一维多原子分子离子与超短激光场作用产生的高次谐波

从经典方程出发，采用克兰克-尼科尔森中心差分法对一维多原子分子离子与一维超短强激光场相互作用产生的高次谐波进行了数值模拟计算，发现激光场的初始相位对高次谐波辐射谱有明显影响；通过进一步研究，给出了初步解释。从而，可以通过调节适当的激光初始相位和选取适当的系统来改善高次谐波的相位匹配，产生清晰的高次谐波辐射谱。     

一维模型原子在组合脉冲辐照下的高次谐波发射

本文采用SMT（sknple man’s theory）仔细分析了一维普薛耳-特勒势（P—T势）模型原子在高、低频组合强激光脉冲辐照下电子的动力学行为。并且，在此基础上，着力讨论了电离电子在激光脉冲策动下回核并与之复合从而发射高次谐波的平台结构，采用一种特殊设计的高、低频脉冲组合方案。使谐波发射效率较之于只用单一低频激光时的谐波发射效率提高两个数量级。     

强激光场中长程势与短程势原子产生高次谐波与电离特性研究

用数值方法求解含时薛定谔方程，研究了具有长程势和短程势的一维原子在强激光场中的高次谐波和电离特性. 在强激光场中，长程势和短程势原子产生的高次谐波具有相似的特性，对应的平台和截止位置相同，但是短程势原子没有低阶的高次谐波，而长程势和短程势原子在激光场中的电离概率明显不同. 研究结果表明，原子的激发态结构对低阶的高次谐波和原子的电离概率有重要影响. 关键词： 强激光场 高次谐波 电离概率     

一维模型原子在组合脉冲辐照下的高次谐波发射

本文采用SMT (simple man's theory) 仔细分析了一维普薛耳-特勒势(P-T势)模型原子在高、低频组合强激光脉冲辐照下电子的动力学行为.并且, 在此基础上,着力讨论了电离电子在激光脉冲策动下回核并与之复合从而发射高次谐波的平台结构.采用一种特殊设计的高、低频脉冲组合方案,使谐波发射效率较之于只用单一低频激光时的谐波发射效率提高两个数量级.     

用TDMA法计算谐振子在强激光脉冲下的高次谐波

用含时薛定谔方程的多态展开(TDMA)方法求解含时薛定谔方程。该方法将含时波函数以基函数展开，通过求解展开系数的一阶微分方程组得到任意时刻的波函数。并将这一方法用于强激光场中谐振子的高次谐波的计算，以HCl分子为例，计算了在脉冲激光作用下高次谐波的产生和对应的激光强度、波长和脉冲宽度。     

晶体环境下高次谐波谱的截止频率分析

通过数值求解中红外飞秒光脉冲与一维单电子多阱势相互作用的含时薛定谔方程, 研究了晶体环境下的高次谐波发射光谱, 发现了晶体谐波谱的截止位置公式.研究发现, 不同于气体环境下的谐波谱截止频率规律, 晶体谐波谱的截止频率与激光电场的峰值振幅及晶格参数成线性关系. 鉴于准经典力学的三步模型对于气体谐波截止频率的解释, 进一步采用准经典力学方法验证了晶体谐波截止位置规律的正确性. 关键词： 中红外飞秒光脉冲 晶体 高次谐波 截止频率     

用TDMA法计算谐振子在强激光脉冲下的高次谐波

用含时薛定谔方程的多态展开(TDMA)方法求解含时薛定谔方程.该方法将含时波函数以基函数展开,通过求解展开系数的一阶微分方程组得到任意时刻的波函数.并将这一方法用于强激光场中谐振子的高次谐波的计算,以HCl分子为例,计算了在脉冲激光作用下高次谐波的产生和对应的激光强度、波长和脉冲宽度.     

激光等离子体中由共振吸收诱发的高次谐波

用电容器模型计算了激光打靶过程中由共振吸收诱发的高效谐波，并在此基础上讨论了超短脉冲强激光的高次谐波作为一种短波长相干辐射源的可能性。     

强激光场中N2分子高次谐波的干涉效应

在强场近似下,利用Lewenstein模型研究了N2分子在强激光场中发射高次谐波的干涉效应,通过对N2分子产生的高次谐波和分子中单个原子产生高次谐波的比较,表明了干涉效应的存在. 得出随着高次谐波阶数的增加,干涉极小值会随着分子轴与激光偏振方向间夹角的增加而减小,在角度接近900附近时干涉效应消失,与两中心干涉模型预测的趋势一致. 通过分析高次谐波产生的机制和相位随取向角的变化,给出了干涉产生的原因.     

强激光和稠密等离子体相互作用产生的三次谐波

研究了超强激光和均匀及线性梯度高密度等离子体相互作用产生的三次谐波，特别研究了等离子体密度为四倍临界密度时的情形，这可能是用相对论效应产生高效谐波的最佳密度。     

超短脉冲谐波截止区量子效应研究

采用Lewenstein路径积分模型和准经典三步模型,计算了不同脉宽的超短脉冲高次谐波波谱。通过比较模型截止频率随载波包络相位的变化关系的差异,对辐射过程中的量子效应进行了研究。结果显示,随脉宽的减小,以上两种模型计算结果出现的偏离增加,谐波辐射中的量子效应愈加明显。当脉宽减小至0.5 T(T为光学周期)时,准经典三步模型已不能用以解释Lewenstein模型的计算结果。     

Effects of Pulse Durations on High-order Harmonic Generation

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Ionization and Harmonic Generation of Diatomic Molecular Ion

l.IntroductionRecentexPerimentshavcdemonstratedthehigh-orderharmonicgenerationinraregasandmoleculargas[1~'j.TherearemanytheoreticalpaPersdealingwithharmonicgen-erationofatom[6~8j,comparativelysPeaking,theoreticalworksabouttheharmonicgen-erationofmolecuIeareless[9j,esPeciallyabouttheevolutionofionizationandharmonicgenerationwiththeinternuclearseparation,andtherelationbetweenionizationandhar-monicgeneration.InthispaPerwegivesomenumericalresultsofdiatomicmolecularionirradiatedbyalinearlyPOlari…     

7 fs超快强激光驱动Ar原子产生支持单个阿秒脉冲的高次谐波连续谱

采用脉冲宽度为7 fs,脉冲能量为0.4 mJ的超快强激光脉冲与气体盒子中Ar原子作用获得了高次谐波截止区连续谱,并发现当驱动激光稳定在不同的载波包络相位时,高次谐波的谱结构、谱调制深度和连续谱的带宽都有很大区别。在某些载波包络相位时获得了平滑的连续谱,调制深度小于17%,连续带宽达10 eV,从而支持时域上获得变换极限500 as的单个阿秒脉冲。     

Harmonic Extension and Enhancement Using a Two-Color Chirped Pulse and an Ultrashort Ultraviolet Pulse

A promising method to both extend the harmonic energy and enhance the harmonic intensity is presented when a He atom is exposed to the combination of a two-color chirped pulse and an ultrashort ultraviolet pulse. It is found that: (1) with the introduction of the two chirps, the harmonic energy has been remarkably extended; (2) by properly adding an ultrashort ultraviolet pulse to this synthesized two-color chirped pulse, the harmonic yield is enhanced by 3 orders of magnitude compared with the two-color chirped case; (3) the harmonic spectrum higher than the 96th order shows an ultrabroad supercontinuum with a 395 eV bandwidth, and the proper superposition over the harmonics directly produced a series of intense 40 as pulses which is 3 orders of magnitude higher than that in the two-color chirped case.     

Extension of Harmonic Cutoff and Generation of Isolated Sub-30 as Pulse in a Two-Color Chirped Laser Field

We theoretically investigate high-order harmonic and isolated attosecond pulse generation in a two-color chirped laser field,which is synthesized by a 9 fs/800 nm fundamental chirped pulse and a 9 fs/1600 nm controlling chirped pulse.Our numerical results show that,by using this method,not only is the harmonic cutoff significantly extended to the 948th order harmonic,but also the bandwidth of the supercontinuum spectrum is effectively broadened to about 1342 eV.In addition,due to the introduction of the chirp,the long quantum path is suppressed and only the short one is selected,and then an isolated 28 as pulse with a bandwidth of 155 eV is obtained directly.     

Single Ultrashort Attosecond Pulse Generation via Combination of Chirped Fundamental Laser and an Ultraviolet Controlling Pulse

We theoretically study the high-order harmonic generation (HHG) from a hydrogen atom in an intense few-cycle chirped fundamental laser in combination with an ultraviolet (uv) controlling pulse.The high-order harmonic spectrum is calculated by solving the time-dependent Schr¨odinger equation using the split-operator method.In our calculation,we present the difference of the high-order harmonic spectrum from one-dimensional (1D) model hydrogen atom and three-dimensional (3D) real hydrogen atom.We found that the plateau of the high-order harmonic generation from the 1D case and 3D case are all extended effectively to I p + 35U p due to the presence of the chirped laser pulse and the HHG supercontinuum spectrum is generated by adding an ultraviolet controlling pulse at a proper time,but the efficiency of the HHG for 3D case is more higher at the near cut-off region than the 1D case.Therefore,the generation of the attosecond pulse by synthesizing the harmonics near cut-off region have some slight differences between 1D and 3D simulations.As a real 3D case study,we show that an isolated 18 as pulse with a bandwidth of 232.5 eV is generated directly by optmizing the combination laser fields.     

椭圆偏振强激光场中准直的乙炔分子的高次谐波发射

We perform an experimental study on high-order harmonic generation (HHG) of aligned acetylene molecules induced by a 35-fs 800-nm strong laser field, by using a home-built HHG spectrometer. It is observed that the molecular HHG probability declines with increasing the laser ellipticity, which is in consistence with the deduction from the well-known tunneling-plus-rescattering scenario. By introducing a weak femtosecond laser pulse to nonadiabatically align the molecules, we investigated the molecular orbital effect on the HHG in both linearly and elliptically polarized driving laser fields. The results show that the harmonic intensity is maximum for the molecular axis aligned perpendicularly to the laser electric field. It indicates that both the highest occupied molecular orbitals (HOMO) and HOMO-1 contribute to the strong-field HHG of acetylene molecules. Our study should pave the way for understanding the interaction of molecules with ultrafast strong laser fields.     

Theoretical Exploration of the Isotopic Effect on Molecular High-Order Harmonic Generation

The isotopic effect on the generation of the molecular high-order harmonics is studied by numerically solving the one-dimensional time-dependent Schrödinger equation when the model hydrogen molecule ions/hydrogen deuterium molecule ions are exposed to an intense laser pulse. To explain the effect more clearly, not only the ionization probabilities but also the electron–nuclear probability density distributions and time-frequency profiles are calculated. The results show that more intense harmonics are generated in the asymmetric diatomic molecule ions/hydrogen deuterium molecule ions than those of hydrogen molecule ions. Moreover, the interference minimum in the harmonic spectra is investigated by adjusting the laser intensity and the initial vibrational state. It is shown that the interference minimum is sensitive to the laser intensity and the initial vibrational level for hydrogen molecule ions; in contrast, it is only dependent on the initial vibrational level for hydrogen deuterium molecule ions.     

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.