EGAS41 - Swansea University
EGAS41 - Swansea University
EGAS41 - Swansea University
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41 st EGAS CP 147 Gdańsk 2009<br />
Corrections to transit time broadening<br />
J. Ulmanis 1 , N.N. Bezuglov 2 , B. Mahrov 1 , C. Andreeva 3 , K. Miculis 1 , M. Bruvelis 1 ,<br />
E. Saks 1 , A. Ekers 1<br />
1 Laser Centre, <strong>University</strong> of Latvia, LV-1002 Riga, Latvia<br />
2 Faculty of Physics, St. Petersburg State <strong>University</strong>, 198904 St. Petersburg, Russia<br />
3 Institute of Electronics, Bulgarian Academy of Sciences, 1784 Sofia, Bulgaria<br />
We reconsider the effect of transit time on line broadening in dilute gases in the weak<br />
excitation limit, when the effects of reabsorption, saturation, and collisions are negligible.<br />
Two-photon excitation of excited molecular levels by counter-propagating laser fields is<br />
used in order to eliminate the Doppler broadening. Both laser fields have Gaussian profiles<br />
and are focused onto the supersonic beam of Na 2 molecules such that transit time is<br />
shorter than natural lifetime of the excited state. In experiment, the field 2 in the 2nd excitation<br />
step is detuned by 1GHz off from one-photon resonance between the intermediate<br />
rovibrational level in the A 1 Σ + u state and the final level 51 Σ + g (v=10,J=9). The excitation<br />
spectrum of the final level is then recorded by scanning the field 1 across the two-photon<br />
resonance.<br />
Usually in such a situation one would describe the absorption profile by a Lorentz<br />
function with the natural width Γ sp and transit time τ tr [1]:<br />
P(∆) = π˜Γ/ ( ∆ 2 + ˜Γ 2) ; ∆ω =<br />
˜Γ<br />
2 = 1 2 (Γ sp + 1/τ tr ), (1)<br />
where ∆ is the detuning of field 1 from the two-photon resonance, and ∆ω is the HWHM.<br />
Transit time τ tr = L/v f is determined by the flow velocity of molecules in the beam v f<br />
and the spot size of the laser beams L. In our case the lifetime is τ sp =42ns and the transit<br />
time is τ tr =23ns.<br />
Analytical solution for two-photon absorption shows that it is described by the Voight<br />
profile, which is in good agreement with the measured line profiles (see Fig. 1). The<br />
HWHM of this profile exceeds the value of ∆ω given by Eq. (1) by a factor of 2.5.<br />
Fluorescence intensity (a.u.)<br />
1,0 Calculated lineshape<br />
Experimental data<br />
0,8<br />
0,6<br />
0,4<br />
0,2<br />
0,0<br />
-800 -700 -600 -500 -400 -300<br />
(MHz)<br />
Figure 1: Doppler-free two-photon excitation spectrum of the Na 2 (5 1 Σ + g ,v=10,J=9).<br />
References<br />
[1] B.W. Shore, The Theory of Coherent Atomic Excitation (Wiley, New York, 1990).<br />
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