Two-pulse excitation for efficient formation of an sp3 nanodomain with frozen shear in a graphite crystal

We propose a two-pulse excitation to efficiently form a novel sp(3)-bonded nanosize domain with frozen shear in a graphite crystal. This sp(3) structure is well stabilized by shear displacement between two neighboring graphite layers. The shearing motion is induced transiently by the first laser pulse, and is frozen by the second pulse before disappearing, resulting in the efficient formation of the sp(3)-bonded domain with frozen shear. We show this dynamical process qualitatively by molecular dynamics calculations.     

High-intensity molecular harmonic generation without ionization

We theoretically investigate high-order harmonic generation from H + 2 in an infrared laser field.Our numerical simulations show that a highly efficient plateau structure exists in the molecular harmonic spectrum.Under the action of the infrared laser pulse,the bound electronic wave packet in a potential well has enough time to tunnel through the effective potential barrier,which is formed by the molecular potential and the infrared laser field,and then recombine with the neighboring nucleus emitting a harmonic photon.During the entire dynamic process,because the wave packet is mainly located in the effective potential,the diffusion effect is of no significance,and thus a highly efficient harmonic plateau can be achieved.Specifically,the cut-off frequency of the plateau is linearly scaled with the peak amplitude of the infrared laser electric field,which may open another route to examine the internuclear distance of the molecule.Furthermore,one may detect the molecular bond lengths using the harmonic plateau.     

Ultrabroadband background-free coherent anti-Stokes Raman scattering microscopy based on a compact Er:fiber laser system

We demonstrate a scheme for efficient coherent anti-Stokes Raman scattering (CARS) microscopy free of nonresonant background. Our method is based on a compact Er:fiber laser source. Impulsive excitation of molecular resonances is achieved by an 11 fs pulse at 1210 nm. Broadband excitation gives access to molecular resonances from 0 cm(-1) up to 4000 cm(-1). Time-delayed narrowband probing at 775 nm enables sensitive and high-speed spectral detection of the CARS signal free of nonresonant background with a resolution of 10 cm(-1).     

Molecular alignment by trains of short laser pulses

We show that a dramatic field-free molecular alignment can be achieved after exciting molecules with proper trains of strong ultrashort laser pulses. Optimal two- and three-pulse excitation schemes are defined, providing an efficient and robust molecular alignment. This opens new prospects for various applications requiring macroscopic ensembles of highly aligned molecules.     

Temporal pulsewidth and the wavelength dependences of the product ions obtained by laser ablation of solid C<Subscript>60</Subscript>

By ablating solid C₆₀ with a laser pulse, we observe various processes such as the prompt- and the delayed-ionization of C₆₀, the fragmentation into molecular ions and the formation of cluster ions. We found these processes show distinct dependences on the temporal pulse width, the power and the wavelength of the ablation laser. From the observations, we could confirm efficient coupling of laser energy to C₆₀ through the molecular absorption even with a laser pulse width less than the electron-phonon coupling time of the C₆₀ molecule.     

一种新颖的全光型表面原子(分子)漏斗

提出了一种产生全光型表面原子(分子)漏斗的新方案.采用红失谐高斯激光束照明由柱面透镜组成的光学系统，可在透镜焦平面附近产生横向漏斗形光强分布，以构成一表面光波导型原子漏斗.计算了漏斗的光强分布及其光学偶极势与偶极力分布.研究结果表明：该原子漏斗可用于冷原子(分子)的表面光波导、分束器和干涉仪以及微阱囚禁的有效装载，因而在集成原子光学及其原子芯片的研究中有着重要的应用. 关键词： 原子漏斗 分子漏斗 光学偶极势 原子芯片     

Surface chemistry and growth mechanisms studies of homo epitaxial (1 0 0) GaAs by laser molecular beam epitaxy

In this paper, GaAs thin film has been deposited on thermally desorbed (1 0 0) GaAs substrate using laser molecular beam epitaxy. Scanning electron microscopy, in situ reflection high energy electron diffraction and in situ X-ray photoelectron spectroscopy are applied for evaluation of the surface morphology and chemistry during growth process. The results show that a high density of pits is formed on the surface of GaAs substrate after thermal treatment and the epitaxial thin film heals itself by a step flow growth, resulting in a smoother surface morphology. Moreover, it is found that the incorporation of As species into GaAs epilayer is more efficient in laser molecular beam epitaxy than conventional molecular beam epitaxy. We suggest the growth process is impacted by surface chemistry and morphology of GaAs substrate after thermal treatment and the growth mechanisms are discussed in details.     

Short-laser-pulse-driven emission of energetic ions into a solid target from a surface layer spalled by a laser prepulse

An efficient emission of picosecond bunches of energetic protons and carbon ions from a thin layer spalled from a organic solid by a laser prepulse is demonstrated numerically. We combine the molecular dynamics technique and multi-component collisional particle-in-cell method with plasma ionization to simulate the laser spallation and ejection of a thin (∼20–30 nm) solid layer from an organic target and its further interaction with an intense femtosecond laser pulse. In spite of its small thickness, a layer produced by laser spallation efficiently absorbs ultrashort laser pulses with the generation of hot electrons that convert their energy to ion energy. The efficiency of the conversion of the laser energy to ions can be as high as 20%, and 10% to MeV ions. A transient electrostatic field created between the layer and surface of the target is up to 10 GV/cm. Received: 13 March 2001 / Accepted: 20 March 2001 / Published online: 20 June 2001     

Double Ionization Dynamics of Molecular Hydrogen in Ultrashort Intense Laser Fields

We experimentally investigate the double ionization of molecular hydrogen subjected to ultrashort intense laser pulses.The total kinetic energy release of the two coincident H~+ ions,which provides a diagnosis of different processes to double ionization of H_2,is measured for two different pulse durations,i.e.,25 and 5fs,and various laser intensities.It is found that,for the long pulse duration(i.e.,25 fs),the double ionization occurs mainly via two processes,i.e.,the charge resonance enhanced ionization and recollision-induced double ionization.Moreover,the contributions from these two processes can be significantly modulated by changing the laser intensity.In contrast,for a few-cycle pulse of 5fs,only the recollsion-induced double ionization survives,and in particular,this process could be solely induced by the first-return recollision at appropriate laser intensities,providing an efficient way to probe the sub-laser-cycle molecular dynamics.     

Tunable carbon monoxide overtone laser sideband system for precision spectroscopy from 2.6 to 4.1 microm

We report a source of tunable laser radiation for high-precision molecular spectroscopy in the 2.6- 4.1-microm spectral region. Laser light from a CO overtone laser is mixed with microwaves, generating tunable sidebands of ~1 mW of power. We achieve very high absolute frequency accuracy by frequency-offset locking the CO laser to a CO(2) laser secondary frequency standard. The uncertainty of the laser frequency is less than 30 kHz (Dnu/nu=3x10(-10)) , and the laser linewidth is of the order of 100 kHz. This tunable and ultrastable laser system is suitable for very accurate molecular spectroscopy and metrology in a most interesting wavelength region. We demonstrate an application of the system to saturated-absorption spectroscopy of a rovibrational transition of carbonyl sulfide.     

fs-pulse synthesis using phase modulation by impulsively excited molecular vibrations

We report the temporal characteristics of laser radiation transmitted through impulsively excited SF6 and exhibiting sideband Raman lines. Even without special dispersion control we observed a sequence of compressed fs pulses following with the period of the excited A(1g) vibrational mode of SF6. The use of both negative and positive group velocity dispersion compensation for the temporal compression was found to be as appropriately efficient. The results prove our new concept of the ultrafast molecular phase modulator.     

Simulation and experiment of the cooling effect of trapped ion by pulsed laser

We investigate the process of pulsed laser cooling using a self-constructed molecular dynamics simulation(MDSimulation) program. We simulate the Doppler cooling process and pulsed laser Doppler cooling process of a single ~(40)Ca~+ ion, and the comparison with the experimental results shows that this self-constructed MD-Simulation program works well in the weak laser intensity situation. Furthermore, we analyze the pulsed laser Doppler cooling process of a single ~(27)Al~+ ion. This program can be used to analyze the molecular dynamic process of various situations of Doppler cooling in an ion trap, which could give predictions and experimental guidance.     

Control the revisit time of the electron wave packet

Ionization of molecules by strong laser fields launches an electron wave packet. This electron wave packet, which can be driven back by the field to recollide with the parent ion, has been widely explored to probe the ultrafast nuclear dynamics. We numerically demonstrate the precise control of the temporal characteristic of the recolliding electron wave packet (REWP) by orthogonally polarized two-color fields. Through changing the relative phase of the two fields, the revisit time of REWP can be manipulated with a resolution of less than 200 attos, thus significantly improving the resolution of the well known molecular clock. This provides an efficient method for real-time observation of the ultrafast molecular dynamics with attosecond resolution.     

Demonstration of highly efficient broadband amplification in a optical parametric chirped-pulse amplifier system

We have demonstrated highly efficient broadband amplification by an optical parametric chirped pulse amplifier (OPCPA) system that uses high energy seed pulses. The OPCPA consists of three type I B-barium borate (BBO) crystals pumped by a Q-switched Nd:YAG laser. We successfully amplified the microjoule level seed pulses to 78 mJ with a pump-to-signal optical conversion efficiency of 26% at a 10 Hz repetition rate. To our knowledge these results represent the most optically efficient OPCPA to date pumped by a typical Q-switched laser.     

2.1 microm continuous-wave Raman laser in GeO2 fiber

We report 33% efficient generation of the first Stokes in a high-concentration GeO(2) fiber Raman laser pumped by a 22 W thulium-doped fiber laser. An output power of 4.6 W at 2.105 microm is demonstrated.     

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.     

Dynamical analysis of the effect of elliptically polarized laser pulses on molecular alignment and orientation

In this Letter, we study the molecular alignment and orientation driven by two elliptically polarized laser pulses.It is shown that the field-free molecular alignment can be achieved in a three-dimensional(3D) case, while the field-free molecular orientation is only along the x and y directions, and that the field-free alignment and orientation along different axes are related to the populations of the rotational states. It is demonstrated that changing the elliptic parameter is efficient for controlling both in-pulse and post-pulse molecular alignment and orientation. The delay time also has an influence on the field-free molecular alignment and orientation.     

Field-free molecular orientation enhanced by tuning the intensity ratio of a three-color laser field

We theoretically study the field-free molecular orientation induced by a three-color laser field. The three-color laser field with a large asymmetric degree can effectively enhance the molecular orientation. In particular, when the intensity ratio of the three-color laser field is tuned to a proper value of I_3: I_2: I_1= 0.09 : 0.5 : 1, the molecular orientation can be improved by ～ 20% compared with that of the two-color laser field at intensity ratio I_2: I_1= 1 : 1 for the same total laser intensity of 2×10~(13)W/cm~2. Moreover, we investigate the effect of the carrier-envelope phase(CEP) on the molecular orientation and use the asymmetric degree of the laser field to explain the result. We also show the influences of the laser intensity, rotational temperature, and pulse duration on the molecular orientation. These results are meaningful for the theoretical and experimental studies on the molecular orientation.     

Diode-pumped continuous-wave Nd:LuVO4 laser operating at 916 nm

We realized an efficient diode-pumped Nd:LuVO4 continuous-wave (CW) laser operating at 916 nm. Laser experiments with 0.5 at. % Nd-doped Nd:LuVO4 crystals of various lengths and cutting directions were also investigated. The maximum output power of 930 mW was obtained with a slope efficiency of 27.2% and an optical conversion efficiency of 20.8% at the absorbed pump power of 4.5 W. The laser experiment shows that Nd:LuVO4 crystal can be used for an efficient diode-pumped laser system.