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Journal of Physics Conference Series

Effects of size and dimension in optic relaxation in Rb vapor

Sergey Nikitich Atutov, V. A. Sorokin

Published Nov 1, 2021• 0 citations
Publisher

Abstract

Abstract We report on an experiment in which the fluorescence decay time of 5P levels of Rb atoms in a coated vapor cell exceeds several of milliseconds that many orders of magnitude longer than normal decay time of excited of rubidium atoms. This effect has been observed by using the pump laser with fixing frequency and the periodically scan the probing laser frequency of which overlap all Rb hyperfine linens of 5P-5S transition. Long time fluorescence decay take place in wide part of the spherical high quality coated cell. In cylindrical part of the cell or in uncoated cell the long time fluorescence decay was disappeared.

DOI
10.1088/1742-6596/2067/1/012004

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Bulletin of the American Physical Society•Jun 11, 2015•0 citations
Abstract We report on an experiment in which the fluorescence decay time of 5P levels of Rb atoms in a coated vapor cell exceeds several of milliseconds that many orders of magnitude longer than normal decay time of excited of rubidium atoms. This effect has been observed by using the pump laser with fixing frequency and the periodically scan the probing laser frequency of which overlap all Rb hyperfine linens of 5P-5S transition. Long time fluorescence decay take place in wide part of the spherical high quality coated cell. In cylindrical part of the cell or in uncoated cell the long time fluorescence decay was disappeared.
We report on an experiment in which the fluorescence decay time of 5P levels of Rb atoms in a coated vapor cell exceeds several of milliseconds, many orders of magnitude longer than normal decay time of excited of rubidium atoms. We found that this peculiarly long - term decay is not exponential and can only be observed in a high quality coated cell with a long lifetime of optical pumped atoms on atomic ground-state sublevels. A numerical simulation based on a complete density matrix is presented. It supports the population pumping process through the ground-state sublevels of Rb atoms as the most plausible mechanism for the observed phenomenon and it consistently demonstrates all the relevant features of the experiment. The investigation can be used, for example, to explore the quality of a various anti-relaxation coatings used for the resonant cells.
Abstract The excitation of long-term fluorescence by variously configured beams of bichromatic laser radiation in a rubidium vapor cell has been studied. From experiments it follows that long-term fluorescence arises only if atoms directly interact both with the pumping beam and with the probing beam tuned in resonance with a three-level Λ-scheme formed by transitions from 52P1/2 to the sublevels of the ground state 52S1/2 F = 3 and 52S1/2 F = 2. It has been shown that the spatial alignment of the pumping and probing beams is not obligatory for this feature of fluorescence to occur. This substantiates the idea that long-term fluorescence is related to the long-lived polarized state of rubidium atoms, which persists even after about 40 collisions with the ceresin-coated walls of the cell.
Enhancement and reduction of the fluorescence intensity in Rb atomic vapor are observed. The reduction is due to a depopulation of the 5P - {3/2 } state upon illumination of a Rb vapor cell with light corresponding to the 5P - {3/2 }→5D - {5/2 } transition. Collisional transfer of the 5D - {5/2 } atoms to the 5D - {3/2 } state, followed by radiative decay to the 5P - {1/2 } state, creates an increase in the population of the 5P - {1/2 } state. The increase in the excited state population results in an increase in the fluorescence intensity of the 5P - {1/2 }→5S - {1/2 } transition. The laser-induced population changes are monitored by the decrease or increase of the corresponding fluorescence signals. Using the steady-state rate equations, the rate constants for the stimulated emission(i.e., 5D - {5/2 }→5P - {3/2 }) is 2.0×10 +8s + {-1 }. The cross section for the fine-structure changing collision(i.e., 5D - {5/2 }→5D - {3/2 }) is 6.4×10 + {-14 }cm +2.
In this communication, we present the results of a systematic study of the new behavior of Rb D1 fluorescence line profiles, for laser frequency detuning over the D1 line hyperfine structure observed in optical cell with anti-relaxation coating of high quality. Experimental spectra are analyzed by means of theoretical calculations of D1 line spectrum obtained by numerical simulation. The provided analysis makes it possible to specify the physical processes responsible for the modification of the shape and the amplitude of the fluorescence line profiles. In addition, the experimentally observed dependences of the measured spectrum on the rate and the direction of laser frequency scan are analyzed.
A high-resolution two-photon spectrum of 5S 1/2 → 5P 3/2 → 5D 5/2 transitions in a thermal 85 Rb vapor cell is presented by using an optical frequency comb and a cw laser. The fluorescence of 6P 3/2 → 5S 1/2 spontaneous emission is detected when the cw laser frequency is scanned from the 5S 1/2 ground state to 5P 3/2 hyperfine levels and the optical frequency comb repetition rate is fixed. The hyperfine splittings (F f = 2–5) of the 5D 5/2 excited state are well resolved. The dependences of fluorescence intensities on the cw laser intensity and temperature of 85 Rb vapor cell are studied, respectively. The experimental results are in good agreement with the theoretical analyses.
An ongoing spectroscopic investigation of atomic rubidium utilizes a two-photon, single-laser excitation process. Transitions accessible with our tunable laser include 5P1/2 (F ′ ) ← 5S1/2 (F) and 5P3/2 (F ′ ) ← 5S1/2 (F). The laser is split into a pump and probe beam to allow for Doppler-free measurements of transitions between hyperfine levels. The pump and probe beams are overlapped in a counter-propagating geometry and the laser frequency scans over a transition. Absorption, fluorescence and polarization spectroscopy techniques are applied to this basic experimental setup. The temperature of the vapor cell and the power of the pump and probe beams have been varied to explore line broadening effects and signal-to-noise of each technique. This humble setup will hopefully grow into a more robust experimental arrangement in which double resonance, two-laser excitations are used to explore hyperfine state changing collisions between rubidium atoms and noble gas atoms. Rb-noble gas collisions can transfer population between hyperfine levels, such as 5P3/2 (F ′ = 3) Collision ←− 5P3/2 (F ′ = 2), and the probe beam couples 7S1/2 (F ′′ = 2) ← 5P3/2 (F ′ = 3). Polarization spectroscopy signal depends on the rate of population transfer due to the collision as well as maintaining the orientation created by the pump laser. Fluorescence spectroscopy relies only on transfer of population due to the collision. Comparison of these techniques yields information regarding the change of the magnetic sublevels, mF , during hyperfine state changing collisions.