Abstract
A time dependent theory for radiative recombination induced by strong pulses is presented. Analytic solutions in the adiabatic limit are derived and found to be in excellent agreement with exact numerical solutions. Both the pump-before-dump "intuitive" and dump-before-pump "counter-intuitive" schemes are considered. Resonantly enhanced two-photon recombination of ultracold atoms is shown to be an efficient mechanism for the production of ultracold molecules. We have performed detailed calculations on the radiative recombination of cold Na atoms by short laser pulses. Our calculations show that, per pulse, it is possible for up to 97% of all head-on Na-Na colliding pairs to end up as v = 0, J = 0 translationally cold Na2 molecules. We show that these findings, translated to thermally cooled ensemble conditions, mean that the fraction of Na atoms at μKelvin which can be recombined by a pulse of 20 ns duration and 108 W/cm2 peak intensity, to form J = 0 molecules is 6 × 10-6 per pulse. With the above parameters, a laser operating at 100 Hz can convert half of an ensemble of cold atoms to cold molecules in ∼25 min. The efficiency of the process can be increased by going to longer pulses of lower intensity, by going to lower temperatures or by increasing the density of the ensemble. In particular, the "counter-intuitive" scheme which allows for use of longer pulses of lower intensities, with no spontaneous emission losses, considerably increases the yield.
Original language | English |
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Pages (from-to) | 6166-6174 |
Number of pages | 9 |
Journal | Journal of Chemical Physics |
Volume | 107 |
Issue number | 16 |
DOIs | |
State | Published - 22 Oct 1997 |
Externally published | Yes |
ASJC Scopus subject areas
- Physics and Astronomy (all)
- Physical and Theoretical Chemistry