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Register a new userModelling laser-atom interactions in the strong field regime
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We consider the ionisation of atomic hydrogen by a strong infrared field. We extend and study in more depth an existing semi-analytical model. Starting from the time-dependent Schroedinger equation in momentum space and in the velocity gauge we substitute the kernel of the non-local Coulomb potential by a sum of N separable potentials, each of them supporting one hydrogen bound state. This leads to a set of N coupled one-dimensional linear Volterra integral equations to solve. We analyze the gauge problem for the model, the different ways of generating the separable potentials and establish a clear link with the strong field approximation which turns out to be a limiting case of the present model. We calculate electron energy spectra as well as the time evolution of electron wave packets in momentum space. We compare and discuss the results obtained with the model and with the strong field approximation and examine in this context, the role of excited states.
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We consider the interaction of atomic hydrogen, in its ground state, with an electromagnetic pulse whose duration is fixed in terms of the number of optical cycles. We study the probability of excitation of the atom in the static field limit i.e. for field frequencies going to zero. Despite the fact that the well known Born-Fock adiabatic theorem is valid only for a system whose energy spectrum is discrete, we show that it is still possible to use this theorem to derive, in the low frequency limit, an analytical formula which gives the probability of transition to any excited state of the atom as a function of the field intensity, the carrier envelope phase and the number of optical cycles within the pulse. The results for the probability of excitation to low-lying excited states, obtained with this formula, agree with those we get by solving the time-dependent Schroedinger equation. The domain of validity is discussed in detail.
The distance-dependence of the anisotropic atom-wall interaction is studied. The central result is the 1/z^6 quadrupolar anisotropy decay in the retarded Casimir-Polder regime. Analysis of the transition region between non-retarded van der Waals regime (in 1/z^3) and Casimir-Polder regime shows that the anisotropy cross-over occurs at very short distances from the surface, on the order of 0.03 Lambda, where Lambda is the atom characteristic wavelength. Possible experimental verifications of this distance dependence are discussed.
We investigate the role of the Coulomb interaction in strong field processes. We find that the Coulomb field of the ion makes its presence known even in highly intense laser fields, in contrast to the assumptions of the strong field approximation. The dynamics of the electron after ionization is analyzed with four models for an arbitrary laser polarization: the Hamiltonian model in the dipole approximation, the strong field approximation, the Coulomb-corrected strong field approximation and the guiding center. These models illustrate clearly the Coulomb effects, in particular Coulomb focusing and Coulomb asymmetry. We show that the Coulomb-corrected strong field approximation and the guiding center are complementary, in the sense that the Coulomb-corrected strong field approximation describes well short time scale phenomena (shorter than a laser cycle) while the guiding center is well suited for describing long time scale phenomena (longer than a laser cycle) like Coulomb-driven recollisions and Rydberg state creation.
Rydberg-atom ensembles are switched from a weakly- into a strongly-interacting regime via adiabatic transformation of the atoms from an approximately non-polar into a highly dipolar quantum state. The resultant electric dipole-dipole forces are probed using a device akin to a field ion microscope. Ion imaging and pair-correlation analysis reveal the kinetics of the interacting atoms. Dumbbell-shaped pair correlation images demonstrate the anisotropy of the binary dipolar force. The dipolar $C_3$ coefficient, derived from the time dependence of the images, agrees with the value calculated from the permanent electric-dipole moment of the atoms. The results indicate many-body dynamics akin to disorder-induced heating in strongly coupled particle systems.
The strong-field approximation can be and has been applied in both length gauge and velocity gauge with quantitatively conflicting answers. For ionization of negative ions with a ground state of odd parity, the predictions of the two gauges differ qualitatively: in the envelope of the angular-resolved energy spectrum, dips in one gauge correspond to humps in the other. We show that the length-gauge SFA matches the exact numerical solution of the time-dependent Schrodinger equation.
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