We demonstrate the feasibility of a laser induced complete population transfer to and from a continuum of states. We study the two-photon dissociation of v = 28; J = 1,...,10 sodium dimers. We demonstrate that using just a pair of "counter intuitively" ordered pulses we can dissociate 100% of the molecules in an ensemble. The scheme is shown to be stable with respect to the initial choice of rotational level and to fluctuations in the laser frequency and intensity. We also study the reverse phenomenon of complete population transfer from the continuum. We perform calculations on the radiative association of Na atoms to form the Na2 molecule in specific vib-rotational states. It is shown that two pulses of 20 nsec duration and as little as 6 MW/cm 2 peak power can photo-associate more than 98% of the atoms within a (pulse and velocity determined) relative effective distance, to yield Na2 molecules in the chosen v = 28; J = 10 vib-rotational state. This means that given a density of 10 16 atoms/cm 3 and a temperature of 7K, a 10Hz pulsed laser source of the above parameters can con- vert half of all the Na atoms in the ensemble to v = 28; J = 10 Na2 molecules within 15 seconds of operation.
Abstract We theoretically investigate the complete population transfer among quantum states of the N a 2 molecule using ultrashort pulse trains using the time-dependent wave packet method. The population accumulation of the target state can be steered by controlling the laser parameters, such as the variable pulse pairs, the different pulse widths, the time delays and the repetition period between two contiguous pulses; in particular, the pulse pairs and the pulse widths have a great effect on the population transfer. The calculations show that the ultrashort pulse train is a feasible solution, which can steer the population transfer from the initial state to the target state efficiently with lower peak intensities.