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Attosecond spectroscopy comprises several techniques to probe matter through electrons and photons. One frontier of attosecond methods is to reveal complex phenomena arising from quantum-mechanical correlations in the matter system, in the photon fields and among them. Recent theories have laid the groundwork for understanding how quantum-optical properties affect high-field photonics, such as strong-field ionization and acceleration of electrons in quantum-optical fields, and how entanglement between the field modes arises during the interaction. Here we demonstrate a new experimental approach that transduces some properties of a quantum-optical state through a strong-field nonlinearity. We perturb high-harmonic emission from a semiconductor with a bright squeezed vacuum field resulting in the emission of sidebands of the high-harmonics with super-Poissonian statistics, indicating that the emitted photons are bunched. Our results suggest that perturbing strong-field dynamics with quantum-optical states is a viable way to coherently control the generation of these states at short wavelengths, such as extreme ultraviolet or soft X-rays. Quantum correlations will be instrumental to advance attosecond spectroscopy and imaging beyond the classical limits.

The increasing interest in chiral light stems from its spiral trajectory along the propagation direction, facilitating the interaction between different polarization states of light and matter. Despite tremendous achievements in chiral light-related research, the generation and control of chiral pulse have presented enduring challenges, especially at the terahertz and ultraviolet spectral ranges, due to the lack of suitable optical elements for effective pulse manipulation. Conventionally, chiral light can be obtained from intricate optical systems, by an external magnetic field, or by metamaterials, which necessitate sophisticated optical configurations. Here, we propose a versatile tunable chiral emitter, composed of only two planar Weyl semimetals slabs, addressing the challenges in both spectral ranges. Our results open the way to a compact tunable chiral emitter platform in both terahertz and ultra-violet frequency ranges. This advancement holds the potential to serve as the cornerstone for integrated chiral photonics.

We develop a quasi-classical theory of high harmonic generation in semiconductors based on an interband current that has been transformed from Bloch to Wannier basis. The Wannier quasi-classical approach reveals a complete picture of the mechanisms shaping high harmonic generation, such that quantitative agreement with full quantum calculations is obtained. The intuitive picture revealed by quasi-classical wavepacket propagation will be helpful in the interpretation and design of high harmonic and attosecond experiments. Beyond that, the capacity to quantitatively model quantum dynamics with classical trajectories should prove useful for a wider spectrum of condensed matter research, including coherent control, transport theory, and strong field physics., Comment: 9 pages; 5 figures; 2 appendices

Strong field driven electric currents in condensed matter systems open new frontiers in petahertz electronics. In this regime new challenges arise as the role of the band structure and the quantum nature of electron-hole dynamics have yet to be resolved. Here we reveal the underlying attosecond dynamics that dictates the temporal evolution of carriers in multi-band solid state systems, via high harmonic generation (HHG) spectroscopy. We demonstrate that when the electron-hole relative velocity approaches zero, enhanced quantum interference leads to the appearance of spectral caustics in the HHG spectrum. Introducing the role of the dynamical joint density of states (JDOS) we identify its direct mapping into the spectrum, exhibiting singularities at the spectral caustics. By probing these singularities, we visualize the structure of multiple unpopulated high conduction bands. Our results open a new path in the control and study of attosecond quasi-particle interactions within the field dressed band structure of crystals.

The finite-difference time-domain (FDTD) method is a flexible and powerful technique for rigorously solving Maxwell's equations. However, three-dimensional optical nonlinearity in current commercial and research FDTD softwares requires solving iteratively an implicit form of Maxwell's equations over the entire numerical space and at each time step. Reaching numerical convergence demands significant computational resources and practical implementation often requires major modifications to the core FDTD engine. In this paper, we present an explicit method to include second and third order optical nonlinearity in the FDTD framework based on a nonlinear generalization of the Lorentz dispersion model. A formal derivation of the nonlinear Lorentz dispersion equation is equally provided, starting from the quantum mechanical equations describing nonlinear optics in the two-level approximation. With the proposed approach, numerical integration of optical nonlinearity and dispersion in FDTD is intuitive, transparent, and fully explicit. A strong-field formulation is also proposed, which opens an interesting avenue for FDTD-based modelling of the extreme nonlinear optics phenomena involved in laser filamentation and femtosecond micromachining of dielectrics., Comment: Final version published in Computer Physics Communications

Using three-dimensional particle-in-cell simulations, we show that few-MeV electrons can be produced by focusing tightly few-cycle radially-polarized laser pulses in a low-density atomic gas. In particular, it is observed that for the few-TW laser power needed to reach relativistic electron energies, longitudinal attosecond microbunching occurs naturally, resulting in femtosecond structures with high-contrast attosecond density modulations. The three-dimensional particle-in-cell simulations show that in the relativistic regime the leading pulse of these attosecond substructures survives to propagation over extended distances, suggesting that it could be delivered to a distant target, with the help of a properly designed transport beamline., Comment: 11 pages, accepted for publication in J. Phys. B

Inclusion of the instantaneous Kerr nonlinearity in the FDTD framework leads to implicit equations that have to be solved iteratively. In principle, explicit integration can be achieved with the use of anharmonic oscillator equations, but it tends to be unstable and inappropriate for studying strong-field phenomena like laser filamentation. In this paper, we show that nonlinear susceptibility can be provided instead by a harmonic oscillator driven by a nonlinear force, chosen in a way to reproduce the polarization obtained from the solution of the quantum mechanical two level equations. The resulting saturable, nonlinearly-driven, harmonic oscillator model reproduces quantitatively the quantum mechanical solutions of harmonic generation in the under-resonant limit, up to the 9th harmonic. Finally, we demonstrate that fully explicit leapfrog integration of the saturable harmonic oscillator is stable, even for the intense laser fields that characterize laser filamentation and high harmonic generation., Comment: 9 pages, 4 figures

We propose a simple laser-driven electron acceleration scheme based on tightly focused radially polarized laser pulses for the production of femtosecond electron bunches with energies in the few-hundreds-of-keV range. In this method, the electrons are accelerated forward in the focal volume by the longitudinal electric field component of the laser pulse. Three-dimensional test-particle and particle-in-cell simulations reveal the feasibility of generating well-collimated electron bunches with an energy spread of 5% and a temporal duration of the order of 1 fs. These results offer a route towards unprecedented time resolution in ultrafast electron diffraction experiments., Comment: 5 pages, 4 figures, published in PRL

We investigate the quantum breathing mode (monopole oscillation) of trapped fermionic particles with Coulomb and dipole interaction in one and two dimensions. This collective oscillation has been shown to reveal detailed information on the many-particle state of interacting trapped systems and is thus a sensitive diagnostics for a variety of finite systems, including cold atomic and molecular gases in traps and optical lattics, electrons in metal clusters and in quantum confined semiconductor structures or nanoplasmas. An improved sum rule formalism allows us to accurately determine the breathing frequencies from the ground state of the system, avoiding complicated time-dependent simulations. In combination with the Hartree-Fock and the Thomas-Fermi approximations this enables us to extend the calculations to large particle numbers $N$ on the order of several million. Tracing the breathing frequency to large $N$ as a function of the coupling parameter of the system reveals a surprising difference of the asymptotic behavior of one-dimensional and two-dimensional harmonically trapped Coulomb systems., Comment: 22 pages, 9 figures

Understanding the damage of DNA bases from hydrogen abstraction by free OH radicals is of particular importance to reveal the effect of hydroxyl radicals produced by the secondary effect of radiation. Previous studies address the problem with truncated DNA bases as ab-initio quantum simulation required to study such electronic spin dependent processes are computationally expensive. Here, for the first time, we employ a multiscale and hybrid Quantum-Mechanical-Molecular-Mechanical simulation to study the interaction of OH radicals with guanine-deoxyribose-phosphate DNA molecular unit in the presence of water where all the water molecules and the deoxyribose-phosphate fragment are treated with the simplistic classical Molecular-Mechanical scheme. Our result illustrates that the presence of water strongly alters the hydrogen-abstraction reaction as the hydrogen bonding of OH radicals with water restricts the relative orientation of the OH-radicals with respective to the the DNA base (here guanine). This results in an angular anisotropy in the chemical pathway and a lower efficiency in the hydrogen abstraction mechanisms than previously anticipated for identical system in vacuum. The method can easily be extended to single and double stranded DNA without any appreciable computational cost as these molecular units can be treated in the classical subsystem as has been demonstrated here., Comment: 7 pages, 9 figures

Dynamical magnetic and nuclear polarization in complex spin systems is discussed on the example of transfer of spin from exciton to the central spin of magnetic impurity in a quantum dot in the presence of a finite number of nuclear spins. The exciton is described in terms of the electron and heavy hole spins interacting via exchange interaction with magnetic impurity, via hypeprfine interaction with a finite number of nuclear spins and via dipole interaction with photons. The time-evolution of the exciton, magnetic impurity and nuclear spins is calculated exactly between quantum jumps corresponding to exciton radiative recombination. The collapse of the wavefunction and the refilling of the quantum dot with new spin polarized exciton is shown to lead to build up of magnetization of the magnetic impurity as well as nuclear spin polarization. The competition between electron spin transfer to magnetic impurity and to nuclear spins simultaneous with the creation of dark excitons is elucidated. The technique presented here opens up the possibility of studying optically induced Dynamical Magnetic and Nuclear Polarization in Complex Spin Systems., Comment: 9 pages and 9 figures

Controlling electron spins strongly coupled to magnetic and nuclear spins in solid state systems is an important challenege in the field of spintronics and quantum computation. We show here that electron droplets with no net spin in semiconductor quantum dots strongly coupled with magnetic ion/nuclear spin systems break down at low temperature and form a non-trivial anti-ferromagnetic spatially ordered spin-texture of magneto-polarons. The spatially ordered combined electron-magnetic ion spin-texture, associated with spontaneous symmetry-breaking in the parity of electronic charge density and magnetization of magnetic ions, emerge from both ab-initio density functional approach to the electronic system coupled with mean-field approximation for the magnetic/nuclear spin system and fully mircoscopic exact diagonalization of small systems. The predicted phase diagram determines the critical temperature as a function of coupling strength and identifies possible phases of the strongly coupled spin system. This prediction may arrest fluctuations in spin system and open the way to control, manipulate and prepare magnetic and nuclear spin ensembles in semiconductor nanostructures., Comment: 4 pages and 3 figures, accepted for publication in Phys. Rev. Lett

Coherent control of OH-free radicals interacting with the spin-triplet state of a DNA molecule is investigated. A model Hamiltonian for molecular spin singlet-triplet resonance is developed. We illustrate that the spin-triplet state in DNA molecules can be efficiently populated, as the spin-injection rate can be tuned to be orders of magnitudes greater than the decay rate due to small spin-orbit coupling in organic molecules. Owing to the nano-second life-time of OH free radicals, a non-equilibrium free energy barrier induced by the injected spin triplet state that lasts approximately longer than one-micro second in room temperature can efficiently block the initial Hydrogen abstraction and DNA damage. For a direct demonstration of the spin-blockade effect, a molecular simulation based on an {\em ab-initio} Car-Parrinello molecular dynamics is deployed., Comment: 5 pages, 5 figures

We employ a large scale molecular simulation based on bond-order ReaxFF to simulate the chemical reaction and study the damage to a large fragment of DNA-molecule in the solution by ionizing radiation. We illustrate that the randomly distributed clusters of diatomic OH-radicals that are primary products of megavoltage ionizing radiation in water-based systems are the main source of hydrogen-abstraction as well as formation of carbonyl- and hydroxyl-groups in the sugar-moiety that create holes in the sugar-rings. These holes grow up slowly between DNA-bases and DNA-backbone and the damage collectively propagate to DNA single and double strand break., Comment: 6 pages and 8 figures. movies and simulations are available at: http://qmsimulator.wordpress.com/

The performance of a quantum computation system is investigated, with qubits represented by magnetic impurities in coupled quantum dots filled with two electrons. Magnetic impurities are electrically manipulated by electrons. The dominant noise source is the electron mediated indirect coupling between magnetic impurities and host spin bath. As a result of the electron mediated coupling, both noise properties and the time needed for elementary gate operations, depend on controllable system parameters, such as size and geometry of the quantum dot, and external electric and magnetic fields. We find that the maximum number of quantum operations per coherence time for magnetic impurities increases as electron spin singlet triplet energy gap decreases. The advantage of magnetic impurities over electrons for weak coupling and large magnetic fields will be illustrated., Comment: 5 page, 2 figure

A 1D model study of charge transport in nano-devices is made by comparing multi-configuration time dependent Hartree-Fock and frozen core calculations. The influence of exchange and Coulomb correlation on the tunneling current is determined. We identify the shape of the tunneling barrier and the resonance structure of the nano-device as the two dominant parameters determining the electron transport. Whereas the barrier shape determines the size of the tunneling current, the resonances determine the structure of the current., Comment: 4 pages