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Dynamic polarizability of a complex atom in strong laser fields

Л. П. Рапопорт, A. F. Klinskikh, V. V. Mordvinov

Published Dec 1, 1997• 0 citations
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Influence of the Stark effect on multiphoton ionization of atoms when the dynamic polarizability depends strongly on the laser frequency

І. І. Бондар, В. В. Суран

The influence of the Stark effect on multiphoton ionization of Ba atoms under conditions when the dynamic polarizability depends strongly on the frequency of the laser radiation is investigated. It is found that for some electric field strengths ε of the laser radiation this effect gives rise to resonance peaks in the Ba + ion yield as a function of the laser radiation frequency at frequencies corresponding to single-photon transitions between the excited states. These frequencies can differ substantially from the frequencies corresponding to the conventional multiphoton excitation of these states from the ground states of the atoms. Peaks in the ion yield as a function of ε behave differently from the conventional Stark effect—their position on the frequency scale does not depend strongly on ε . The conditions under which such an induced resonance structure appears are determined.

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Dynamic hyperpolarizability and two-photon detachment in the presence of a strong static electric field: Application to H^{-}

M. V. Frolov, Nikolai L. Manakov, Anthony F. Starace

Our recent analysis [J. Phys. B 33, R141 (2000)] of the problem of ${\mathrm{H}}^{\ensuremath{-}}$ in both laser and strong static electric fields, which treated effects that are linear in the laser intensity I (e.g., the dynamic polarizability and the single-photon detachment cross section), is extended here to treat effects of higher order $(\ensuremath{\sim}{I}^{2})$ in the laser intensity (e.g., the dynamic hyperpolarizability, the two-photon detachment cross section, the linear in I corrections to the single-photon detachment rate, etc). We introduce the concept of the dynamic hyperpolarizability of an atom in the presence of a strong electric field based on the complex quasienergy approach with properly normalized, quasistationary quasienergy wave functions. Our analysis of the general structure of the dynamic hyperpolarizability tensor of an atom in a nondegenerate $(S$-) state is performed for arbitrary field geometries and laser polarizations. The connection of the hyperpolarizability $\ensuremath{\gamma}(\mathcal{F};\ensuremath{\omega})$ to the complex quasienergy and to atomic ionization rates is established. Analytic results (in terms of Airy functions) are obtained for five irreducible components of a hyperpolarizability tensor (that are independent of the laser polarization and the field geometry) for the case of a weakly bound electron in a three-dimensional, zero-range potential. These results are used for the analysis of the frequency, field geometry, and laser polarization dependence of the two-photon detachment rate as well as of the linear in laser intensity corrections to the single-photon detachment rate. It is shown that the oscillatory behavior of the frequency dependence of both the real and the imaginary parts of $\ensuremath{\gamma}(\mathcal{F};\ensuremath{\omega})$ exists for both the coplanar and orthogonal field geometries, and that this behavior is qualitatively different for frequencies below and above the single-photon detachment threshold. The threshold behavior of the two-photon detachment rate is analyzed in detail and the static electric-field-induced modification of Wigner's threshold law for a short-range potential is discussed.

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Stabilization of Atoms in a Strong Laser Field

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Dynamic polarizabilities and magic wavelengths for dysprosium

V. A. Dzuba, V. V. Flambaum, Benjamin Lev

We theoretically study dynamic scalar polarizabilities of the ground and select long-lived excited states of dysprosium, a highly magnetic atom recently laser cooled and trapped. We demonstrate that there is a set of magic wavelengths of the unpolarized lattice laser field for each pair of states, which includes the ground state and one of these excited states. At these wavelengths, the energy shift due to laser field is the same for both states, which can be useful for resolved sideband cooling on narrow transitions and precision spectroscopy. We present an analytical formula that, near resonances, allows for the determination of approximate values of the magic wavelengths without calculating the dynamic polarizabilities of the excited states.

arXiv:1011.4738•Physical Review A•Mar 4, 2011•39 citations
The influence of the Stark effect on multiphoton ionization of Ba atoms under conditions when the dynamic polarizability depends strongly on the frequency of the laser radiation is investigated. It is found that for some electric field strengths ε of the laser radiation this effect gives rise to resonance peaks in the Ba + ion yield as a function of the laser radiation frequency at frequencies corresponding to single-photon transitions between the excited states. These frequencies can differ substantially from the frequencies corresponding to the conventional multiphoton excitation of these states from the ground states of the atoms. Peaks in the ion yield as a function of ε behave differently from the conventional Stark effect—their position on the frequency scale does not depend strongly on ε . The conditions under which such an induced resonance structure appears are determined.
Our recent analysis [J. Phys. B 33, R141 (2000)] of the problem of ${\mathrm{H}}^{\ensuremath{-}}$ in both laser and strong static electric fields, which treated effects that are linear in the laser intensity I (e.g., the dynamic polarizability and the single-photon detachment cross section), is extended here to treat effects of higher order $(\ensuremath{\sim}{I}^{2})$ in the laser intensity (e.g., the dynamic hyperpolarizability, the two-photon detachment cross section, the linear in I corrections to the single-photon detachment rate, etc). We introduce the concept of the dynamic hyperpolarizability of an atom in the presence of a strong electric field based on the complex quasienergy approach with properly normalized, quasistationary quasienergy wave functions. Our analysis of the general structure of the dynamic hyperpolarizability tensor of an atom in a nondegenerate (S(S(S-) state is performed for arbitrary field geometries and laser polarizations. The connection of the hyperpolarizability $\ensuremath{\gamma}(\mathcal{F};\ensuremath{\omega})$ to the complex quasienergy and to atomic ionization rates is established. Analytic results (in terms of Airy functions) are obtained for five irreducible components of a hyperpolarizability tensor (that are independent of the laser polarization and the field geometry) for the case of a weakly bound electron in a three-dimensional, zero-range potential. These results are used for the analysis of the frequency, field geometry, and laser polarization dependence of the two-photon detachment rate as well as of the linear in laser intensity corrections to the single-photon detachment rate. It is shown that the oscillatory behavior of the frequency dependence of both the real and the imaginary parts of $\ensuremath{\gamma}(\mathcal{F};\ensuremath{\omega})$ exists for both the coplanar and orthogonal field geometries, and that this behavior is qualitatively different for frequencies below and above the single-photon detachment threshold. The threshold behavior of the two-photon detachment rate is analyzed in detail and the static electric-field-induced modification of Wigner's threshold law for a short-range potential is discussed.
We theoretically study dynamic scalar polarizabilities of the ground and select long-lived excited states of dysprosium, a highly magnetic atom recently laser cooled and trapped. We demonstrate that there is a set of magic wavelengths of the unpolarized lattice laser field for each pair of states, which includes the ground state and one of these excited states. At these wavelengths, the energy shift due to laser field is the same for both states, which can be useful for resolved sideband cooling on narrow transitions and precision spectroscopy. We present an analytical formula that, near resonances, allows for the determination of approximate values of the magic wavelengths without calculating the dynamic polarizabilities of the excited states.