Rubidium vapor (1011 - 1014 cm-3) was irradiated by a dye-laser beam (10 kW(DOT)cm-2 - 2 MW(DOT)cm-2, pulse duration approximately 30 nsec, linewidth <EQ 0.25 cm-1), which was tuned to the D1,2-resonance lines. The mutual competition of the two photon ionization, associative ionization and Penning ionization of the laser excited rubidium atoms was investigated. The data of laser intensities and a rubidium vapor concentrations, which results in domination of the each ionization channels were founded. On the basis of the received experimental results, the cross-section values for the multiphoton and collisional ionization channels of laser-excited atoms were determined.
An investigation of the resonant interaction of the rubidium atoms with an intensity (10 kWcm-2 ≤ I ≤ 2 MWcm-2) and a wavelength close to that of the D1 and D2 transitions of the rubidium atom (5S1/2 → 5P3/2 or 5S1/2 → 5P1/2, λD1 = 780 nm, λD2 = 795 nm), which has passes through rubidium vapor with density (1011 - 1014 cm-3) been studied theoretically. The system of equations describing the processes of Collisional ionization and multiphoton ionization of rubidium vapour resonantly excited with nanosecond pulsed laser is solved. The dependence of the ion density on the laser intensity and the atomic density of rubidium are considered. The result of calculations revealed that, both quadratic ion density dependence on laser intensity and linear behaviour of the ion density versus rubidium density for 5S1/2 → 5P3/2 transition is due to photoioization process. In contrast, for 5S1/2 → 5P1/2 transition, the ion density dependence is nonlinear and indicates that the collisional processes play the major contribution in the total ionization. Also, the obtained results showed reasonable agreement with the experimentally measured values of the ion density dependence given by Bakhramov et al. In addition, the analysis of mutual competition between the different ionization processes considered for the ion yield as a function of both laser intensity and atoms density are also presented this work.
Diode laser excitation of rubidium atoms at the D2 line followed by (1 + 1) ionization using a pulsed dye laser was examined. Mass-resolved D2 spectra were recorded for both natural isotopes. Excitation using two sequential diode laser photons was accomplished by counterpropagating the beam from the 780 nm laser and one from a 775.8 laser; the latter excites Rb from the {sup 5}P{sub 3/2} level to the {sup 5}D{sub 5/2} level at 25704 cm{sup {minus}1}. A photon from the R6G laser then ionized the atom. Spectra resulting from scanning the second diode laser -- with the first an an off-resonance fixed frequency revealed both two-photon and sequential (1 + 1) processes.
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.
The multiphoton excitation of rubidium has been investigated over the 4600-6500-\AA{} wavelength region with a tunable dye-laser source having a linewidth better than 0.1 \AA{} and a space-charge ionization detector sensitive to a few ions per second. Multiphoton transitions have been observed to occur both through intermediate atomic states and through intermediate continuum states of the rubidium molecule. In the former case two-photon transitions have been observed from the
52S ground state of atomic rubidium to higher-lying
n2D levels for values of
n ranging from 9 to 34 and to
n2S levels for values of
n from 11 through 20. The fine-structure intervals of the
n2D levels for
n=9toc13 were measured together with the line-strength ratios and were found to be in good agreement with the predictions of a simple theoretical model. At the shorter wavelengths hybrid two-photon resonances were observed to be excited through resonant intermediate continuum states of
Rb2. As a result the dispersion curve for two-photon absorption in rubidium showed what appears to be resonant intermediate $p\ensuremath{\pi}(^{3}\ensuremath{\Sigma}_{u1})$ and
0g+ terms dissociating to give a
5P23 atom and resulting in the strong development of features corresponding to the $5^{2}P_{\frac{3}{2}}\ensuremath{\rightarrow}n^{2}D_{\frac{3}{2},\frac{5}{2}}$ part of the diffuse series, for $n\ensuremath{\le}50$ in absorption and the $5^{2}P_{\frac{3}{2}}\ensuremath{\rightarrow}n^{2}S_{\frac{1}{2}}$ part of the sharp series. Components to
322D and
302S were recorded to a precision of 0.3 ${\mathrm{cm}}^{\ensuremath{-}1}$ and quantum defects for these previously unobserved terms were derived. The corresponding hybrid two-photon resonances involving intermediate states dissociating to give a
52P21 atom were not observed in the wavelength interval available in this experiment.
Atomic potassium is ionized by three channels when it is excited by a pulse dye laser. They are energy pooling induced ionization, 4S→6S and 4S→4D two photon resonant three photon ionization. The ionization current intensity at various vapor temperature and laser intensity were investigated for the former two ionization channels. The atomic radiation trapping and nonlinear ionization were found in ionization current spectra. The qualitative explanations for above phenomena are given.
Abstract We have studied the formation of the molecular ion Rb2+ and the atomic ion Rb+. These are created in laser excited rubidium vapor at the first resonance, 5s–5p and 5p-nl transitions. A theoretical model is applied to this interaction to explain the time evolution and the laser-power dependence of the population density of Rb+ and Rb2+. A set of rate equations which describe: the temporal variation of the population density of the excited states; the atomic ion density; and the electron density, were solved numerically under the experimental conditions of Barbier and Cheret. In their experiment the Rb concentration was 1×1013cm−3 and the laser power was taken to be 50–500 mW at vapor temperature = 450 K. The results showed that the main processes for producing Rb2+ are associative ionization and Hornbeck-Molnar ionization. The calculations have also showed that, the atomic ions Rb+ are formed through the Penning Ionization (PI) and photoionization processes. Moreover, a reasonable agreement between the experimental results and our calculations for the ion currents of the Rb+ and Rb2+ is obtained.