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Chinese Physics

Two-colour coherent control of multiphoton ionization: a comparison between long-range and short-range potential model atoms

Peng-Cheng Li, Zhou Xiaoxin

Published Oct 1, 2007• 1 citation
Publisher

Abstract

Using the numerical solution of the time-dependent Schrödinger equation of a one-dimensional model atom in a two-colour laser field, we have investigated the effects of the potential models on coherent control of atomic multiphoton ionization. It is found that the photoelectron spectra are obviously different for the long-range (Coulomb-like) and short-range (with no excited bound states) potential model atoms, which are produced by two-colour coherent control of atomic multiphoton ionization in a few laser cycles. Our results indicate that two-colour coherent control of atomic multiphoton ionization can be observed in simulations, depending on the choice of the model potentials.

DOI
10.1088/1009-1963/16/10/021

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Using the numerical solution of the time-dependent Schrödinger equation of a one-dimensional model atom in a two-colour laser field, we have investigated the effects of the potential models on coherent control of atomic multiphoton ionization. It is found that the photoelectron spectra are obviously different for the long-range (Coulomb-like) and short-range (with no excited bound states) potential model atoms, which are produced by two-colour coherent control of atomic multiphoton ionization in a few laser cycles. Our results indicate that two-colour coherent control of atomic multiphoton ionization can be observed in simulations, depending on the choice of the model potentials.
We examine the excitation dynamics of a model atom excited by a two-colour laser field. Here the two colours or frequencies are the fundamental and its third harmonic. The atomic model consists of two bound states which are near-resonantly coupled by a three-photon excitation by the fundamental and a one-photon excitation by the third harmonic, and a structureless continuum. We investigate how the laser parameters (intensity and frequency) and the relative phase between the two colours affects the degree of phase modulation in the ionization signal. We compare our findings from this simple model atom with those from more realistic atomic models by carrying out numerical integration of the hydrogenic Schrodinger equation in both one and three dimensions.
We present a theoretical study of the main characteristics of two-color photoionization spectra obtained when atoms are subjected to an intense radiation pulse containing the fundamental of an infrared laser and one of its higher harmonics. The frequency of the latter is chosen to be high enough that the atom can be ionized by a single photon. The calculation is performed by numerical integration of the time-dependent Schrödinger equation for a (three-dimensional) hydrogen atom. We present the general properties of the spectra and angular distributions as well as the possible occurrence of interferences between the laser-assisted process and above-threshold ionization. Our results indicate that such interference effects, which can lead to partial coherent control of the photoionization process, can be observed at moderate laser intensities within the reach of currently operated laser and harmonic sources.
Coherent control provides a quantum interference based method for controlling atomic and molecular dynamics. We report two experimental observations of different ways to achieve such a control in atomic photoionization continuum. One is the photoionization of sodium atoms, initially prepared in the 3P1/2 excited state, by a non resonant three-photon interaction with 1064-nm laser light and by a one-photon interaction with the third-harmonic field, at 355 nm. Interference between the two transition paths allows the control of the total ionization rate by varying the relative phase of the laser fields. The second experiment is the observation of the modification of the ionization continua of xenon through laser induced continuum structure (LICS). The multiphoton radiative decay of the xenon ground state into the two electronic continua, that correspond to the two fine structure levels of the ground state of the xenon ion, is varied by electromagnetically embedding a bound state of the atom into the two continua. Both experiments are performed on an atomic beam apparatus which uses a time-of-flight spectrometer for energy analyzing the emitted photoelectrons.
Weak-field coherent phase control of atomic non-resonant multiphoton excitation induced by shaped femtosecond pulses is studied theoretically in the single-cycle regime. The carrier-envelope phase (CEP) of the pulse, which in the multi-cycle regime does not play any control role, is shown here to be a new effective control parameter that its effect is highly sensitive to the spectral position of the ultrabroad spectrum. Rationally chosen position of the ultrabroadband spectrum coherently induces several groups of multiphoton transitions from the ground state to the excited state of the system: transitions involving only absorbed photons as well as Raman transitions involving both absorbed and emitted photons. The intra-group interference is controlled by the relative spectral phase of the different frequency components of the pulse, while the inter-group interference is controlled jointly by the CEP and the relative spectral phase. Specifically, non-resonant two- and three-photon excitation is studied in a simple model system within the perturbative frequency-domain framework. The developed intuition is then applied to weak-field multiphoton excitation of atomic cesium (Cs), where the simplified model is verified by non-perturbative numerical solution of the time-dependent Schrödinger equation. We expect this work to serve as a basis for a new line of femtosecond coherent control experiments.
A simple, "exactly solvable" atomic model will be presented that helps to discuss some of the interesting features of multiphoton ionization of atoms. The electromagnetic field is treated non-perturbatively, it can be strong. The atomic electrons are assumed to be non-interacting (Hartree model). They are bound in a harmonic oscillator potential (one- or three-dimensional). At the ionization energy, the potential is cut off and the free electron has no Coulomb attraction. The Schrodinger equation has exact analytic solutions valid in the inner or outer regions. If the field is turned on adiabatically, the exact solution can be found by matching these solutions at the boundary; both of their value and the normal derivative at all times. Thus the machine calculation reduces to repeated application of fast Fourier transforms and to the solution of linear equations (unfortunately a lot of them).