52P1/2 ↔ 52P3/2 excitation transfer in rubidium induced in collisions with CH4, CH2D2, and CD4 molecules

1980 ◽  
Vol 58 (7) ◽  
pp. 1047-1048 ◽  
Author(s):  
R. A. Phaneuf ◽  
L. Krause
Keyword(s):  
Energy Transfer ◽  
Temperature Dependence ◽  
Isotope Effect ◽  
Cross Sections ◽  
Noble Gas ◽  
Rotational Energy ◽  
Excitation Transfer ◽  
Sensitized Fluorescence ◽  
Temperature Range ◽  
Rotational Energy Transfer

The temperature dependence of cross sections for 52P1/2 ↔ 52P3/2 excitation transfer in rubidium, induced in collisions with CH4, CH2D2, and CD4 molecules, has been investigated using methods of sensitized fluorescence over a temperature range 300–650 K. The cross sections, which are of the order of 30 Å2 and which exceed similar cross sections for collisions with noble gas atoms by at least two orders of magnitude, exhibit an isotope effect which is ascribed to the phenomenon of electronic-to-rotational energy transfer.

Temperature dependence of cross sections for 72P1/2 ↔ 72P3/2 excitation transfer and for quenching in cesium, induced in collisions with H2, N2, CH4, and CD4

1982 ◽  
Vol 60 (2) ◽  
pp. 239-244 ◽  
Author(s):  
I. N. Siara ◽  
R. U. Dubois ◽  
L. Krause
Keyword(s):  
Energy Transfer ◽  
Temperature Dependence ◽  
Cross Sections ◽  
Rotational Energy ◽  
Excitation Transfer ◽  
Sensitized Fluorescence ◽  
Temperature Range ◽  
Rotational Energy Transfer ◽  
Order Of Magnitude

The temperature dependence of cross sections for 72P1/2 ↔ 72P3/2 excitation transfer in cesium, as well as the effective quenching of these states, induced in collisions with H2, N2, CH4, and CD4 molecules have been investigated in a series of sensitized fluorescence experiments over a temperature range 390–640 K. The 72P mixing cross sections are of the order of 10−15 cm2 and exceed by at least one order of magnitude similar cross sections for mixing by collisions with Ne, Ar, Kr, and Xe. The large sizes of the mixing cross sections and their variation with temperature are ascribed to a phenomenon of electronic-to-rotational energy transfer.

Inelastic Collisions Between Excited Alkali Atoms and Molecules X. Temperature Dependence of Cross Sections for 2P1/2↔2P3/2 Mixing in Cesium, Induced in Collisions with Deuterated Hydrogens, Ethanes, and Propanes

1974 ◽  
Vol 52 (7) ◽  
pp. 589-591 ◽  
Author(s):  
E. Walentynowicz ◽  
R. A. Phaneuf ◽  
L. Krause
Keyword(s):  
Energy Transfer ◽  
Temperature Dependence ◽  
Isotope Effect ◽  
Cross Sections ◽  
Rotational Energy ◽  
Inelastic Collisions ◽  
Atoms And Molecules ◽  
Rotational Energy Transfer ◽  
Alkali Atoms ◽  
The Cross

The dependence on temperature of the cross sections for 2P1/2 ↔ 2P3/2 mixing in cesium, induced in collisions with various deuterated hydrogen, ethane and propane molecules, has been studied in the range 290–650 K. In the cases of hydrogen and ethane, the behavior of the cross sections was found to depend on the degree of deuteration of the molecules. The very large sizes of the mixing cross sections and the isotope effect observed in their variation with temperature, are ascribed to the phenomenon of electronic to rotational energy transfer.

Sensitized Fluorescence in Vapors of Alkali Atoms XIV. Temperature Dependence of Cross Sections for 72P1/2–72P3/2 Mixing in Cesium, Induced in Collisions with Noble Gas Atoms

1974 ◽  
Vol 52 (11) ◽  
pp. 945-949 ◽  
Author(s):  
I. N. Siara ◽  
H. S. Kwong ◽  
L. Krause
Keyword(s):  
Temperature Dependence ◽  
Cross Sections ◽  
Noble Gas ◽  
Excitation Transfer ◽  
Sensitized Fluorescence ◽  
Alkali Atoms ◽  
Resonance Doublet ◽  
The Cross ◽  
Adiabatic Case

The cross sections for 72P1/2–72P3/2 excitation transfer in cesium, induced in collisions with noble gas atoms, have been determined in a series of sensitized fluorescence experiments at temperatures ranging from 405 to 630 K. The cross sections which lie in the range 0.06–20 Å2, exhibit a temperature dependence which, however, is less pronounced than in the more adiabatic case of the cesium resonance doublet.

Inelastic Collisions Between Excited Alkali Atoms and Molecules IX. An Isotope Effect in the Cross Sections for 62P1/2↔62P3/2 Mixing in Cesium, Induced in Collisions with Deuterated Methanes

1974 ◽  
Vol 52 (7) ◽  
pp. 584-588 ◽  
Author(s):  
E. Walentynowicz ◽  
R. A. Phaneuf ◽  
W. E. Baylis ◽  
L. Krause
Keyword(s):  
Energy Transfer ◽  
Isotope Effect ◽  
Cross Sections ◽  
Noble Gas ◽  
Inelastic Collisions ◽  
Semiclassical Theory ◽  
Vibrational States ◽  
Rotational Energy Transfer ◽  
Alkali Atoms ◽  
The Cross

The temperature dependence of cross sections for 62P1/2 ↔ 62P3/2 mixing in cesium, induced in collisions with CH4, CH3D, CH2D2, CHD3, and CD4 molecules, has been investigated in a series of sensitized fluorescence experiments over a temperature range 290–650 K. The various cross sections which are of the order of 10−15 cm2, and which exceed similar cross sections for cesium–noble gas collisions by 4 – 6 orders of magnitude, exhibit differences in their variation with temperature. This isotope effect in the collision cross sections is interpreted on the basis of a novel semiclassical theory of electronic to rotational energy transfer. The cross section for mixing induced by collisions with CF4, which was determined in a subsidiary experiment, and which is 2–3 times larger than the methane cross sections, does not show comparable behavior with temperature, probably because the energy transfer takes place to closely lying molecular vibrational states.

Rotational Energy Transfer within the A1Σu+ State of Na2 Induced by Collisions with (2S1/2) Na

2007 ◽  
Vol 62 (3-4) ◽  
pp. 176-178
Author(s):  
Rami Haj Mohamad ◽  
Khaled Hussein ◽  
Abdel-Monhem Nachabé
Keyword(s):  
Energy Transfer ◽  
Cross Section ◽  
Cross Sections ◽  
Ground State ◽  
Rhodamine 6G ◽  
Rotational Energy ◽  
Spectral Lines ◽  
Rotational Energy Transfer ◽  
Rotational Transitions ◽  
Electronic Ground

The (v’ = 34, J’ = 14) level of the A1Σ+u electronic state of Na2 has been selectively populated by excitation with the 578.1 nm line of a ring dye-laser with rhodamine 6G. Through collisions with (2S1/2) Na atoms, energy is transferred to neighbouring rotational levels in Na2, and the density of these levels is determined by observing the fluorescence to the electronic ground state. From previous measurements of the lifetime of the A1Σ+u state and new measurements of the intensities of collision-induced spectral lines, absolute collision cross-sections for all rotational transitions up to ΔJ = ±6 have been obtained; the total cross-section for all rotational transitions observed is: rotσtotal = 0.41 nm2.

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