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M. F. Ciappina

Publications and source records attributed to M. F. Ciappina.

At least 37 records · Page 2Linked to original sources

Two-photon absorption in semiconductors: a multi-band length-gauge analysis

The simplest approach to deal with light excitations in direct-gap semiconductors is to model them as a two-band system: one conduction and one valence band. For such models, particularly simple analytical expressions are known to exist for the optical response such as multi-photon absorption coefficients. Here we show that generic multi-band models do not require much more complicated expressions. Our length-gauge analysis is based on the semiconductors Bloch equations in the absence of all scattering processes. In the evaluation, we focus on two-photon excitation by a pump-probe scheme with possibly non-degenerate and arbitrarily polarized configurations. The theory is validated by application to graphene and its bilayer, described by a tight-binding model, as well as bulk Zincblende semiconductors described by k.p theory.

cond-mat.mtrl-sci↗

Polarization in Strong-Field Ionization of Excited Helium

We analyze how bound-state excitation, electron exchange and the residual binding potential influence above-threshold ionization (ATI) in Helium prepared in an excited $p$ state, oriented parallel and perpendicular to a linearly polarized mid-IR field. Using ab initio B-spline Algebraic Diagrammatic Construction (ADC), and several one-electron methods with effective potentials, including the Schrödinger solver Qprop, modified versions of the Strong-Field Approximation and the Coulomb-Quantum Orbit Strong-Field Approximation (CQSFA), we find that these specific physical mechanisms leave significant imprints in ATI spectra and photoelectron momentum distributions. Examples are changes of up to two orders of magnitude in the high-energy photoelectron region, and ramp-like structures that can be traced back to Coulomb-distorted trajectories. The present work also shows that electron exchange renders rescattering less effective, causing suppressions in the ATI plateau. Due to the long-range potential, the electron continuum dynamics are no longer confined to the polarization axis, in contrast to the predictions of traditional approaches. Thus, one may in principle probe excited-state configurations perpendicular to the driving-field polarization without the need for orthogonally polarized fields.

physics.atom-ph↗

Manipulating Twisted Electrons in Strong-Field Ionization

We investigate the discrete orbital angular momentum (OAM) of photoelectrons freed in strongfield ionization. We use these `twisted' electrons to provide an alternative interpretation on existing experimental work of vortex interferences caused by strong field ionization mediated by two counterrotating circularly polarized pulses separated by a delay. Using the strong field approximation, we derive an interference condition for the vortices. In computations for a neon target we find very good agreement of the vortex condition with photoelectron momentum distributions computed with the strong field approximation, as well as with the time-dependent methods Qprop and R-Matrix. For each of these approaches we examine the OAM of the photoelectrons, finding a small number of vortex states localized in separate energy regions. We demonstrate that the vortices arise from the interference of pairs of twisted electron states. The OAM of each twisted electron state can be directly related to the number of arms of the spiral in that region. We gain further understanding by recreating the vortices with pairs of twisted electrons and use this to determine a semiclassical relation for the OAM. A discussion is included on measuring the OAM in strong field ionization directly or by employing specific laser pulse schemes as well as utilizing the OAM in time-resolved imaging of photo-induced dynamics.

physics.atom-ph↗

Focal-shape effects on the efficiency of the tunnel-ionization probe for extreme laser intensities

We examine the effect of laser focusing on the potential of a recently discussed scheme [M.F. Ciappina {\em et al}, Phys. Rev. A 99, 043405 (2019); Las. Phys. Lett. 17, 025301 (2020)] for in situ determination of ultra-high intensities of electromagnetic radiation delivered by multi-petawatt laser facilities. Using two model intensity distributions in the focus of a laser beam, we show how the resulting yields of highly charged ions generated in the process of multiple sequential tunneling of electrons from atoms, depend on the shape of these distributions. Our findings lead to the conclusion that an accurate extraction of the peak laser intensity can be made either in the near-threshold regime when the production of the highest charge state happens only in a small part of the laser focus close to the point where the intensity is maximal, or through the determination of the points where the ion yields of close charges become equal. We show that, for realistic parameters of the gas target, the number of ions generated in the central part of the focus in the threshold regime should be sufficient for a reliable measurement with highly sensitive time-of-flight detectors. Although positions of the intersection points generally depend on the focal shape, they can be used to localize the peak intensity value in a certain interval. Additionally to this analysis, we discuss the method in comparison to other recently proposed approaches for direct measurement of extreme laser intensities.

physics.atom-ph↗

Perspective on petahertz electronics and attosecond nanoscopy

The field of attosecond nanophysics, combining the research areas of attosecond physics with nanoscale physics, has experienced a considerable rise in recent years both experimentally and theoretically. Its foundation rests on the sub-cycle manipulation and sampling of the coupled electron and near-field dynamics on the nanoscale. Attosecond nanophysics not only addresses questions of strong fundamental interest in strong-field light-matter interactions at the nanoscale, but also could eventually lead to a considerable number of applications in ultrafast, petahertz-scale electronics, and ultrafast metrology for microscopy or nanoscopy. In this perspective, we outline the current frontiers, challenges, and future directions in the field, with particular emphasis on the development of petahertz electronics and attosecond nanoscopy.

physics.optics↗

Diagnostics of ultra-intense laser pulses using tunneling ionization

We revisit a recently proposed scheme [M.F. Ciappina et al 2019 Phys. Rev. A 99 043405] for accurate measurement of electromagnetic radiation intensities in a focus of high-power laser beams. The method is based on the observation of multiple sequential tunneling ionization of atoms and suggests the determination of the peak intensity value from the appearance in the focal area ions with a certain charge number. Here we study the sensitivity of the approach to two essential factors: the focal volume effect and the tunneling ionization model chosen to calculate ionization rates. We show, on the one hand, that the results appear almost model-independent for ionization of helium- and hydrogen-like ions and, on the other hand, that the focal averaging leaves the intensity-dependent features visible. Our findings are in favor to a practical implementation of the atomic diagnostics of extreme laser intensities.

physics.atom-ph↗

CEP-Controlled Molecular Dissociation by Ultrashort Chirped Laser Pulses

We demonstrate and characterize that a carrier-envelope-phase (CEP)-controlled ultrashortchirped field is an efficient and robust mechanism to modify the dissociation dynamics of molecularhydrogen. Different dissociation pathways are collectively induced and their interference contributeto the kinetic energy release spectra. Chirping is able to efficiently manipulate the interferencesof different dissociation pathways. We demonstrate a linear relationship between chirp and CEP-dependence, dissociation as well as directional electron localization.

physics.atom-ph↗

Determination of the spectral variation origin in high-order harmonic generation in noble gases

One key parameter in the high-order harmonic generation (HHG) phenomenon is the exact frequency of the generated harmonic field. Its deviation from perfect harmonics of the laser frequency can be explained considering (i) the single-atom laser-matter interaction and (ii) the spectral changes of the driving laser. In this work, we perform an experimental and theoretical study of the causes that generate spectral changes in the HHG radiation. We measured the driving laser spectral shift after high harmonic generation in long medium using a correction factor to take into account the multiple possible HHG initiation distances along the laser path. We separate out the contribution of laser spectral shift from the resultant high harmonic spectral shift in order to elucidate the microscopic effect of spectral shift in HHG. Therefore, in some cases we are able to identify the dominant electron trajectory from the experimental data. Our investigations lead to valuable conclusions about atomic dipole phase contribution to a high harmonic spectral shift. We demonstrate that the significant contribution of a long electron path leads to a high harmonic shift, which differs from that expected from the driving laser. Moreover, we assess the origin of the high-order harmonics spectral broadening and provide an explanation for the narrowest high harmonic spectral width in our experiment.

physics.atom-ph↗

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↗

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↗

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↗

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↗

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↗

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↗

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↗

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↗

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↗