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Physical Review A

Excitation-transfer collisions in cesium vapor: Cs(5 D5/2 )+Cs(6 S1/2 )→Cs (5 D3/2 )+ Cs(6 S1/2 )

B. Keramati, Mark F. Masters, John Huennekens

Published Nov 1, 1988• 10 citations
Publisher

Abstract

We report an experimental investigation of the excitation-transfer collision Cs(5${D}_{5/2}$)+Cs(6S)\ensuremath{\rightarrow}CS ((5${D}_{3/2}$)+Cs(6S). The upper 5${D}_{5/2}$ state was excited by a cw dye laser tuned to the one-photon, quadrupole-allowed 6S\ensuremath{\rightarrow}5${D}_{5/2}$ transition. Since the direct 5D\ensuremath{\rightarrow}6P fluorescence could not be detected with our apparatus, we monitored instead the cascade 6P\ensuremath{\rightarrow}6S fluorescence. The ratio of 6${P}_{1/2}$ to 6${P}_{3/2}$ fluorescence contains information on the collisional mixing that takes place in the 5D levels but also includes a significant contribution from mixing in the 6P levels. This latter contribution could effectively be subtracted out using the results of a second experiment in which a tunable cw diode laser was used to pump the 6${P}_{3/2}$ state, and the same fluorescence ratio monitored. The 5D mixing cross section we obtain, 70 A${\r{}}^{2}$, is significantly larger than previous indirect determinations.

DOI
10.1103/physreva.38.4518

Related papers

Energy transfer in collisions between two Cs(5D) atoms

Yifan Shen

Using stepwise excitation of the cesium 8S atoms level in Cs vapor,several collisional and radiative processes have been identified from the intensities and spectra of the Cs fluorescence.The 5D state was populated by 8S→7P→5D transitions.In cesium densities 1016-1017?cm-3,the energy pooling collisions 5D+5D→nL+6S(nL=9D,11S,7F are studied.Since the 5D→6P(3.0-3.6 μm) fluorescence could not be detected with this experiment,the EP rate coefficients have been measured relative to the known rate coefficient of the collision,i.e.,6P+5D→6S+7D.The excited-atom density and spatial distribution were mapped by monitoring the absorption of a counterpropagating single-mode laser beam,tuned to 6P3/2→8S1/2 transition,which could be translated parallel to the pump beam.The excited atom densities are combined with measured fluorescene ratios to determine cross sections for the cesium energy pooling process.The average values(in units of 10-10?cm3s-1) for nL=9D,11S and 7F are 8.4±4.2,7.3±3.6,and 9.7±4.8,respectively.Influence on k11S and k7F of the energy transfer process 11S+6S7F+6S is also dicussed.

Journal of Atomic and Molecular Physics•Jan 1, 2007•0 citations

Radiative lifetimes, collisional mixing, and quenching of the cesium 5DJ levels

Antonio Sasso, Wolfgang Demtröder, T. Colbert +3 more

We report the results of a series of pulsed and cw laser experiments which measure spontaneous and effective lifetimes of the Cs(5DJ) levels and investigate excitation-transfer collisions involving Cs(5DJ) atoms and ground-state-cesium perturbers. With cw excitation of the dipole-forbidden but electric-quadrupole-allowed 6S1/2\ensuremath{\rightarrow}5D5/2 transition, we monitor the ratio of sensitized to direct fluorescence, i.e., I5D3/2\ensuremath{\rightarrow}6P1/2/I5D5/2\ensuremath{\rightarrow}6P3/2. A rate-equation analysis of these data yields values for the Cs(5D5/2)+Cs(6S)\ensuremath{\rightarrow}Cs(5D3/2)+Cs(6S) excitation-transfer rate, and for the rate of quenching of Cs(5D) by ground-state perturbers. The role of out-of-multiplet quenching is discussed at length, and we have demonstrated that quenching by ground-state atoms dominates over that by cesium dimers under these conditions. In the pulsed-laser experiments, the temporal evolution of the 5DJ\ensuremath{\rightarrow}6S and cascade 6PJ\ensuremath{'}\ensuremath{\rightarrow}6S fluorescence was observed following either direct forbidden-line pumping of one fine-structure level, or indirect excitation of both fine-structure levels (i.e., molecular excitation followed by predissociation). Analysis of the buildup and decay rates of the various levels as a function of cesium density yields values for the natural lifetimes of the Cs(5DJ) levels, as well as for the excitation transfer and quenching rates. Best values for the lifetimes and cross sections for Cs-Cs collisions obtained from these combined experiments are \ensuremath{\tau}5D=1250\ifmmode\pm\else\textpm\fi{}115 ns, \ensuremath{\sigma}5/2\ensuremath{\rightarrow}3/2=36\ifmmode\pm\else\textpm\fi{}8 \AA{}2, and \ensuremath{\sigma}5D=30\ifmmode\pm\else\textpm\fi{}3 \AA{}2. In addition, numbers for the 6P level-quenching cross sections due to collisions with Cs atoms and Cs2 molecules, respectively, were obtained: \ensuremath{\sigma}6P(Cs)=6.6\ifmmode\pm\else\textpm\fi{}3.0 \AA{}2 and \ensuremath{\sigma}6P(Cs2)=863\ifmmode\pm\else\textpm\fi{}260 \AA{}2. In the discussion, we show how these new values can be used to reconcile the seemingly discrepant results of several previous studies.

Physical Review A•Feb 1, 1992•23 citations

ENERGY TRANSFER IN COLLISIONS BETWEEN TWO EXCITED CESIUM ATOMS

SHEN YI-FAN, LI WAN-XING, 新疆大学物理系,乌鲁木齐830046

Cesium molecules are pumped by a CW dye laser. Some of the excited molecules then pre-dissociate or collisionally transfer excitation to produce excited atoms at the 5D and 6P levels. The cross sections (in units of 10-14cm2) for the excitation transfer process Cs(6P)+Cs(5D) →Cs(7DJ)+Cs(6S)for J being 5/2 and 3/2 are 5. 4 ± 50% and 4. 9 ± 50%, respectively. The cross sections (in units of 10-14cm2) for the excitation transfer out of the 7D doublet [i. e. , Cs(7DJ)+Cs(6S) →states other than Cs(7D)] for J being 5/2 and 3/2 are 1. 6 ±50% and 0. 34±50%, respectively. To obtain these cross sections, the intensities of 7D and 5D fluorescence emissions and the 6P atom density are measured by using the absorption equivalent width technique. The results are discussed in eomparison with those of other experiments.

Acta Physica Sinica•Jan 1, 1993•1 citation

[Experimental evaluation of the cross sections in Cs (6D(1/2)) + Cs(6S(1/2)) inelastic collisions].

Qi-cun Guo, Hongping Wu, Li-kui Kang +3 more

At a Cs density higher than 9 x 10(14) cm(-3), cesium vapor was irradiated in a glass fluorescence cell with pulses of radiation from an YAG-laser-pumped OPO laser, populating 6D(5/2) state by two-photon absorption. Energy transfer in Cs6(D(5/2)) + Cs (6S) collisions was studied using methods of atomic fluorescence. At the different Cs densities, we have measured the time-integrated intensities of the components and fitted a three-state rate equation model to obtain the cross sections. The experimental points were fitted to a straight line very well. The authors converted the gradient and intercept into cross sections. The cross section for 6D(5/2)-->6D(3/2) transfer is (2.1 +/- 0.4) x 10(14) cm2. The cross section for excitation transfer out of the 6D doublet is sigmaQ = (1.6 +/- 0.4) x 10(-14) cm2. The cross section on contains information on reverse energy pooling collisions [i.e., Cs(6D(3/2)) + Cs (6S(1/2))-->Cs(6P) + 6Cs(P)] and contribution from mining in 6Dj-->7P(J'), This latter contribution could be subtracted out using the results of a second experiment. At a Cs density lower than 6.0 x 10(12) cm3, the laser was used to pump the 6D(3/2) and 6D(5/2) states, respectively. The resulting fluorescence included the direct component emitted in the decay of the 6D(J) state and the sensitized component arising from the collisionally populated 7P(J') state. Relative intensities of the components yielded the cross sections. The cross-sections for the processes Cs(6D(5/2)) + Cs(6S(1/2))-->Cs(7P(J')) + Cs(6S(1/2)) are (1.6 +/- 0.5) x 10(-15) cm2. for J'= 3/2 and (6.5 +/- 2.1) x 10(-16) cm2, for J' = 1/2, respectively. The cross-sections for the processes Cs(6D(3/2) + Cs(6S(1/2))-->Cs (7P(J')) + Cs(6S(1/2)) are (1.9 +/- 0.6) x 10(-15) cm2. for J' = 3/2 and (7.6 + 2.4) x 10(-16) cm2, for J' = 1/2, respectively. The 6D(J) -->7P(J'), energy transfer rate coefficient is small. The total quenching rate coefficient out of the 6D(J) state is much larger. Evidence suggests that the quenching of the 6D(J) state is caused predominantly by reverse energy-pooling process. The cross section for this process, i.e., Cs(6D(3/2))+Cs(6S(1/2))-->Cs(6P) + Cs(6P) is (1.3 +/- 0.4) x 10(-14) cm2.

•Sep 1, 2009•0 citations

Energy-pooling collisions in cesium: 6 PJ +6 PJ →6S+(nl=7P,6D,8S,4F)

Z. J. Jabbour, R. K. Namiotka, John Huennekens +3 more

We report experimental rate coefficients for the energy-pooling collisions Cs(6${\mathit{P}}_{1/2}$)+Cs(6${\mathit{P}}_{1/2}$)\ensuremath{\rightarrow}Cs(6${\mathit{S}}_{1/2}$)+Cs(${\mathit{nl}}_{\mathit{J}\ensuremath{'}}$) and Cs(6${\mathit{P}}_{3/2}$)+Cs(6${\mathit{P}}_{3/2}$)\ensuremath{\rightarrow}Cs(6${\mathit{S}}_{1/2}$)+Cs(${\mathit{nl}}_{\mathit{J}\ensuremath{'}}$) where ${\mathit{nl}}_{\mathit{J}\ensuremath{'}}$=7${\mathit{P}}_{1/2}$, 7${\mathit{P}}_{3/2}$, 6${\mathit{D}}_{3/2}$, 6${\mathit{D}}_{5/2}$, 8${\mathit{S}}_{1/2}$, 4${\mathit{F}}_{5/2}$, or 4${\mathit{F}}_{7/2}$. Atoms were excited to either the 6${\mathit{P}}_{1/2}$ or 6${\mathit{P}}_{3/2}$ state using a single-mode Ti:sapphire laser. The excited-atom density and spatial distribution were mapped by monitoring the absorption of a counterpropagating single-mode ring dye laser beam, tuned to either the 6${\mathit{P}}_{1/2}$\ensuremath{\rightarrow}8${\mathit{S}}_{1/2}$ or 6${\mathit{P}}_{3/2}$\ensuremath{\rightarrow}7${\mathit{D}}_{3/2,5/2}$ transitions, which could be translated parallel to the pump beam. Transmission factors, which describe the average probability that photons emitted within the fluorescence detection region can pass through the optically thick vapor without being absorbed, were calculated for all relevant transitions. Effective lifetimes of levels populated by energy-pooling collisions are modified by radiation trapping, and these factors were calculated using the Molisch theory. These calculated quantities have been combined with the measured excited-atom densities and fluorescence ratios to yield absolute energy-pooling rate coefficients. It was found that the rate for production, in all cases, is greatest for 6D, but that 1/2-1/2 collisions are significantly more efficient than 3/2-3/2 collisions for populating 7P. It was also found that 7${\mathit{P}}_{1/2}$ is populated two to three times more efficiently than 7${\mathit{P}}_{3/2}$ in 1/2-1/2 collisions, but that the 7P fine-structure levels are approximately equally populated in 3/2-3/2 collisions. \textcopyright{} 1996 The American Physical Society.

Physical Review A•Aug 1, 1996•63 citations

Experimental study of cesium 5D+5D-g6S+(nL=9D,11S,7F) energy pooling collisions

Qing Wang, Kang Dai, Yifan Shen

We report experimentally the measured rate coefficients for the energy pooling (EP) collisions process Cs(5D)+Cs(5D)-gCs(6S)+Cs(nL=9D,11S,7F) in cesium densities of 10^(16)-10^(17) cm^(-3). The 5D state was populated via 8S-g7P-g5D spontaneous emission following two-step pumping 6S-g6P_(3/2)-g8S. Since the 5D-g6P (3.0-3.6 microns) fluorescence could not be detected in this experiment, we carried out a relative measurement for the process 6P+5D-g6S+7D. The excited-atom density and spatial distribution were mapped by monitoring the absorption of a counterpropagating single-mode laser beam, tuned to 6P_(3/2)-g9S_(1/2) transition, which could be translated parallelly to the pump beam. The excited atom densities have been combined with the measured fluorescence ratios to yield EP rate coefficients. The average values for nL=9D,11S and 7F are 8.0+-4.0, 7.0+-3.5, and 9.3+-4.6 (in units of 10^(-10) cm3/s), respectively. Influence of the energy transfer process 11S+6S-g7F+6S on the rate coefficients k_(11S) and k_(7F) is also discussed.

Chinese Optics Letters•Jul 10, 2007•0 citations
We report an experimental investigation of the excitation-transfer collision Cs(5D5/2{D}_{5/2}D5/2​)+Cs(6S)\ensuremath{\rightarrow}CS ((5D3/2{D}_{3/2}D3/2​)+Cs(6S). The upper 5D5/2{D}_{5/2}D5/2​ state was excited by a cw dye laser tuned to the one-photon, quadrupole-allowed 6S\ensuremath{\rightarrow}5D5/2{D}_{5/2}D5/2​ transition. Since the direct 5D\ensuremath{\rightarrow}6P fluorescence could not be detected with our apparatus, we monitored instead the cascade 6P\ensuremath{\rightarrow}6S fluorescence. The ratio of 6P1/2{P}_{1/2}P1/2​ to 6P3/2{P}_{3/2}P3/2​ fluorescence contains information on the collisional mixing that takes place in the 5D levels but also includes a significant contribution from mixing in the 6P levels. This latter contribution could effectively be subtracted out using the results of a second experiment in which a tunable cw diode laser was used to pump the 6P3/2{P}_{3/2}P3/2​ state, and the same fluorescence ratio monitored. The 5D mixing cross section we obtain, 70 A˚2{\r{}}^{2}˚2, is significantly larger than previous indirect determinations.
Using stepwise excitation of the cesium 8S atoms level in Cs vapor,several collisional and radiative processes have been identified from the intensities and spectra of the Cs fluorescence.The 5D state was populated by 8S→7P→5D transitions.In cesium densities 1016-1017?cm-3,the energy pooling collisions 5D+5D→nL+6S(nL=9D,11S,7F are studied.Since the 5D→6P(3.0-3.6 μm) fluorescence could not be detected with this experiment,the EP rate coefficients have been measured relative to the known rate coefficient of the collision,i.e.,6P+5D→6S+7D.The excited-atom density and spatial distribution were mapped by monitoring the absorption of a counterpropagating single-mode laser beam,tuned to 6P3/2→8S1/2 transition,which could be translated parallel to the pump beam.The excited atom densities are combined with measured fluorescene ratios to determine cross sections for the cesium energy pooling process.The average values(in units of 10-10?cm3s-1) for nL=9D,11S and 7F are 8.4±4.2,7.3±3.6,and 9.7±4.8,respectively.Influence on k11S and k7F of the energy transfer process 11S+6S7F+6S is also dicussed.
We report the results of a series of pulsed and cw laser experiments which measure spontaneous and effective lifetimes of the Cs(5DJ) levels and investigate excitation-transfer collisions involving Cs(5DJ) atoms and ground-state-cesium perturbers. With cw excitation of the dipole-forbidden but electric-quadrupole-allowed 6S1/2\ensuremath{\rightarrow}5D5/2 transition, we monitor the ratio of sensitized to direct fluorescence, i.e., I5D3/2\ensuremath{\rightarrow}6P1/2/I5D5/2\ensuremath{\rightarrow}6P3/2. A rate-equation analysis of these data yields values for the Cs(5D5/2)+Cs(6S)\ensuremath{\rightarrow}Cs(5D3/2)+Cs(6S) excitation-transfer rate, and for the rate of quenching of Cs(5D) by ground-state perturbers. The role of out-of-multiplet quenching is discussed at length, and we have demonstrated that quenching by ground-state atoms dominates over that by cesium dimers under these conditions. In the pulsed-laser experiments, the temporal evolution of the 5DJ\ensuremath{\rightarrow}6S and cascade 6PJ\ensuremath{'}\ensuremath{\rightarrow}6S fluorescence was observed following either direct forbidden-line pumping of one fine-structure level, or indirect excitation of both fine-structure levels (i.e., molecular excitation followed by predissociation). Analysis of the buildup and decay rates of the various levels as a function of cesium density yields values for the natural lifetimes of the Cs(5DJ) levels, as well as for the excitation transfer and quenching rates. Best values for the lifetimes and cross sections for Cs-Cs collisions obtained from these combined experiments are \ensuremath{\tau}5D=1250\ifmmode\pm\else\textpm\fi{}115 ns, \ensuremath{\sigma}5/2\ensuremath{\rightarrow}3/2=36\ifmmode\pm\else\textpm\fi{}8 \AA{}2, and \ensuremath{\sigma}5D=30\ifmmode\pm\else\textpm\fi{}3 \AA{}2. In addition, numbers for the 6P level-quenching cross sections due to collisions with Cs atoms and Cs2 molecules, respectively, were obtained: \ensuremath{\sigma}6P(Cs)=6.6\ifmmode\pm\else\textpm\fi{}3.0 \AA{}2 and \ensuremath{\sigma}6P(Cs2)=863\ifmmode\pm\else\textpm\fi{}260 \AA{}2. In the discussion, we show how these new values can be used to reconcile the seemingly discrepant results of several previous studies.
Cesium molecules are pumped by a CW dye laser. Some of the excited molecules then pre-dissociate or collisionally transfer excitation to produce excited atoms at the 5D and 6P levels. The cross sections (in units of 10-14cm2) for the excitation transfer process Cs(6P)+Cs(5D) →Cs(7DJ)+Cs(6S)for J being 5/2 and 3/2 are 5. 4 ± 50% and 4. 9 ± 50%, respectively. The cross sections (in units of 10-14cm2) for the excitation transfer out of the 7D doublet [i. e. , Cs(7DJ)+Cs(6S) →states other than Cs(7D)] for J being 5/2 and 3/2 are 1. 6 ±50% and 0. 34±50%, respectively. To obtain these cross sections, the intensities of 7D and 5D fluorescence emissions and the 6P atom density are measured by using the absorption equivalent width technique. The results are discussed in eomparison with those of other experiments.
At a Cs density higher than 9 x 10(14) cm(-3), cesium vapor was irradiated in a glass fluorescence cell with pulses of radiation from an YAG-laser-pumped OPO laser, populating 6D(5/2) state by two-photon absorption. Energy transfer in Cs6(D(5/2)) + Cs (6S) collisions was studied using methods of atomic fluorescence. At the different Cs densities, we have measured the time-integrated intensities of the components and fitted a three-state rate equation model to obtain the cross sections. The experimental points were fitted to a straight line very well. The authors converted the gradient and intercept into cross sections. The cross section for 6D(5/2)-->6D(3/2) transfer is (2.1 +/- 0.4) x 10(14) cm2. The cross section for excitation transfer out of the 6D doublet is sigmaQ = (1.6 +/- 0.4) x 10(-14) cm2. The cross section on contains information on reverse energy pooling collisions [i.e., Cs(6D(3/2)) + Cs (6S(1/2))-->Cs(6P) + 6Cs(P)] and contribution from mining in 6Dj-->7P(J'), This latter contribution could be subtracted out using the results of a second experiment. At a Cs density lower than 6.0 x 10(12) cm3, the laser was used to pump the 6D(3/2) and 6D(5/2) states, respectively. The resulting fluorescence included the direct component emitted in the decay of the 6D(J) state and the sensitized component arising from the collisionally populated 7P(J') state. Relative intensities of the components yielded the cross sections. The cross-sections for the processes Cs(6D(5/2)) + Cs(6S(1/2))-->Cs(7P(J')) + Cs(6S(1/2)) are (1.6 +/- 0.5) x 10(-15) cm2. for J'= 3/2 and (6.5 +/- 2.1) x 10(-16) cm2, for J' = 1/2, respectively. The cross-sections for the processes Cs(6D(3/2) + Cs(6S(1/2))-->Cs (7P(J')) + Cs(6S(1/2)) are (1.9 +/- 0.6) x 10(-15) cm2. for J' = 3/2 and (7.6 + 2.4) x 10(-16) cm2, for J' = 1/2, respectively. The 6D(J) -->7P(J'), energy transfer rate coefficient is small. The total quenching rate coefficient out of the 6D(J) state is much larger. Evidence suggests that the quenching of the 6D(J) state is caused predominantly by reverse energy-pooling process. The cross section for this process, i.e., Cs(6D(3/2))+Cs(6S(1/2))-->Cs(6P) + Cs(6P) is (1.3 +/- 0.4) x 10(-14) cm2.
We report experimental rate coefficients for the energy-pooling collisions Cs(6P1/2{\mathit{P}}_{1/2}P1/2​)+Cs(6P1/2{\mathit{P}}_{1/2}P1/2​)\ensuremath{\rightarrow}Cs(6S1/2{\mathit{S}}_{1/2}S1/2​)+Cs(${\mathit{nl}}_{\mathit{J}\ensuremath{'}}$) and Cs(6P3/2{\mathit{P}}_{3/2}P3/2​)+Cs(6P3/2{\mathit{P}}_{3/2}P3/2​)\ensuremath{\rightarrow}Cs(6S1/2{\mathit{S}}_{1/2}S1/2​)+Cs(${\mathit{nl}}_{\mathit{J}\ensuremath{'}}$) where ${\mathit{nl}}_{\mathit{J}\ensuremath{'}}$=7P1/2{\mathit{P}}_{1/2}P1/2​, 7P3/2{\mathit{P}}_{3/2}P3/2​, 6D3/2{\mathit{D}}_{3/2}D3/2​, 6D5/2{\mathit{D}}_{5/2}D5/2​, 8S1/2{\mathit{S}}_{1/2}S1/2​, 4F5/2{\mathit{F}}_{5/2}F5/2​, or 4F7/2{\mathit{F}}_{7/2}F7/2​. Atoms were excited to either the 6P1/2{\mathit{P}}_{1/2}P1/2​ or 6P3/2{\mathit{P}}_{3/2}P3/2​ state using a single-mode Ti:sapphire laser. The excited-atom density and spatial distribution were mapped by monitoring the absorption of a counterpropagating single-mode ring dye laser beam, tuned to either the 6P1/2{\mathit{P}}_{1/2}P1/2​\ensuremath{\rightarrow}8S1/2{\mathit{S}}_{1/2}S1/2​ or 6P3/2{\mathit{P}}_{3/2}P3/2​\ensuremath{\rightarrow}7D3/2,5/2{\mathit{D}}_{3/2,5/2}D3/2,5/2​ transitions, which could be translated parallel to the pump beam. Transmission factors, which describe the average probability that photons emitted within the fluorescence detection region can pass through the optically thick vapor without being absorbed, were calculated for all relevant transitions. Effective lifetimes of levels populated by energy-pooling collisions are modified by radiation trapping, and these factors were calculated using the Molisch theory. These calculated quantities have been combined with the measured excited-atom densities and fluorescence ratios to yield absolute energy-pooling rate coefficients. It was found that the rate for production, in all cases, is greatest for 6D, but that 1/2-1/2 collisions are significantly more efficient than 3/2-3/2 collisions for populating 7P. It was also found that 7P1/2{\mathit{P}}_{1/2}P1/2​ is populated two to three times more efficiently than 7P3/2{\mathit{P}}_{3/2}P3/2​ in 1/2-1/2 collisions, but that the 7P fine-structure levels are approximately equally populated in 3/2-3/2 collisions. \textcopyright{} 1996 The American Physical Society.
We report experimentally the measured rate coefficients for the energy pooling (EP) collisions process Cs(5D)+Cs(5D)-gCs(6S)+Cs(nL=9D,11S,7F) in cesium densities of 10^(16)-10^(17) cm^(-3). The 5D state was populated via 8S-g7P-g5D spontaneous emission following two-step pumping 6S-g6P_(3/2)-g8S. Since the 5D-g6P (3.0-3.6 microns) fluorescence could not be detected in this experiment, we carried out a relative measurement for the process 6P+5D-g6S+7D. The excited-atom density and spatial distribution were mapped by monitoring the absorption of a counterpropagating single-mode laser beam, tuned to 6P_(3/2)-g9S_(1/2) transition, which could be translated parallelly to the pump beam. The excited atom densities have been combined with the measured fluorescence ratios to yield EP rate coefficients. The average values for nL=9D,11S and 7F are 8.0+-4.0, 7.0+-3.5, and 9.3+-4.6 (in units of 10^(-10) cm3/s), respectively. Influence of the energy transfer process 11S+6S-g7F+6S on the rate coefficients k_(11S) and k_(7F) is also discussed.