Dielectric breakdown of Mott insulators in dynamical mean-field theory

Using nonequilibrium dynamical mean-field theory, we compute the time evolution of the current in a Mott insulator after a strong electric field is turned on. We observe the formation of a quasistationary state in which the current is almost time independent although the system is constantly excited. At moderately strong fields this state is stable for quite long times. The stationary current exhibits a threshold behavior as a function of the field, in which the threshold increases with the Coulomb interaction and vanishes as the metal-insulator transition is approached.     

Free‐electron laser multiplex driven by a superconducting linear accelerator

Free‐electron lasers (FELs) generate femtosecond XUV and X‐ray pulses at peak powers in the gigawatt range. The FEL user facility FLASH at DESY (Hamburg, Germany) is driven by a superconducting linear accelerator with up to 8000 pulses per second. Since 2014, two parallel undulator beamlines, FLASH1 and FLASH2, have been in operation. In addition to the main undulator, the FLASH1 beamline is equipped with an undulator section, sFLASH, dedicated to research and development of fully coherent extreme ultraviolet photon pulses using external seed lasers. In this contribution, the first simultaneous lasing of the three FELs at 13.4 nm, 20 nm and 38.8 nm is presented.     

Excimer laser ablation of gold-loaded inverse polystyrene-block-poly (2-vinylpyridine) micelles

Diblock-copolymers (PS(1700)-b-P2VP(450) or PS(1350)-b-P2VP(400)) forming spherical micelles, can be loaded with a Au-salt and deposited on top of various substrates. Such polymer films have been exposed to a pulsed ArF excimer laser in order to remove the polymer matrix and, in parallel, to chemically reduce the salt into metallic Au nanodots. To analyze this process in detail, it was subdivided into three steps: (a) laser ablation of thick and thin diblock-copolymer films; (b) laser irradiation of Au-salt loaded diblock-copolymer films; and (c) laser irradiation of arrays of metallic Au nanodots. In (a) it was found that a complete removal of the polymer by laser ablation is only possible in air under ambient conditions while identical laser irradiations under vacuum result in a residual layer of approximately 14 nm. Substep (b) revealed a nucleation process of the resulting metallic Au within the micellar core leading to clusters of small Au dots. Furthermore, this substep provided evidence for an asymmetric interplay between the macroscopic temperature of a polymer film during laser treatment and the energy density per laser pulse. In (c) it could be demonstrated that metallic Au nanodots on mica are stable against laser irradiation under conditions leading to a polymer removal. Received: 7 August 2000 / Accepted: 2 November 2000 / Published online: 3 April 2001     

Simulations of turbulent asymptotic suction boundary layers

A series of large-eddy simulations of a turbulent asymptotic suction boundary layer (TASBL) was performed in a periodic domain, on which uniform suction was applied over a flat plate. Three Reynolds numbers (defined as ratio of free-stream and suction velocity) of Re = 333, 400 and 500 and a variety of domain sizes were considered in temporal simulations in order to investigate the turbulence statistics, the importance of the computational domain size, the arising flow structures as well as temporal development length required to achieve the asymptotic state. The effect of these two important parameters was assessed in terms of their influence on integral quantities, mean velocity, Reynolds stresses, higher order statistics, amplitude modulation and spectral maps. While the near-wall region up to the buffer region appears to scale irrespective of Re and domain size, the parameters of the logarithmic law (i.e. von Kármán and additive coefficient) decrease with increasing Re, while the wake strength decreases with increasing spanwise domain size and vanishes entirely once the spanwise domain size exceeds approximately two boundary-layer thicknesses irrespective of Re. The wake strength also reduces with increasing simulation time. The asymptotic state of the TASBL is characterised by surprisingly large friction Reynolds numbers and inherits features of wall turbulence at numerically high Re. Compared to a turbulent boundary layer (TBL) or a channel flow without suction, the components of the Reynolds-stress tensor are overall reduced, but exhibit a logarithmic increase with decreasing suction rates, i.e. increasing Re. At the same time, the anisotropy is increased compared to canonical wall-bounded flows without suction. The reduced amplitudes in turbulence quantities are discussed in light of the amplitude modulation due to the weakened larger outer structures. The inner peak in the spectral maps is shifted to higher wavelength and the strength of the outer peak is much less than for TBLs. An additional spatial simulation was performed, in order to relate the simulation results to wind tunnel experiments, which – in accordance with the results from the temporal simulation – indicate that a truly TASBL is practically impossible to realise in a wind tunnel. Our unique data set agrees qualitatively with existing literature results for both numerical and experimental studies, and at the same time sheds light on the fact why the asymptotic state could not be established in a wind tunnel experiment, viz. because experimental studies resemble our simulation results from too small simulation boxes or insufficient development times.     

Damping of Bloch oscillations in the Hubbard model

Using nonequilibrium dynamical mean-field theory, we study the isolated Hubbard model in a static electric field in the limit of weak interactions. Linear response behavior is established at long times, but only if the interaction exceeds a critical value, below which the system exhibits an ac-type response with Bloch oscillations. The transition from ac to dc response is defined in terms of the universal long-time behavior of the system, which does not depend on the initial condition.     

Photoinduced reversible changes in the electronic structure of photochromic diarylethene films

The change in the valence electronic structure upon switching of two photochromic diarylethene derivatives, i.e. 1,2-bis(2-methyl-5-p-tolylthiophen-3-yl)cyclopent-1-ene (DAE1) and 1,2-bis(5-(4-hexyloxycarbonylphenyl)-2-methylthiophen-3-yl)cyclopent-1-ene (DAE2), was measured by photoelectron spectroscopy. Switching between open and closed forms was followed in situ upon illumination. The increase of the ionization energy from the closed to the open form was 0.85 eV for DAE1 and 0.80 eV for DAE2. For DAE1, the work function also decreased by 0.25 eV upon switching, which is explained by a decrease of the intrinsic molecular dipole moment and a preferential orientation of molecules in thin films.     

A nanofiber-based optical conveyor belt for cold atoms

We demonstrate optical transport of cold cesium atoms over millimeter-scale distances along an optical nanofiber. The atoms are trapped in a one-dimensional optical lattice formed by a two-color evanescent field surrounding the nanofiber, far red- and blue-detuned with respect to the atomic transition. The blue-detuned field is a propagating nanofiber-guided mode while the red-detuned field is a standing-wave mode which leads to the periodic axial confinement of the atoms. Here, this standing wave is used for transporting the atoms along the nanofiber by mutually detuning the two counter-propagating fields which form the standing wave. The performance and limitations of the nanofiber-based transport are evaluated and possible applications are discussed.     

Coarse-grained model for gold nanocrystals with an organic capping layer

We have developed a coarse-grained interaction potential between icosahedral nanocrystals and united CH _x or SH atoms that interact via Lennard–Jones interactions. This interaction potential can be used to efficiently compute thermodynamic and structural properties of alkyl-thiol capping layers adsorbed on gold nanocrystals.     

Ligand-free gold–silver nanoparticle alloy polymer composites generated by picosecond laser ablation in liquid monomer

Polymer matrix nanocomposites filled with metallic and alloy nanoparticles add functionality in various applications such as optical devices and in the energy sector. However, matrix coupling agents or nanoparticle ligands may be unwanted additives, potentially inhibiting the resulting nanocomposite to be processed by injection molding. The generation of stabilizer-free Au, Ag, and AuAg alloy nanoparticle acrylate composites is achieved by picosecond-pulsed laser ablation of the respective metal target in the liquid monomer. Complementary to laser ablation of the solid alloy, we have alloyed nanoparticles by post-irradiation of Au and Ag colloids in the liquid monomer. The optical properties of the colloidal nanoparticles are successfully transferred to the solid poly(methyl methacrylate) matrix and characterized by their plasmon resonance that can be easily tuned between 400 and 600 nm by laser alloying in the liquid monomer.