Dissociation and ionization of H+2 by ultrashort intense laser pulses probed by coincidence 3D momentum imaging

Laser-induced dissociation and ionization of H(+)(2) were simultaneously measured using coincidence 3D momentum imaging, allowing direct separation of the two processes, even where the fragment kinetic energy is the same for both processes. The results for 45 and 135 fs 790 nm pulses with an intensity of approximately 2.5 x 10(14) W/cm(2) differ from each other much more than one would expect from previous measurements with longer pulses. Ionization was negligible for the longer pulse and was strongly aligned along the laser polarization for the shorter pulse, but showed no structure in its kinetic energy distribution. In addition, the ionization to dissociation ratio was found to be much smaller than theoretically predicted for H(+)(2).     

Nonsequential double ionization of Xe by mid-infrared laser pulses

With the three-dimensional semiclassical ensemble model, we studied the correlated electron dynamics in strong-field nonsequential double ionization of Xe by mid-infrared laser pulses over a wide range of laser intensities. Numerical results show that the correlated electron momentum distribution exhibits the strong back-to-back pattern at the lower laser intensity. It evolves into the side-by-side behavior as the laser intensity increases and presents the experimentally observed crosslike shape at high laser intensity. Different from the case of near-infrared region where recollision mainly occurs at the first returning, at the mid-infrared region recollision dominantly occurs at the later returnings. The windows of initial transverse velocity for the various multiple-returning recollision trajectories are different and are unambiguously determined by this semiclassical ensemble model.     

Electron wavepacket phases in ionization and rescattering processes by intense laser pulses

Exact numerical solutions of the time-dependent Schrödinger equation, TDSE, are presented for the H atom and H^2/+ molecular ion ionized by short (10 optical cycles), intense I ₀ ≥ 10¹⁴ W/cm², 800 nm laser pulses. Calculations of the time dependent expectation values of the dipole moment d(t), velocity $ \dot d Exact numerical solutions of the time-dependent Schr?dinger equation, TDSE, are presented for the H atom and H^2/+ molecular ion ionized by short (10 optical cycles), intense I ₀ ≥ 10¹⁴ W/cm², 800 nm laser pulses. Calculations of the time dependent expectation values of the dipole moment d(t), velocity (t), and acceleration (t) are used to identify the phase of these physical parameters with respect to the laser field during the harmonic generation process. It is found in general that electron wavepackets in an inner region near the parent ion are out of phase with the response expected from the classical laser induced recollision model, whereas wavepackets in an outer region, far from the parent ion, are in phase with the field force. It is found furthermore that it is the inner electron wavepacket which contributes mainly to the high order harmonic generation, HHG, process, even though its acceleration is out of phase with the field force. This suggests strong Coulomb refocussing effects in the HHG process, especially in the case of H^2/+. Original Russian Text ? Astro, Ltd., 2009. In honor of Prof. N.B. Delone. The article is published in the original.     

Nonsequential double ionization with few-cycle laser pulses

We investigate differential electron momentum distributions in nonsequential double ionization with linearly polarized, few-cycle pulses, using a classical model based on a laser-assisted inelastic (e(-),2e(-)) rescattering mechanism. These yields, as functions of the momentum components parallel to the laser polarization, are highly asymmetric and strongly influenced by the phase difference between the pulse envelope and its carrier oscillation, radically changing their sign around a critical phase. This behavior provides a powerful tool for absolute-phase measurements.     

Independent electron theory of multiple ionization of xenon by intense laser pulses

The intensity dependence of the multiphoton ionization spectra of Xe atoms has been investigated with an improved accuracy and well-controlled laser parameters. In particular, we have examined the ionization rates for X³⁺, X²⁻, X⁺ as functions of the laser intensity and the pressure in the target chamber. The apparatus used for these measurements is characterized by a high-energy resolution (better than 200 meV) and a completely digital acquisition system. The time-of-flight spectra clearly show the contributions of the different isotopes present in Xe gas. The laser pulses have been characterized with great accuracy by monitoring the energy, pulse width and divergence shot by shot. The ionization rates of the different ions have been used for testing the basic assumption of the Geltman theory of multiple ionization based on the single electron ionization model. We have found that for the small intensity range investigated the quantity (dXe ⁺/dI)·(dXe ³⁺/dI)/(dXe ²⁺/dI)² appears to be quite close to the value 0.5 predicted by this model.     

Enhancement and control of H2 dissociative ionization by femtosecond VUV laser pulses

We report ab initio calculations of H2 ionization by VUV/fs 10(12) W/cm2 laser pulses including correlation and all electronic and vibrational degrees of freedom (DOF). Inclusion of the nuclear DOF leads to a substantial increase of resonance enhanced multiphoton ionization. By varying pulse duration, it is possible to control the ratio of dissociative to nondissociative ionization as well as the final H+(2) vibrational distribution. For pulses longer than 10 fs and proportional to omega>0.46 a.u., dissociative ionization entirely dominates, which is a very unusual situation in photoionization studies.     

Time-resolved double ionization with few cycle laser pulses

Ionization of D2 launches a vibrational wave packet on the ground state of D+2. Removal of the second electron places a pair of D+ ions onto a Coulombic potential. Measuring the D+ kinetic energy determines the time delay between the first and the second ionization. Caught between a falling ionization and a rapidly rising intensity, the typical lifetime of the D+2 intermediate is less than 5 fs when an intense 8.6 fs laser pulse is used. We simulate Coulomb explosion imaging of the ground state wave function of D2 by a 4 fs optical pulse and compare with our experimental observations.     

Nonsequential double ionization of diatomic molecules by elliptically polarized laser pulses

Using the classical ensemble method, we investigate nonsequential double ionization （NSDI） of diatomic molecules by elliptically polarized laser pulses. The results show that the ellipticity of the laser field has a strong suppression effect on NSDI probabilities both in parallel and perpendicular alignments. The double ionization （DI） channel is commonly dominated by NSDI, and the NSDI channel changes with ellipticity. As ellipticity increases, more and more NSDIs occur through recollision excitation with subsequent field ionization （RESI）. Moreover, like the case of linear polarization, the two electrons involved in NSDI for perpendicularly aligned molecules are more likely to emit into the opposite hemispheres as compared to the case of parallel alignment. Additionally, this alignment effect increases as ellipticity increases.     

Photoelectron angular distributions at the ionization of atoms by intense sub-one-cycle laser pulses

The phase sensitivity of the photoelectron angular distributions by intense sub-one-cycle linearly polarized laser pulses has been discussed within the analytic Landau-Dykhne approximation. In both cases of sine and cosine laser pulses most of the electrons are ejected along the polarization axis of the laser field. Nevertheless the electron yield and the electron kinetic energies are much larger for the cosine waveform pulse.     

Enhanced ionization of perpendicularly aligned H2 in intense laser fields

Using three-dimensional classical ensembles, we have investigated the enhancement of double ionization of perpendicularly aligned H₂ molecules by a 800 nm laser pulse with intensity ranging from 1 × 10¹⁴ W/cm² to 6 × 10¹⁴ W/cm². The simulated results show that double ionization probability of H₂ strongly depends on R and reaches a maximum at an intensity independent critical distance R_C ≈ 5 a.u. Furthermore, the enhancement of double ionization is more pronounced in the cases of weaker or stronger fields. These results, a well indication of the influence of molecular structures and laser–molecule interactions on double ionization of diatomic molecules, are analyzed in detail and qualitatively explained based on the field-induced barrier suppression model and back analysis.     

Two-color ionization of hydrogen by short intense pulses

Photoelectron energy spectra resulting by the interaction of hydrogen with two short pulses having carrier frequencies, respectively, in the range of the infrared and XUV regions have been calculated. The effects of the pulse duration and timing of the X-ray pulse on the photoelectron energy spectra are discussed. 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. It is found that, depending on the duration of the X-ray pulse, ripples in the energy spectra separated by the infrared photon energy may appear. Moreover, the temporal shape of the low frequency radiation field may be inferred by the breadth of the photoelectron energy spectra.     

Subcycle electron emission in sequential double ionization by elliptical laser pulses

Using a classical ensemble method, we have investigated sequential double ionization (SDI) of Ar atoms driven by elliptical laser pulses. The results show that the ion momentum distribution of the Ar atoms depends strongly on the pulse duration. As the pulse duration increases, the ion momentum distribution changes from two bands to four bands and then to six bands and finally to an eight-band structure. Back analysis of double ionization trajectories shows that the variation of the band structure originates from pulse duration dependent multiple ionization bursts of the second electron. Our calculations indicate that the subcycle electron emission in the SDI could be more easily accessed by using elliptical laser pulses with a longer wavelength. Moreover, we show that there is good correspondence between the scaled radial momentum and the ionization time.     

Effect of electron excitation in nonsequential double ionization by intense laser fields

We study the double ionization process of atoms in intense laser fields. The momentum distributions of the correlated electrons are calculated. Contrary to the general expectation, we show an increasing proportion of the electrons ionized via excitation with the increasing laser intensity. These electrons generally have small energy thus they concentratedly distribute on the central region of the momentum diagram. Consequently, the central part of the momentum diagram becomes more notable in higher intensity laser fields. Further study suggests that this phenomenon is general in double ionization.     

Dynamics of H9+ in intense laser pulses

We discuss the response of the H9+ cluster to an excitation by an intense laser beam. Calculations are done within the framework of TDLDA-MD, an approach which has proven to provide a robust tool for investigations in metal cluster dynamics. We first discuss static and low energy properties of H9+ and make comparisons with other existing ab initio results. We then explore the various excitation/deexcitation scenarios as a function of the laser parameters.     

Electron energy spectra from intense laser double ionization of helium

The double ionization of helium in the strong-field limit has been studied using an electron-ion coincidence technique. The observed double ionization electron energy spectra differ significantly from the single ionization distributions. This gives new support to the rescattering model of double ionization and explicitly reveals the role of backward electron emission following the e-2e ionizing collision.     

Single attosecond burst generation during ionization of excited atoms by intense ultrashort laser pulses

We develop an analytical approach to describing the generation of a single attosecond burst during barrier-suppression ionization of a hydrogen atom by an intense laser pulse. We derive analytical expressions that describe the evolution of the electron wave packet in the time interval between the detachment from the atom and the collision with the parent ion for an arbitrary initial atomic state by assuming the atom to be fully ionized in one laser-field half-period. For various s-states, we derive expressions for the profile of the attosecond burst generated when the electron packet collides with the ion and analyze the dependence of its generation efficiency on the principal quantum number n of the initial atomic state. The results obtained are compared with the results of three-dimensional numerical calculations. We show that the attosecond pulse generation efficiency can be several orders of magnitude higher than that in the case of ionization from the ground state when pre-excited atomic states are used.     

Strong orientation effects in ionization of H+2 by short, intense, high-frequency light pulses

We present three-dimensional time-dependent calculations of ionization of arbitrarily spatially oriented H+2 by attosecond, intense, high-frequency laser fields. The ionization probability shows a strong dependence on both the internuclear distance and the relative orientation between the laser field and the internuclear axis. The physical features are explained in terms of two-center interference effects.     

Improved carrier-envelope phase locking of intense few-cycle laser pulses using above-threshold ionization

A robust nonoptical carrier-envelope phase (CEP) locking feedback loop, which utilizes a measurement of the left-right asymmetry in the above-threshold ionization (ATI) of Xe, is implemented, resulting in a significant improvement over the standard slow-loop f-to-2f technique. This technique utilizes the floating average of a real-time, every-single-shot CEP measurement to stabilize the CEP of few-cycle laser pulses generated by a standard Ti:sapphire chirped-pulse amplified laser system using a hollow-core fiber and chirped mirror compression scheme. With this typical commercially available laser system and the stereographic ATI method, we are able to improve short-term (minutes) CEP stability after a hollow-core fiber from 450 to 290 mrad rms and long-term (hours) stability from 480 to 370 mrad rms.