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Register a new userStatic field limit of excitation probabilities in laser-atom interactions
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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.
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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.
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.
We present experimental and theoretical results showing the improved beam quality and reduced divergence of an atom laser produced by an optical Raman transition, compared to one produced by an RF transition. We show that Raman outcoupling can eliminate the diverging lens effect that the condensate has on the outcoupled atoms. This substantially improves the beam quality of the atom laser, and the improvement may be greater than a factor of ten for experiments with tight trapping potentials. We show that Raman outcoupling can produce atom lasers whose quality is only limited by the wavefunction shape of the condensate that produces them, typically a factor of 1.3 above the Heisenberg limit.
Application of a parallel-projection inversion technique to z-scan spectra of multiply charged xenon and krypton ions, obtained by non-resonant field ionization of neutral targets, has for the first time permitted the direct observation of intensity-dependent ionization probabilities. These ionization efficiency curves have highlighted the presence of structure in the tunnelling regime, previously unobserved under full-volume techniques.
This work reports on the application of a novel electric field-ionization setup for high-resolution laser spectroscopy measurements on bunched fast atomic beams in a collinear geometry. In combination with multi-step resonant excitation to Rydberg states using pulsed lasers, the field ionization technique demonstrates increased sensitivity for isotope separation and measurement of atomic parameters over non-resonant laser ionization methods. The setup was tested at the Collinear Resonance Ionization Spectroscopy experiment at ISOLDE-CERN to perform high-resolution measurements of transitions in the indium atom from the 5s$^2$5d~$^2$D$_{5/2}$ and 5s$^2$5d~$^2$D$_{3/2}$ states to 5s$^2$($n$)p~$^2$P and 5s$^2$($n$)f~$^2$F Rydberg states, up to a principal quantum number of $n$ = 72. The extracted Rydberg level energies were used to re-evaluate the ionization potential of the indium atom to be 46670.1055(21) cm$^{-1}$. The nuclear magnetic dipole and nuclear electric quadrupole hyperfine structure constants and level isotope shifts of the 5s$^2$5d~$^2$D$_{5/2}$ and 5s$^2$5d~$^2$D$_{3/2}$ states were determined for $^{113,115}$In. The results are compared to calculations using relativistic coupled-cluster theory. A good agreement is found with the ionization potential and isotope shifts, while disagreement of hyperfine structure constants indicates an increased importance of electron correlations in these excited atomic states. With the aim of further increasing the detection sensitivity for measurements on exotic isotopes, a systematic study of the field-ionization arrangement implemented in the work was performed and an improved design was simulated and is presented. The improved design offers increased background suppression independent of the distance from field ionization to ion detection.
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