FORMATION OF ULTRACOLD CESIUM MOLECULES IN THE GROUND ELECTRONIC STATE

2012 ◽  
Vol 11 (06) ◽  
pp. 1323-1330 ◽  
Author(s):  
XUE-JIN HU ◽  
WEI ZHANG ◽  
YIN HUANG ◽  
JUN-FENG YANG ◽  
SHU-LIN CONG

We investigate theoretically the preparation of ultracold photoassociated Cs 2 molecules in the lowest vibrational level of the ground electronic state via the stimulated Raman adiabatic passage (STIRAP) by solving the time-dependent Schrödinger equation using the mapped Fourier grid method. A negative chirped laser pulse is used to produce the unstable photoassociated molecules in the excited electronic state. A dump pulse is utilized to transfer a partial population of the unstable photoassociated molecules to the vibrational v″ = 18 level of the ground electronic state. This part of population is then transferred to the v″ = 0 level of the ground electronic state by the pump and Stokes laser pulses via an intermediate state which is taken to be the v′ = 7 level of the excited electronic state, forming the stable photoassociated molecules. The population transfer efficiency from v″ = 18 to v″ = 0 in the ground electronic state reaches 96.2% via the STIRAP.

2014 ◽  
Vol 17 (1) ◽  
pp. 79-92 ◽  
Author(s):  
Jinglun Li ◽  
Yin Huang ◽  
Ting Xie ◽  
Shuo Chai ◽  
Shulin Cong

AbstractThe 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.


1997 ◽  
Vol 107 (8) ◽  
pp. 2930-2941 ◽  
Author(s):  
S. Mahapatra ◽  
R. Vetter ◽  
Ch. Zuhrt ◽  
H. T. Nguyen ◽  
T. Ritschel ◽  
...  

2013 ◽  
Vol 138 (9) ◽  
pp. 094318 ◽  
Author(s):  
T. Rajagopala Rao ◽  
Sugata Goswami ◽  
S. Mahapatra ◽  
B. Bussery-Honvault ◽  
P. Honvault

2017 ◽  
Vol 96 (2) ◽  
Author(s):  
Jim L. Hicks ◽  
Chakree Tanjaroon ◽  
Susan D. Allen ◽  
Matt Tilley ◽  
Steven Hoke ◽  
...  

1993 ◽  
Vol 71 (10) ◽  
pp. 1556-1561 ◽  
Author(s):  
J.K.G. Watson

The a″ vibrational frequencies of all possible H and D isotopomers of propynal (HCCCHO) are shown to allow two solutions for the a″ harmonic potential constants. Equations relating the solutions are given. In the [Formula: see text] ground electronic state one solution can be rejected as chemically unrealistic, but in the [Formula: see text] excited electronic state the choice is more difficult. It is shown that a choice can be made on the basis of the observed cross-sequence intensities in the [Formula: see text] band system.


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