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Now showing 1 - 10 of 225
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    Endurance of quantum coherence due to particle indistinguishability in noisy quantum networks
    (London : Nature Publ. Group, 2018) Perez-Leija, Armando; Guzmán-Silva, Diego; León-Montiel, Roberto de J.; Gräfe, Markus; Heinrich, Matthias; Moya-Cessa, Hector; Busch, Kurt; Szameit, Alexander
    Quantum coherence, the physical property underlying fundamental phenomena such as multi-particle interference and entanglement, has emerged as a valuable resource upon which modern technologies are founded. In general, the most prominent adversary of quantum coherence is noise arising from the interaction of the associated dynamical system with its environment. Under certain conditions, however, the existence of noise may drive quantum and classical systems to endure intriguing nontrivial effects. In this vein, here we demonstrate, both theoretically and experimentally, that when two indistinguishable non-interacting particles co-propagate through quantum networks affected by non-dissipative noise, the system always evolves into a steady state in which coherences accounting for particle indistinguishabilty perpetually prevail. Furthermore, we show that the same steady state with surviving quantum coherences is reached even when the initial state exhibits classical correlations.
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    Kinematic origin for near-zero energy structures in mid-IR strong field ionization
    (Bristol : IOP Publ., 2016) Pisanty, Emilio; Ivanov, Misha
    We propose and discuss a kinematic mechanism underlying the recently discovered 'near-zero energy structure' in the photoionization of atoms in strong mid-infrared laser fields, based on trajectories which revisit the ion at low velocities exactly analogous to the series responsible for low-energy structures. The different scaling of the new series, as $E\sim {I}_{p}^{2}/{U}_{p}$, suggests that the near-zero energy structure can be lifted to higher energies, where it can be better resolved and studied, using harder targets with higher ionization potential.
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    Sub-laser-cycle control of coupled electron–nuclear dynamics at a conical intersection
    ([London] : IOP, 2015) Richter, Maria; Bouakline, Foudhil; González-Vázquez, Jesús; Martínez-Fernández, Lara; Corral, Inés; Patchkovskii, Serguei; Morales, Felipe; Ivanov, Misha; Martín, Fernando; Smirnova, Olga
    Nonadiabatic processes play a fundamental role in the understanding of photochemical processes in excited polyatomic molecules. A particularly important example is that of radiationless electronic relaxation at conical intersections (CIs). We discuss new opportunities for controlling coupled electron–nuclear dynamics at CIs, offered by the advent of nearly single-cycle, phase-stable, mid-infrared laser pulses. To illustrate the control mechanism, a two-dimensional model of the NO2 molecule is considered. The key idea of the control scheme is to match the time scale of the laser field oscillations to the characteristic time scale of the wave packet transit through the CI. The instantaneous laser field changes the shape and position of the CI as the wave packet passes through. As the CI moves in the laser field, it 'slices' through the wave packet, sculpting it in the coordinate and momentum space in a way that is sensitive to the carrier-envelope phase of the control pulse. We find that the electronic coherence imparted on the sub-laser-cycle time scale manifests during much longer nuclear dynamics that follow on the many tens of femtosecond time scale. Control efficiency as a function of molecular orientation is analyzed, showing that modest alignment is sufficient for showing the described effects.
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    Characterization of self-modulated electron bunches in an argon plasma
    (Bristol : IOP Publ., 2018) Gross, M.; Lishilin, O.; Loisch, G.; Boonpornprasert, P.; Chen, Y.; Engel, J.; Good, J.; Huck, H.; Isaev, I.; Krasilnikov, M.; Li, X.; Niemczyk, R.; Oppelt, A.; Qian, H.; Renier, Y.; Stephan, F.; Zhao, Q.; Brinkmann, R.; Martinez de la Ossa, A.; Osterhoff, J.; Grüner, F.J.; Mehrling, T.; Schroeder, C.B.; Will, I.
    The self-modulation instability is fundamental for the plasma wakefield acceleration experiment of the AWAKE (Advanced Wakefield Experiment) collaboration at CERN where this effect is used to generate proton bunches for the resonant excitation of high acceleration fields. Utilizing the availability of flexible electron beam shaping together with excellent diagnostics including an RF deflector, a supporting experiment was set up at the electron accelerator PITZ (Photo Injector Test facility at DESY, Zeuthen site), given that the underlying physics is the same. After demonstrating the effect [1] the next goal is to investigate in detail the self-modulation of long (with respect to the plasma wavelength) electron beams. In this contribution we describe parameter studies on self-modulation of a long electron bunch in an argon plasma. The plasma was generated with a discharge cell with densities in the 1013 cm-3 to 1015 cm-3 range. The plasma density was deduced from the plasma wavelength as indicated by the self-modulation period. Parameter scans were conducted with variable plasma density and electron bunch focusing.
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    Molecular above-threshold ionization spectra as an evidence of the three-point interference of electron wave packets
    (Bristol : IOP Publ., 2015) Hasović, Elvedin; Milošević, Dejan B.; Gazibegović-Busuladži, Azra; Čerkić, Aner; Busuladžić, Mustafa
    We consider high-order above-threshold ionization (HATI) of polyatomic molecules ionized by a strong linearly polarized laser field. Improved molecular strong-field approximation by which the HATI process on polyatomic molecular species can be described is developed. Using this theory we calculate photoelectron angular-energy spectra for different triatomic molecules. Special attention is devoted to the minima that are observed in the calculated high-energy electron spectra of the ozone and carbon dioxide molecules. A key difference between these minima and minima that are observed in the corresponding spectra of diatomic molecules are presented.
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    Preparation of clay mineral samples for high resolution x-ray imaging
    (Bristol : Institute of Physics Publishing, 2013) Abbati, G.; Seim, C.; Legall, H.; Stiel, H.; Thomas, N.; Wilhein, T.
    In the development of optimum ceramic materials for plastic forming, it is of fundamental importance to gain insight into the compositions of the clay minerals. Whereas spectroscopic methods are adequate for determining the elemental composition of a given sample, a knowledge of the spatial composition, together with the shape and size of the particles leads to further, valuable insight. This requires an imaging technique such as high resolution X-ray microscopy. In addition, fluorescence spectroscopy provides a viable element mapping technique. Since the fine particle fraction of the materials has a major effect on physical properties like plasticity, the analysis is focused mainly on the smallest particles. To separate these from the bigger agglomerates, the raw material has to pass through several procedures like centrifugation and filtering. After that, one has to deposit a layer of appropriate thickness on to a suitable substrate. These preparative techniques are described here, starting from the clay mineral raw materials and proceeding through to samples that are ready to analyze. First results using high resolution x-ray imaging are shown.
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    Differential Cross Sections for the H + D2 → HD(v′ = 3, j′ = 4-10) + D Reaction above the Conical Intersection
    (Washington, DC : Soc., 2015) Gao, Hong; Sneha, Mahima; Bouakline, Foudhil; Althorpe, Stuart C.; Zare, Richard N.
    We report rovibrationally selected differential cross sections (DCSs) of the benchmark reaction H + D2 → HD(v′ = 3, j′ = 4–10) + D at a collision energy of 3.26 eV, which exceeds the conical intersection of the H3 potential energy surface at 2.74 eV. We use the PHOTOLOC technique in which a fluorine excimer laser at 157.64 nm photodissociates hydrogen bromide (HBr) molecules to generate fast H atoms and the HD product is detected in a state-specific manner by resonance-enhanced multiphoton ionization. Fully converged quantum wave packet calculations were performed for this reaction at this high collision energy without inclusion of the geometric phase (GP) effect, which takes into account coupling to the first excited state of the H3 potential energy surface. Multimodal structures can be observed in most of the DCSs up to j′ = 10, which is predicted by theory and also well-reproduced by experiment. The theoretically calculated DCSs are in good overall agreement with the experimental measurements, which indicates that the GP effect is not large enough that its existence can be verified experimentally at this collision energy.
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    Attosecond time delays in C60 valence photoemissions at the giant plasmon
    (Bristol : IOP Publ., 2015) Barillot, T.; Magrakvelidze, M.; Loriot, V.; Bordas, C.; Hervieux, P.-A.; Gisselbrecht, M.; Johnsson, P.; Laksman, J.; Mansson, E.P.; Sorensen, S.; Canton, S.E.; Dahlström, J.M.; Dixit, G.; Madjet, M.E.; Lépine, F.; Chakraborty, H.S.
    We perform time-dependent local density functional calculations of the time delay in C60 HOMO and HOMO-1 photoionization at giant plasmon energies. A semiclassical model is used to develop further insights.
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    The Bend+Libration Combination Band Is an Intrinsic, Collective, and Strongly Solute-Dependent Reporter on the Hydrogen Bonding Network of Liquid Water
    (Washington, DC : Americal Chemical Society, 2017) Verma, Pramod Kumar; Kundu, Achintya; Puretz, Matthew S.; Dhoonmoon, Charvanaa; Chegwidden, Oriana S.; Londergan, Casey H.; Cho, Minhaeng
    Water is an extensively self-associated liquid due to its extensive hydrogen bond (H-bond) forming ability. The resulting H-bonded network fluid exhibits nearly continuous absorption of light from the terahertz to the near-IR region. The relatively weak bend+libration water combination band (centered at 2130 cm-1) has been largely overlooked as a reporter of liquid water's structure and dynamics despite its location in a convenient region of the IR for spectroscopic study. The intermolecular nature of the combination band leads to a unique absorption signal that reports collectively on the rigidity of the H-bonding network in the presence of many different solutes. This study reports comprehensively how the combination band acts as an intrinsic and collective probe in various chemically and biologically relevant solutions, including salts of varying character, denaturants, osmolytes, crowders, and surfactants that form reverse micelles and micelles. While we remark on changes in the line width and intensity of this combination band, we mainly focus on the frequency and how the frequency reports on the collective H-bonding network of liquid water. We also comment on the "association band" moniker often applied to this band and how to evaluate discrete features in this spectral region that sometimes appear in the IR spectra of specific kinds of aqueous samples of organic solutes, especially those with very high solute concentrations, with the conclusion that most of these discrete spectral features come exclusively from the solutes and do not report on the water. Contrasts are drawn throughout this work between the collective and delocalized reporting ability of the combination band and the response of more site-specific vibrations like the much-investigated OD stretch of HDO in H2O: the combination band is a unique reporter of H-bonding structure and dynamics and fundamentally different than any local mode probe. Since this band appears as the spectroscopic "background" for many local-mode reporter groups, we note the possibility of observing both local and collective solvent dynamics at the same time in this spectral region.
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    Laser stripping of hydrogen atoms by direct ionization
    ([London] : IOP, 2015) Brunetti, E.; Becker, W.; Bryant, H.C.; Jaroszynski, D.A.; Chou, W.
    Direct ionization of hydrogen atoms by laser irradiation is investigated as a potential new scheme to generate proton beams without stripping foils. The time-dependent Schrödinger equation describing the atom-radiation interaction is numerically solved obtaining accurate ionization cross-sections for a broad range of laser wavelengths, durations and energies. Parameters are identified where the Doppler frequency up-shift of radiation colliding with relativistic particles can lead to efficient ionization over large volumes and broad bandwidths using currently available lasers.