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Physical Review A

Lifetime measurements using the cascade-photon-coincidence technique with a sputtered-atom source

S. David Rosner, R. A. Holt, Timothy J. Scholl

Published May 1, 1997• 8 citations
Publisher

Abstract

We have developed an interesting and widely applicable technique for measuring lifetimes of low-lying levels of neutral atoms and their first few ionization states. The cascade-photon-coincidence method has been extended by using a light source consisting of excited atoms sputtered from a solid by 10-keV argon ions. We have measured the lifetimes of the ${4\mathrm{p}}^{2}$${\mathrm{P}}_{3\mathrm{/}2}^{\mathrm{o}}$ state of Ca II, the ${6\mathrm{p}}^{2}$${\mathrm{P}}_{3\mathrm{/}2}^{\mathrm{o}}$ state of Ba II, and the ${4\mathrm{p}}^{2}$${\mathrm{P}}_{3\mathrm{/}2}^{\mathrm{o}}$ state of Al III. These measurements are in good agreement with earlier work.

DOI
10.1103/physreva.55.3469

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We have developed an interesting and widely applicable technique for measuring lifetimes of low-lying levels of neutral atoms and their first few ionization states. The cascade-photon-coincidence method has been extended by using a light source consisting of excited atoms sputtered from a solid by 10-keV argon ions. We have measured the lifetimes of the {4\mathrm{p}}^{2}$${\mathrm{P}}_{3\mathrm{/}2}^{\mathrm{o}} state of Ca II, the {6\mathrm{p}}^{2}$${\mathrm{P}}_{3\mathrm{/}2}^{\mathrm{o}} state of Ba II, and the {4\mathrm{p}}^{2}$${\mathrm{P}}_{3\mathrm{/}2}^{\mathrm{o}} state of Al III. These measurements are in good agreement with earlier work.
A direct measurement of the natural lifetime for the (3p54s3{p}^{5}4s3p54s) 3P1^{3}P_{1}3P1​ state of argon has been made using a modified delayed-coincidence method. Argon atoms are repetitively excited by pulses of electrons. For each pulse, the decaying light signal is sampled for a time $\ensuremath{\Delta}t$ at some delay time t1{t}_{1}t1​ after the excitation is terminated. The exponential decay is then reconstructed as the delay time is changed. Collision effects are not important in the pressure region (5.0\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}6}$-2.0\ifmmode\times\else\texttimes\fi{}${10}^{\ensuremath{-}4}$ Torr) of the experiment and the effects due to cascading are eliminated by keeping the energy of the bombarding electrons low enough so that excitation of the 3p54p3{p}^{5}4p3p54p levels is negligible. The measured lifetime is dependent upon the argon pressure, and this effect is attributed to resonance trapping; a value of 21\ifmmode\pm\else\textpm\fi{}2 nsec is obtained for the natural lifetime by using the existing theories of resonance trapping to extrapolate the data to zero pressure.
The lifetimes of the 5p2P325p^{2}P_{\frac{3}{2}}5p2P23​​ and 5p2P125p^{2}P_{\frac{1}{2}}5p2P21​​ states of Sr+{\mathrm{Sr}}^{+}Sr+ and the 6p2P326p^{2}P_{\frac{3}{2}}6p2P23​​ and 6p2P126p^{2}P_{\frac{1}{2}}6p2P21​​ states of Ba+{\mathrm{Ba}}^{+}Ba+ have been measured by the Hanle-effect technique with optical excitation from the ion ground state. (The lifetimes of the Mg+{\mathrm{Mg}}^{+}Mg+ 3p2P323p^{2}P_{\frac{3}{2}}3p2P23​​ and Ca+{\mathrm{Ca}}^{+}Ca+ 4p2P324p^{2}P_{\frac{3}{2}}4p2P23​​ states were obtained by the same technique and reported previously.) These Ca+{\mathrm{Ca}}^{+}Ca+, Sr+{\mathrm{Sr}}^{+}Sr+, and Ba+{\mathrm{Ba}}^{+}Ba+ states each decay to a 2D32,52^{2}D_{\frac{3}{2},\frac{5}{2}}2D23​,25​​ doublet as well as to the ground 2S12^{2}S_{\frac{1}{2}}2S21​​ state, and the branching ratios for these transitions have been measured. The ions were produced by introducing traces of the atomic vapor into an argon discharge. Consequently, the cross sections for collisional depolarization of these 2PJ^{2}P_{J}2PJ​ states due to collisions with argon were also obtained from the measurements. The experimental results are given in Tables I and II. A discussion of the ion-atom collisional depolarization cross sections is included.
We present a lifetime measurement of the 6s6s6s level of rubidium. We use a time-correlated single-photon counting technique on two different samples of rubidium atoms, a vapor cell with variable rubidium density, and a sample of atoms confined and cooled in a magneto-optical trap. The 5P1∕25{P}_{1∕2}5P1∕2​ level serves as the resonant intermediate step for the two-step excitation to the 6s6s6s level. We detect the decay of the 6s6s6s level through the cascade fluorescence of the 5P3∕25{P}_{3∕2}5P3∕2​ level at 780 nm. The two samples have different systematic effects, but we obtain consistent results that averaged give a lifetime of $45.57\ifmmode\pm\else\textpm\fi{}0.17\phantom{\rule{0.3em}{0ex}}\mathrm{ns}$.
The lifetimes of the n 2{\mathrm{}}^{2}2P1/2{P}_{1/2}P1/2​ and n 2{\mathrm{}}^{2}2P3/2{P}_{3/2}P3/2​ states of thallium, n=7--11, have been determined through measurements of the fluorescence signal resulting from two-photon excitation in an atomic beam. The temporal dependence of the fluorescence signal is determined by solving the equations governing cascade spontaneous fluorescence from higher-lying initial states. It is shown that under conditions applicable to our experiments, the asymptotic decay of the fluorescence is a measure of the lifetime of the initial state. The possibility of self-absorption of the fluorescence within the atomic beam is investigated; it is found to be negligible over the range of thallium densities used in the experiment. Our lifetime measurements for these eight 2P^{2}\mathrm{P}2P states are compared with other known experimental data and with the results of previous semiempirical calculations.