Thanks to the rapid advances in laser technology, laser pulses are becoming increasingly shorter and intense which make them an adequate tool to probe the ultrafast dynamics in atoms and molecules [1-5]. Experimentalists with theoreticians have worked consistently toward mastering the ionization control techniques by intense temporal pulses [6]. Depending on the characteristics of an incident laser pulse, different features could appear in the spectra of the emitted electrons or light from an atomic or a molecular system. Transform-limited pulses, which are ideal and bandwidth limited, have been extensively used to investigate laser-matter interaction [7]. A particular attention was given, in the past few years, to the effect of the carrier-phase envelope of a transform-limited pulse in controlling the ionization yield in some asymmetric molecular systems [8,9].

Recently, there is an increasing interest to investigate the interaction of atoms and molecules with chirped laser pulses [10-14]. These pulses that are frequency modulated have an advantage over unchirped laser pulses, i.e., transform-limited laser pulses. Their characterization and shaping make them more tailored to achieve complete electronic population inversion in molecular systems [15] and induce resonant multiphoton population transfer in Rydberg atoms [16-20]. It is important to note that the ability to control population transfer from an initial state to a desired final state is of crucial importance as it will open the way to the control of a chemical reaction’s end product.

In this paper, we show the efficiency of the chirped laser pulses to control the ionization yield in a real hydrogen atom. We used intense short chirped laser pulses of central carrier frequency which correspond to the 7^th harmonic of the Ti:Sapphire laser. A chirped laser pulse is experimentally produced by chirp filtering of a transform-limited laser pulse. We consider, in this paper, alistic experimental representation of a linearly polarized chirped laser pulse, in which the chirp parameter increases the pulse duration of the original transform-limited laser pulse and decreases its intensity. The frequency bandwidth of the resulting chirped pulse remains the same as that of the corresponding transform-limited laser pulse. The theoretical approach we used to calculate the unperturbed energetic structure of the hydrogen atom is based on an accurate L² discretization technique using B-spline functions [21,22]. We calculated the ionization probability by numerically solving the three-dimensional time-dependent Schrödinger equation using a spectral method [23-25]. We show how the sign of the chirp parameter induces an asymmetry in the ionization process in the hydrogen atom. We present results of the time evolution of the 1s and 2p bound states population from the switch-on to the switch-off of the chirped pulses and then we analyze the role of the first excited state 2p in the ionization process.

Atomic units are used throughout the paper unless otherwise mentioned.

For the numerical calculations, we have considered a set of N_b =1200 B-splines of order k = 7 defined on the radial box of maximum length R_max = 1000 a.u. We have fixed the maximum electron angular momentum to l = 12. As we choose the laser pulse to be polarized linearly along the z axis, only electronic transitions between states of m = 0 magnetic quantum number are permitted. We kept in all our calculations the CEP constant and set to φ = 0. The convergence of our numerical results has been checked by increasing the number of B-spline functions, the radial box size and the number of angular moment a. We have also checked that the results are gauge independent.

We consider in this paper a transform-limited pulse (ξ = 0) of central carrier frequency ω₀ = 0.399 a.u. (10.85 eV), which corresponds to the 7^th harmonic of Ti:Sa laser (λ = 114 nm). The pulse has an intensity and a FWHM duration.

We plot, in Figure 1, the transform-limited pulse vector potential variation with time. In experiment, upon transmission through a chirp filter, an initially transform-limited pulse becomes chirped with a chirp parameter. The filtered pulse will be up-chirped if is positive and will be down-chirped if is negative. In Figure 1, we compare between the shape of the and the vector potentials of a simulated up-chirped pulse of and a down-chirped pulse of. Both chirped pulses, according to Equations (9) and (12), have an intensity of

and a FWHM duration. The form of the vector potential we use in this paper (see Equation (7)) simulates a realistic experimental case in which the chirp filtering decreases the intensity of the transform limited pulse and increases its to talduration. We present also, in Figure 1, the spectral profile of the three pulses and the variation of their instantaneous frequency with time. Specifically, an up-chirped pulse (down-chirped) with a positive (negative) value of means that the instantaneous laser frequency increases (decreases) with time. Nevertheless, the frequency bandwidth of the up-

and down-chirped pulses remains the same that the transform-limited pulse.

We submit the atom taken initially in its fundamental electronic state 1s to each of the three pulses presented in Figure 1. As the energy of the 1s state is, the atom needs to absorb two photons to be ionized. We present, in Figure 2, the results of the ionization probability as a function of the time duration of each of the unchirped pulse and the chirped pulses of. We notice that the up-chirped pulse ionizes more the atom than both the unchirped and the downchirped pulses. More interesting, the ionization probability obtained at the end of the up-chirped laser pulse is three and a half times higher than that obtained with the down-chirped laser pulse. Figure 2 clearly indicates that the sign of the chirp parameter induces an asymmetry in the ionization yield.

To understand how the sign of the chirp influences the two-photon ionization yield, we analyzed the transfer of the population from the 2p bound state involved in the ionization path to the continuum states. In the present study, the absorption of the first photon by the atominduces a transfer of the population from the fundamental state 1s to the 2p state, whereas the absorption of the second photon results in a transfer of 2p state population to the continuum states. We follow in time the survival population of the 1s state and the amount of the population transferred to the 2p state. We show in Figure 3 (Figure 4) how the 1s (2p) state is depopulated (populated) as each of the three pulses progresses.

We notice from both figures that when the chirped pulses reach their higher intensity, the up-chirped pulse, in contrast with the down-chirped pulse, makes a large amounts of the 1s population transferred to the 2p excited state which considerably depopulates the 1s state and hence enormously populates the 2p sates. Consequently, higher amount of the population is transferred from the 2p bound state to the continuum channel when than when. The upand down-chirped laser pulses are of the same intensity and duration, however, the excitation process they induce inside the atom is different. The sign of the chirp parameter influences the variation of the instantaneous frequency with

time, which affects the average of the population transferred to the 2p state and then to the continuum states. When the atom is under a chirped laser pulse of a positive, the instantaneous frequency increases as the pulse progresses (see Figure 1). The 2p bound state becomes close to resonance in the first half duration of the laser pulse when the latter is gaining in intensity which reinforces the transfer of the population from the 1s to the 2p state and then to the continuum states. In contrast, when the atom is under a chirped pulse of negative, the instantaneous frequency decreases as the pulse progresses. Here, the 2p bound state becomes close to resonance in the second half duration of the pulse when the intensity of the latter is decreasing which weakens the transfer of the population from the 1s to the 2p state and then to the continuum states.

We have numerically investigated in this paper the ionization process in a real hydrogen atom by short and intense chirped laser pulses. We have observed an asymmetry in the ionization yield induced by the sign of the chirp parameter. We found that an up-chirped laser pulse is more efficient to ionize the atom than a down-chirped laser pulse. Our study has proven that chirped laser pulses that are selective are an efficient tool to control the atomic ionization process. The study presented in this paper could be applicable in another atomic or molecular target.

The present research was supported by the NSERC and by the New Brunswick Innovation Foundation (NBIF). Allocation of CPU time and assistance with the computer facilities from the Atlantic Computational Excellence Network (ACEnet, St-John’s, NL, Canada) and from the “Réseau Québecois de Calcul de Haute Performance” are acknowledged.