwide employing these Yb3 + -doped materials.

The hyperfine structure splitting in the 6p3S3/24→6p27sP1/24 transition at 307 nm in atomic 208Bi was measured with collinear laser spectroscopy at ISOLDE, CERN. The hyperfine A and B factors of both states were determined with an order of magnitude improved accuracy. Based on these measurements, theoretical input for the hyperfine structure anomaly, and results from hyperfine measurements on hydrogen-like and lithium-like 209Bi80+,82+, the nuclear magnetic moment of 208Bi has been determined to μ(Bi208)=+4.570(10) μN. Using this value, the transition energy of the ground-state hyperfine splitting in hydrogen-like and lithium-like 208Bi80+,82+ and their specific difference of −67.491(5)(148) meV are predicted. This provides a means for an experimental confirmation of the cancellation of nuclear structure effects in the specific difference in order to exclude such contributions as the cause of the hyperfine puzzle, the recently reported 7-σ discrepancy between experiment and bound-state strong-field QED calculations of the specific difference in the hyperfine structure splitting of 209Bi80+,82+.

We study the trident process in inhomogeneous plane-wave background fields. We obtain compact analytical expressions for all terms in the probability, including the exchange part, for an arbitrarily shaped plane wave. We evaluate the probability numerically using complex deformation of light-front time integrals and derive various analytical approximations. Our results provide insights into the importance of the one-step and exchange parts of the probability relative to the two-step process, and into the convergence to the locally constant field approximation.

Ultrafast spectroscopy with attosecond resolution has enabled the real time observation of ultrafast electron dynamics in atoms, molecules and solids. These experiments employ attosecond pulses or pulse trains and explore dynamical processes in a pump–probe scheme that is selectively sensitive to electronic state of matter via photoelectron or XUV absorption spectroscopy or that includes changes of the ionic state detected via photo-ion mass spectrometry. Here, we demonstrate how the implementation of combined photo-ion and absorption spectroscopy with attosecond resolution enables tracking the complex multidimensional excitation and decay cascade of an Auger auto-ionization process of a few femtoseconds in highly excited krypton. In tandem with theory, our study reveals the role of intermediate electronic states in the formation of multiply charged ions. Amplitude tuning of a dressing laser field addresses different groups of decay channels and allows exerting temporal and quantitative control over the ionization dynamics in rare gas atoms.

The feasibility of an experiment for the observation of parity nonconserving effects using He-like highly charged ions in storage rings is discussed theoretically. The basic idea is the observation of an asymmetry in the emission of the hyperfine quenched transition (1s2s)¹S₀\to (1s)²¹S₀+γ with respect to the direction of a beam of ions with polarized nuclei. It will be shown, that for such an experiment 151Eu^61+ ions with nuclear spin I=5/2 in the excited electronic state (1s2s)¹S₀ with zero total electron angular momentum and polarized nuclei are the best available candidates. The nuclei can be polarized if H-like Eu^62+ ions capture an electron from a polarized electron beam which overlays the ion beam on some part of the ring and travels with nearly the same velocity. It is suggested, to monitor steadily the degree of the nuclear polarization by the observation of the selective laser excitation and subsequent decay of the Zeeman sublevels of the excited hyperfine states of the ionic ground state. Estimates for the observation time aiming at an accuracy of PNC measurement of about 0.1 % are given.

A description of the spectral and angular distributions of Compton scattered light in collisions of intense laser pulses with high-energy electrons is unwieldy and usually requires numerical simulations. However, due to the large number of parameters affecting the spectra such numerical investigations can become computationally expensive. Using methods of catastrophe theory we predict higher-dimensional caustics in the spectra of the Compton scattered light, which are associated with bright narrow-band spectral lines, and in the simplest case can be controlled by the value of the linear chirp of the pulse. These findings require no full-scale calculations and have direct consequences for the photon yield enhancement of future nonlinear Compton scattering x-ray or gamma-ray sources.

Often, the interpretation of experiments concerning the manipulation of the energy distribution of laser-accelerated ion bunches is complicated by the multitude of competing dynamic processes simultaneously contributing to recorded ion signals. Here we demonstrate experimentally the acceleration of a clean proton bunch. This was achieved with a microscopic and three-dimensionally confined near critical density plasma, which evolves from a 1 µm diameter plastic sphere, which is levitated and positioned with micrometer precision in the focus of a Petawatt laser pulse. The emitted proton bunch is reproducibly observed with central energies between 20 and 40 MeV and narrow energy spread (down to 25%) showing almost no low-energetic background. Together with three-dimensional particle-in-cell simulations we track the complete acceleration process, evidencing the transition from organized acceleration to Coulomb repulsion. This reveals limitations of current high power lasers and viable paths to optimize laser-driven ion sources.

We measured the fluorescence photon yield of neon upon soft x-ray ionization (∼1200 eV) from the x-ray free-electron laser at Linac Coherent Light Source, and demonstrated the usage of a grazing incidence spectrometer with a variable line spacing grating to perform x-ray fluorescence spectroscopy on a gas phase system. Our measurements also allowed us to estimate the focal size of the beam from the theoretical description developed, in terms of the rate equation approximation accounting for photoionization shake off of neutral neon and double auger decay of single core holes.

We summarize results for local and global properties of the effective potential for the Higgs boson obtained from the functional renormalization group, which allows one to describe the effective potential as a function of both scalar field amplitude and renormalization group scale. This sheds light onto the limitations of standard estimates which rely on the identification of the two scales and helps in clarifying the origin of a possible property of meta-stability of the Higgs potential. We demonstrate that the inclusion of higher-dimensional operators induced by an underlying theory at a high scale (GUT or Planck scale) can relax the conventional lower bound on the Higgs mass derived from the criterion of absolute stability. This article is part of the Theo Murphy meeting issue "Higgs cosmology".

The fast evaporative cooling of micrometer-sized water droplets in a vacuum offers the appealing possibility to investigate supercooled water—below the melting point but still a liquid—at temperatures far beyond the state of the art. However, it is challenging to obtain a reliable value of the droplet temperature under such extreme experimental conditions. Here, the observation of morphology-dependent resonances in the Raman scattering from a train of perfectly uniform water droplets allows us to measure the variation in droplet size resulting from evaporative mass losses with an absolute precision of better than 0.2%. This finding proves crucial to an unambiguous determination of the droplet temperature. In particular, we find that a fraction of water droplets with an initial diameter of 6379±12  nm remain liquid down to 230.6±0.6  K. Our results question temperature estimates reported recently for larger supercooled water droplets and provide valuable information on the hydrogen-bond network in liquid water in the hard-to-access deeply supercooled regime.

We investigate the emergence of N = 1 supersymmetry in the long-range behavior of three-dimensional parity-symmetric Yukawa systems. We discuss a renormalization approach that manifestly preserves supersymmetry whenever such symmetry is realized, and use it to prove that supersymmetry-breaking operators are irrelevant, thus proving that such operators are suppressed in the infrared. All our findings are illustrated with the aid of the ϵ-expansion and a functional variant of perturbation theory, but we provide numerical estimates of critical exponents that are based on the non-perturbative functional renormalization group.

Noncollinear pulse characterization methods can be applied to over-octave spanning waveforms, but geometrical effects in the nonlinear medium such as beam smearing and critical sensitivity to beam alignment hinder their accurate application. Here, a method is introduced for the temporal and spatial characterization of two pulses by interferometric, spectrally resolved imaging of self-diffraction. Geometrical effects are resolved by the method and, therefore, do not limit the accuracy. Two methods for quantitative pulse retrieval are presented. One method is analytical and very fast; the other method is iterative and more robust if applied to noisy data.

We have systematically investigated the ground-state hyperfine structure for alkali-metal atoms 87Rb, 33Cs, and 211Fr and alkali-metal-like ions 135Ba^+ and 225Ra^+, which are of particular interest for parity violation studies. The quantum electrodynamic one-loop radiative corrections have been rigorously evaluated within an extended Furry picture employing core-Hartree and Kohn-Sham atomic potentials. Moreover, the effect of the nuclear magnetization distribution on the hyperfine structure intervals has been studied in detail and its uncertainty has been estimated. Finally, the theoretical description of the hyperfine structure has been completed with full many-body calculations performed in the all-orders correlation potential method.

We have conceived, built, and operated a cryogenic Penning trap with an electrically conducting yet optically transparent solid electrode. The trap, dedicated to spectroscopy and imaging of confined particles under large solid angles, is of “half-open” design with one open endcap and one closed endcap that mainly consists of a glass window coated with a highly transparent conductive layer. This arrangement allows for the trapping of externally or internally produced particles and yields flexible access for optical excitation and efficient light collection from the trapping region. At the same time, it is electrically closed and ensures long-term ion confinement under well-defined conditions. With its superior surface quality and its high as well as homogeneous optical transmission, the window electrode is an excellent replacement for partially transmissive electrodes that use holes, slits, metallic meshes, and the like.

In this article, we provide analytical expressions for the photon polarization tensor in pulsed Hermite- and Laguerre-Gaussian laser beams. Our results are based on a locally constant field approximation of the one-loop Heisenberg-Euler effective Lagrangian for quantum electrodynamics. Hence, by construction they are limited to slowly varying electromagnetic fields, varying on spatial and temporal scales significantly larger than the Compton wavelength/time of the electron. The latter criterion is fulfilled by all laser beams currently available in the laboratory. Our findings will, e.g., be relevant for the study of vacuum birefringence experienced by probe photons brought into collision with a high-intensity laser pulse which can be represented as a superposition of either Hermite- or Laguerre-Gaussian modes.

The possibility of utilizing plasma undulators and plasma accelerators to produce compact ultraviolet and X-ray sources, has attracted considerable interest for a few decades. This interest has been driven by the great potential to decrease the threshold for accessing such sources, which are mainly provided by a few dedicated large-scale synchrotron or free-electron laser (FEL) facilities. However, the broad radiation bandwidth of such plasma devices limits the source brightness and makes it difficult for the FEL instability to develop. Here, using multi-dimensional particle-in-cell (PIC) simulations, we demonstrate that a plasma undulator generated by the beating of a mixture of high-order laser modes propagating inside a plasma channel, leads to a few percent radiation bandwidth. The strength of the undulator can reach unity, the period can be less than a millimeter, and the number of undulator periods can be significantly increased by a phase locking technique based on the longitudinal tapering. Polarization control of such an undulator can be achieved by appropriately choosing the phase of the modes. According to our results, in the fully beam loaded regime, the electron current in the plasma undulator can reach 0.3âEUR%0kA level, making such an undulator a potential candidate towards a table-top FEL.

Ultrafast supercontinuum generation in gas-filled waveguides is an enabling technology for many intriguing applications ranging from attosecond metrology towards biophotonics, with the amount of spectral broadening crucially depending on the pulse dispersion of the propagating mode. In this study, we show that structural resonances in a gas-filled antiresonant hollow core optical fiber provide an additional degree of freedom in dispersion engineering, which enables the generation of more than three octaves of broadband light that ranges from deep UV wavelengths to near infrared. Our observation relies on the introduction of a geometric-induced resonance in the spectral vicinity of the ultrafast pump laser, outperforming gas dispersion and yielding a unique dispersion profile independent of core size, which is highly relevant for scaling input powers. Using a krypton-filled fiber, we observe spectral broadening from 200 nm to 1.7 μm at an output energy of ∼ 23 μJ within a single optical mode across the entire spectral bandwidth. Simulations show that the frequency generation results from an accelerated fission process of soliton-like waveforms in a non-adiabatic dispersion regime associated with the emission of multiple phase-matched Cherenkov radiations on both sides of the resonance. This effect, along with the dispersion tuning and scaling capabilities of the fiber geometry, enables coherent ultra-broadband and high-energy sources, which range from the UV to the mid‐infrared spectral range.

A high-precision, single-shot, and real-time carrier-envelope phase (CEP) measurement at 1.8 μm laser wavelength based on stereographic photoelectron spectroscopy is presented. A precision of the CEP measurement of 120 mrad for each and every individual laser shot for a 1 kHz pulse train with randomly varying CEP is demonstrated. Simultaneous to the CEP measurement, the pulse lengths are characterized by evaluating the spatial asymmetry of the measured above-threshold ionization (ATI) spectra of xenon and referenced to a standard pulse-duration measurement based on frequency-resolved optical gating. The validity of the CEP measurement is confirmed by implementing phase tagging for a CEP-dependent measurement of ATI in xenon with high energy resolution.

Semiconductor nanowire (NW) lasers attract a lot of attention as potential elements of nanophotonic circuits and lab-on-a chip devices. Here, we report on the experimental investigation of stimulated near ultraviolet (NUV) emission, pumped by three-photon absorption from near infrared femtosecond laser pulses, from ZnO NW arrays of different morphologies and compare it to the bulk. The spectrally and temporally resolved measurements of the NUV emission show both strong enhancements in the absorption and emission properties of the nanowire arrays compared to bulk samples. Thus, we determine a many times higher three-photon absorption in the nanostructure morphology compared to the bulk material. Furthermore, the threshold pumping intensity for stimulated emission in a vertically oriented nanowire array is twice lower and the emission onset time is shorter than in randomly oriented arrays, revealing strong influence of the macroscopic nanowire arrangement.