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Theoretical Chemistry Accounts

Isotope effects on the formation of the lowest rovibrational level of NaH molecule via pump–dump photoassociation

Binbin Wang, Yong‐Chang Han, Yuhui Pang, Shu‐Lin Cong, Ying‐Yu Niu

Published Jun 10, 2015• 4 citations
Publisher
DOI
10.1007/s00214-015-1680-0

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Chinese Physics Letters•Sep 1, 2010•5 citations
The formation of NaH molecules in the lowest rovibrational level of the ground electronic state is investigated using a pump-dump photoassociation (PA) scheme. In short-range region, two colliding atoms Na and H are efficiently associated into the NaH molecule in the rovibrational |0,0〉 state of the ground electronic state via the intermediately rovibrational |10,1〉 state of the excited electronic state. The changes of populations with the electric field amplitudes, frequency detunings, dump pulse duration and delay time between two laser pulses are calculated and discussed. The PA probability reaches 0.623 with a high state-selectivity.
The photoassociation processes via the pump-dump scheme for the heternuclear (Na + H → NaH) and the homonuclear (Na + Na → Na2) molecular systems are studied, respectively, using the time-dependent quantum wavepacket method. For both systems, the initial atom pair in the continuum of the ground electronic state (X(1)Σ(+)) is associated into the molecule in the bound states of the excited state (A(1)Σ(+)) by the pump pulse. Then driven by a time-delayed dumping pulse, the prepared excited-state molecule can be transferred to the bound states of the ground electronic state. It is found that the pump process can induce a superposition of the rovibrational levels |v, j〉 on the excited state, which can lead to the field-free alignment of the excited-state molecule. The molecular alignment can affect the dumping process by varying the effective coupling intensity between the two electronic states or by varying the population transfer pathways. As a result, the final population transferred to the bound states of the ground electronic state varies periodically with the delay time of the dumping pulse.
The formation of the NaH molecule from unaligned ultracold atoms via photoassociation (PA) is theoretically investigated by numerically solving the time-dependent Schrödinger equation including the vibrational and rotational degrees of freedom. The PA processes via one- and two-photon excitations are described. The calculated results show that the associated molecule can be prepared to a desired rovibrational state of the ground electronic state for NaH. Compared with the one-photon association probability, the two-photon association probability is obviously enhanced.