Three-dimensional localized coherent structures of surface turbulence. III Experiment and model validation

The paper continues a series of publications devoted to the 3D nonlinear localized coherent structures on the surface of vertically falling liquid films. The work is primarily focussed on experimental investigations. We study: (i) instabilities and transitions leading to 3D coherent structures; (ii) characteristics of these structures. Some nonstationary effects are also studied numerically. Our experimental results, as well as the results of other investigators, are in a good agreement with our theoretical and numerical predictions.Comment: 42 pages, 15 figure

Linear and Nonlinear Evolution and Diffusion Layer Selection in Electrokinetic Instability

In the present work fournontrivial stages of electrokinetic instability are identified by direct numerical simulation (DNS) of the full Nernst-Planck-Poisson-Stokes (NPPS) system: i) The stage of the influence of the initial conditions (milliseconds); ii) 1D self-similar evolution (milliseconds-seconds); iii) The primary instability of the self-similar solution (seconds); iv) The nonlinear stage with secondary instabilities. The self-similar character of evolution at intermediately large times is confirmed. Rubinstein and Zaltzman instability and noise-driven nonlinear evolution to over-limiting regimes in ion-exchange membranes are numerically simulated and compared with theoretical and experimental predictions. The primary instability which happens during this stage is found to arrest self-similar growth of the diffusion layer and specifies its characteristic length as was first experimentally predicted by Yossifon and Chang (PRL 101, 254501 (2008)). A novel principle for the characteristic wave number selection from the broadbanded initial noise is established.Comment: 13 pages, 8 figure

Overcoming blockade in producing doubly-excited dimers by a single intense pulse and their decay

Excitation of two identical species in a cluster by the absorption of two photons of the same energy is strongly suppressed since the excitation of one subunit blocks the excitation of the other one due to the binding Coulomb interaction. Here, we propose a very efficient way to overcome this blockade in producing doubly-excited homoatomic clusters by a single intense laser pulse. For Ne$_2$ it is explicitly demonstrated that the optimal carrier frequency of the pulse is given by half of the energy of the target state, which allows one to doubly excite more than half of the dimers at moderate field intensities. These dimers then undergo ultrafast interatomic decay bringing one Ne to its ground state and ionizing the other one. The reported \emph{ab initio} electron spectra present reliable predictions for future experiments by strong laser pulses.Comment: 5 fig

Emitter-site selective photoelectron circular dichroism of trifluoromethyloxirane

The angle-resolved inner-shell photoionization of R-trifluoromethyloxirane, C3H3F3O, is studied experimentally and theoretically. Thereby, we investigate the photoelectron circular dichroism (PECD) for nearly-symmetric O 1s and F 1s electronic orbitals, which are localized on different molecular sites. The respective dichroic $\beta_{1}$ and angular distribution $\beta_{2}$ parameters are measured at the photoelectron kinetic energies from 1 to 16 eV by using variably polarized synchrotron radiation and velocity map imaging spectroscopy. The present experimental results are in good agreement with the outcome of ab initio electronic structure calculations. We report a sizable chiral asymmetry $\beta_{1}$ of up to about 9% for the K-shell photoionization of oxygen atom. For the individual fluorine atoms, the present calculations predict asymmetries of similar size. However, being averaged over all fluorine atoms, it drops down to about 2%, as also observed in the present experiment. Our study demonstrates a strong emitter- and site-sensitivity of PECD in the one-photon inner-shell ionization of this chiral molecule

Dynamic interference of photoelectrons produced by high-frequency laser pulses

The ionization of an atom by a high-frequency intense laser pulse, where the energy of a single-photon is sufficient to ionize the system, is investigated from first principles. It is shown that as a consequence of an AC Stark effect in the continuum, the energy of the photoelectron follows the envelope of the laser pulse. This is demonstrated to result in strong dynamic interference of the photoelectrons of the same kinetic energy emitted at different times. Numerically exact computations on the hydrogen atom demonstrate that the dynamic interference spectacularly modifies the photoionization process and is prominently manifested in the photoelectron spectrum by the appearance of a distinct multi-peak pattern. The general theory is shown to be well approximated by explicit analytical expressions which allow for a transparent understanding of the discovered phenomena and for making predictions on the dependence of the measured spectrum on the properties of the pulse.Comment: 5 figure

Technical Design Report for the PANDA Solenoid and Dipole Spectrometer Magnets

This document is the Technical Design Report covering the two large spectrometer magnets of the PANDA detector set-up. It shows the conceptual design of the magnets and their anticipated performance. It precedes the tender and procurement of the magnets and, hence, is subject to possible modifications arising during this process.Comment: 10 pages, 14MB, accepted by FAIR STI in May 2009, editors: Inti Lehmann (chair), Andrea Bersani, Yuri Lobanov, Jost Luehning, Jerzy Smyrski, Technical Coordiantor: Lars Schmitt, Bernd Lewandowski (deputy), Spokespersons: Ulrich Wiedner, Paola Gianotti (deputy