Femtosecond laser induced nanostructuring of zirconium in liquid confined environment

The surface, structural, and mechanical properties of zirconium after irradiation with Ti: sapphire laser(800 nm, 30 fs,1 k Hz) have been investigated. The zirconium targets were exposed for a varying number of laser pulses ranging from 500 to 2000 at a fixed fluence of 3.6 J/cm~2 corresponding to an intensity of 1.2×10~(14)W/cm~2 in ambient environments of deionized water and propanol. A scanning electron microscope(SEM) was employed to investigate the surface morphology of the irradiated zirconium. The SEM analysis shows the formation of various kinds of features including nanoscale laser induced periodic surface structures(LIPSS), sponge like surface structure, flakes, conical structures, droplets, pores, and cavities. The energy dispersive x-ray spectroscopy(EDS) analysis exhibits the variation in chemical composition along with an enhanced diffusion of oxygen under both ambient conditions. The crystal structure and phase analyses of the exposed targets were explored by x-ray diffraction(XRD) and Raman spectroscopy techniques, respectively. The XRD analysis confirms the presence of various phases of zirconium hydride and zirconia after ablation in both de-ionized water and propanol. However, excessive hydrides are formed in the case of propanol. The Raman analysis supports the EDS and XRD results. It also reveals the presence of oxides(zirconia) after irradiation in both de-ionized water and propanol environments.The chemical reactivity of zirconium was significantly improved in the presence of liquids which were accountable for the growth of novel phases and modification in the chemical composition of the irradiated Zr. A nanohardness tester was employed to measure the nanohardness of the laser treated targets. The initial increase and then decrease in nanohardness was observed with an increase in the number of laser pulses in the de-ionized water environment. In the case of propanol,a continuous decrease in hardness was observed.     

PTCDA分子基态的飞秒激光控制研究

将优化控制理论和多组态含时Hartree（MCTDH）方法相结合,建立了适合于MCTDH方法的计算具有平面结构的PTCDA分子的多自由度振动量子模型,研究了在PTCDA分子激发后从分子激发态回落至分子基态的动力学过程.在理论上分析了约化目标态产生率与激发脉冲、分子的演变时间及优化场的有效能量之间的关系,对分子在各个振动坐标下波函数的振动分布做了分析与比较.研究发现,增加分子的回落演变时间在提高目标态产生率的同时可以使优化激光控制场的强度降低,这为实验上用低能量激光最大程度地实现目标态提供了有效手段. 关键词： PTCDA 多组态含时Hartree方法 飞秒激光控制     

Femtosecond laser induced nanostructure formation: self-organization control parameters

In self-organized nanostructure formation upon femtosecond laser ablation, the laser polarization is an important control parameter. Experiments on fluoride crystals, using circular and elliptical polarization, study this influence in more detail. For circular polarization, spherical nanoparticles of about 100 nm diameter are formed. With increasing ellipticity, longer and longer ordered chains and linear structures are generated, oriented perpendicular to the long axis of the polarization ellipse. A similar effect occurs when, for circular polarization, the angle of incidence is varied from normal to 45°: the s-component of the incident field, not attenuated by the projection, determines length and orientation of the ordered ripples. However, surface defects like scratches exert an even stronger influence on the ripples orientation than the polarization, resulting in curved structures bending from polarization-controlled to defect-controlled orientation. Since the structure formation takes place only long after the end of the laser pulse, a certain electrical field memorizer is required to account for this polarization dependence. A promising approach assumes directional atomic surface diffusion anisotropies, arising, e.g. from plasmon-coupled metal–colloid arrays.     

Femtosecond laser nanostructuring of a tungsten surface

Tungsten surface nanostructuring is performed using the radiation of a Yb:KGW femtosecond laser in air and in liquid nitrogen. Arrays of linear nanostructures and nanorods of tungsten and tungsten nitride are fabricated on the surfaces of targets. Possible scenarios of transforming surface nanostructures of one type into another and the formation of network-like relief are considered.     

Femtosecond petawatt laser

The high‐power femtosecond laser has now become an excellent scientific tool for the study of not only relativistic laser–matter interactions but also scientific applications. The high‐power femtosecond laser depends on the Kerr‐lens modelocking (KLM) and chirped‐pulse amplification (CPA) technique. An all‐Ti:sapphire‐based 30‐fs PW CPA laser, which is called the PULSER (Petawatt Ultrashort Laser System for Extreme Science Research) has been recently constructed and is being used for accelerating the charged particles (electrons and protons) and generating ultrashort high‐energy photon (X‐ray and γ‐ray) sources. In this review, the world‐wide PW‐level femtosecond laser systems are first summarized, the output performances of the PULSER‐I & II are described, and the future upgrade plan of the PULSER to the multi‐PW level is also discussed. Then, several experimental results on particle (electron and proton) acceleration and X‐ray generation in the intensity range of mid‐10¹⁸ W/cm² to mid‐10²⁰ W/cm² are described. Experimental demonstrations for the newly proposed phenomena and the understanding of physical mechanisms in relativistic and ultrarelativistic regimes are highly expected as increasing the laser peak intensity up to over 10²² W/cm² ～10²³ W/cm².     

飞秒激光精密微纳加工的研究进展

飞秒激光由于其超快时间特性和超高峰值功率特性在精密微纳加工领域引起了人们广泛的重视．在与物质的相互作用中它能快速、准确地将能量作用在特定的区域内，从而可以获得极高的分辨率和加工精度。文章综述了飞秒激光精密微纳加工的最新研究进展，分别就飞秒激光烧蚀微加工和飞秒激光双光子聚合产生三维微纳结构进行了介绍，阐述了各自的物理机制．最后对飞秒激光微纳加工的研究前景做了初步探讨。     

Femtosecond laser ablation of DAST

High rate femtosecond (fs) laser ablation of the organic salt 4-N,N-dimethylamino-4-N-methyl-stilbazolium tosylate (DAST), an organic crystal with very high optical nonlinearities has been demonstrated. The threshold fluence and the ideal fluence range for damage free ablation for the wavelengths 550, 600, and 775 nm have been determined and the quality of the produced grooves has been investigated. The threshold fluences are in the order of 10–70 mJ/cm² and the ideal fluence range for damage free ablation is ranging from 30 to 300 mJ/cm², depending on the wavelength. The optimal focussing for ablation has been investigated and first results towards the structuring of a ridge waveguide are presented. We conclude that this method is most promising for waveguide patterning of DAST surfaces for integrated optics applications.     

Femtosecond laser ablation of aluminium

We investigate femtosecond laser ablation of aluminium using a hybrid simulation scheme. Two equations are solved simultaneously: one for the electronic system, which accounts for laser energy absorption and heat conduction, the other for the dynamics of the lattice where the ablation process takes place. For the electron-temperature a generalized heat-conduction equation is solved by applying a finite difference scheme. For the lattice properties, e.g. pressure, density or temperature, we use common molecular dynamics. Energy transfer between the subsystems is allowed by introducing an electron-phonon coupling term. This combined treatment of the electronic and atomic systems is an extension of the well known two-temperature model [Anisimov, Kapeliovich, Perel’man, Electron emission from metal surfaces exposed to ultra short laser pulses, JETP Lett. 39 (2)].     

Femtosecond multipulse polarization spectroscopy of molecular vibrations and rotations in liquids

Simultaneous control over the vibrational and rotational molecular responses in ultrafast optical Kerr-effect signals in acetonitrile, toluene, and chloroform at room temperature is achieved by means of non-resonance excitation with two 30-fs orthogonal linearly polarized laser pulses. It is shown that the orientational response of the molecules can be suppressed and their vibrational response isolated by enhanced the delay between the exciting pulses and their relative intensity.     

Femtosecond uv excimer laser ablation

Experiments on the ablation of polymethylmethacrylate (PMMA) with 300 fs uv excimer laser pulses at 248 nm are reported for the first time. With these ultrashort pulses, ablation can be done at fluences up to five times lower than the threshold fluence for 16 ns ablation of PMMA, and the surface morphology is improved, also for several other materials. A model for ablation is proposed, assuming a non-constant absorption coefficient _eff depending on the degree of incubation of the irradiated material and the intensity of the incoming excimer laser pulse. The agreement between our model and our experimental observations is excellent for 16 ns excimer laser pulses, also predicting perfectly the shape of a pulse transmitted through a thin PMMA sample under high fluence irradiation. Qualitative agreement for 300 fs excimer laser pulses is obtained so far.     

飞秒激光相干场诱导材料功能微结构

飞秒激光在整个脉冲宽度内具有极好的相干性，因而当从同一光束分出的两束或两束以上的光束时间与空间上实现相互叠加时将会形成强度周期性调制的电磁场．这种周期调制的电磁场与材料产生相互作用，能诱导出相应的周期微结构．最近通过两束或两束以上飞秒激光干涉诱导功能微结构得到了广泛研究．文章综合了国内外飞秒激光研究小组在干涉诱导微结构方面的一些最新成果以及作者在这方面开展的工作，对飞秒激光干涉技术的原理及其在诱导微结构方面的应用进行了介绍．     

Femtosecond control of photoionization and photodissociation of sodium iodine molecules by laser pulse

Wave packet propagation techniques are used to find experimentally reliable laser parameters that yield optimal production.The photoionization and photodissociation dynamics of sodium iodine molecules are interpreted into several channels.Several frequencies are found to be suitable for NaI molecules during the photoionization and dissociation processes.Photon-dressed excited states and electron-dressed ionic continuum states facilitate the search for available laser parameters.     

Femtosecond pulse generation in a linear passive mode-locked dye laser

The femtosecond pulse generation in a c.w. pumped linear passive mode-locked rhodamine 6G-DODCI (3,3-diethyloxadicarbo cyanine iodide) dye laser is studied experimentally. Colliding pulse mode-locking (CPM) is achieved by placing the saturable absorber jet in the centre of the linear ring resonator. The laser performance is studied as a function of the saturable absorber concentration and of the absorber jet detuning from the central position (CPM position). Without a prism pair in the resonator pulse durations down to 140 fs were obtained. Detuning the absorber jet from the CPM position resulted in a trailing pulse tail ofcirca 900 fs duration. The dependence of the laser performance on the prism pair positioning is investigated experimentally and analysed theoretically. At the prism pair balanced position, stable pulses of about 50 fs duration were generated independent of the lateral detuning of the absorber jet out of the resonator centre. The dependence of the laser wavelength on the absorber concentration is compared with theoretical predictions. In an appendix the ray-tracing inside the linear resonator is simulated by an ABCD matrix calculation for Gaussian beams.     

Femtosecond laser pulse energy self-stabilization

A photoconductive switch driving a Pockels cell ensures energy self-stabilization of ultra-fast laser pulses from single shot to hundreds of kHz. In this kind of stabilization, the pulse corrects itself. In a first experiment, the self-stabilization of a 20-Hz, 800-nm femtosecond Chirped Pulse Amplification laser shows a reduction of the energy fluctuations from 7% rms to 0.64% rms. PACS 42.60.Lh; 42.60.Mi; 42.65.Re     

Femtosecond laser near field ablation

The high field strength of femtosecond laser pulses leads to nonlinear effects during the interaction with condensed matter. One such effect is the ablation process, which can be initiated below the threshold of common thermal ablation if the excitation pulses are sufficiently short. This effect leads to structure formation, which is anisotropic because of the polarization properties of the near field and can result in pattern sizes below the resolution limit of light. These effects are explored by temporally resolved scattering methods and by post‐mortem analysis to show the non‐thermal and anisotropic nature of this process. The near‐field distribution of plasmon modes can be tailored to a large extent in order to obtain control of the pattern formation.     

Femtosecond laser nanostructuring of silver film

In this paper, we report an evolution of surface morphology of silver film irradiated by a 1 kHz femtosecond laser. By SEM observations, it is noted that different nanostructures with respective surface features depend highly on the number of pulses and the laser fluence. Especially when the laser fluence is below the threshold fluence of film breakdown, a textured nanostructure including many nanobumps and nanocavities will appear on the surface of silver film. In order to determine an optimal regime for nanostructuring silver film and to further study the underlying mechanism, we perform a quantitative analysis of laser fluence and pulse number. The results show that this nanostructure formation should be due to a sequential process of laser melting, vapor bubbles bursting, heat stress confinement, and subsequent material redistribution. As a potential application, we find this nanostructured silver film can be used as the active substrate for surface enhanced Raman scattering effect.     

Femtosecond laser machining of electrospun membranes

We demonstrate that a femtosecond laser can be used to machine arbitrary patterns and pattern arrays into free-standing electrospun polycaprolactone (PCL) membranes. We also examine the influence of various laser irradiation settings on the final microstructure of electrospun membranes. A beam fluence of 0.6 J/cm² is used to ablate holes in 100 μm thick PCL membranes. The machined holes have an average diameter of 436 μm and a center-to-center spacing of 1000 μm. Based on these results, the femtosecond ablation of electrospun membranes shows great potential for fabricating a variety of functional tissue scaffolds. This technique will advance scaffold design by providing the ability to rapidly tailor surface morphology, while minimizing and controlling the deformation of the electrospun fibers.     

Femtosecond laser microstructuring of nickel foil

We observe the morphological change and grain structure of Ni foil when it is ablated with femtosecond laser pulses. Scanning electron microscopy and field emission transmission electron microscopy are used to study the nature of the morphology and grain structure of nickel foil and determine the essential features. The results indicate that there are many random uanostructures in the center of the ablated region composed of nanocrystalline grains as well as some core-shell structures phase explosion and extremely high cooling rate are the for the formation of surface nanostructures. The observed morphologies seem to suggest that most probable physical mechanisms responsible