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Optics Letters

Temperature dependence of Rb 5P fine-structure transfer induced by He4 collisions

M. A. Gearba, J. F. Sell, Brian M. Patterson, R. Lloyd, J. Plyler, R. J. Knize

Published May 9, 2012• 7 citations
Publisher

Abstract

Employing ultrafast laser excitation and time-correlated single-photon counting, we have measured the fine-structure transfer between Rb 5P states induced by collisions with 4He buffer gas at temperatures up to 150 °C. The temperature dependence of the binary cross section agrees with earlier measurements. Our data show that the temperature dependence of the three-body rate is about the same as that of the binary rate. The three-body rate can be described as arising from the reduction of the rubidium fine-structure splitting due to nearby helium atoms.

DOI
10.1364/ol.37.001637

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Collisional excitation transfer and quenching in Rb(5P) -methane mixtures

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We have examined fine-structure mixing between the rubidium $5\phantom{\rule{0.16em}{0ex}}^{2}P_{3/2}$ and $5\phantom{\rule{0.16em}{0ex}}^{2}P_{1/2}$ states along with quenching of these states due to collisions with methane gas. Measurements are carried out using ultrafast laser-pulse excitation to populate one of the Rb $5{\phantom{\rule{0.16em}{0ex}}}^{2}P$ states, with the fluorescence produced through collisional excitation transfer observed using time-correlated single-photon counting. Fine-structure mixing rates and quenching rates are determined by the time dependence of this fluorescence. As $\mathrm{Rb}(5\phantom{\rule{0.16em}{0ex}}^{2}P$) collisional excitation transfer is relatively fast in methane gas, measurements were performed at methane pressures of $2.5--25$ Torr, resulting in a collisional transfer cross section ($5\phantom{\rule{0.16em}{0ex}}^{2}P_{3/2}\ensuremath{\rightarrow}5\phantom{\rule{0.16em}{0ex}}^{2}P_{1/2}$) of $(4.23\ifmmode\pm\else\textpm\fi{}0.13)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}15}\phantom{\rule{4pt}{0ex}}{\mathrm{cm}}^{2}$. Quenching rates were found to be much slower and were performed over methane pressures of $50--4000$ Torr, resulting in a quenching cross section of $(7.52\ifmmode\pm\else\textpm\fi{}0.10)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}19}\phantom{\rule{4pt}{0ex}}{\mathrm{cm}}^{2}$. These results represent a significant increase in precision compared to previous work, and also resolve a discrepancy in previous quenching measurements.

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Mixture and Quenching of the Rb (5P_J) States Induced by Collisions with Helium Atoms

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Applying the cw laser absorption and fluorescence method,the cross sections for the fine structure mixing and quenching of the Rb(5PJ) state,induced by collisions with He atoms have been measured,Rubidium atoms were optically excited to 5 P3/2states.The excited atom density and spatial distribution were mapped by monitoring the absorption of a counterpropagating single mode laser beam,tuned to the 5PJ→ 7S1/2 transitions.Transmission factors were calculated for the 5PJ→ 5S transitions.The fluorescence intensity I795 of the sensitized 5P1/2→ 5S1/2emission was measured as a function of He density in the range 0.5×1017 N 4× 1017cm-3at constant temperature T = 340 K.It was found that the quantity N/ I795 exhibited a parabolic dependence on N,confirming that the quenching of the 5PJ states is due to collision with He atoms,not due to Rb ground state atoms.The coefficients of the second-order polynomial fitted through the measured date yielded the cross sectionsσ3/2→1/2=(1.84± 0.61)× 10-17cm2 andσD=(1.07± 0.30)× 10-17cm2 for the 5PJfine-structure mixing and quenching,respectively,due to collision with He atoms.

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Fine-structure mixing in 5~2P Rb atoms studied through excitation transfer and energy-pooling collisions

Yifan Shen

Rb atoms were excited to the 5P3/2 level using a single-mode laser diode. The 5P3/2 state atom density was measured by the absorption of line from a Rb hollow-cathode lamp. The excited atom density is combined with measured fluorescence ratio to determine collisional cross section for the energy pooling process [i.e. Rb(5P3/2)+Rb(5P3/2)→Rb(5D)+Rb(5S)]. The cross section is (5.0±1.9)(?)10-14cm2. Cross section for 5P3/2 →5P1/2 transfer in Rb, induced in collision with ground-state Rb atoms, has been determined using methods of atomic fluorescence. The resulting fluorescence included a direct component arising from the optically excited state and a sensitized component due to the collisionally populated fine-structure state and the energy-pooling collisions. Measurement of relative intensities of the two components yielded the following cross section: σ(5P3/2→5P1/2)=(3.0±0.9)×10-15cm2. It is found that the rate for the energy pooling is an order of magnitude more efficient than 5P3/2→5P1/2 mixture. Comparisons of our result with other experiments have been made.

Chinese Journal of Quantum Electronics•Jan 1, 2005•1 citation

82D3/2 ↔ 82D5/2 excitation transfer in rubidium induced in collisions with ground-state Rb atoms

Małgorzata Głódź, J. B. Atkinson, L. Krause

Cross sections for inelastic transfer between the 82D3/2 and 82D5/2 fine-structure states in rubidium, induced in resonant collisions with ground-state Rb atoms, have been determined using an experimental method involving two-photon excitation of atomic fluorescence. Rubidium vapor in a fluorescence cell was irradiated with pulses of 641 nm radiation from a N2 laser-pumped dye-laser tuned to excite one of the 82D states. The resulting fluorescence included the direct component originating from the optically excited state and a sensitized component arising from the other fine-structure state populated by collisions. Relative intensities of the fluorescent components, determined by photon-counting techniques, yielded the cross sections for excitation transfer: Q(2D3/2 → 2D5/2) = 8.1 × 10−13 cm2; Q(2D3/2 ← 2D5/2) = 5.5 × 1013 cm2; as well as [Formula: see text], the effective quenching cross section. The excitation transfer cross sections which are considered accurate to within ±20% are in the ratio predicted by the principle of detailed balancing.

Canadian Journal of Physics•Apr 1, 1981•8 citations
Employing ultrafast laser excitation and time-correlated single-photon counting, we have measured the fine-structure transfer between Rb 5P states induced by collisions with 4He buffer gas at temperatures up to 150 °C. The temperature dependence of the binary cross section agrees with earlier measurements. Our data show that the temperature dependence of the three-body rate is about the same as that of the binary rate. The three-body rate can be described as arising from the reduction of the rubidium fine-structure splitting due to nearby helium atoms.
Using ultrafast laser excitation and time-correlated single-photon counting techniques, we have measured the collisional mixing rates between the rubidium 5(2)P fine-structure levels in the presence of (4)He gas. A nonlinear dependence of the mixing rate with (4)He density is observed. We find Rb fine-structure transfer is primarily due to binary collisions at (4)He densities of < or = 10(19) cm(-3), while at greater densities, three-body collisions become significant. We determine a three-body collisional transfer rate coefficient (5(2)P(3/2) --> 5(2)P(1/2)) of 1.25(9)x10(-32) cm(6)/s at 22 degrees C.
Measurements of the mixing rates and cross sections for collisional excitation transfer between the 5P 1/2 and 5P 3/2 states of rubidium (Rb) in the presence of 4 He buffer gas are presented. Selected pulses from a high repetition rate, mode-locked femtosecond laser are used to excite either Rb state with the fluorescence due to collisional excitation transfer observed by time-correlated single-photon counting. The time dependence of this fluorescence is fitted to the solution of rate equations which include the mixing rate, atomic lifetimes and any quenching processes. The variation in the mixing rate over a large range of buffer gas densities allows the determination of both the binary collisional transfer cross section and a three-body collisional transfer rate. We do not observe any collisional quenching effects at 4 He pressures up to 6 atm and discuss in detail other systematic effects considered in the experiment.
We have examined fine-structure mixing between the rubidium 52P3/25\phantom{\rule{0.16em}{0ex}}^{2}P_{3/2}52P3/2​ and 52P1/25\phantom{\rule{0.16em}{0ex}}^{2}P_{1/2}52P1/2​ states along with quenching of these states due to collisions with methane gas. Measurements are carried out using ultrafast laser-pulse excitation to populate one of the Rb 52P5{\phantom{\rule{0.16em}{0ex}}}^{2}P52P states, with the fluorescence produced through collisional excitation transfer observed using time-correlated single-photon counting. Fine-structure mixing rates and quenching rates are determined by the time dependence of this fluorescence. As Rb(52P\mathrm{Rb}(5\phantom{\rule{0.16em}{0ex}}^{2}PRb(52P) collisional excitation transfer is relatively fast in methane gas, measurements were performed at methane pressures of 2.5−−252.5--252.5−−25 Torr, resulting in a collisional transfer cross section ($5\phantom{\rule{0.16em}{0ex}}^{2}P_{3/2}\ensuremath{\rightarrow}5\phantom{\rule{0.16em}{0ex}}^{2}P_{1/2}$) of $(4.23\ifmmode\pm\else\textpm\fi{}0.13)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}15}\phantom{\rule{4pt}{0ex}}{\mathrm{cm}}^{2}$. Quenching rates were found to be much slower and were performed over methane pressures of 50−−400050--400050−−4000 Torr, resulting in a quenching cross section of $(7.52\ifmmode\pm\else\textpm\fi{}0.10)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}19}\phantom{\rule{4pt}{0ex}}{\mathrm{cm}}^{2}$. These results represent a significant increase in precision compared to previous work, and also resolve a discrepancy in previous quenching measurements.
Applying the cw laser absorption and fluorescence method,the cross sections for the fine structure mixing and quenching of the Rb(5PJ) state,induced by collisions with He atoms have been measured,Rubidium atoms were optically excited to 5 P3/2states.The excited atom density and spatial distribution were mapped by monitoring the absorption of a counterpropagating single mode laser beam,tuned to the 5PJ→ 7S1/2 transitions.Transmission factors were calculated for the 5PJ→ 5S transitions.The fluorescence intensity I795 of the sensitized 5P1/2→ 5S1/2emission was measured as a function of He density in the range 0.5×1017 N 4× 1017cm-3at constant temperature T = 340 K.It was found that the quantity N/ I795 exhibited a parabolic dependence on N,confirming that the quenching of the 5PJ states is due to collision with He atoms,not due to Rb ground state atoms.The coefficients of the second-order polynomial fitted through the measured date yielded the cross sectionsσ3/2→1/2=(1.84± 0.61)× 10-17cm2 andσD=(1.07± 0.30)× 10-17cm2 for the 5PJfine-structure mixing and quenching,respectively,due to collision with He atoms.
Rb atoms were excited to the 5P3/2 level using a single-mode laser diode. The 5P3/2 state atom density was measured by the absorption of line from a Rb hollow-cathode lamp. The excited atom density is combined with measured fluorescence ratio to determine collisional cross section for the energy pooling process [i.e. Rb(5P3/2)+Rb(5P3/2)→Rb(5D)+Rb(5S)]. The cross section is (5.0±1.9)(?)10-14cm2. Cross section for 5P3/2 →5P1/2 transfer in Rb, induced in collision with ground-state Rb atoms, has been determined using methods of atomic fluorescence. The resulting fluorescence included a direct component arising from the optically excited state and a sensitized component due to the collisionally populated fine-structure state and the energy-pooling collisions. Measurement of relative intensities of the two components yielded the following cross section: σ(5P3/2→5P1/2)=(3.0±0.9)×10-15cm2. It is found that the rate for the energy pooling is an order of magnitude more efficient than 5P3/2→5P1/2 mixture. Comparisons of our result with other experiments have been made.
Cross sections for inelastic transfer between the 82D3/2 and 82D5/2 fine-structure states in rubidium, induced in resonant collisions with ground-state Rb atoms, have been determined using an experimental method involving two-photon excitation of atomic fluorescence. Rubidium vapor in a fluorescence cell was irradiated with pulses of 641 nm radiation from a N2 laser-pumped dye-laser tuned to excite one of the 82D states. The resulting fluorescence included the direct component originating from the optically excited state and a sensitized component arising from the other fine-structure state populated by collisions. Relative intensities of the fluorescent components, determined by photon-counting techniques, yielded the cross sections for excitation transfer: Q(2D3/2 → 2D5/2) = 8.1 × 10−13 cm2; Q(2D3/2 ← 2D5/2) = 5.5 × 1013 cm2; as well as [Formula: see text], the effective quenching cross section. The excitation transfer cross sections which are considered accurate to within ±20% are in the ratio predicted by the principle of detailed balancing.