Steering Vibrational Population Transfer via Double-∑-Type Laser Scheme  

通过双∑型激光方案控制振动态布居转移

作　　者：李立航[1] 韩永昌[1] 丛书林[1] 

机构地区：[1]大连理工大学、物理与光电工程学院,大连116024

出　　处：《Chinese Journal of Chemical Physics》2015年第1期43-48,I0001,共7页化学物理学报（英文）

基　　金：Li-hang Li thanks Dr. Yin Huang for assistance. The project is supported by the Specialized Research Fund for the Doctoral Program of Higher Education （No.20130041120053）, SRF for ROCS, SEM, the Sci- ence and Technology Research Funds of the Depart- ment of Education of Liaoning Province （L2013014）, the National Magnetic Confinement Fusion Science Pro- gram （No.2013GB109005）, the Fundamental Research Funds for the Central Universities （DUT12RC（3）60）, and the NationM Natural Science Foundation of China （No.21473018, No.10974024, and No.11274056）.

摘　　要：The vibrational state-selected population transfer from a highly vibrationally excited level to the ground level is of great importance in the preparation of ultra-cold molecules. By using the time-dependent quantum-wave-packet method, the population transfer dynamics is investigated theoretically for the HF molecule. A double-E-type laser scheme is proposed to transfer the population from the ｜v=16〉 level to the ground vibrational level ｜v=0〉 on the ground electronic state. The scheme consists of two steps： The first step is to transfer the population from ｜v=16〉 to ｜v=7〉 via an intermediate level ｜v=11〉, and the second one is to transfer the population from ｜v=7〉 to ｜v=0〉 via ｜v=3〉. In each step, three vibrational levels form a E-type population transfer path under the action of two temporally overlapped laser pulses. The maximal population-transfer efficiency is obtained by optimizing the laser inten- sities, frequencies, and relative delays. Cases for the pulses in intuitive and counterintuitive sequences are both calculated and compared. It is found that for both cases the population can be efficiently （over 90%） transferred from the ｜v=-16〉 level to the ｜v=0〉 level.

关 键 词：Population transfer Wave packet dynamics Vibrational state 

分 类 号：O561.3[理学—原子与分子物理] TN241[理学—物理]