Diffraction grating fabrication in lithium niobate and KDP crystals with femtosecond laser pulses

We report studies of the modifications induced inside lithium niobate and KDP crystals by Yb:KGW ultrafast laser pulses, having 300-fs pulse duration and operating at 100-kHz repetition rate. By focusing the laser beam with a 0.42 numerical-aperture objective, we have recorded homogeneous volume Bragg gratings in the bulk of the niobate crystal that showed excellent diffraction efficiencies, reaching up to 87%, and remained permanent after thermal annealing for one hour at 150°C. The refractive index modification level was found to be 0.002 in lithium niobate. The results show that lithium niobate is a very promising crystal candidate for microphotonics applications. On the contrary, in the KDP crystal no smoothly modified refractive index zones were created.     

Storing energy in lithium fluoride crystals irradiated with femtosecond laser pulses

The release of energy in the form of the light sum of thermally stimulated luminescence (TSL), stored under conditions of self-focusing and the multiple filamentation of femtosecond laser radiation during the interaction between model wide-bandgap dielectric crystals of lithium fluoride is studied. It is shown that F₂ color centers are important centers of emission in the TSL process.     

Color center formation in KCl and KBr single crystals with femtosecond laser pulses

Because of their extremely high instantaneous powers, femtosecond lasers can color many nominally transparent materials. Although the excitations responsible for this defect formation occur on subpicosecond time scales, subsequent interactions between the resulting electronic and lattice defects complicate the evolution of color center formation and decay. These interactions must be understood in order to account for the long-term behavior of coloration. In this work, we probe the evolution of color centers generated by femtosecond laser radiation in potassium chloride and potassium bromide single crystals on time scales from microseconds to hundreds of seconds. By using an appropriately chosen probe laser focused through the femtosecond laser spot, we follow the changes in coloration due to individual or multiple femtosecond pulses and the evolution of that coloration for long times after femtosecond laser radiation is terminated.     

Linear photogalvanic current excited in sillenite crystals by femtosecond laser pulses

We observe electric pulses generated in sillenite crystals (Bi₁₂SiO₂₀ and Bi₁₂TiO₂₀) by 100-fs laser pulses at the wavelength of 400 nm (below the band gaps of both crystals). The peak value of the current pulses scales linearly with the intensity of laser pulses up to ∼45 GW/cm². The direction of the induced current depends on the polarization state of the laser pulse. This polarization dependence and features of the current detection via charge accumulation at the sample electrodes allow us to conclude that the electric pulses are generated due to the linear photogalvanic effect.     

Towards nanostructuring with femtosecond laser pulses

Detailed investigations of the possibilities for using femtosecond lasers for the nanostructuring of metal layers and transparent materials are reported. The aim is to develop a simple laser-based technology for fabricating two- and three-dimensional nanostructures with structure sizes on the order of several hundred nanometers. This is required for many applications in photonics, for the fabrication of photonic crystals and microoptical devices, for data storage, displays, etc. Measurements of thermionic electron emission from metal targets, which provide valuable information on the dynamics of femtosecond laser ablation, are discussed. Sub-wavelength microstructuring of metals is performed and the minimum structure size that can be fabricated in transparent materials is identified. Two-photon polymerization of hybrid polymers is demonstrated as a promising femtosecond laser-based nanofabrication technology. Received: 20 November 2002 / Accepted: 20 January 2003 / Published online: 28 May 2003 RID="*" ID="*"Corresponding author. Fax: +49-511/2788-100, E-mail: ch@lzh.de     

Surface enhanced Raman scattering silica substrate fast fabrication by femtosecond laser pulses

We report the fabrication of surface enhanced Raman spectroscopy (SERS) fused silica glass substrates using fast femtosecond-laser (fs-laser) scan, followed by silver chemical plating. A cross-section enhancement factor (EF) of 2.5×10⁶, evaluated by Rhodamine 6G (10⁻⁷ M solution), was obtained. The Raman mapping indicated a good uniformity over the fs-laser scanned area. The dimension and pattern of the SERS activated region can be conveniently controlled by laser 2D scanning, potentially enabling integration of SERS into a high-order optical–chemical analysis system on a glass chip.     

Modification of the fused silica glass network associated with waveguide fabrication using femtosecond laser pulses

Atomic-scale structural changes have been observed in the glass network of fused silica after modification by tightly focused 800-nm, 130-fs laser pulses at fluences between 5 and 200 J cm^-2. Raman spectroscopy of the modified glass shows an increase in the 490 and 605-cm^-1 peaks, indicating an increase in the number of 4- and 3-membered ring structures in the silica network. These results provide evidence that densification of the glass occurs after exposure to fs pulses. Fluorescence spectroscopy of the modified glass shows a broad fluorescence band at 630 nm, indicating the formation of non-bridging oxygen hole centers (NBOHC) by fs pulses. Waveguides that support the fundamental mode at 633 nm have been fabricated inside fused silica by scanning the glass along the fs laser beam axis. The index changes are estimated to be approximately 0.07×10^-3. Received: 17 December 2001 / Accepted: 9 July 2002 / Published online: 25 October 2002 RID="*" ID="*"Corresponding author. Fax: +1-925/423-2463, E-mail: dmkrol@ucdavis.edu     

Color center formation in soda lime glass and NaCl single crystals with femtosecond laser pulses

The high instantaneous powers associated with femtosecond lasers can color many nominally transparent materials. Although the excitations responsible for this defect formation occur on subpicosecond time scales, subsequent interactions between the resulting electronic and lattice defects complicate the evolution of color center formation and decay. These interactions must be understood in order to account for the long term behavior of coloration. In this work, we probe the evolution of color centers produced by femtosecond laser radiation in soda lime glass and single crystal sodium chloride on different time scales, from microseconds to hundreds of seconds. By using an appropriately chosen probe laser focused through the femtosecond laser spot, we can follow the changes in coloration due to individual or multiple femtosecond pulses, and follow the evolution of that coloration for a long time after femtosecond laser radiation is terminated. For the soda lime glass, the decay of color centers is well described in terms of bimolecular annihilation reactions between electron and hole centers. Similar processes appear to operate in single crystal sodium chloride. PACS 82.50.Pt; 78.55.Qr; 78.55.Fv; 78.47.+p     

飞秒激光制备彩色镍

采用飞秒脉冲激光在空气条件下扫描处理镍片表面,制备了彩色镍。用扫描电子显微镜、紫外-可见-近红外分光光度计、拉曼光谱仪等对其进行了表征。扫描电子显微镜测量显示,彩色镍表面出现了纳米激光诱导周期表面结构,结构周期为480～510 nm;紫外-可见-近红外分光光度计测量表明,彩色镍对波长为200～2 200 nm的光的反射率大大降低;拉曼谱表明样品表面形成了一定含量的氧化镍。     

Nanostructuring with spatially localized femtosecond laser pulses

Spatially localized femtosecond pulses have been produced by a combination of scanning near-field optical microscopy with ultrashort pulse lasers. With these pulses direct ablative writing on metal surfaces is demonstrated. Possible applications of this technique for nanostructuring, repair, and production of lithographic masks are discussed.     

Nanocomposites based on globular photonic crystals grown by laser ablation using femtosecond laser pulses

The prepared samples were characterized by reflection and transmission spectra of broadband visible-range radiation, and the volume fraction of substances introduced into pores of artificial opals is estimated. It is found that the introduction of solid-state nanoparticles with negative real part of the permittivity into opal pores results in a decrease in the effective refractive index and a short-wavelength shift in the spectral position of the stop band in artificial opal.     

飞秒激光制备彩色镍

 采用飞秒脉冲激光在空气条件下扫描处理镍片表面,制备了彩色镍。用扫描电子显微镜、紫外-可见-近红外分光光度计、拉曼光谱仪等对其进行了表征。扫描电子显微镜测量显示,彩色镍表面出现了纳米激光诱导周期表面结构,结构周期为480～510 nm;紫外-可见-近红外分光光度计测量表明,彩色镍对波长为200～2 200 nm的光的反射率大大降低;拉曼谱表明样品表面形成了一定含量的氧化镍。     

整形飞秒激光金属材料精细加工

实验通过二极管记录透射光信号随脉冲个数变化关系以及观测样品烧蚀形貌来研究不同实验条件对激光烧蚀的影响。使用的样品是厚度为50 m铝箔。实验中通过研究不同变量:激光焦点与样品的相对位置、激光的能量、背景气体压强以及脉冲形状对烧蚀加工过程和结果的影响,从而获得较好烧蚀效果的条件,达到控制烧蚀加工过程的目的。特别是通过使用不同形状的脉冲和具有一定规律的脉冲序列对样品进行烧蚀,发现某些形状的整形脉冲烧蚀结果明显优于变换极限脉冲。说明脉冲整形作为一种新的技术可以在激光精细钻孔领域得到更深入的研究和应用。     

飞秒激光在晶体中传输的级联非线性过程

系统地回顾了有关级联过程导致的各种非线性效应的工作,指出了级联效应可导致不同光谱成分间出现能量转移现象,且二阶级联过程中产生的白光还能够提供种子光进而得到基于参量放大过程的宽带锥形辐射。在此基础上,进一步研究了入射的基频波长对于超连续白光能量转移效果及产生倍频效率的影响以及二阶级联过程引起的偏振调制现象,指出当入射波长越靠近相位匹配波长时倍频效率越高,发现二阶级联效应还可以引起显著的基频光偏振调制。     

飞秒激光在晶体中传输的级联非线性过程

系统地回顾了有关级联过程导致的各种非线性效应的工作,指出了级联效应可导致不同光谱成分间出现能量转移现象,且二阶级联过程中产生的白光还能够提供种子光进而得到基于参量放大过程的宽带锥形辐射。在此基础上,进一步研究了入射的基频波长对于超连续白光能量转移效果及产生倍频效率的影响以及二阶级联过程引起的偏振调制现象,指出当入射波长越靠近相位匹配波长时倍频效率越高,发现二阶级联效应还可以引起显著的基频光偏振调制。     

Amplitude autocorrelation of femtosecond laser pulses using linear photogalvanic effect in sillenite crystals

We demonstrate excitation of the linear photogalvanic current in a Bi₁₂TiO₂₀ crystal by two orthogonally polarized femtosecond laser pulses with detecting the electrical current via charge accumulation on the sample electrodes. Such a setup was used to implement an interferometric autocorrelation technique for characterization of ultrashort light pulses. Integration of the detected current in femtosecond time domain leads to vanishing of a bipolar component of the photogalvanic current which arises due to a pulse chirping. The advantage of the proposed technique is that it produces the electric field correlation function directly without the need for data processing using a compact, robust, and non-expensive detector in the form of a photoconductive cell of a non-centrosymmetric crystal.     

Ablation experiments on polyimide with femtosecond laser pulses

Some applications of polymer films require the microstructuring of partly uneven substrates. This cannot be achieved by conventional photolithography, usually performed with ultraviolet short-pulse lasers (excimer, fourth harmonic Nd:YAG). When processing thermally sensitive or undoped polymers with low optical absorption, the use of femtosecond laser pulses can improve the ablation precision, also reducing the heat-affected zone. Therefore, a Ti:sapphire laser system was employed to perform ablation experiments on polyimide (PI). The irradiated areas were evaluated by means of optical and scanning electron microscopy. Highly oriented ripple structures, which are related to the polarization state of the laser pulses, were observed in the cavities. The relationship between the ablation threshold fluence and the number of laser pulses applied to the same spot is described in accordance with an incubation model.     

Three-dimensional second-harmonic generation imaging with femtosecond laser pulses

A three-dimensional reflectance scanning optical microscope based on the nonlinear optical phenomenon of second-harmonic generation is presented. A mode-locked Ti:sapphire laser producing <90-fs pulses at ~790nm was used, and the images were constructed by scanning of an object, which possessed local second-order nonlinearity, relative to a focused spot from the laser. The second-harmonic light at ~395nm generated by the specimen was separated from the fundamental beam by use of dichroic and interference filters and was detected by a photodiode. The technique was then used to characterize the distribution of second-order nonlinearity and microstructure of the nonlinear material lithium triborate.     

采用飞秒激光诱导制备彩色金属

采用脉宽为35～65fs,中心波长为800nm的飞秒脉冲激光对经抛光的镍片进行表面扫描处理,并在金属表面上制备了彩色镍图案;设置不同的激光扫描速度和能量密度扫描处理不锈钢表面,亦制备了彩色图案。介绍了实验过程,分析了实验结果,扫描电子显微镜（SEM）形貌分析显示,经过飞秒激光扫描处理的金属表面出现了纳米量级的激光诱导周期表面结构（NC—LIPSS）,在镍上形成的结构周期约为480—510nm,在不锈钢上形成的结构周期约为480～540nm。     

采用飞秒激光诱导制备彩色金属

采用脉宽为35～65 fs,中心波长为800 nm的飞秒脉冲激光对经抛光的镍片进行表面扫描处理,并在金属表面上制备了彩色镍图案;设置不同的激光扫描速度和能量密度扫描处理不锈钢表面,亦制备了彩色图案。介绍了实验过程,分析了实验结果,扫描电子显微镜(SEM)形貌分析显示,经过飞秒激光扫描处理的金属表面出现了纳米量级的激光诱导周期表面结构(NC-LIPSS),在镍上形成的结构周期约为480～510 nm,在不锈钢上形成的结构周期约为480～540 nm。