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The high-harmonic generation from a structured quantum ring (SQR) driven by an intense laser field is presented within the single active electron approximation. The spectrum is studied by varying the symmetry of the physical system. The standard SQR (six identical and equidistant dots in a ring) presents a 60° rotational symmetry, that in this work is broken, moving or changing only one potential hole. We find that careful designed breaking of the geometrical symmetry of the SQR opens the possibility of controlling the characteristics of the harmonic lines such as intensity and polarization. HHG analysis of the emission spectrum performed through a Morlet wavelet, shows that the high-frequency emission occurs during short time intervals.

The dynamics of a one-dimensional atom driven by three-laser fields is investigated. The total electric field is made up of a fundamental laser field of intensity W cm−2 and wavelength λ = 820 nm and two weak lasers with larger wavelengths. The intensity of the two weak fields is with k = 0.25. The frequencies of the weak fields are and , with and . The three lasers have a Gaussian envelope of 72 fs FWHM. It is shown, by numerical computation and using the semiclassical theory of high-harmonic generation, that the atom interacting with this combined field is able to emit an isolated attosecond burst of radiation.

The electron of a H 2 + driven by a strong electromagnetic field induces molecular vibrations. Numerical and analytical results show that the molecule behaves as a parametric oscillator and can be treated as a kicked oscillator. The results are discussed from the point of view of the electron's periodic dressing and undressing processes.

We use a 5-level system to investigate the HHG spectrum emitted by an atom driven by a linearly or elliptically polarized laser field. For this model the Schrodinger equation is numerically solved and we study the dipendence of the spectra, harmonic intensity and polarization of emitted radiation on the laser field ellipticity. Studying the intensity of the emitted radiation we find that un alsoder high laser ellipticity the harmonic emission is greatly reduced; the analysis of results shows that the harmonic intensity and the emitted radiation depend on the laser ellipticity.

Atomic and molecular systems, subjected to intense laser pulse, emit typical High-Order Armonic Generation (HHG) spectra. This work aims to investigate the possibility to obtain a laser device by HHG. At this end, we analyzed the emission spectra by a molecular ion driven by a linearly polarized laser field. The temporal behaviour is obtained using the Morlet wavelets transform of emission. The results show that, after filtration of the electromagnetic radiation emitted, it is possible to select a frequency which seems to have almost constant intensity and phase. This characteristic makes possible that HHG from a molecule can be used as high frequency laser fields.

We report on numerical results of energy spectra of photoelectrons emitted by irradiating an hydrogen atom with a relatively weak single attosecond XUV pulse in the presence of a two-color IR laser pulse. The densities of probabilities have been obtained by treating the interaction of the atom with the XUV radiation at the first order of the time-dependent perturbation theory and describing the emitted electron through the Coulomb-Volkov wavefunction. The results of the calculations agree with the ones found by numerically solving the time-dependent Schrödinger equation. Specifically, we use an algorithm that implements an high recision variant of the Cranck Nicolson integration method and allows to take into account the singularity in the Coulomb potential. Analysis of the spectra obtained for very long pulses show that certain features may be explained in terms of quantum interferences in the time domain.

We study the high harmonic generation and the polarization of the harmonics emitted by a nanoring driven by two laser fields of angular frequency ?1 and ?2, with ?2?=?2?1, and ?1 resonant between the ground and the first excited state. We show that by varying parameters, such as laser intensity, photon energy and the delay between the two laser pulses, we can control the number of harmonics and the polarization of the radiation. In particular we show that with this choice of two-laser photon frequency rate we obtain more harmonics with respect to other configurations. We also calculated the average absorbed energy and the average angular momentum acquired by the electron as a function of the intensity of the two lasers obtaining spikes of angular momentum.

We discuss the physical properties of a noninteracting electron gas constrained to a spherical surface. In particular we consider its chemical potentials, its ionization potential, and its electric static polarizability. All these properties are discussed analytically as functions of the number $N$ of electrons. The trends obtained with increasing $N$ are compared with those of the corresponding properties experimentally measured or theoretically evaluated for quasispherical hollow atomic and molecular clusters. Most of the properties investigated display similar trends, characterized by a prominence of shell effects. This leads to the definition of a scale-invariant distribution of magic numbers which follows a power law with critical exponent $\ensuremath{-}0.5$. We conclude that our completely mechanistic and analytically tractable model can be useful for the analysis of self-assembling complex systems.

In this paper we discuss isotopic effects in simple molecular ions subjected to strong laser fields. We show that the intensity of the emitted spectra strongly depends upon both the nuclear mass of the molecular ions and the laser pulse duration. In particular, for short pulse duration [up to 8 optical cycles (o.c.)], we confirm the trend described in the most studied case in which the high-order harmonic generation is more efficient for heavier isotopes; in contrast, an interesting physical phenomenon is predicted for pulses longer than 16 o.c. characterized by an inverse effect in which lighter molecular species are responsible for higher-order harmonic emission.

The time dependent Schrodinger equation of a homonuclear diatomic molecule in the presence of a linearly polarized laser field is numerically solved by means of a split-operator parallel code. The calculations are carried out by assuming a single active electron model with fixed nuclei; a simplified two-dimensional model of the system is used. The highly nonlinear response of the electron wave function to the laser electric field stimulates the molecule to emit electromagnetic radiation consisting of a wide plateau of odd harmonics of the laser field. It is shown that the emitted spectrum can be finely controlled by changing the angle between the laser electric field and the molecular axis; this can be used to achieve a tunable source of high frequency radiation.

We show that it is possible to use a piecewise constant Hamiltonian to describe the main features of the dynamics of an atom interacting with a laser field. In particular we show that using this approximation we are able to give a good description of the ionization signal, of the HHG spectra and of the attosecond pulses generated by the radiating electron. Finally, we give an explicit formula to evaluate the ionization rate in the time dependent laser field. This formula, which is a generalization of the Landau formula for the ionization rate of an atom in a static electric field, fairly well reproduces the numerical ionization rates for a broad range of laser frequency and intensity. The main advantage of this formula is that it can be used well beyond the limits of the quasi-static formula for the ionization rate of an atom.

A new scheme to generate isolated attosecond pulses is presented that involves the use of a laser field and of a unipolar field. The laser field has a pulse of intensity I = 1.5×1014 W cm−2 and wavelength λ = 820 nm. The unipolar pulse is an asymmetric pulse consisting of a sharp peak, lasting approximately half a laser period, i.e. nearly 1.4 fs, followed by a long and shallow tail. We show that on combining these two fields, it is possible to generate isolated attosecond pulses as short as 1/10 of a laser period, i.e. approximately 270 as. Moreover, it is argued that this scheme is robust either against small variations of the laser envelope, or against small changes in the delay between the laser pump and the unipolar pulse.

In this paper we investigate the single and double ionization signals of ${\text{H}}_{2}$ molecules, with fixed and moving nuclei, as a function of laser intensity, for two different values of laser wavelength ($\ensuremath{\lambda}=390\text{ }\text{nm}$ and $\ensuremath{\lambda}=780\text{ }\text{nm}$), using an approach for evaluating the ionization signals which allows the investigation of relatively long-lasting pulses. The He system is first investigated to benchmark our calculation against already known results. We confirm the evidence of nonsequentiality in the ionization processes of all the systems investigated. Furthermore, we show that the nuclei motion enhances the double ionization signals by means of a mechanism which is very similar to a charge-resonant enhanced ionization (CREI) effect [Zuo and Bandrauk, Phys. Rev. A 52, R2511 (1995)].

We study the dynamics of an electron constrained over the surface of a rigid sphere, with geometrical parameters similar to those of the C60 fullerene, embedded in a low intensity linearly polarized laser field. The model is shown to emit odd harmonics of the laser even at very low field intensity. For more intense laser fields, the spectrum presents odd harmonics and hyper-Raman lines shaped in a broad plateau. The spectrum of the model is compared to that theoretically obtained by other authors for more realistic models of C60. It is concluded that the model can be used as a paradigm for mesoscopic molecules in the fullerene family, particularly in practical applications where it is convenient to have a simple model of fullerene molecules. It is also concluded that the model is an example lending support to the concept of universality introduced by other authors some time ago.

In this paper we show how it is possible to investigate the nuclear dynamics of simple molecular ions and molecules by looking at the high-order harmonic generation spectra they emit in the presence of a laser field. In particular we investigate two different effects: the presence of sidebands in the emitted spectra around the usual odd harmonics and an isotopic effect which affects the height of the plateau lines. We further study the advantages and the limitations of the semiclassical approach.

We propose a new scheme to produce isolated attosecond pulses, involving the use of three laser pulses: a fundamental laser field of intensity I = 3.5 × 1014 W cm−2 and of wavelength λ = 820 nm, and two properly chosen weak lasers with wavelengths 1.5λ and 0.5λ. The three lasers have a Gaussian envelope of 36 fs full width at half maximum. The resulting total field is an asymmetric electric field with an isolated peak. We show that a model atom, interacting with the above-defined total field, generates an isolated attosecond pulse as short as 1/10 of a laser period, i.e. approximately 270 as.

We study the single and double ionization yields and the dissociation dynamics of a one-dimensional two-electron molecule exposed to a laser pulse of intensity IL in the range 1013 − 1015 W/cm2 and photon energy hω¯L =3.18 eV. The calculations are carried out in the case of both fixed and movable nuclei. At low IL the ionization curves have a power law shape In that is interrupted by a knee at higher intensity.

The dynamics of hydrogen-like molecules is investigated beyond the usual fixed nuclei approximation. The nuclear motion introduces in the familiar spectrum of emitted radiation additional regular lines whose separation is essentially given by the vibrational frequency of nuclear motion. A wavelet analysis of the emitted spectrum shows that the intensity of the harmonic lines is modulated with the same period of the nuclear motion; this suggests the possibility of the real-time control of the nuclear dynamics.

In this paper we show how it is possible to investigate the nuclei dynamics of a D2+ molecular ion by using the high harmonic generation spectra emitted by the system when subjected to an intense laser field. In particular, the emitted spectra contains, in addition to the usual odd harmonic peaks, additional satellite peaks whose frequency spacing is equal to the vibrational frequency of the nuclei.

The dynamics of a diatomic one-dimensional homonuclear molecule driven by a two-laser field is investigated beyond the usual fixed nuclei approximation. The dynamics of the nuclei is treated by means of Newton equations of motion; the full quantum description is used for the single active electron. The first laser pulse (pump) excites vibrations of the nuclei, while the second very short pulse (probe) has the role of confining the electron around one of the nuclei. We show how to use the radiation scattered in these conditions by the molecule to achieve real-time control of the molecular dynamics.

We describe, using a semiclassical approach, the molecular dynamics of a one-dimensional H2 molecule interacting with a laser, beyond the Born–Oppenheimer approximation. We observe and discuss different molecular behaviors, such as ionization and dissociation.

The dynamics of an electron wave packet in the presence of laser radiation and of a one-dimensional repulsive soft-core potential is investigated. For different laser intensities and for different initial positions of the electron wave packet, these results are compared with those for an attractive potential. The repulsive potential is capable of confining the electron quite efficiently under appropriate conditions. In these conditions, the electron is shown to emit a high harmonic spectrum similar to that emitted by the more conventional attractive potential. It is thus argued that recombination into an atomic bound state as required by the three step model is not essential for the emission of high harmonics.

We present the results of experimental and theoretical studies of high-order harmonic generation (HHG) in plasmas containing fullerenes using pulses of different duration and wavelength. We find that the harmonic cutoff is extended in the case of few-cycle pulses (3.5 fs, 29th harmonic) compared to longer laser pulses (40 fs, 25th harmonic) at the same intensity. Our studies also include HHG in fullerenes using 1300 and 780 nm multicycle (35 and 40 fs) pulses. For 1300 nm pulses, an extension of the harmonic cutoff to the 41st order was obtained, with a decrease in conversion efficiency that is consistent with theoretical predictions based on wave packet spreading for single atoms. Theoretical calculations of fullerene harmonic spectra using the single active electron approximation were carried out for both few-cycle and multicycle pulses.

The collision of an electron against a repulsive potential in the presence of a laser field is investigated. It is found that a sufficiently strong laser field forces the electron to remain in the neighbourhood of the repulsive potential causing bremsstrahlung. By appropriately filtering the emitted signal, an electron in the presence of a repulsive potential is capable of generating attosecond pulses.