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Now showing 1 - 10 of 11
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    Signatures of Light-Induced Potential Energy Surfaces in H2+
    (Bristol : IOP Publ., 2020) Kübel, M.; Spanner, M.; Dube, Z.; Naumov, A. Yu; Vrakking, M.J.J.; Corkum, P.B.; Villeneuve, D.M.; Staudte, A.
    Using theory and Cold Target Recoil Ion Momentum Spectroscopy we find signatures of light-induced molecular potential energy surfaces in the 3-dimensional proton momentum distributions of dissociating H+2. © 2020 Journal of Physics: Conference Series. All rights reserved.
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    General Time-Dependent Configuration-Interaction Singles II: The Atomic Case
    (Woodbury, NY : Inst., 2022-10-10) Carlström, Stefanos; Bertolino, Mattias; Dahlström, Jan Marcus; Patchkovskii, Serguei
    We present a specialization of the grid-based implementation of the time-dependent configuration-interaction singles described in the preceding paper [S. Carlström et al., preceding paper, Phys. Rev. A 106, 043104 (2022)]. to the case of spherical symmetry. We describe the intricate time propagator in detail and conclude with a few example calculations. Among these, of note are high-resolution photoelectron spectra in the vicinity of the Fano resonances in photoionization of neon and spin-polarized photoelectrons from xenon, in agreement with recent experiments.
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    General Time-Dependent Configuration-Interaction Singles I: The Molecular Case
    (Woodbury, NY : Inst., 2022-10-10) Carlström, Stefanos; Spanner, Michael; Patchkovskii, Serguei
    We present a grid-based implementation of the time-dependent configuration-interaction singles method suitable for computing the strong-field ionization of small gas-phase molecules. After outlining the general equations of motion used in our treatment of this method, we present example calculations of strong-field ionization of He, LiH, H2O, and C2H4 that demonstrate the utility of our implementation. The following paper [S. Carlström et al., following paper, Phys. Rev. A 106, 042806 (2022)] specializes to the case of spherical symmetry, which is applied to various atoms.
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    Optimization of quantum trajectories driven by strong-field waveforms
    (College Park : American Institute of Physics Inc., 2014) Haessler, S.; Balciunas, T.; Fan, G.; Andriukaitis, G.; Pugžlys, A.; Baltuška, A.; Witting, T.; Squibb, R.; Zaïr, A.; Tisch, J.W.G.; Marangos; Chipperfield, L.E.
    Quasifree field-driven electron trajectories are a key element of strong-field dynamics. Upon recollision with the parent ion, the energy transferred from the field to the electron may be released as attosecondduration extreme ultaviolet emission in the process of high-harmonic generation. The conventional sinusoidal driver fields set limitations on the maximum value of this energy transfer and the efficient return of the launched electron trajectories. It has been predicted that these limits can be significantly exceeded by an appropriately ramped-up cycle shape [L. E. Chipperfield et al., Phys. Rev. Lett. 102, 063003 (2009)]. Here, we present an experimental realization of similar cycle-shaped waveforms and demonstrate control of the high-harmonic generation process on the single-atom quantum level via attosecond steering of the electron trajectories.With our improved optical cycles, we boost the field ionization launching the electron trajectories, increase the subsequent field-to-electron energy transfer, and reduce the trajectory duration. We demonstrate, in realistic experimental conditions, 2 orders of magnitude enhancement of the generated extreme ultraviolet flux together with an increased spectral extension. This application, which is only one example of what can be achieved with cycle-shaped high-field light waves, has significant implications for attosecond spectroscopy and molecular self-probing.
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    Intercalant-mediated Kitaev exchange in Ag3LiIr2O6
    (College Park, MD : APS, 2022) Yadav, Ravi; Reja, Sahinur; Ray, Rajyavardhan; van den Brink, Jeroen; Nishimoto, Satoshi; Yazyev, Oleg V.
    The recently synthesized Ag3LiIr2O6 has been proposed as a Kitaev magnet in proximity to the quantum spin liquid phase. We explore its microscopic Hamiltonian and magnetic ground state using many-body quantum chemistry methods and exact diagonalization techniques. Our calculations establish a dominant bond dependent ferromagnetic Kitaev exchange between Ir sites and find that the inclusion of Ag 4d orbitals in the configuration interaction calculations strikingly enhances the Kitaev exchange. Furthermore, using exact diagonalization of the nearest-neighbor fully anisotropic J−K−Γ Hamiltonian, we obtain the magnetic phase diagram as a function of further neighbor couplings. We find that the antiferromagnetic off-diagonal coupling stabilizes long range order, but the structure factor calculations suggest that the material is very close to the quantum spin liquid phase and the ordered state can easily collapse into a liquid by small perturbations such as structural distortion or bond disorder.
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    Static Disorder in Excitation Energies of the Fenna-Matthews-Olson Protein: Structure-Based Theory Meets Experiment
    (Washington, DC : ACS, 2020) Chaillet, Martin L.; Lengauer, Florian; Adolphs, Julian; Müh, Frank; Fokas, Alexander S.; Cole, Daniel J.; Chin, Alex W.; Renger, Thomas
    Inhomogeneous broadening of optical lines of the Fenna-Matthews-Olson (FMO) light-harvesting protein is investigated by combining a Monte Carlo sampling of low-energy conformational substates of the protein with a quantum chemical/electrostatic calculation of local transition energies (site energies) of the pigments. The good agreement between the optical spectra calculated for the inhomogeneous ensemble and the experimental data demonstrates that electrostatics is the dominant contributor to static disorder in site energies. Rotamers of polar amino acid side chains are found to cause bimodal distribution functions of site energy shifts, which can be probed by hole burning and single-molecule spectroscopy. When summing over the large number of contributions, the resulting distribution functions of the site energies become Gaussians, and the correlations in site energy fluctuations at different sites practically average to zero. These results demonstrate that static disorder in the FMO protein is in the realm of the central limit theorem of statistics. © 2020 American Chemical Society.
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    From atomistic tight-binding theory to macroscale drift–diffusion: Multiscale modeling and numerical simulation of uni-polar charge transport in (In,Ga)N devices with random fluctuations
    (Melville, NY : American Inst. of Physics, 2021) O’Donovan, Michael; Chaudhuri, Debapriya; Streckenbach, Timo; Farrell, Patricio; Schulz, Stefan; Koprucki, Thomas
    Random alloy fluctuations significantly affect the electronic, optical, and transport properties of (In,Ga)N-based optoelectronic devices. Transport calculations accounting for alloy fluctuations currently use a combination of modified continuum-based models, which neglect to a large extent atomistic effects. In this work, we present a model that bridges the gap between atomistic theory and macroscopic transport models. To do so, we combine atomistic tight-binding theory and continuum-based drift–diffusion solvers, where quantum corrections are included via the localization landscape method. We outline the ingredients of this framework in detail and present first results for uni-polar electron transport in single and multi- (In,Ga)N quantum well systems. Overall, our results reveal that both random alloy fluctuations and quantum corrections significantly affect the current–voltage characteristics of uni-polar electron transport in such devices. However, our investigations indicate that the importance of quantum corrections and random alloy fluctuations can be different for single and multi-quantum well systems.
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    Mapping the dissociative ionization dynamics of molecular nitrogen with attosecond resolution
    (Bristol : IOP Publ., 2015) Klinker, M.; Trabattoni, A.; González-Vázquez, J.; Liu, C.; Sansone, G.; Linguerri, R.; Hochlaf, M..; Klei, J.; Vrakking, M.J.J.; Martin, F.; Nisoli, M.; Calegari, F.
    We wish to understand the processes underlying the ionization dynamics of N2 as experimentally induced and studied by recording the kinetic energy release (KER) in a XUV-pump/IR-probe setup. To this end a theoretical model was developed describing the ionization process using Dyson Orbitals and, subsequently, the dissociation process using a large set of diabatic potential energy surfaces (PES) on which to propagate. From said set of PES, a small subset is extracted allowing for the identification of one and two photon processes chiefly responsible for the experimentally observed features.
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    Quantum chemical insights into hexaboride electronic structures: correlations within the boron p-orbital subsystem
    (London : Springer Nature, 2022) Petersen, Thorben; Rößler, Ulrich K.; Hozoi, Liviu
    The notion of strong electronic correlations arose in the context of d-metal oxides such as NiO but can be exemplified on systems as simple as the H2 molecule. Here we shed light on correlation effects on B62− clusters as found in MB6 hexaborides and show that the B 2p valence electrons are fairly correlated. B6-octahedron excitation energies computed for CaB6 and YbB6 agree with peak positions found by resonant inelastic x-ray scattering, providing a compelling picture for the latter. Our findings characterize these materials as very peculiar p-electron correlated systems and call for more involved many-body investigations within the whole hexaboride family, both alkaline- and rare-earth compounds, not only for N- but also (N ± 1)-states defining e. g. band gaps.
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    Photon transport in one-dimensional systems coupled to three-level quantum impurities
    (Bristol : IOP, 2013) Martens, C.; Longo, P.; Busch, K.
    We discuss the transport properties of a single photon in a one-dimensional waveguide with an embedded three-level atom and utilize both stationary plane-wave solutions and time-dependent transport calculations to investigate the interaction of a photon with driven and undriven V- and Λ-systems. Specifically, for the case of an undriven V-system, we analyze the phenomenon of long-time occupation of the upper atomic levels in conjunction with almost dark states. For the undriven Λ-system, we find non-stationary dark states and we explain how the photon's transmittance can be controlled by an initial phase difference between the energetically lower-lying atomic states. With regard to the driven three-level systems, we discuss electromagnetically induced transparency in terms of the pulse propagation of a single photon through a Λ-type atom. In addition, we demonstrate how a driven V-type atom can be utilized to control the momentum distribution of the scattered photon.