激光诱导硬币等离子体特征参数的研究

利用1064 nm调Q Nd:YAG激光诱导产生壹圆硬币等离子体,为了提高等离子体特征参数的求解精度,利用改进型迭代Boltzmann算法,建立镍原子谱线(225.47 nm、303.19 nm、304.50 nm、323.30 nm、339.29 nm、491.84 nm、495.32 nm、500.03 nm、501.76 nm)的Boltzmann图,计算得到硬币等离子体电子温度为28144 K.通过测量镍原子谱线341.48 nm的Stark展宽,得到硬币等离子体的电子数密度为8.6×1017cm-3.基于实验结果,证明激光诱导硬币等离子体满足局部热力学平衡模型.     

激光脉冲能量对激光诱导铝合金等离子体物理特性的影响

为研究激光脉冲能量对激光诱导等离子体辐射特性和膨胀过程的影响,采用ICCD相机对不同激光脉冲能量激发的铝合金等离子体进行快速成像,并利用Boltzmann斜线法和Stark展宽法分析等离子体的电子温度和电子数密度随激光脉冲能量的演化规律.实验结果表明,激光诱导等离子体呈现明显的分层结构,等离子体的激发阈值约为3mJ,等离子体不同区域的面积随激光脉冲能量变化呈现不同的特征.当激光脉冲能量低于10mJ时,等离子体的分层结构不显著.激光脉冲能量从10mJ增加到100mJ过程中,等离子体电子温度从4 980K升高到7 221K,等离子体的电子数密度在1017 cm-3量级并随激光能量增加而增大且趋于饱和.     

纳秒激光诱导紫铜黄铜等离子体特征参数的对比研究

基于1064 nm Nd:YAG激光器,对比研究了紫铜和黄铜等离子的特征参数。洛仑兹函数拟合Cu I 324.75 nm得到紫铜和黄铜等离子体的电子密度分别是3.61017 cm-3和3.31017 cm-3。为了减小谱线自发辐射跃迁几率不确定性和测量误差带来的计算误差,采用改进型迭代玻耳兹曼算法精确求解紫铜等离子体和黄铜等离子体的电子温度分别是6316 K和6051 K,分析表明,两种等离子体特征参数的差异主要是由于黄铜中的锌元素的电离能（9.39 eV）大于铜元素的电离能（7.72 eV）而造成的。实验数据证实激光诱导的紫铜和黄铜等离子体满足局部热力学平衡模型和光学薄模型。     

纳秒激光诱导紫铜黄铜等离子体特征参数的对比研究(英文)

基于1064nm Nd:YAG激光器,对比研究了紫铜和黄铜等离子的特征参数。洛仑兹函数拟合Cu I 324.75nm得到紫铜和黄铜等离子体的电子密度分别是3.6×1017 cm-3和3.3×1017 cm-3。为了减小谱线自发辐射跃迁几率不确定性和测量误差带来的计算误差,采用改进型迭代玻耳兹曼算法精确求解紫铜等离子体和黄铜等离子体的电子温度分别是6316K和6051K,分析表明,两种等离子体特征参数的差异主要是由于黄铜中的锌元素的电离能(9.39eV)大于铜元素的电离能(7.72eV)而造成的。实验数据证实激光诱导的紫铜和黄铜等离子体满足局部热力学平衡模型和光学薄模型。     

缓冲气体对激光等离子体光谱特性影响的实验研究

准分子激光(波长:308 nm,脉宽:10 ns)诱导Al等离子体.详细研究了缓冲气体对激光等离子体光谱特性的影响,测量了不同延时下激光诱导Al等离子体的电子温度和不同缓冲气压下光谱线的Stark展宽并由此计算了等离子体的电子密度,最后根据电子碰撞激发理论对实验结果进行了讨论.     

LIBS技术对羊毛脂复合物中重金属元素的成分分析

利用激光诱导击穿光谱技术对市面上某型号口红的羊毛脂复合物中重金属元素进行分析,使用波长为532nm的激光在口红表面击穿诱导高温等离子体,通过对MCP增益、延迟、门宽三个参数的优化来获得最佳光谱.由发射光谱线的强度计算等离子体的电子温度,研究了激光诱导等离子体的电子温度随时间演化的特性.     

飞秒激光诱导铝等离子体时间分辨光谱研究

在大气环境下利用中心波长800nm、脉宽为30fs的激光聚焦在铝靶上,测定了激光诱导铝等离子体中铝原子的时间分辨发射谱。在局部热平衡条件近似下,根据实验测定的谱线相对强度得到了等离子体的电子温度;研究了激光脉冲能量对等离子体电子温度的影响和等离子体电子温度的时间演化特性。同时,实验发现了394.4nm和396.1nm两条铝原子谱线存在较强的自吸收效应,实验结果表明随着激光脉冲能量的减少和延时的增加,自吸收现象逐渐消失。     

激光诱导Ni等离子体特性的研究

以Nd·YAG激光器的二倍频输出作为激发源,获得了激光诱导Ni等离子体的发射光谱,基于发射光谱,对等离子体电子激发温度和电子密度进行了测量,其典型值分别为3 714 K,4.67×1016 cm-3。测量了等离子体电子激发温度和电子密度的空间分布,发现沿垂直于激光传播方向的径向,随到中心点距离的增加,等离子体辐射的强度减小,但线型和线宽不变,表明等离子体电子激发温度和电子密度沿径向均匀分布。沿激光传播方向,随到样品表面距离的增加,等离子体辐射强度、电子激发温度和电子密度先增加后降低,在距样品表面1.5 mm处,达到最大值。采用激光诱导击穿光谱技术进行相关探测时,收集距离样品表面1.5 mm处的发射谱,有利于提高探测灵敏度。     

样品温度对纳秒激光诱导Cu等离子体特征参数的影响

为了研究样品温度对激光诱导击穿Cu等离子体特征参数的影响,以黄铜为研究对象,在优化的实验条件下采用波长为532 nm的Nd∶YAG纳秒脉冲激光诱导激发不同温度下的块状黄铜,测量了Cu等离子体的特征谱线强度和信噪比;同时在局部热平衡条件下利用Boltzmann斜线法和Stark展宽法分析计算了不同的样品温度条件下等离子体电子温度和电子密度。实验结果表明,在激光功率为60 mW时,随着样品温度的升高,Cu的特征谱线强度和信噪比逐渐增加,样品温度为130 ℃时达到最大值,然后趋于饱和。计算表明,黄铜样品中Cu元素Cu Ⅰ 329.05 nm,Cu Ⅰ 427.51 nm,Cu Ⅰ 458.71 nm,Cu Ⅰ 510.55 nm,Cu Ⅰ 515.32 nm,Cu Ⅰ 521.82 nm, Cu Ⅰ 529.25 nm,Cu Ⅰ 578.21 nm八条谱线在130℃的相对强度相较于室温（18 ℃）下分别提高了11.55倍、4.53倍、4.72倍,3.31倍、4.47倍、4.60倍、4.25倍、4.55倍,光谱信噪比分别增大了1.35倍,2.29倍、1.76倍、2.50倍、2.45倍、2.28倍、2.50倍,2.53倍。分析认为,升高样品温度会增大样品的烧蚀质量,相对于温度较低状态增加了等离子体中样品粒子浓度,进而提高等离子体发射光谱强度。所以,适当升高样品温度能够提高谱线强度和信噪比,从而增强LIBS技术检测分析光谱微弱信号的测量精度,改善痕量元素的检测灵敏度。同时研究了改变样品温度时等离子体电子温度和电子密度的变化趋势。计算表明,当样品温度从室温上升到130 ℃的过程中,等离子体的电子温度由4 723 K上升到7 121 K时基本不再变化。这种变化规律与发射谱线强度和信噪比变化趋势一致。分析认为,这主要是由于在升高样品温度的初始阶段,激光烧蚀量增大,等离子体内能增大,从而导致等离子体电子温度升高。当激光烧蚀样品的量达到一定值后不再变化,激光能量被激发溅射出来的样品蒸发物以及尘粒的吸收、散射和反射,导致激光能量密度降低,电子温度趋于饱和,达到某种动态平衡。选用一条Cu原子谱线（324.75 nm）的Stark展宽系数计算激光等离子体的电子密度,同时研究改变样品温度时等离子电子密度的变化趋势,计算表明在样品温度为130 ℃时,Cu Ⅰ 324.75 nm对应的等离子电子密度相较于室温（18 ℃）条件下增大了1.74×1017 cm-3。该变化趋势与电子温度的变化趋势一致。适当升高样品温度使得电子密度增大,从而提高电子和原子的碰撞几率,激发更多的原子,这是增强光谱谱线强度的原因之一。由此可见,升高样品温度是一种便捷的提高LIBS检测灵敏度的有效手段。     

基于发射光谱法锡等离子体特征参数的求解研究

利用调QNd:YAG 1064 nm激光器诱导产生锡等离子体,基于9条锡发射谱线,构建二维玻尔兹曼图,得到锡等离子体电子温度5063 K,利用洛伦兹函数拟合锡发射谱线Sn(I) 228.66 nm,得到锡等离子体电子密度3.8×10¹⁷ cm^-3,结果证实激光诱导的锡等离子体处于热力学平衡状态.     

Diagnostics of Tin Plasma Produced by Visible and IR Nanosecond Laser Ablation

We present the optical emission spectroscopic studies of the Tin (Sn) plasma, produced by the fundamental (1064 nm) and second (532 nm) harmonics of a Q switched Nd: YAG pulsed laser having pulse duration of 5 ns and 10 Hz repetition rate which is capable of delivering 400 mJ at 1064 nm, and 200 mJ at 532 nm using Laser Induced Breakdown Spectroscopy (LIBS). The laser beam was focused on target material by placing it in air at atmospheric pressure. The experimentally observed line profiles of four neutral tin (Sn I) lines at 231.72, 248.34, 257.15 and 266.12 nm were used to extract the electron temperature (T_e) using the Boltzmann plot method and determined its value 6360 and 5970 K respectively for fundamental and second harmonics of the laser. Whereas, the electron number density (N_e) has been determined from the Stark broadening profile of neutral tin (Sn I) line at 286.33 nm and determined its value 5.85 x 10¹⁶ and 6.80 x 10¹⁶cm^–3 for fundamental and second harmonics of the laser respectively. Both plasma parameters (T_e and N_e) have also been calculated by varying distance from the target surface along the line of propagation of plasma plume and also by varying the laser irradiance. (© 2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Quantitative studies of copper plasma using laser induced breakdown spectroscopy

In the present work, we present the spatial evolution of the copper plasma produced by the fundamental harmonic (1064 nm) and second harmonic (532 nm) of a Q-switched Nd:YAG laser. The experimentally observed line profiles of neutral copper have been used to extract the electron temperature using the Boltzmann plot method, whereas, the electron number density has been determined from the Stark broadening. Besides we have studied the variation of electron temperature and electron number density as a function of laser energy at atmospheric pressure. The Cu I lines at 333.78, 406.26, 465.11 and 515.32 nm are used for the determination of electron temperature. The relative uncertainty in the determination of electron temperature is ≈10%. The electron temperature calculated for the fundamental harmonic (1064 nm) of Nd:YAG laser is 10500–15600 K, and that for the second harmonic (532 nm) of Nd:YAG laser is 11500–14700 K at a Q Switch delay of 40 μs. The electron temperature has also been calculated as a function of laser energy from the target surface for both modes of the laser. We have also studied the spatial behavior of the electron number density in the plume. The electron number densities close to the target surface (0.05 mm), in the case of fundamental harmonic (1064 nm) of Nd:YAG laser having pulse energy 135 mJ and second harmonic (532 nm) of Nd:YAG laser with pulse energy 80 mJ are 2.50×10¹⁶ and 2.60×10¹⁶ cm⁻³, respectively.     

Quantum cascade laser-based carbon monoxide detection on a second time scale from human breath

We present three different detection schemes for measuring carbon monoxide (CO) in direct absorption using a thermoelectrically cooled, distributed-feedback pulsed quantum cascade (qc) laser operating between 2176 and 2183 cm^-1. The laser emission has overlap with the strong R(8)1 ro-vibrational transition in CO at 2176.2835 cm^-1. Firstly, by utilizing the frequency chirp of the qc-laser with long laser pulses, a minimal detectable absorption of 1.2×10^-5 cm^-1 is achieved at an acquisition rate of 3 Hz. Additionally, with short laser pulses and slow frequency scanning a minimal detectable absorption 8.2×10^-7 cm^-1 is reported, with an acquisition time of 60 s. Finally, a novel amplitude modulation technique is developed to facilitate real-time measurement of CO in exhaled air. The application of this detector to detection of CO in a single breath as a potential non-invasive diagnostic tool is shown. PACS 07.07.Df; 42.62.Be     

Optical characterization of laser-induced crystallized silicon films

Optical absorption coefficient spectra of thin silicon films were precisely investigated using a simple reflectance system with total reflectance mirrors placed on the rear side of samples in order to cancel an interference effect in a range between 1.1 eV and 3 eV. The absorption coefficient decreased according to crystallization as the laser energy increased and it got similar to that of single crystalline silicon in the range of 1.7 eV 3 eV. However, the absorption coefficient was higher than 10² cm^–1 in the photon energy lower than 1.3 eV. This probably results from band tail states caused by defect states localized at grain boundaries in the crystallized films. 2.5%-phosphorus doped laser crystallized silicon films had a high optical absorption coefficient ( > 10⁴ cm^–1) in the low photon energy range (1.1 eV 1.7 eV) caused by free carriers produced from the dopant atoms activated in the silicon films. The experimental results gave the carrier density of 1.3 × 10²¹ cm³ and the carrier mobility of 20 cm²/Vs.     

X-ray emission from plasma generated by nanosecond laser irradiating tantalum

A continuum spectrum of X-rays, originating from the interaction of a moderate intensity nanosecond Nd:Yag laser (1064 nm, 9 ns, 30 Hz, 900 mJ, 10¹¹ W/cm²) with metal targets producing plasma, is investigated. The photon emission intensity is particularly high when the plasma expands in a low-pressure gas. The photon energy is measured through selective thin absorber films employed in front of the solid state detector. The temperature of the hot electrons generated from the plasma, responsible for the continuum spectrum emission, is calculated from the fit of the X-ray spectrum with a Maxwellian distribution, and it is about 1–2 keV.     

Optical absorption in early stage low temperature laser produced plasma

We describe a new technique to measure the UV/visible absorption spectrum of the ablated material during the laser pulse. The technique utilizes the continuum emission from one laser produced plasma as a light source to measure the absorption properties of a second laser produced plasma which is formed on a semi-transparent target with an array of 40 μm holes. A 6 ns, 1064 nm laser was used to ablate a Ag target and the plasma absorption was measured in the range 450–625 nm for a laser fluence of 1 J cm⁻². The total absorption cross-section is (0.5–1.5)×10⁻¹⁷ cm² in the range 450–540 nm. By comparing the measured absorption with a calculation using the plasma spectroscopy code FLYCHK it can be concluded that, in the wavelength region examined here, the absorption is mainly due to bound-bound transitions.     

Threshold and saturation properties of a solid-state XeF (C-A) excimer laser

A dielectric laser cavity of 1 cm length has been optimized for high gain (7 cm^–1) operation which is achieved in XeF doped Ar crystals. Mode structures on the C-A spectral distribution around 540 nm and far field transverse mode patterns are reported. Photchemical gain burning is observed in the spectral mode structures. The dependence of the laser threshold on pump energy, pumped length and on cavity losses is studied. XeF densities of 7×10¹⁷ cm^–3 and distributed losses of 1.2 cm^–1 are derived. The measured quantum efficiency of 14% and the saturation behaviour are consistently described. Losses by transient aborption and two photon absorption are discussed.     

Expansion velocities of 0.5 ps KrF excimer laser induced plasma by Doppler-shift analysis of pump and probe measurements

High gradient laser plasma is formed by focused KrF laser pulses (248.3 nm, 450 fs, 10¹³ W/cm²) on liquids (water, styrene) and solids (silicon, aluminum, and polyimide). The hydrodynamic expansion of the plasma was studied by measuring the blue Doppler-shift of reflected probe pulses which was produced by a delayed dye laser (496.6 nm, 450 fs). The Doppler-shift corresponds to the velocity of the reflecting surface of the plasma which is defined by the critical electron density. Expansion is investigated as a function of delay time and laser intensity. The reflecting surface of the plasma accelerates over 1–2 ps after the onset of the ablating laser pulse. With increasing intensity up to 2×10¹³ W/cm² the maximum average velocities are monotonously increasing up to 1–2×10⁵ m/s. PACS 52.38.Kd; 52.50.Jm, 52.70.Kz     

Application of a continuous-wave tunable erbium-doped fiber laser to molecular spectroscopy in the near infrared

Development of a continuous-wave tunable fiber laser-based spectrometer for applied spectroscopy is reported. Wide wavelength tunability of an erbium-doped fiber laser (EDFL) was investigated in the near-infrared region of 1543–1601 nm. Continuous mode-hop free fine frequency tuning has been accomplished by temperature tuning in conjunction with mechanical tuning. The overall spectroscopic performance of the EDFL was evaluated in terms of frequency tunability along with its suitability for molecular spectroscopy. High-resolution absorption spectra of acetylene (C₂H₂) were recorded near 1544 nm with a minimum measurable absorption coefficient of about 3.5×10^-7 cm^-1/Hz^1/2 for direct absorption spectroscopy associated with a 100-m long multipass cell. Detections of C₂H₂ at different concentration levels were performed as well with high dynamic detection range varying from 100% purity to sub ppmv using cavity ring down spectroscopy. A 3σ-detection-limited minimum detectable concentration (MDC) of 400 ppbv has been obtained by using the transition line P_e(22) of the ν₁+ν₃+ν₅ ¹(Π_g)-ν₅ ¹(Π_u) hot band near 1543.92 nm with a detection bandwidth of 2.3 Hz. This corresponds to a minimum detectable absorption coefficient of 6.6×10^-11 cm^-1/Hz^1/2. The sensitivity limit could be further improved by almost one order of magnitude (down to ∼60 ppbv) by use of the P_e(27) line of the ν₁+ν₃(Σ_u ⁺)-0(Σ_g ⁺)combination band near 1543.68 nm. PACS 42.55.Wd; 42.62.Fi; 07.57.Ty; 07.88.+y