arXiv subjects

M. Lewenstein

Publications and source records attributed to M. Lewenstein.

At least 55 records · Page 3Linked to original sources

arXiv2018

High-order harmonic generation driven by inhomogeneous plasmonics fields spatially bounded: influence on the cut-off law

We study high-order harmonic generation (HHG) in model atoms driven by plasmonic-enhanced fields. These fields result from the illumination of plasmonic nanostructures by few-cycle laser pulses. We demonstrate that the spatial inhomogeneous character of the laser electric field, in a form of Gaussian-shaped functions, leads to an unexpected relationship between the HHG cutoff and the laser wavelength. Precise description of the spatial form of the plasmonic-enhanced field allows us to predict this relationship. We combine the numerical solutions of the time-dependent Schrödinger equation (TDSE) with the plasmonic-enhanced electric fields obtained from 3D finite element simulations. We additionally employ classical simulations to supplement the TDSE outcomes and characterize the extended HHG spectra by means of their associated electron trajectories. A proper definition of the spatially inhomogeneous laser electric field is instrumental to accurately describe the underlying physics of HHG driven by plasmonic-enhanced fields. This characterization opens new perspectives for HHG control with various experimental nano-setups

physics.atom-ph↗

arXiv2017

Exploring Interacting Topological Insulators with Ultracold Atoms: the Synthetic Creutz-Hubbard Model

Understanding the robustness of topological phases of matter in the presence of strong interactions, and synthesising novel strongly-correlated topological materials, lie among the most important and difficult challenges of modern theoretical and experimental physics. In this work, we present a complete theoretical analysis of the synthetic Creutz-Hubbard ladder, which is a paradigmatic model that provides a neat playground to address these challenges. We put special attention to the competition of correlated topological phases and orbital quantum magnetism in the regime of strong interactions. These results are furthermore confirmed and extended by extensive numerical simulations. Moreover we propose how to experimentally realize this model in a synthetic ladder, made of two internal states of ultracold fermionic atoms in a one-dimensional optical lattice. Our work paves the way towards quantum simulators of interacting topological insulators with cold atoms.

cond-mat.quant-gas↗

arXiv2017

Above-threshold ionization (ATI) in multicenter molecules: the role of the initial state

A possible route to extract electronic and nuclear dynamics from molecular targets with attosecond temporal and nanometer spatial resolution is to employ recolliding electrons as `probes'. The recollision process in molecules is, however, very challenging to treat using {\it ab initio} approaches. Even for the simplest diatomic systems, such as H$_2$, today's computational capabilities are not enough to give a complete description of the electron and nuclear dynamics initiated by a strong laser field. As a consequence, approximate qualitative descriptions are called to play an important role. In this contribution we extend the work presented in N. Suárez {\it et al.}, Phys.~Rev. A {\bf 95}, 033415 (2017), to three-center molecular targets. Additionally, we incorporate a more accurate description of the molecular ground state, employing information extracted from quantum chemistry software packages. This step forward allows us to include, in a detailed way, both the molecular symmetries and nodes present in the high-occupied molecular orbital. We are able to, on the one hand, keep our formulation as analytical as in the case of diatomics, and, on the other hand, to still give a complete description of the underlying physics behind the above-threshold ionization process. The application of our approach to complex multicenter - with more than 3 centers, targets appears to be straightforward.

physics.atom-ph↗

arXiv2017

Detection of Zak phases and topological invariants in a chiral quantum walk of twisted photons

Topological insulators are fascinating states of matter exhibiting protected edge states and robust quantized features in their bulk. Here, we propose and validate experimentally a method to detect topological properties in the bulk of one-dimensional chiral systems. We first introduce the mean chiral displacement, and we show that it rapidly approaches a multiple of the Zak phase in the long time limit. Then we measure the Zak phase in a photonic quantum walk, by direct observation of the mean chiral displacement in its bulk. Next, we measure the Zak phase in an alternative, inequivalent timeframe, and combine the two windings to characterize the full phase diagram of this Floquet system. Finally, we prove the robustness of the measure by introducing dynamical disorder in the system. This detection method is extremely general, as it can be applied to all one-dimensional platforms simulating static or Floquet chiral systems.

cond-mat.mes-hall↗

arXiv2017

Nonergodic subdiffusion from transient interactions with heterogeneous partners

Spatiotemporal disorder has been recently associated to the occurrence of anomalous nonergodic diffusion of molecular components in biological systems, but the underlying microscopic mechanism is still unclear. We introduce a model in which a particle performs continuous Brownian motion with changes of diffusion coefficients induced by transient molecular interactions with diffusive binding partners. In spite of the exponential distribution of waiting times, the model shows subdiffusion and nonergodicity similar to the heavy-tailed continuous time random walk. The dependence of these properties on the density of binding partners is analyzed and discussed. Our work provide an experimentally-testable microscopic model to investigate the nature of nonergodicity in disordered media.

cond-mat.stat-mech↗

arXiv2017

Single atom edge-like states via quantum interference

We demonstrate how quantum interference may lead to the appearance of robust edge-like states of a single ultracold atom in a two-dimensional optical ribbon. We show that these states can be engineered either within the manifold of local ground states of the sites forming the ribbon, or of states carrying one unit of angular momentum. In the former case, we show that the implementation of edge-like states can be extended to other geometries, such as tilted square lattices. In the latter case, we suggest to use the winding number associated to the angular momentum as a synthetic dimension.

quant-ph↗

arXiv2016

Loading Ultracold Gases in Topological Floquet Bands: Current and Center-of-Mass Responses

Topological band structures can be designed by subjecting lattice systems to time-periodic modulations, as was recently demonstrated in cold atoms and photonic crystals. However, changing the topological nature of Floquet Bloch bands from trivial to non-trivial, by progressively launching the time-modulation, is necessarily accompanied with gap-closing processes: this has important consequences for the loading of particles into a target Floquet band with non-trivial topology, and hence, on the subsequent measurements. In this work, we analyse how such loading sequences can be optimized in view of probing the topology of Floquet bands through transport measurements. In particular, we demonstrate the robustness of center-of-mass responses, as compared to current responses, which present important irregularities due to an interplay between the micro-motion of the drive and inter-band interference effects. The results presented in this work illustrate how probing the center-of-mass displacement of atomic clouds offers a reliable method to detect the topology of Floquet bands, after realistic loading sequences.

cond-mat.quant-gas↗

arXiv2016

Spin-valley dynamics of electrically driven ambipolar carbon-nanotube quantum dots

An ambipolar $n$-$p$ double quantum dot defined by potential variation along a semiconducting carbon-nanotube is considered. We focus on the (1e,1h) charge configuration with a single excess electron in the conduction band state confined in the $n$-type dot and a single missing electron in the valence band state of the $p$-dot for which lifting of the Pauli blockade of the current was observed in the electric-dipole spin resonance [E. A. Laird et al. Nat. Nanotech. 8 , 565 (2013)]. The dynamics of the system driven by periodic electric field is studied with the Floquet theory and the time-dependent configuration interaction method with the single-electron spin-valley-orbitals determined for atomistic tight-binding Hamiltonian. We find that the transitions lifting the Pauli blockade are strongly influenced by coupling to a vacuum state with an empty $n$ dot and a fully filled $p$ dot. The coupling shifts the transition energies and strongly modifies the effective $g$ factors for axial magnetic field. The coupling is modulated by the bias between the dots but it appears effective for surprisingly large energy splitting between the (1e,1h) ground state and the vacuum (0e,0h) state. Multiphoton transitions and high harmonic generation effects are also discussed.

cond-mat.mes-hall↗

arXiv2016

Double-electron ionization driven by inhomogeneous fields

Electron-electron correlation effects play an instrumental role in our understanding of sequential (SDI) and non-sequential double ionization (NSDI) mechanisms. Here, we present a theoretical study of NSDI driven by plasmonic-enhanced spatial inhomogeneous fields. By numerically solving the time-dependent Schrödinger equation for a linear reduced model of He and a double-electron time-evolution probability analysis, we provide evidence for the enhancement effects in NSDI showing that the double ionization yield at lower laser peak intensities is increased due to the inhomogeneity of the laser field. Furthermore, our quantum mechanical model, as well as classical trajectory Monte Carlo simulations, show that inhomogeneous fields are a useful tool for splitting the binary and recoil processes in the rescattering scenario.

physics.atom-ph↗

arXiv2016

Emergence of a higher energy structure in strong field ionization with inhomogeneous electric fields

Studies of strong field ionization have historically relied on the strong field approximation, which neglects all spatial dependence in the forces experienced by the electron after ionization. More recently, the small spatial inhomogeneity introduced by the long-range Coulomb potential has been linked to a number of important features in the photoelectron spectrum, such as Coulomb asymmetry, Coulomb focusing, and the low energy structure (LES). Here, we demonstrate by combined quantum and classical simulations that a small time-varying spatial dependence in the laser electric field creates a prominent higher energy peak at energies above the "classical cut-off" for direct electrons. This higher energy structure (HES) originates from direct electrons ionized near the peak of a single half-cycle of the laser pulse. The HES is separated from all other ionization events (providing sub-cycle resolution) and is highly sensitive to the carrier envelope phase (CEP). The large accumulation of electrons with tuneable energy suggests a promising method for creating a localized source of electron pulses of attosecond duration using tabletop laser technology.

physics.atom-ph↗

arXiv2016

Above-Threshold Ionization and Laser-Induced Electron Diffraction in Diatomic Molecules

Strong field photoemission and electron recollision provide a viable route to extract electronic and nuclear dynamics from molecular targets with attosecond temporal resolution. However, since an {\em ab-initio} treatment of even the simplest diatomic systems is beyond today's capabilities approximate qualitative descriptions are warranted. In this paper, we develop such a theoretical approach to model the photoelectrons resulting from intense laser-molecule interaction. We present a general theory for symmetric diatomic molecules in the single active electron approximation that, amongst other capabilities, allows adjusting both the internuclear separation and molecular potential in a direct and simple way. More importantly we derive an analytic approximate solution of the time dependent Schrödinger equation (TDSE), based on a generalized strong field approximation (SFA) version. Using that approach we obtain expressions for electrons emitted transition amplitudes from two different molecular centres, and accelerated then in the strong laser field. One innovative aspect of our theory is the fact that the dipole matrix elements are free from non-physical gauge and coordinate system dependent terms -- this is achieved by adapting the coordinate system, in which SFA is performed, to the centre from which the corresponding part of the time dependent wave function originates. Our analytic results agree very well with the numerical solution of the full three-dimensional TDSE for the H$_2^+$ molecule. Moreover, the theoretical model was applied to describe laser-induced electron diffraction (LIED) measurements of O$_2^+$ molecules, obtained at ICFO, and reproduces the main features of the experiment very well. Our approach can be extended in a natural way to more complex molecules and multi-electron systems.

physics.atom-ph↗

arXiv2016

Attosecond physics at the nanoscale

Recently two emerging areas of research, attosecond and nanoscale physics, have started to come together. Attosecond physics deals with phenomena occurring when ultrashort laser pulses, with duration on the femto- and sub-femtosecond time scales, interact with atoms, molecules or solids. The laser-induced electron dynamics occurs natively on a timescale down to a few hundred or even tens of attoseconds, which is comparable with the optical field. On the other hand, the second branch involves the manipulation and engineering of mesoscopic systems, such as solids, metals and dielectrics, with nanometric precision. Although nano-engineering is a vast and well-established research field on its own, the merger with intense laser physics is relatively recent. In this article we present a comprehensive experimental and theoretical overview of physics that takes place when short and intense laser pulses interact with nanosystems, such as metallic and dielectric nanostructures. In particular we elucidate how the spatially inhomogeneous laser induced fields at a nanometer scale modify the laser-driven electron dynamics. Consequently, this has important impact on pivotal processes such as ATI and HHG. The deep understanding of the coupled dynamics between these spatially inhomogeneous fields and matter configures a promising way to new avenues of research and applications. Thanks to the maturity that attosecond physics has reached, together with the tremendous advance in material engineering and manipulation techniques, the age of atto-nano physics has begun, but it is in the initial stage. We present thus some of the open questions, challenges and prospects for experimental confirmation of theoretical predictions, as well as experiments aimed at characterizing the induced fields and the unique electron dynamics initiated by them with high temporal and spatial resolution.

physics.atom-ph↗

arXiv2016

Entanglement and coherence in quantum state merging

Understanding the resource consumption in distributed scenarios is one of the main goals of quantum information theory. A prominent example for such a scenario is the task of quantum state merging where two parties aim to merge their parts of a tripartite quantum state. In standard quantum state merging, entanglement is considered as an expensive resource, while local quantum operations can be performed at no additional cost. However, recent developments show that some local operations could be more expensive than others: it is reasonable to distinguish between local incoherent operations and local operations which can create coherence. This idea leads us to the task of incoherent quantum state merging, where one of the parties has free access to local incoherent operations only. In this case the resources of the process are quantified by pairs of entanglement and coherence. Here, we develop tools for studying this process, and apply them to several relevant scenarios. While quantum state merging can lead to a gain of entanglement, our results imply that no merging procedure can gain entanglement and coherence at the same time. We also provide a general lower bound on the entanglement-coherence sum, and show that the bound is tight for all pure states. Our results also lead to an incoherent version of Schumacher compression: in this case the compression rate is equal to the von Neumann entropy of the diagonal elements of the corresponding quantum state.

quant-ph↗

arXiv2016

Assisted distillation of quantum coherence

We introduce and study the task of assisted coherence distillation. This task arises naturally in bipartite systems where both parties work together to generate the maximal possible coherence on one of the subsystems. Only incoherent operations are allowed on the target system while general local quantum operations are permitted on the other, an operational paradigm that we call local quantum-incoherent operations and classical communication (LQICC). We show that the asymptotic rate of assisted coherence distillation for pure states is equal to the coherence of assistance, an analog of the entanglement of assistance, whose properties we characterize. Our findings imply a novel interpretation of the von Neumann entropy: it quantifies the maximum amount of extra quantum coherence a system can gain when receiving assistance from a collaborative party. Our results are generalized to coherence localization in a multipartite setting and possible applications are discussed.

quant-ph↗

arXiv2016

Competing valence bond and symmetry breaking Mott states of spin-3/2 fermions on a honeycomb lattice

We investigate magnetic properties of strongly interacting four component spin-3/2 ultracold fermionic atoms in the Mott insulator limit with one particle per site in an optical lattice with honeycomb symmetry. In this limit, atomic tunneling is virtual, and only the atomic spins can exchange. We find a competition between symmetry breaking and liquid like disordered phases. Particularly interesting are valence bond states with bond centered magnetizations, situated between the ferromagnetic and conventional valence bond phases. In the framework of a mean-field theory, we calculate the phase diagram and identify an experimentally relevant parameter region where a homogeneous SU(4) symmetric Affleck-Kennedy-Lieb-Tasaki-like valence bond state is present.

cond-mat.quant-gas↗

arXiv2015

High-order harmonic generation from Rydberg atoms driven by plasmonic-enhanced laser fields

We theoretically investigate high-order harmonic generation (HHG) in Rydberg atoms driven by spatially inhomogeneous laser fields, induced, for instance, by plasmonic enhancement. It is well known that the laser intensity should to exceed certain threshold in order to generate HHG, when noble gas atoms in their ground state are used as an active medium. One way to enhance the coherent light coming from a conventional laser oscillator is to take advantage of the amplification obtained by the so-called surface plasmon polaritons, created when a low intensity laser field is focused onto a metallic nanostructure. The main limitation of this scheme is the low damage threshold of the materials employed in the nanostructures engineering. In this work we propose to use Rydberg atoms, driven by spatially inhomogeneous, plasmonic-enhanced laser fields, for HHG. We exhaustively discuss the behaviour and efficiency of these systems in the generation of coherent harmonic emission. To this aim we numerically solve the time-dependent Schrödinger equation for an atom with an electron initially in a highly excited $n$-th Rydberg state, located in the vicinity of a metallic nanostructure, where the electric field changes spatially on the scales relevant for the dynamics of the laser-ionized electron. We first use a one-dimensional model to investigate the phenomena systematically. We then employ a more realistic situation, when the interaction of a plasmonic-enhanced laser field with a three-dimensional Hydrogen atom is modelled. We discuss the scaling of the relevant input parameters with the principal quantum number $n$ of the Rydberg state in question, and demonstrate that harmonic emission could be achieved from Rydberg atoms well below the damage threshold, thus without deteriorating the geometry and properties of the metallic nanostructure.

physics.atom-ph↗

arXiv2015

Controlling electron localization of H$_2^+$ by intense plasmon-enhanced laser fields

We present a theoretical study of the wave packet dynamics of the H$_2^+$ molecular ion in plasmon-enhanced laser fields. Such fields may be produced, for instance, when metallic nano-structures are illuminated by a laser pulse of moderated intensity. Their main property is that they vary in space on nanometer scales. We demonstrate that the spatial inhomogeneous character of these plasmonic fields leads to an enhancement of electron localization, an instrumental phenomenon that controls molecular fragmentation. We suggest that the charge-imbalance induced by the surface-plasmon resonance near the metallic nano-structures is the origin of the increase in the electron localization.

physics.atom-ph↗

arXiv2015

Signatures of double-electron re-combination in high-order harmonic generation driven by spatially inhomogeneous fields

We present theoretical studies of high-order harmonic generation (HHG) driven by plasmonic fields in two-electron atomic systems. Comparing the two-active electron and single-active electron approximation models of the negative hydrogen ion atom, we provide strong evidence that a double non-sequential two-electron recombination appears to be the main responsible for the HHG cutoff extension. Our analysis is carried out by means of a reduced one-dimensional numerical integration of the two-electron time-dependent Schrödinger equation (TDSE), and on investigations of the classical electron trajectories resulting from the Newton's equation of motion. Additional comparisons between the negative hydrogen ion and the helium atom suggest that the double recombination process depends distinctly on the atomic target. Our research paves the way to the understanding of strong field processes in multi-electronic systems driven by spatially inhomogeneous fields.

physics.atom-ph↗