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Now showing 1 - 8 of 8
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    Ultrafast structural changes in SrTiO3 due to a superconducting phase transition in a YBa2Cu3O7 top layer
    (College Park, MD : Institute of Physics Publishing, 2010) Lübcke, A.; Zamponi, F.; Loetzsch, R.; Kämpfer, T.; Uschmann, I.; Große, V.; Schmidl, F.; Köttig, T.; Thürk, M.; Schwoerer, H.; Förster, E.; Seidel, P.; Sauerbrey, R.
    We investigate the structural response of SrTiO3 when Cooper pairs are broken in an epitaxially grown YBa2Cu3O 7 top layer due to both heating and optical excitation. The crystal structure is investigated by static, temperaturedependent and time-resolved x-ray diffraction. In the static case, a large strain field in SrTiO3 is formed in the proximity of the onset of the superconducting phase in the top layer, suggesting a relationship between both effects. For the time-dependent studies, we likewise find a large fraction of the probed volume of the SrTiO3 substrate strained if the top layer is superconducting. Upon optical breaking of Cooper pairs, the observed width of the rocking curve is reduced and its position is slightly shifted towards smaller angles. The dynamical theory of x-ray diffraction is used to model the measured rocking curves. We find that the thickness of the strained layer is reduced by about 200 nm on a sub-ps to ps timescale, but the strain value at the interface between SrTiO3 and YBa2Cu3O7 remains unaffected. © IOP Publishing Ltd and Deutsche Physikalische Gesellschaft.
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    A cascaded laser acceleration scheme for the generation of spectrally controlled proton beams
    (College Park, MD : Institute of Physics Publishing, 2010) Pfotenhauer, S.M.; Jäckel, O.; Polz, J.; Steinke, S.; Schlenvoigt, H.-P.; Heymann, J.; Robinson, A.P.L.; Kaluza, M.C.
    We present a novel, cascaded acceleration scheme for the generation of spectrally controlled ion beams using a laser-based accelerator in a 'double-stage' setup. An MeV proton beam produced during a relativistic laser-plasma interaction on a thin foil target is spectrally shaped by a secondary laser-plasma interaction on a separate foil, reliably creating well-separated quasi-monoenergetic features in the energy spectrum. The observed modulations are fully explained by a one-dimensional (1D) model supported by numerical simulations. These findings demonstrate that laser acceleration can, in principle, be applied in an additive manner. © IOP Publishing Ltd and Deutsche Physikalische Gesellschaft.
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    Laser-driven ion acceleration using isolated mass-limited spheres
    (College Park, MD : Institute of Physics Publishing, 2010) Sokollik, T.; Paasch-Colberg, T.; Gorling, K.; Eichmann, U.; Schnürer, M.; Steinke, S.; Nickles, P.V.; Andreev, A.; Sandner, W.
    We report on our experiments on laser-driven ion acceleration using fully isolated mass-limited spheres with a diameter down to 8μm for the first time. Two-dimensional (2D) particle-in-cell (PIC) and hydro-code simulations were used to show that the pre-plasma at both the front and rear sides of the target strongly affect the efficiency of the ion acceleration. The mechanism of the plasma flow around mass-limited targets has not yet been identified for laser-driven ion acceleration. Our models indicate that this effect is the cause of the observed limitation to the ion-beam energy in both previous experiments and in our own. © IOP Publishing Ltd and Deutsche Physikalische Gesellschaft.
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    Imaging of carrier-envelope phase effects in above-threshold ionization with intense few-cycle laser fields
    (College Park, MD : Institute of Physics Publishing, 2008) Kling, M.F.; Rauschenberger, J.; Verhoef, A.J.; Hasović, E.; Uphues, T.; Milošević, D.B.; Muller, H.G.; Vrakking, M.J.J.
    Sub-femtosecond control of the electron emission in above-threshold ionization of the rare gases Ar, Xe and Kr in intense few-cycle laser fields is reported with full angular resolution. Experimental data that were obtained with the velocity-map imaging technique are compared to simulations using the strong-field approximation (SFA) and full time-dependent Schrödinger equation (TDSE) calculations. We find a pronounced asymmetry in both the energy and angular distributions of the electron emission that critically depends on the carrier-envelope phase (CEP) of the laser field. The potential use of imaging techniques as a tool for single-shot detection of the CEP is discussed. © IOP Publishing Ltd and Deutsche Physikalische Gesellschaft.
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    Attosecond electron thermalization in laser-induced nonsequential multiple ionization: Hard versus glancing collisions
    (College Park, MD : Institute of Physics Publishing, 2008) Liu, X.; De Morisson Faria, C.F.; Becker, W.
    A recollision-based largely classical statistical model of laser-induced nonsequential multiple (N-fold) ionization of atoms is further explored. Upon its return to the ionic core, the first-ionized electron interacts with the other N - 1 bound electrons either through a contact or a Coulomb interaction. The returning electron may leave either immediately after this interaction or join the other electrons to form a thermalized complex which leaves the ion after the delay Δt, which is the sum of a thermalization time and a possible additional dwell time. Good agreement with the available triple and quadruple ionization data in neon and argon is obtained with the contact scenario and delays of Δt = 0.17 T and 0.265 T, respectively, with T the laser period. © IOP Publishing Ltd and Deutsche Physikalische Gesellschaft.
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    Towards time resolved core level photoelectron spectroscopy with femtosecond x-ray free-electron lasers
    (College Park, MD : Institute of Physics Publishing, 2008) Pietzsch, A.; Föhlisch, A.; Beye, M.; Deppe, M.; Hennies, F.; Nagasono, M.; Suljotil, E.; Wurth, W.; Gahl, C.; Dörich, K.; Melnikov, A.
    We have performed core level photoelectron spectroscopy on a W(110) single crystal with femtosecond XUV pulses from the free-electron laser at Hamburg (FLASH). We demonstrate experimentally and through theoretical modelling that for a suitable range of photon fluences per pulse, time-resolved photoemission experiments on solid surfaces are possible. Using FLASH pulses in combination with a synchronized optical laser, we have performed femtosecond time-resolved core-level photoelectron spectroscopy and observed sideband formation on the W 4f lines indicating a cross correlation between femtosecond optical and XUV pulses. © IOP Publishing Ltd and Deutsche Physikalische Gesellschaft.
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    Interference in strong-field ionization of a two-centre atomic system
    (College Park, MD : Institute of Physics Publishing, 2008) Ansari, Z.; Böttcher, M.; Manschwetus, B.; Rottke, H.; Sandner, W.; Verhoef, A.; Lezius, M.; Paulus, G.G.; Saenz, A.; Milošević, D.B.
    Strong-field photoionization of argon dimers by a few-cycle laser pulse is investigated using electron-ion coincidence momentum spectroscopy. The momentum distribution of the photoelectrons exhibits interference due to the emission from the two atomic argon centres, in analogy with a Young's doubleslit experiment. However, a simulation of the dimer photoelectron momentum spectrum based on the atomic spectrum supplemented with a theoretically derived interference term leads to distinct deviations from the experimental result. The deviations may have their origin in a complex electron dynamics during strong-field ionization of the Ar2 dimer. © IOP Publishing Ltd and Deutsche Physikalische Gesellschaft.
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    Ultrafast optical excitations of metallic nanostructures: From light confinement to a novel electron source
    (College Park, MD : Institute of Physics Publishing, 2007) Ropers, C.; Elsaesser, T.; Cerullo, G.; Zavelani-Rossi, M.; Lienau, C.
    Combining ultrafast coherent spectroscopy with nano-optical microscopy techniques offers a wealth of new possibilities for exploring the structure and function of nanostructures. In this paper, we describe newly developed nano-optical methods based on short-pulse laser sources with durations in the 10 fs regime. These techniques are used to unravel some of the intricate dynamics of elementary excitations in metallic nanostructures. Specifically, we explore light localization and storage in plasmonic crystals, demonstrate field enhancement and second harmonic generation from metallic nanotips and describe a novel nanometre-sized source of electron pulses. The rapid progress in this area offers exciting new prospects for probing and controlling electron dynamics in metallic nanostructures with femtosecond temporal and nanometre spatial resolution. © IOP Publishing Ltd and Deutsche Physikalische Gesellschaft.