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Journal of the Optical Society of America B

Measurement of photoionization cross section in atomic uranium using simultaneous observation of laser-induced photoionization and fluorescence signals

M.L. Shah, Gomati Prasad Gupta, Vas Dev, Bishwaranjan Dikshit, Manmohan Singh Bhatia, B. M. Suri

Published Mar 16, 2012• 4 citations
Publisher

Abstract

Laser-induced photoionization and fluorescence signals were simultaneously observed in atomic uranium using a single Nd:YAG-pumped dye laser. These signals were recorded in two specific cases. In the first case, the dye laser was resonant to the first-step transition (0–16900.38 cm−1). In the second case, the laser was near-resonant to the first-step transition with a slight detuning (0.15 cm−1) so that it became two-photon resonant at 33801.06 cm−1. The uranium atoms in the ground state were ionized by a single-color, three-photon photoionization technique resulting in the photoionization signal, and the fluorescence signal was simultaneously obtained from the first excited state involved in the photoionization process. The photoionization and the fluorescence signals in the above-mentioned cases were also estimated theoretically for several values of the photoionization cross section for the transition between the second excited state at 33801.06 cm−1 and the autoionization state at 50701.59 cm−1 using density matrix formalism. From the comparison of theoretically calculated ratios of fluorescence signals in the two specific cases with the experimentally obtained values, the photoionization cross section for the 33801.06–50701.59 cm−1 transition has been obtained, which is found to be (5±1)×10−16 cm2.

DOI
10.1364/josab.29.000600

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Laser-induced photoionization and fluorescence signals were simultaneously observed in atomic uranium using a single Nd:YAG-pumped dye laser. These signals were recorded in two specific cases. In the first case, the dye laser was resonant to the first-step transition (0–16900.38 cm−1). In the second case, the laser was near-resonant to the first-step transition with a slight detuning (0.15 cm−1) so that it became two-photon resonant at 33801.06 cm−1. The uranium atoms in the ground state were ionized by a single-color, three-photon photoionization technique resulting in the photoionization signal, and the fluorescence signal was simultaneously obtained from the first excited state involved in the photoionization process. The photoionization and the fluorescence signals in the above-mentioned cases were also estimated theoretically for several values of the photoionization cross section for the transition between the second excited state at 33801.06 cm−1 and the autoionization state at 50701.59 cm−1 using density matrix formalism. From the comparison of theoretically calculated ratios of fluorescence signals in the two specific cases with the experimentally obtained values, the photoionization cross section for the 33801.06–50701.59 cm−1 transition has been obtained, which is found to be (5±1)×10−16 cm2.
We report two-step photoionization studies from the 5ppp 2{}^{2}2P3/2{P}_{3/2}P3/2​ excited state of rubidium using two dye lasers simultaneously pumped by a common Nd:YAG laser in conjunction with a thermionic diode ion detector. The photoionization cross section at the first ionization threshold is measured as 18.8 \ifmmode\pm\else\textpm\fi{} 3 Mb and at excess energies of 0.013, 0.106, 0.229, and 0.329 eV is measured as 15, 13.6, 12.6, and 12.5 Mb, respectively. The measured value of the photoionization cross section at the threshold is used to calibrate the oscillator strengths of the 5ppp 2{}^{2}2P3/2{P}_{3/2}P3/2​ \ensuremath{\rightarrow} nnnd 2{}^{2}2D5/2{D}_{5/2}D5/2​ (22 \ensuremath{\leqslant} nnn \ensuremath{\leqslant} 52) Rydberg transitions.
Two-step resonant photoionization of free Ni atoms is studied by one-color and two-color processes, using pulsed lasers with photon energies around half the ground-state ionization energy. Two-color two-step resonance ionization from the ground state a3{\mathrm{}}^{3}3F4{\mathit{F}}_{4}F4​ and the first metastable state a3{\mathrm{}}^{3}3D3{\mathit{D}}_{3}D3​ via the triplet states z3{\mathrm{}}^{3}3G3,4,50{\mathit{G}}_{3,4,5}^{0}G3,4,50​ was used to probe the autoionizing states just above the ionization limit. Several strong lines in the one-color ionization spectrum are explained as direct two-photon transitions to autoionizing states. Photoionization cross sections were deduced from saturation measurements. The large cross sections observed for specific one-color two-step transitions are due to the near double resonant excitation into autoionizing states. \textcopyright{} 1996 The American Physical Society.
We have observed fluorescence and ionization signals resulting from two-photon resonant excitation of thallium in an atomic beam. The output of a pulsed dye laser is used to excite the resonance between the ground state (6('2)P(,1/2)) and an excited n('2)P state of thallium. Both two-photon absorption and three-photon absorption occur simultaneously; the latter results in photoionization of the atom. The excited states populated by two-photon absorption decay via cascade fluorescence back to the ground state; one or more of these spectral components constitute our fluorescence signal. The lifetimes of the excited n('2)P states of thallium have been measured directly by observing the exponential decay of this fluorescence. Calculations are included to ascertain the time required for the fluorescence signal to reach within 2% of a simple exponential decay. This decay is a measure of the lifetime of the initial state, under the condition that none of the fluorescence components arise from states which are populated by cascade through longer-lived states. The lifetimes of the n('2)P(,1/2) and n('2)P(,3/2) states of thallium for n = 7 to 11 are determined in this manner and compared with the values deduced from semi-empirical calculations of oscillator strengths by various authors. For calculations employing the effects of core polarizability in the electron wavefunctions and in the transition matrix elements, the agreement is very good--to within our experimental uncertainty, which is typically(, )<5%. Our measurements are also compared to the four other known experimental values for such excited states of thallium. Some of these previous experiments and calculations were carried out in conjunction with parity non-conservation experiments in thallium. Our measurements may provide useful checks on the accuracy of some of the calculations performed in the evaluation of such experiments. The ionization and fluorescence signals are also studied under conditions of strong saturation of the two-photon resonance with the 7('2)P states. The manifestation of saturation in the ionization signal is a broadening of the excitation spectrum, which is found to greatly exceed that of the fluorescence signal. Furthermore, the ratio of the ionization signal to the fluorescence signal at the peak of the resonance is found to vary linearly at intensities below about 10('9) W/cm('2); this too saturates at higher intensities. Various models are employed to simulate the observed behavior, encompassing both rate equations as well as density matrix formulations. The numerical solutions to these models are compared with the observed behavior; the agreement is found to depend strongly on the assumed experi- mental conditions to which the ensemble of atoms is subjected.
The two-photon excitation and three-photon ionization of atomic cesium is investigated over the 6550-6950-\AA{} wavelength region with a tunable-dye-laser source having a 0.06-0.08-\AA{} linewidth and a space-charge ionization detector sensitive to a few ions per second. An online data-acquisition computer provides significant signal-to-noise recovery. The resulting dispersion curve for photoionization is interpreted in terms of the two-photon transitions from the ground 62S126^{2}S_{\frac{1}{2}}62S21​​ level to resonant n2Dn^{2}Dn2D and n2Sn^{2}Sn2S intermediate states, and represents, to the authors' knowledge, the first such two-photon absorption spectrum of Cs. Transitions from n=9to13n=9\mathrm{to}13n=9to13 have been recorded for the $6^{2}S_{\frac{1}{2}}\ensuremath{-}n^{2}D_{\frac{5}{2},\frac{3}{2}}$ series and from n=11to14n=11\mathrm{to}14n=11to14 for the $6^{2}S_{\frac{1}{2}}\ensuremath{-}n^{2}S_{\frac{1}{2}}$ series.
Stimulated by a recent measurement of coherent control in photoionization of atomic barium, we have calculated one- and two-photon ionization cross sections of the aligned 6s6p 1P16s6p\text{ }{^{1}P}_{1}6s6p 1P1​ state of barium in the energy range between the 5d3/25{d}_{3/2}5d3/2​ and 5d5/25{d}_{5/2}5d5/2​ states of Ba+{\text{Ba}}^{+}Ba+. We have also measured these photoionization spectra in the same energy region, driving the one- or two-photon processes with the second or first harmonic of a tunable dye laser, respectively. Our calculations employ the eigenchannel RRR-matrix method and multichannel quantum defect theory to calculate the rich array of autoionizing resonances in this energy range. The nonresonant two-photon process is described using lowest-order perturbation theory for the photon-atom interactions, with a discretized intermediate-state one-electron continuum. The calculations provide an absolute normalization for the experiment, and they accurately reproduce the rich resonance structures in both the one- and two-photon cross sections, and confirm other aspects of the experimental observations. These results demonstrate the ability of these computationally inexpensive methods to reproduce experimental observables in one- and two-photon ionization of heavy alkaline earths, and they lay the groundwork for future studies of the phase-controlled interference between one- and two-photon ionization processes.