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Physical Review A

Resonance shifts in the multiphoton ionization of cesium atoms

J. Morellec, Didier Normand, G. Petite

Published Jul 1, 1976• 107 citations
Publisher

Abstract

This work reports the multiphoton ionization of cesium atoms, via resonance with the $6F$ level, by interaction with a single transverse and longitudinal mode neodymium-glass laser beam. At a low rate of ion production, when the laser frequency is tuned through resonance, the laser intensity necessary to create a constant number of ions passes through a minimum, as expected, for a three-photon energy equal to the unperturbed $6S\ensuremath{\rightarrow}6F$ transition energy. But for a higher ionization rate, involving larger laser intensities, a departure from expectation is observed which is interpreted as a consequence of an energy shift of the transition. The level shifts are demonstrated in another way by their strong effect on the experimental order of nonlinearity of the interaction, ${K}_{\mathrm{expt}}$. A sharp variation of ${K}_{\mathrm{expt}}$ is observed when the energy shift of the $6S\ensuremath{\rightarrow}6F$ transition exactly compensates the wavelength detuning of the laser. The latter method gives shift values which are found to be independent of the large variations of the interaction volume under conditions of resonance. Both methods give a linear dependence of the shifts on the laser intensity. Identification of these shifts with energy shifts of the $6S\ensuremath{\rightarrow}6F$ transition is subject to theoretical reservations and needs further experimentation.

DOI
10.1103/physreva.14.300

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This work reports the multiphoton ionization of cesium atoms, via resonance with the 6F6F6F level, by interaction with a single transverse and longitudinal mode neodymium-glass laser beam. At a low rate of ion production, when the laser frequency is tuned through resonance, the laser intensity necessary to create a constant number of ions passes through a minimum, as expected, for a three-photon energy equal to the unperturbed 6S\ensuremath→6F6S\ensuremath{\rightarrow}6F6S\ensuremath→6F transition energy. But for a higher ionization rate, involving larger laser intensities, a departure from expectation is observed which is interpreted as a consequence of an energy shift of the transition. The level shifts are demonstrated in another way by their strong effect on the experimental order of nonlinearity of the interaction, Kexpt{K}_{\mathrm{expt}}Kexpt​. A sharp variation of Kexpt{K}_{\mathrm{expt}}Kexpt​ is observed when the energy shift of the 6S\ensuremath→6F6S\ensuremath{\rightarrow}6F6S\ensuremath→6F transition exactly compensates the wavelength detuning of the laser. The latter method gives shift values which are found to be independent of the large variations of the interaction volume under conditions of resonance. Both methods give a linear dependence of the shifts on the laser intensity. Identification of these shifts with energy shifts of the 6S\ensuremath→6F6S\ensuremath{\rightarrow}6F6S\ensuremath→6F transition is subject to theoretical reservations and needs further experimentation.
The present paper applies the method of high-intensity quantum electrodynamics developed earlier to several problems of current experimental interest. In this paper the intensitydependent shifts and widths of atomic levels are calculated and applied to a given transition near resonance. The technique is demonstrated with three examples: the multiphoton ionization of atomic cesium and hydrogen in atomic beams and third-harmonic production in an atomic vapor. It is found that the multiphoton-ionization rate in a relatively weak laser beam (of order 108{10}^{8}108 W/cm2{\mathrm{cm}}^{2}cm2) is determined by the intensity-dependent level width (6f6f6f configuration) as well as the interference of the fine-structure states, and that the rates for hydrogen, in a much more intense beam (of order 1012{10}^{12}1012 W/cm2{\mathrm{cm}}^{2}cm2) are determined by both the intensity-dependent widths and shifts as‘\stackrel{\mathrm{`}}{\mathrm{s}}s‘ well as the wave-function renormalization constants. The agreement of these two examples of calculations with the experiments done recently is satisfactory. For third-harmonic production the role of two-photon resonance is emphasized, and the dependence of the generated third-harmonic intensity on the intensity and frequency of the fundamental is discussed. Near resonance, the ratio of third-harmonic intensity to fundamental intensity saturates.
The narrow spectral bandwith (0.4 \AA{}) of a Nd-glass laser was tuned over a range of 40 \AA{} to populate selectively the 6f6f6f level of cesium atoms. The resulting variation of the multiphoton ionization probability was investigated as a function of the laser wavelength.
This paper reports the four-photon ionization of caesium atoms when the laser frequency is tuned through the resonant three-photon transition 6S → 6F. This experiment was performed by using a tunable-wavelength bandwidth-limited subnanosecond laser pulse at 1.06 μm, in the 108-109 W.cm-2 laser intensity range. Pulse widths of 1.5 ns, 50 ps, and 15 ps were used. The resonant character of the multiphoton ionization process was observed, even with the shortest pulse of 15 ps. Nevertheless the influence of a temporal effect is demonstrated according to theoretical predictions. The resonance shift ΔE of the 6S → 6F transition energy was found to be linear with the laser intensity I within the range 108-109 W.cm-2. ΔE = α I, with α = 2 cm-1/GW.cm-2. This result confirms previous measurements performed with single-mode 35 ns laser pulses and is in very good agreement with calculated resonance shifts.
Experimental and theoretical results are presented for resonantly enhanced three-photon ionization of cesium atoms in the wavelength range from 830 to 950 nm. The accidental near resonance of the 6p2P32,126p^{2}P_{\frac{3}{2},\frac{1}{2}}6p2P23​,21​​ levels at the one-photon energy and the near resonance at the two-photon level with the 6d2D32,526d^{2}D_{\frac{3}{2},\frac{5}{2}}6d2D23​,25​​ states gives rise to large ionization signals and interesting anomalies in the relative intensities of the fine-structure levels. "Hybrid resonances" are observed which involve the production of 6p2P126p ^{2}P_{\frac{1}{2}}6p2P21​​ atoms from molecular cesium. One hybrid resonance involves ionization of the 6p2P126p ^{2}P_{\frac{1}{2}}6p2P21​​ state via an electric quadrupole transition ($6p ^{2}P_{\frac{1}{2}}\ensuremath{-}7p ^{2}P_{\frac{3}{2}}$). Both experimental and theoretical photoelectron angular distributions are compared for all of the observed resonances except for the 6p2P326p ^{2}P_{\frac{3}{2}}6p2P23​​ state where the signals were too weak for such a measurement. Agreement between experiment and theory is fair for three-photon ionization via the 6p2P126p^{2}P_{\frac{1}{2}}6p2P21​​ state. Comparison of experiment and theory for the case of the 6d2D32,526d^{2}D_{\frac{3}{2},\frac{5}{2}}6d2D23​,25​​ states indicates that hyperfine coupling during the laser-pulse duration may be important. The angular distributions for the hybrid resonances show the general behavior predicted by theory but the features appear broadened.
We have studied two-photon resonant three-photon ionization of atomic sodium vapor. A dye laser tuned to either the 4d or 5s two-photon allowed transition was used to excite the atom and a second more intense laser (λ = 7000 Å) was used for ionization. The ion yield was measured as a function of resonant laser intensity and detuning, the nonresonant laser intensity, and the temporal overlap of the exciting and ionizing laser pulses. We have found1 that at high laser intensities the photoionization yield decreases as the nonresonant laser intensity is increased. When tuned to the 5s level a value of ~−0.6 was obtained for the exponential index even with the resonant laser tuned to maximize the ion yield. A theoretical model including the effects of Stark shift of the ground state, power broadening of the intermediate level due to saturation of the two-photon transition and by rapid transitions to the ionization continuum was used to predict the experimental results. Good agreement between theory and experiment required the use of a photoionization cross section for the 5s level which was ~20 times greater than the accepted value. Results for photoionization from the 4d level are also presented.
This paper studies the resonant multiphoton ionization (RMPI) phenomenon, in the case of caesium atoms interacting with the intense field of a neodymium-Glass laser. In the first part, we present a recent theory of RMPI, in a simplified form in order to obtain the main informations on the physics of RMPI. Then we present two experiments of RMPI : four-photon ionization of the caesium atom in its ground state, with a three-photon resonance on the 6F level and three-photon ionization of the caesium atom is its 62P3/2 state with a two-photon resonance on the 12F level. In the first experiment, the internal structure of the resonant transition is resolved, enabling us to point out and analyse the important effect of pulse shapes and focusing conditions on our experimental results, which are discussed in detail. We also give some new interpretations of results published previously [1]. In the second experiment, we measure the 12F fine structure — which is found to be (0.016 ± 0.008) cm-1 — and show that we have reached the limits imposed by the Doppler effect. These experimental results are in good agreement with the theoretical predictions suggesting that the physical picture given of RMPI by recent works on this subject is satisfactory.