Molecular state reconstruction by nonlinear wave packet interferometry

We show that time- and phase-resolved two-color nonlinear wave packet interferometry can be used to reconstruct the probability amplitude of an optically prepared molecular wave packet without prior knowledge of the underlying potential surface. We analyze state reconstruction in pure- and mixed-state model systems excited by shaped laser pulses and propose nonlinear wave packet interferometry as a tool for identifying optimized wave packets in coherent control experiments.     

分子的飞秒强光电离

文章以一个实验者的角度，介绍了分子的飞秒强光电离的研究现状。文章从对比飞秒激光电离质谱与纳秒激光电离质谱开始，接着介绍分子在激光场作用下的可能电离机理，着重描述了几个处理分子场致电离的理论模型和实验验证，最后对飞秒激光导致的分子在激光脉冲作用后取向研究进行了简单介绍。     

分子的飞秒强光电离

文章以一个实验者的角度,介绍了分子的飞秒强光电离的研究现状.文章从对比飞秒激光电离质谱与纳秒激光电离质谱开始,接着介绍分子在激光场作用下的可能电离机理,着重描述了几个处理分子场致电离的理论模型和实验验证,最后对飞秒激光导致的分子在激光脉冲作用后取向研究进行了简单介绍.     

Theoretical study of the influence of intense femtosecond laser field on the evolution of the wave packet and the population of NaRb molecule

Employing the two-state model and the time-dependent wave packet method, we have investigated the influences of the parameters of the intense femtosecond laser field on the evolution of the wave packet, as well as the population of ground and double-minimum electronic states of the NaRb molecule. For the different laser wavelengths, the evolution of the wave packet of 6{ }^1\Sigma ^ + state with time and internuclear distance is different, and the different laser intensity brings different influences on the population of the electronic states of the NaRb molecule. One can control the evolutions of wave packet and the population in each state by varying the laser parameters appropriately, which will be a benefit for the light manipulation of atomic and molecular processes.     

The shift of atomic ground state by a limited nonresonant moderately strong laser field

The shift of the atomic ground state due to the interaction with an external limited nonresonant laser field and vacuum fluctuation is calculated in resolvent formalism. The shift operator ¯R is taken to the fourth order of perturbation expansion. It is shown that the term which mixes these two interactions gives a slight correction to the total shift, which can be expressed by the Lamb shift of the excited state.     

Controlling vibrational wave packet motion with intense modulated laser fields

Intense, nonresonant laser fields produce Stark shifts that strongly modify the potential energy surfaces of a molecule. A vibrational wave packet can be guided by this Stark shift if the laser field is appropriately modulated during the wave packet motion. We modulated a 70 fs laser pulse with a period on the time scale of the vibrational motion (approximately 10 fs) by mixing the signal and idler of an optical parametric amplifier. We used ionization of H2 or D2 to launch a vibrational wave packet on the ground state of H2(+) or D2(+). If the laser intensity was high as the wave packet reached its outer turning point, the Stark shift allowed the molecule to dissociate through bond softening. On the other hand, if the field was small at this critical time, little dissociation was measured. By changing the modulation period, we achieved control of the dissociation yield with a contrast of 90%.     

Quantum reconstruction of an intense polarization squeezed optical state

We perform a reconstruction of the polarization sector of the density matrix of an intense polarization squeezed beam starting from a complete set of Stokes measurements. By using an appropriate quasidistribution, we map this onto the Poincaré space, providing a full quantum mechanical characterization of the measured polarization state.     

Selective excitation of the molecular rotational wave packet by two time-delayed laser pulses

In this paper, we investigate the control of the molecular wave packet of a linear molecule by two femtosecond laser pulses. It is shown that the odd and the even rotational wave packets created by a single laser pulse can be selectively excited by accurately controlling the time delay of another laser pulse. By inserting the peak of the second laser pulse at the position of maximum or minimum value around quarter or three quarter rotational period of the slope curve with odd (or even) rotational wave packet contribution that is created by the first laser pulse, the odd rotational wave packet can be enhanced (or suppressed) while the even rotational wave packet is suppressed (or enhanced). As a result, the molecular alignments around quarter and three quarter rotational periods can be obtained. Moreover, it is also shown that by inserting the second laser pulse around the quarter or three quarter rotational periods, the changes in the maximum degree of the molecular alignment for the odd and the even rotational wave packet contributions are consistent with their corresponding slope curves at these positions.     

Photoemission of a single-electron wave packet in a strong laser field

The radiation emitted by a single-electron wave packet in an intense laser field is considered. A relation between the exact quantum formulation and its classical counterpart is established via the electron's Wigner function. In particular, we show that the wave packet, even when it spreads to the scale of the wavelength of the driving laser field, cannot be treated as an extended classical charge distribution, but rather behaves as a pointlike emitter carrying information on its initial quantum state. We outline an experimental setup dedicated to put this conclusion to the test.     

Quantum control by selective population of dressed states using intense chirped femtosecond laser pulses

The physical mechanism of strong field quantum control using chirped femtosecond laser pulses is investigated. Dressed state control is exerted by making explicit use of the temporal phase changes of the pulse. In our experiment, the dressed state population is mapped by photoelectron spectra from simultaneous excitation and ionization of potassium atoms as a function of the chirp parameter. We show that chirped pulses can be used to selectively steer ground state atoms temporarily into a single dressed state realizing transient Selective Population of Dressed States (SPODS). PACS 32.80.Qk; 32.80.Rm; 33.80.Rv     

飞秒强激光场中氢原子团簇的各向异性膨胀

利用LAMMPS程序研究了氢原子团簇在飞秒强激光场下的动力学行为, 讨论了引起小氢原子团簇各向异性膨胀的原因.通过对外电离过程中团簇内部电子的行为以及团簇各个方向上最外层质子距离团簇中心的距离随时间的变化情况的分析, 发现团簇的膨胀呈现各向异性,且引起这种各向异性的根源在于团簇内部电子的抖动以及逃逸.对氢原子团簇与强激光场相互作用过程中质子各能量分量以及各向异性程度随时间变化情况进行了研究,发现各向异性程度是随时间变化的, 这种各向异性程度首先随着激光电场的增强而增加,随后又逐渐减小,直到最后趋于某一大于1的稳定值.分析了激光脉冲结束后质子的平均能量与观测角之间的关系, 并将分析结果与Ditmire小组的实验结果进行了比较,发现我们的模拟结果在定性上与实验相符合.     

Quantum interference of a time-dependent wave packet of atom irradiated by an ultra-short laser pulse

The wave packet evolution of an atom irradiated by an intense laser pulse is systematically investigated by using the numerical solution of the time-dependent Schr ?dinger equation. There are two types of spatial interference structures in the time-dependent evolution of the atomic wave packet. With the increasing of the evolution time, the interference fringe spacing for type Ⅰ(type Ⅱ) becomes larger(smaller). As the wavelength of the incident laser increases, the interference of the wave packet is changed from type Ⅱ to type Ⅰ, and the shift of interference type can be attributed to the contribution of excited states by using the energy analysis of the time-dependent wave function.     

Quantum teleportation of a single-photon wave packet

A quantum teleportation scheme based on the EPR-pair entangled with respect to the “energy+time” variables is proposed. Teleportation of the multimode state of a single-photon wave packet is considered.     

Achromatic reconstruction of the wave front of femtosecond laser pulses

Wave-front reconstruction by geometric-optical reflection of the reconstructing radiation from interference surfaces of a structure recorded in the bulk of a medium by counterpropagating laser pulses is observed. The recording is done with the aid of a sapphire titanate laser. Pulse durations of 30–40 fs are used. Pis’ma Zh. éksp. Teor. Fiz. 65, No. 5, 388–390 (10 March 1997)     

Hard X-ray emission by clusters in an intense femtosecond laser field during collective recombination

We consider the new mechanism of X-ray generation by clusters under irradiation by femtosecond laser pulses, the so-called collective photorecombination. We develop the theory of the photo-recombination of electrons that pass from atomic clusters at the outer ionization to the ground level of a homogeneously charged cluster. Such a cluster is considered to be a quantum potential well. The dipole approximation is inapplicable for this process. We conclude that X-ray photons in collective photorecombination on a charged cluster as a whole have an energy that is much larger than that for photorecombination on separate atomic ions inside the cluster. For a typical cluster of 2.25 × 10⁶ electrons, with a radius R = 300 Å, and a number density of plasma electrons n _e = 2 × 10²² cm^?3, we find that at a 5% outer ionization of this cluster, the energy of hard X-ray photons is 7.2 keV.     

Chirping-dependent ionization and dissociation of methane in an intense femtosecond laser field

We studied the ionization and dissociation of polyatomic molecule methane in an intense femtosecond laserfield with wavelength of 810 nm and intensities ranging from 1.4×10~(14)to 2.6×10~(15) W/cm~2 by massspeetroscopy.Abundant fragment inos were observed in addition to the strong parent ion.The effect offrequency chirp was investigated and it was found that the negatively chirped pulses dramatically enhancedthe dissociation probability,which might be used to control the dissociation pathways.     

Coulomb explosion of CS_2 molecule under an intense femtosecond laser field

We experimentally demonstrate the Coulomb explosion process of CS_2 molecule under a near-infrared(800 nm)intense femtosecond laser field by a DC-sliced ion imaging technique. We obtain the DC-sliced images of these fragment ions S~+, S~(2+), CS~+, and CS~(2+)by breaking one C–S bond, and assign their Coulomb explosion channels by considering their kinetic energy release and angular distribution. We also numerically simulate the dissociation dynamics of parent ions CS_2~(k+)(k = 2–4) by a Coulomb potential approximation, and obtain the time evolution of Coulomb energy and kinetic energy release, which indicates that the dissociation time of parent ions CS_2~(k+) decreases with the increase of the charge number k.These experimental and theoretical results can serve as a useful benchmark for those researchers who work in the related area.     

Ultracold atom-atom collisions in a nonresonant laser field

Using a recently developed approach for treating the three-dimensional anisotropic scattering we find considerable influence of a nonresonant laser field with intensity I> or =10(5) W/cm(2) on the Cs-Cs ultracold collisions. Strong dependence on the laser wavelength lambda(L) is shown at the optical region as lambda(L) becomes shorter than the critical value lambda(0) approximately 3000 nm (of the atomic de Broglie wave lambda) defining the region lambda(0)< or =lambda of the s-wave domination in the absence of the external field. Dependence on the laser polarization is also essential. The found effect can be applicable for controlling atom-atom interactions at ultralow temperatures.     

Photoelectron imaging on time-dependent molecular alignment created by a femtosecond laser pulse

Rotational wave packet revivals on an excited electronic state have been measured by femtosecond time-resolved photoelectron imaging for the first time. The first full revival at 82 ps of S1 (n,pi*) pyrazine was clearly observed in the time dependencies of the photoelectron intensity and the photoelectron angular distribution (PAD). The PAD, measured for laser aligned pyrazine, clearly reflects the different characters of pi* and 3s molecular orbitals.     

Quantum instability for a wave packet kicked periodically by a quadratic potential

The quantal behaviour of wave packet periodically kicked by a quadratic potential has been investigated using Floquet theory. The wave function of the particle afterN kicks has been determined. This wave function has been utilized to obtain the packet width, energy and loss of memory as a function of the number of kicks. It has also been shown that the free particle wave packet quasienergy spectrum makes a transition from discrete to absolutely continuous atɛ T=2. The behaviour forɛT>2 is quantum mechanically irregular.