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超冷原子向异核四聚物分子A3B的绝热转化
引用本文:李冠强,彭娉,曹振洲,薛具奎.超冷原子向异核四聚物分子A3B的绝热转化[J].物理学报,2012,61(9):90301-090301.
作者姓名:李冠强  彭娉  曹振洲  薛具奎
作者单位:1. 陕西科技大学理学院,西安,710021
2. 中南民族大学电子信息工程学院,武汉,430074
3. 西北师范大学物理与电子工程学院,兰州,730070
基金项目:国家自然科学基金 (批准号: 10774120, 10975114), 中南民族大学中央高校基本科研业务专项基金(批准号: CZQ11001)和 陕西科技大学自然科学基金(批准号: ZX11-33)资助的课题.
摘    要:提出了利用Efimov共振辅助的受激拉曼绝热通道(ER-STIRAP) 过程实施超冷原子向异核四聚物分子A3B转化的理论方案, 得到了转化过程中中间态分别为同核Efimov三聚物A3和 异核Efimov三聚物A2B两种途径下系统的暗态解, 证实了ER-STIRAP技术对超冷异核四聚物分子A3B合成的可行性和有效性. 研究了外场参数, 包括缔合光脉冲的强度、脉宽、磁耦合强度及其失谐量等对A3B形成的影响. 对两种不同中间态的转化途径进行比较发现, 与中间态为异核Efimov三聚物A2B的途径相比, 经历中间态为同核Efimov三聚物A3的途径时系统实现最终四聚物分子A3B的产率更高. 另外, 还讨论了系统内禀的非线性和中间态的自发辐射损失对异核四聚物分子合成的影响.

关 键 词:异核四聚物分子  受激拉曼绝热通道  绝热保真度  转化效率
收稿时间:2011-06-25

Adiabatic conversion from ultracold atoms to heteronuclear tetrameric molecule A3B
Li Guan-Qiang,Peng Ping,Cao Zhen-Zhou,Xue Ju-Kui.Adiabatic conversion from ultracold atoms to heteronuclear tetrameric molecule A3B[J].Acta Physica Sinica,2012,61(9):90301-090301.
Authors:Li Guan-Qiang  Peng Ping  Cao Zhen-Zhou  Xue Ju-Kui
Institution:1. College of Science, Shaanxi University of Science and Technology, Xi'an 710021, China;2. College of Electronics and Information Engineering, South-Central University for Nationalities, Wuhan 430074, China;3. College of Physics and Electronic Engineering, Northwest Normal University, Lanzhou 730070, China
Abstract:We present a theoretical scheme for conversion from ultracold atoms to heteronuclear tetrameric molecule A3B via Efimov resonace-assisted stimulated Raman adiabatic passage (ER-STIRAP). The dark state solutions of the system are obtianed for two different pathways. For the first pathway, the intermediate state is populated by homonuclear Efimov trimer A3, and the second one by heteronuclear Efimov trimer A2B. The feasibility and the effectiveness of the scheme are also verified. Meanwhile, we investigate the effects of external field parameters, including the intensity of associated laser pulses, its width, magnetic coupling strength and its detuning, on the fomation of heteronuclear tetrameric molecules. By comparison, it is found that the ultimate yield of the tetrameric molecules for the second pathway is less than ones for the first pathway. In addition, the effects of the intrinsic nolinearity of the system and the spontaneous decay in the intermediate state on the tetramer formation are discussed.
Keywords:heteronuclear tetrameric molecule  stimulated Raman adiabatic passage  adiabatic fidelity  conversion efficiency
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