在双色场中使用相干叠加态来提高高次谐波的发射

本文提出了一种在双色场中使用相干叠加态来提高高次谐波发射效率的方法. 我们首先通过在800nm基本激光脉冲上添加一束控制激光脉冲在理论上得到双色合成激光场;其次,通过求解一维含时薛定谔方程,计算得到了体系处于不同初始态时的高次谐波谱,并结合时频分布图对其微观机理进行分析. 计算结果表明,使用相干叠加态作为体系的初始态,通过调节两束激光的相对相位可以有效实现提高高次谐波的发射效率的目的.     

在双色场中使用相干叠加态来提高高次谐波的发射

本文提出了一种在双色场中使用相干叠加态来提高高次谐波发射效率的方法.我们首先通过在800 nm基本激光脉冲上添加一束控制激光脉冲在理论上得到双色合成激光场;其次,通过求解一维含时薛定谔方程,计算得到了体系处于不同初始态时的高次谐波谱,并结合时频分布图时其微观机理进行分析.计算结果表明,使用相干叠加态作为体系的初始态,通过调节两束激光的相对相位可以有效实现提高高次谐波的发射效率的目的.     

通过双色激光场和低频电场合成获得孤立40阿秒脉冲

本文提出了一个在双色激光场上叠加低频电场来拓宽高次谐波谱平台区域,从而获得孤立40阿秒脉冲的方案.计算中,我们针对氦原子数值求解了一维含时薛定谔方程,并结合电子的经典回碰动能随时间分布图以及时频分析图,分析了低频电场对高次谐波谱产生过程的影响.计算结果表明,该方案可以有效的拓宽谐波谱的平台区域.通过叠加适当阶数的谐波谱,我们得到了孤立40阿秒脉冲.     

通过双色激光场和低频电场合成获得孤立40阿秒脉冲

本文提出了一个在双色激光场上叠加低频电场来拓宽高次谐波谱平台区域,从而获得孤立40阿秒脉冲的方案.计算中,我们针对氯原子数值求解了一维含时薛定谔方程,并结合电子的经典回碰动能随时间分布图以及时频分析图,分析了低频电场对高次谐波谱产生过程的影响.计算结果表明,该方案可以有效的拓宽谐波谱的平台区域.通过叠加适当阶数的谐波谱,我们得到了孤立40阿秒脉冲.     

外加静电场下CO高次谐波谱

利用分子在强激光中产生的高次谐波谱可以实现对分子结构及分子中电子迁移动力学过程的探测和研究.本文采用Lewenstein模型,计算了确定取向的CO分子在线偏振光与静电场组合作用下产生的高次谐波谱.结果表明,针对外加静电场相对分子朝向的两种不同指向,高次谐波谱分别展现了双平台结构和拉长的单平台结构.理论分析表明这些谐波谱的结构特点主要来自于不同跃迁通道贡献的相干叠加.本文为极性分子在非对称场下的高次谐波的形成提供了一个清晰的物理图像,对调控极性分子的高次谐波,进而产生可控阿秒脉冲具有科学意义.     

相干叠加脉冲锁模激光器调制特性的研究

本文在理论上发现了相干叠加脉冲锁模激光器的调制特性,并对其进行了全面的分析和计算.对于相干叠加脉冲锁模激光器的脉冲压缩及调制特性给予了详尽的数值计算结果和清晰的物理图象的解释,并提出利用相干叠加脉冲锁模激光器的调制特性产生更短脉冲的可能性.     

双色激光脉冲辐照叠加态生成强的38 as孤立脉冲

采用多周期800 nm激光组合1 600 nm红外激光脉冲辐照氦离子He⁺叠加态生成强、短孤立阿秒脉冲. 结果表明,相对于800 nm单色激光辐照基态情形,截止频率由70次谐波大幅度展宽到280次谐波,且获得频宽为108 eV并由单一短量子路径贡献的连续辐射谱,叠加该连续谱210次到280次谐波获得了脉宽为38 as的强、短孤立脉冲,其强度比单色场情形提高了11个数量级. 研究进一步表明,两束激光脉冲的时间延迟从0.05π到－0.05π之间获得的孤立阿秒脉冲是最优化的,且脉冲持续时间 关键词： 组合激光脉冲 相干叠加态 阿秒脉冲     

双Λ型原子系统中制备相干叠加态的研究(英文)

本文讨论了在双Λ型原子系统中制备相干叠加态的方法:一个Λ型系统通过控制激光而另一个Λ型系统采用部分受激拉曼绝热通道的方法.在理论上分析了产生任意相干叠加态的可能性并且讨论了透热系统在产生相干叠加态过程中的重要性.研究表明,没有透热过程是不可能制备出任意的叠加态.应用数值方法验证理论分析是正确,并且指出任意叠加态的产生只与控制脉冲的时间延迟有关.     

强激光场中原子的束缚态和连续态对高次谐波的影响

利用基函数展开结合线性最小二乘法方法求解含时薛定谔方程,研究了一维原子在强激光场中产生高次谐波过程中,束缚态和连续态以及它们的干涉效应对高次谐波的影响.结果表明,低能的高次谐波是由束缚态束缚态之间的相互作用产生的,高能的高次谐波是由束缚态连续态之间的相互作用产生的,而截断频率后消失的高次谐波是由于束缚态束缚态与束缚态连续态之间存在干涉效应的结果 关键词： 线性最小二乘法 强激光场 高次谐波的产生     

原子相干对里德伯原子稳定性的影响

研究了含级联双光子过程的多束缚态激光场诱导原子连续态结构系统中原子的相干捕获,给出了产生相干捕获的条件及暗态的表达式,讨论了原子初态和激光强度对原子相干捕获及粒子布居值在束缚态上分布的影响,揭示了原子相干对稳定里德伯原子的重要作用。     

Ultrahigh Harmonic Generation from an Atom with Superposition of Ground State and Highly Excited States

We investigate the high-order harmonic generation from an atom prepared in a superposition of ground state and highly excited state. When the atom is irradiated by an ultrashort pulse, the cutoff position of the plateau in the harmonic spectrum is largely extended compared with the case that the atom is initially in the ground state. The physics of the extension of the high-order harmonic plateau can be interpreted by the spatial structure of the atomic initial wave packet. We can optimize the generation of high-order harmonics by substituting the excited state for a particular coherent superposition of some highly excited states to form a spatially localized excited wave packet.     

Decoding the electron dynamics in high-order harmonic generation from asymmetric molecular ions in elliptically polarized laser fields

The high-order harmonic generation from an asymmetric molecular ion is theoretically investigated based on the Born-Oppenheimer model with two-dimensional electron dynamics. It is shown that the harmonic intensity changes periodically in elliptically polarized laser fields. The periodical character is ellipticity-dependent. By establishing the physical image, the periodicity of the harmonic intensity can be ascribed to the contributions of the ground state and the excited state. Furthermore, the electron dynamics from different electronic states can be selected via combining the elliptically polarized laser field with a static electric field. The harmonics dominated either by ground state or excited state are emitted once in an optical cycle in the combined laser field.     

利用三束中红外空间非均匀激光场产生超长平台区

数值研究了氦离子在三束中红外激光场下发射高次谐波以及阿秒脉冲的特点. 计算结果表明, 通过适当调节三束激光场的延迟时间和相位角, 不仅谐波发射的截止能量得到了延伸, 而且单一的量子路径也被选择出来对谐波发射起作用, 随后通过适当的引入空间非均匀参数,谐波截止能量得到了进一步扩展,形成了一个超长的1773eV的平台区. 并且我们发现当选择氦离子的基态和第一激发态为叠加初始态时,谐波的强度被增强了4-6个数量级. 最后, 通过叠加谐波谱上的谐波, 可获得一系列脉宽为32as左右的阿秒X射线光源. 并且这些光源的强度比氦离子基态作为初始态时增强了4-6个数量级.     

利用三束中红外空间非均匀激光场产生超长平台区

数值研究了氦离子在三束中红外激光场下发射高次谐波以及阿秒脉冲的特点. 计算结果表明, 通过适当调节三束激光场的延迟时间和相位角, 不仅谐波发射的截止能量得到了延伸, 而且单一的量子路径也被选择出来对谐波发射起作用, 随后通过适当的引入空间非均匀参数,谐波截止能量得到了进一步扩展,形成了一个超长的1773eV的平台区. 并且我们发现当选择氦离子的基态和第一激发态为叠加初始态时,谐波的强度被增强了4-6个数量级. 最后, 通过叠加谐波谱上的谐波, 可获得一系列脉宽为32as左右的阿秒X射线光源. 并且这些光源的强度比氦离子基态作为初始态时增强了4-6个数量级.     

Multi-photon resonance enhanced super high-order harmonic generation

This paper proposes highly charged ions pumped by intense laser to produce very high order harmonics.Numerical simulations and full quantum theory of Ne 9+ ions driven by laser pulses at 1064 nm in the power range of 10 9 W/cm 2 ～ 10 15 W/cm 2 show that the emission spectrum corresponds to the electronic transitions from the excited states to the ground state,which is very different from the spectrum of general high-order harmonic generation.In such situation,harmonic order as high as 1000 can be obtained without producing lower order harmonics and the energy conversion efficiency is close to general high order harmonic generation of hydrogen atom in the same laser field.     

Formation mechanism of ethanol-water excimer

The fluorescent spectrum and the excitation spectrum were used to present the cluster molecular structure feature in ethanol-water solutions.Through analyzing the fluorescent characteristics of an excimer,it is proposed that the excimers are formed between the ethanol-water cluster molecules in the excited state and in the ground state.The fluorescent lifetime and the fluorescent intensity decay process give information about the photo-physical and photo-chemical processes of the formation and the dissociation of an excimer.The theoretical calculation and physical analysis coincide with the experimental results.The preliminary conclusion about the structure feature of ethanol-water cluster molecule is that it has a planar one like a sandwich.     

迭加态原子高次谐波发射的选频提高

本文研究了由体系的基态和较高激发态迭加形成的原子在强激光场作用下的高次谐波发射.观察电离波包的演化过程,阐明了谐波发射效率提高的原因.在给定入射激光条件下,通过选择不同的激发态,可以实现对谐波发射的控制.     

Harmonic Enhancement Mechanism of a Superposition State Atom Irradiated by Short Pulses

We investigate the high-order harmonic generation （HHG） of a model atom whose initial state is prepared in a superposition of its ground state and an excited state irradiated by different duration laser pulses. Compared to the HHG generated from an atom whose initial state is in its ground state, its conversion efficiency obtains some enhancement. The enhancement originates from the higher ionization rate （rather than the ionization yield） of the atom with superposition initial state.     

Theoretical Study of High-Order Harmonic Generation From a Coherent Superposition State in a Chirp-Free Pulse Combined with a Chirped Control Pulse

In this paper, we theoretically investigate high-order harmonic generation (HHG) from a helium atom prepared in a coherent superposition state in a two-color laser field. Numerical results show that the emission efficiency of the harmonic spectrum in a coherent superposition state is enhanced by approximately eight orders of magnitude compared with the case of the ground state. In addition, the effect of the initial population of the excited state on the HHG is presented to reveal the physical origin of the enhancement of HHG. By adjusting the laser parameters of the driving pulse, such as the chirping parameter, the relative phase, and the intensity of the driving pulse, an ultrabroad continuum with a width of 275 eV can be observed. Finally, an isolated 12-as pulse is generated after phase compensation.     

Isolated ultrashort attosecond pulse generation from a coherent superposition state in a few-cycle chirped laser pulse

We theoretically demonstrate an efficient method for producing an isolated ultrashort attosecond pulse by high-order harmonic generation in an intense few-cycle chirped laser pulse. Our simulation calculations show that the harmonic spectrum reveals an ultrabroad extreme ultraviolet supercontinuum when the initial state is prepared in a coherent superposition of the ground and first excited states. It is also shown that the method can enhance the short quantum path and eliminate the long one, and then an isolated 23-attosecond pulse is produced. By properly adjusting the chirp parameter, a clean single attosecond pulse as short as 11 attoseconds is directly obtained.