journal article·2018-11-01Open access

Adiabatic population transfer between electronic states of LiH molecule in two picosecond laser pulses

Ying-Yu Niu, Rong Wang

AIP Advances· Volume 8· Issue 11

Abstract

The population transfer of stimulated Raman adiabatic passage (STIRAP) is investigated using a time-dependent quantum wave packet method. The population is transferred from an initial state to a target state through the interaction of the external laser field with the permanent dipole moment and the transition dipole moment. The laser field is composed of an infrared pulse and a near ultraviolet pulse. The two pulses with small detunings are more efficient to achieve the STIRAP transition. The process of STIRAP is sensitive to the detunings of the two pulses. When the two detunings are the same in a Λ transition or the positive detuning of the pump pulse is equal to the negative detuning of the Stokes pulse in a ladder transition, the final population in the intermediate state can be eliminated and the target population is increased.
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Research context

OpenAlex topics: Quantum optics and atomic interactions · Cold Atom Physics and Bose-Einstein Condensates · Atomic and Subatomic Physics Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Science, Dalian Jiaotong University , Dalian 116028, China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Liaoning Province

References (34)

Show source-provided references
1. Rev. Mod. Phys. · 1998 · 70 · 100310.1103/revmodphys.70.1003 ↗
2. New J. Phys. · 2010 · 12 · 07500810.1088/1367-2630/12/7/075008 ↗
3. Phys. Rev. Lett. · 2008 · 101 · 02360110.1103/physrevlett.101.023601 ↗
4. Phys. Rev. Lett. · 2014 · 113 · 20530110.1103/physrevlett.113.205301 ↗
5. AIP Adv. · 2014 · 4 · 01713410.1063/1.4864057 ↗
6. Chem. Phys. Lett. · 1988 · 149 · 46310.1016/0009-2614(88)80364-6 ↗
7. J. Chem. Phys. · 1990 · 92 · 536310.1063/1.458514 ↗
8. Phys. Rev. A · 1999 · 59 · 291010.1103/physreva.59.2910 ↗
9. Phys. Rev. A · 2006 · 73 · 05340210.1103/physreva.73.053402 ↗
10. Phys. Rev. Lett. · 2014 · 113 · 25530110.1103/physrevlett.113.255301 ↗
11. J. Chem. Phys. · 2015 · 142 · 17090110.1063/1.4916903 ↗
12. Rev. Mod. Phys. · 2017 · 89 · 01500610.1103/revmodphys.89.015006 ↗
13. Phys. Rev. A · 1996 · 53 · 250110.1103/physreva.53.2501 ↗
14. Phys. Rev. A · 2005 · 72 · 02340510.1103/physreva.72.023405 ↗
15. Phys. Rev. A · 2008 · 78 · 05341010.1103/physreva.78.053410 ↗
16. Phys. Rev. A · 2007 · 76 · 01340610.1103/physreva.76.013406 ↗
17. J. Phys. B. · 2017 · 50 · 22540110.1088/1361-6455/aa90d9 ↗
18. Phys. Rev. A · 2009 · 79 · 02341810.1103/physreva.79.023418 ↗
19. Phys. Rev. A · 1999 · 59 · 213410.1103/physreva.59.2134 ↗
20. J. Phys. B. · 2017 · 50 · 21510110.1088/1361-6455/aa8d9d ↗
21. Chem. Phys. · 2007 · 342 · 1610.1016/j.chemphys.2007.09.007 ↗
22. J. Chem. Phys. · 2006 · 125 · 23410310.1063/1.2403880 ↗
23. Phys. Rev. A · 1998 · 58 · 468310.1103/physreva.58.4683 ↗
24. J. Chem. Phys. · 2003 · 118 · 736610.1063/1.1545773 ↗
25. Phys. Rev. A · 2001 · 63 · 031403(R)10.1103/physreva.63.031403 ↗
26. Phys. Rev. A · 2001 · 64 · 02340410.1103/physreva.64.023404 ↗
27. J. Chem. Phys. · 1981 · 74 · 236110.1063/1.441355 ↗
28. Phys. Rev. A · 2014 · 90 · 05341810.1103/physreva.90.053418 ↗
29. Phys. Rev. A · 2016 · 93 · 02250610.1103/physreva.93.022506 ↗
30. J. Comput. Phys. · 1982 · 47 · 41210.1016/0021-9991(82)90091-2 ↗
31. J. Chem. Phys. · 2015 · 143 · 09430310.1063/1.4929388 ↗
32. J. Chem. Phys. · 2007 · 127 · 08411510.1063/1.2762222 ↗
33. Phys. Rev. Lett. · 1998 · 80 · 93210.1103/physrevlett.80.932 ↗
34. Phys. Rev. A · 2000 · 62 · 05341310.1103/physreva.62.053413 ↗