里德堡钾原子的布居数在受激拉曼绝热通道中的相干迁移

本文用含时多态展开方法研究了在两束部分重叠的脉冲场驱动下布居数在钾原子量子态中的相干迁移。结果表明，布居数能否实现完全迁移取决于两个脉冲的持续时间和重叠程度，当脉冲的持续时间和重叠合适时，将发生布居数的完全迁移，并形成布居数囚禁。     

里德伯钠原子经绝热快速通道的布居数跃迁相干控制

运用含时多态展开方法和B-样条函数研究了啁啾频率微波场中里德伯钠原子的量子态之间的布居数迁移.计算了里德伯钠原子n=70-77的开普勒频率.计算了在不同的微波场中六个态的布居数从n=70到n=77随时间的迁移,布居数跃迁到最终态n=77达到了98%,这可以通过连续的单光子跃迁来实现.结果表明,通过优化微波脉冲参数可以实现从低态到较高态的布居跃迁的相干控制.     

Observation of wave packet dichotomy and adiabatic stabilization in an optical waveguide

We report on the first experimental observation of wave packet dichotomy and adiabatic stabilization of light in a periodically bent optical waveguide in analogy with similar behavior of atoms in high-frequency strong laser fields.     

Quantum state transfer via adiabatic passage

Based on adiabatic passage, we propose a scheme for implementing the quantum transfer of an unknown atomic state. In our scheme, we utilize photons for ideal quantum transmission between two cavities with the successful probability being about 1. Meanwhile, the scheme is robust against the effects of atomic spontaneous emission. It may be useful for transferring quantum information among spatially distant atoms.     

Suppression of decoherence in a wave packet via nonlinear resonance

We propose a simple approach for suppressing decoherence of a wave packet excited in an anharmonic oscillator. We show that when a resonant external field forces the oscillator to follow the driving force, motion around the resonant trajectory inside a stable resonant island can be made almost completely immune to the environment. As an example, we study suppression of decoherence due to coupling to thermally populated rotations in vibrational wave packets in a Na2 molecule.     

Mid-range adiabatic wireless energy transfer via a mediator coil

A technique for efficient mid-range wireless energy transfer between two coils via a mediator coil is proposed. By varying the coil frequencies, three resonances are created: emitter–mediator (EM), mediator–receiver (MR) and emitter–receiver (ER). If the frequency sweeps are adiabatic and such that the EM resonance precedes the MR resonance, the energy flows sequentially along the chain emitter–mediator–receiver. If the MR resonance precedes the EM resonance, then the energy flows directly from the emitter to the receiver via the ER resonance; then the losses from the mediator are suppressed. This technique is robust against noise, resonant constraints and external interferences.     

Perturbative and nonperturbative processes in adiabatic population transfer

With the help of superadiabatic techniques for quantum systems depending slowly on time, we demonstrate how the total transition amplitude, tracked in time in the usual adiabatic basis, can be decomposed into a perturbative part consisting of terms proportional to powers of the adiabaticity parameter, and a nonperturbative component. The interference of both components underlies the oscillations that accompany transitions in the adiabatic basis. Whereas for traditionally considered systems the final nonadiabatic transition probability is determined by the nonperturbative part alone, this is no longer correct for models describing stimulated Raman adiabatic passage (STIRAP). We explain the recently discovered breakdown of the Dykhne-Davis-Pechukas formula on general grounds, and provide simple, but accurate approximations for transition amplitudes in STIRAP systems. Received: 22 January 1998 / Revised: 17 March 1998 / Accepted: 31 March 1998     

IBr分子含时波包的理论探究

本文主要对IBr分子的飞秒含时光电子能谱进行了模拟计算.运用含时量子波包方法,对不同延迟时间的光电子能谱进行模拟计算与理论分析.应用波包和光诱导势理论,对光电子能谱共同的两峰系特征及多峰现象给予合理解释.光电子能谱的峰值随延迟时间的增加而递减现象,是由于波包在势能面上因分子解离发散,使整个波包在势能曲线上的振荡递减造成的.研究表明：波包的传播是一个能量减弱的过程;跃迁过程中不同电离通道之间的竞争,也对能谱存在一定的影响.     

Isotope-selective femtosecond wave packet dynamics: The rare molecule

For the first time, the femtosecond real-time vibrational dynamics of the rare ^41,41K₂ isotope, excited to the electronic state, could be selectively studied by means of time-resolved three photon ionization. A vibrational period of fs is determined. Superimposed, a beat structure with a period of 20 ps is observed. A detailed Fourier analysis reveals a strong band of three lines centered around 65.5 cm^-1. A significant perturbation of the wave packet caused by spin-orbit coupling of the A and the crossing state is found. This perturbation is the reason for the fast dephasing of the initially generated wave packet within about 10 ps. The spectrogram of the real-time data shows total revivals of the wave packet at 20 ps and 40 ps. Fractional revivals are found for times around 10 ps and 30 ps. Due to high intensity effects a remarkable slightly broadened line at 90 cm^-1 appears and can be assigned to the wave packet propagation generated in the dimer's ground state by impulsive stimulated Raman scattering. Revivals of this ground state wave packet are found at 17ps and 34ps. A comparison with other isotopes of K₂ is given. Received: 9 February 1998 / Revised: 15 May 1998 / Accepted: 2 June 1998     

IBr分子含时波包的理论探究

本文主要对IBr分子的飞秒含时光电子能谱进行了模拟计算.运用含时量子波包方法,对不同延迟时间的光电子能谱进行模拟计算与理论分析.应用波包和光诱导势理论,对光电子能谱共同的两峰系特征及多峰现象给予合理解释.光电子能谱的峰值随延迟时间的增加而递减现象,是由于波包在势能面上因分子解离发散,使整个波包在势能曲线上的振荡递减造成的.研究表明：波包的传播是一个能量减弱的过程;跃迁过程中不同电离通道之间的竞争,也对能谱存在一定的影响.     

Dependence of adiabatic population transfer on pulse profile

Control of population transfer by rapid adiabatic passage has been an established technique wherein the exact amplitude profile of the shaped pulse is considered to be insignificant. We study the effect of ultrafast shaped pulses for two-level systems, by density-matrix approach. However, we find that adiabaticity depends simultaneously on pulse profile as well as the frequency modulation under non-resonant conditions     

Piecewise adiabatic passage with a series of femtosecond pulses

We develop a method of executing complete population transfers between quantum states in a piecewise manner using a series of femtosecond laser pulses. The method can be applied to a large class of problems as it benefits from the high peak powers and large spectral bandwidths afforded by femtosecond pulses. The degree of population transfer is robust to a wide variation in the absolute and relative intensities, durations, and time ordering of the pulses. The method is studied in detail for atomic sodium where piecewise adiabatic population transfer, as well as the induction of Ramsey-type interferences, is demonstrated.     

Population transfer via adiabatic passage in the Rydberg potassium atom

Using the time-dependent multilevel approach, we have calculated the coherent population transfer between the quantum states of potassium atom by a single frequency-chirped laser pulse. The result shows that a pair of sequential `broadband' frequency-chirped laser pulses can efficiently transfer population from the initial state of the ladder system to the target state. It is also found that the population can be efficiently transferred to a target state and trapped there by using an `intuitive' or a `counterintuitive' frequency sweep laser pulse in the case of `narrowband' frequency-chirped laser pulse. Our research shows that the complete population transfer is related to the pulse duration, chirp rate, and amplitude of the laser pulse.     

Coherent population transfer in an atom by multiphoton adiabatic rapid passage

Coherent population transfer in an atom using a sequence of adiabatic rapid passages through single-photon resonances is well-known, but it requires that the frequency sweep match the changing frequencies of the atomic transitions. The same population transfer can be effected via a single multiphoton adiabatic rapid passage, which requires only a small frequency sweep, if it is possible to select the desired multiphoton transition from the many possible transitions. Here we report the observation of population transfer between Rydberg states by high order multiphoton adiabatic rapid passage.     

Li2分子含时波包动力学的理论研究

利用含时量子波包方法计算得到了Li2分子的光电子能谱,并运用波包动力学理论对含有不同参量的光电子能谱现象给出了合理的解释。通过分析文中的直观图像,研究了波包的动力学过程。结果表明,泵浦-探测脉冲的延迟时间对光电子能谱的形状有重要的影响;在较短延迟时间下,能谱独特的四峰现象是由光诱导势的产生引起的。     

Inversion in an extended three-level medium produced by adiabatic population transfer

Features of the adiabatic population transfer are studied with the spatial evolution of interacting pulses propagating in an optically dense medium of three-level Λ-atoms taken into account. A self-consistent analytical solution describing the spatial-temporal dynamics of interacting short pulses under the conditions of adiabatic population transfer is constructed in the adiabatic approximation with consideration for the first nonadiabatic correction. Practically complete inversion on a forbidden transition determined by coherent (adiabatic) population transfer is shown to take place over a length of the medium, which may exceed the absorption length of a weak probing pulse in the absence of control radiation on the adjacent transition by several orders of magnitude.     

Li2分子含时波包动力学的理论研究

利用含时量子波包方法计算得到了Li2分子的光电子能谱,并运用波包动力学理论对含有不同参量的光电子能谱现象给出了合理的解释.通过分析文中的直观图像,研究了波包的动力学过程.结果表明,泵浦-探测脉冲的延迟时间对光电子能谱的形状有重要的影响;在较短延迟时间下,能谱独特的四峰现象是由光诱导势的产生引起的.     

Probing the launching position of the electron wave packet in molecule strong-field tunneling ionization

Strong-field tunneling ionization is the first step for a broad class of phenomena in intense laser-atom/molecule interactions. Accurate information about the electron wave packet from strong-field tunneling ionization of atoms and molecules is of essential importance for understanding various tunneling ionization triggered processes. Here, we survey the property of the electron wave packet in tunneling ionization of molecules with a method based on strong-field photoelectron holography. By solving the time-dependent Schr ¨odinger equation, it is shown that the holographic interference in the photoelectron momentum distribution exhibits the asymmetric behavior with respect to the laser polarization direction, when the molecule is aligned with a nonzero angle to the linearly polarized laser field. We demonstrate that this asymmetry is due to the nonzero initial transverse displacement of the electron wave packet at tunneling. By analyzing the holographic interference, this transverse displacement for the launching of electron wave packet tunneling from the molecules is accurately retrieved. This displacement is directly related to the electron density distribution in molecules, and thus our work developed a novel concept for probing electronic structure in molecules.