Selective excitation of singly-ionized silver emission lines by Grimm glow discharge plasmas using several different plasma gases

The relative intensities of silver emission lines from Grimm glow discharge plasmas were investigated in the wavelength range from 160 to 600 nm when using different plasma gases. It was characteristic of the plasma excitation that the spectral patterns were strongly dependent on the nature of the plasma gas employed. Intense emission lines of silver ion were observed when argonhelium mixed gases were employed as the plasma gas. Selective excitation of the ionic lines could be principally attributed to the charge transfer collisions between silver atoms and helium ions.     

Laser-induced breakdown spectroscopy at a water/gas interface: A study of bath gas-dependent molecular species

Single-pulse laser-induced breakdown spectroscopy has been performed on the surface of a bulk water sample in an air, argon, and nitrogen gas environment to investigate emissions from hydrogen-containing molecules. A microplasma was formed at the gas/liquid interface by focusing a Nd:YAG laser beam operating at 1064 nm onto the surface of an ultra-pure water sample. A broadband Echelle spectrometer with a time-gated intensified charge-coupled device was used to analyze the plasma at various delay times (1.0–40.0 μs) and for incident laser pulse energies ranging from 20–200 mJ. In this configuration, the dominant atomic spectral features at short delay times are the hydrogen H-alpha and H-beta emission lines at 656 and 486 nm, respectively, as well as emissions from atomic oxygen liberated from the water and air and nitrogen emission lines from the air bath gas. For delay times exceeding approximately 8 μs the emission from molecular species (particularly OH and NH) created after the ablation process dominates the spectrum. Molecular emissions are found to be much less sensitive to variations in pulse energy and exhibit a temporal decay an order of magnitude slower than the atomic emission. The dependence of both atomic hydrogen and OH emission on the bath gas above the surface of the water was studied by performing the experiment at standard pressure in an atmospheric purge box. Electron densities calculated from the Stark broadening of the H-beta and H-gamma lines and plasma excitation temperatures calculated from the ratio of H-beta to H-gamma emission were measured for ablation in the three bath gases.     

Fast quantitative determination of platinum in liquid samples by laser-induced breakdown spectroscopy

The potential of laser-induced breakdown spectroscopy (LIBS) for the rapid determination of platinum in liquid silicone oils has been evaluated in the framework of on-line process control. A comparison of LIBS sensitivity between three setups designed for liquid analysis (static, liquid jet and flowing liquid) was performed using a 266 nm Nd/YAG laser irradiation. Best results were obtained using the flowing liquid setup and a similar limit of detection was obtained using the liquid jet. The effect of different buffer gases (Ar, He, N(2), etc.) on the signal sensitivity was studied in liquid jet analysis and best values were obtained with a nitrogen sheath gas. Detection limits were in the 100 mg/kg range for both setups. Quantitative determination of platinum in real liquid samples was also investigated using both liquid jet and flowing liquid setups. Calibration curves were plotted for Pt with the liquid jet and the flowing liquid setups under optimised temporal acquisition parameters (delay time and gate width). A normalisation using a silicon line was applied and recovery ranged from 3 to 15% for Pt in catalyst samples with both setups showing that LIBS is a sensitive and accurate method for on-line applications.     

A novel single frequency stabilized Fabry-Perot laser diode at 1590 nm for gas sensing

A novel single frequency stabilized Fabry-Perot (SFP) laser diode with an emission wavelength of lambda = 1590 nm for H2S gas sensing is reported. Sculpting of the multi-mode spectral distribution of a FP laser to achieve single frequency emission is carried out using post growth photolitographic processing of the device. The resulting longitudinal-mode controlled FP laser has a stabilized single frequency emission with a side mode suppression ratio (SMSR) of 40 dB. The application of this device to spectroscopic based H2S sensing is demonstrated by targeting absorption lines in the wavelength range 1588 < or = lambda < or = 1591 nm. Using wavelength modulation spectroscopy (WMS), a low detection limit of 120 ppm x m x Hz(-1/2) was estimated while targeting the absorption line at 1590.08 nm. These initial results demonstrate the potential of the stabilized FP laser diode at this wavelength as a tunable, single frequency source for spectroscopic based gas sensing.     

Laser ablation solid sampling: vertical spatial emission intensity profiles in inductively coupled plasma

Spectral emission intensity in the inductively coupled plasma (ICP) was measured versus height above the load coil during laser ablation solid-sample introduction. The laser-beam pulse width, power density, and wavelength, and the sample composition are know to effect the particle size distribution of the ablated mass. Ceramic and metal samples were ablated using nanosecond and picosecond pulses, and provided similar emission intensity profiles for common elements, indicating that changes in the particle size distribution are not manifested in the vertical spatial emission profile. The gas environment in the ablation chamber also influences the particle size distribution as well as the ablation interaction. Gas composition will influence the spatial emission intensity profile because of changes in the excitation characteristics of the ICP. A preliminary study using noble gases in the ablation interaction was conducted by keeping the spatial profile constant, maintaining a constant total gas composition to the ICP.     

Enhancements in laser ablation inductively coupled plasma-atomic emission spectrometry based on laser properties and ambient environment

Analytical performance of laser ablation inductively coupled plasma-atomic emission spectrometry (ICP-AES) depends critically on the interaction between the laser light and the sample. The analyte emission line intensity in ICP-AES depends on the quantity of mass ablated. The effect of laser parameters (wavelength, pulse duration, and power density) was investigated for increasing the quantity of ablated mass. For fixed laser beam energy, the ablated mass can change 2 to 3 orders of magnitude by changing the laser beam spot size on the sample. The ablated mass quantity also depends on laser pulse duration and wavelength; and on ambient gas in the sample chamber. The shorter the pulse duration and wavelength, the higher the quantity of ablated mass. By using He in the chamber, the amount of mass increases by a factor of 2 for 30 ns excimer laser ablation and by an order of magnitude for ps-laser ablation.     

Characterization of laser ablation and ionization in helium and argon: A comparative study by time-of-flight mass spectrometry

Laser ablation and ionization in ambient helium and argon gases were studied by multiple-stage time-of-flight mass spectrometry. Measurements made at different gas pressures indicated that there exists an optimal pressure for adequately cooling energetic ions and reducing multiply charged ions that are higher for He than for Ar. The temporal distributions of ions were compared at various laser fluences and gas pressures, and the broad distributions for He could be ascribed to elastic scattering and thermodynamic processes. The diffusion of ions in He resulted in a longer delay before the instrument registered its maximal signal. Ions with different masses were observed to have the same kinetic energies in He, which was confirmed using the SIMION software, while ion movement was hydrodynamically controlled in Ar. The velocities of singly and doubly charged ions were also studied, and doubly charged ions showed much higher kinetic energy because of their frontal location in the plasma expansion.     

Basic investigations for laser microanalysis: I. Optical emission spectrometry of laser-produced sample plumes

In order to find optimum conditions for laser ablation and atomization for analytical purposes, time resolved emission spectra of Nd:YAG laser-produced plasma plumes propagating into noble gas atmospheres of different pressures were measured with an optical multichannel analyzer. The time evolution of the plasma temperature was determined. Strong temperature changes were observed depending on the matrix composition. The analytical figures of merit of optical emission spectrometry (OES) of laser-produced sample plasmas were determined using, as examples, measurements of two analytes (silicon and chromium) in homogeneous and low-alloyed standard steel samples.     

The effect of sequential dual-gas testing on laser-induced breakdown spectroscopy-based discrimination: Application to brass samples and bacterial strains

Four Cu–Zn brass alloys with different stoichiometries and compositions have been analyzed by laser-induced breakdown spectroscopy (LIBS) using nanosecond laser pulses. The intensities of 15 emission lines of copper, zinc, lead, carbon, and aluminum (as well as the environmental contaminants sodium and calcium) were normalized and analyzed with a discriminant function analysis (DFA) to rapidly categorize the samples by alloy. The alloys were tested sequentially in two different noble gases (argon and helium) to enhance discrimination between them. When emission intensities from samples tested sequentially in both gases were combined to form a single 30-spectral line “fingerprint” of the alloy, an overall 100% correct identification was achieved. This was a modest improvement over using emission intensities acquired in argon gas alone. A similar study was performed to demonstrate an enhanced discrimination between two strains of Escherichia coli (a Gram-negative bacterium) and a Gram-positive bacterium. When emission intensities from bacteria sequentially ablated in two different gas environments were combined, the DFA achieved a 100% categorization accuracy. This result showed the benefit of sequentially testing highly similar samples in two different ambient gases to enhance discrimination between the samples.     

X射线荧光光谱法快速测定FeSiB非晶合金薄带中硅、硼、铁

提出了以自制的标准样品,采用单点法绘制校准曲线,利用X射线荧光光谱仪测定FeSiB非晶薄带样品中硅、硼和铁的含量。对于4个FeSiB非晶合金薄带样品中硅、硼和铁进行了10次测定,其分析结果的相对标准偏差分别为0.4%~0.5%、1.3%~4.2%和0.2%~0.4%。方法的分析结果与火花源原子发射光谱法、化学重量法和电感耦合等离子体原子发射光谱(ICP-AES)法的测定值吻合较好。方法快速、简便,薄带样品无需制样,适用于FeSiB非晶合金薄带的快速成分分析。     

Fast Imaging of Laser-induced Plasma Emission from a ZnO Target

The spatio-temporal evolution of plasma plume laser ablation zinc oxide target was investigated by ICCD camera fast imaging. The plasma was created by a KrF excimer laser of 248 nm wavelength and 25 ns pulse. The laser fluence was set at 2 J/cm². This study was performed under vacuum and oxygen atmosphere at a pressure range of 10^− 6 to 10 mbar.Free expansion, splitting and stopping of the plume were observed at different pressures and time delays following the laser pulse. Moreover, depending on the gas pressures, the photography shows some turbulence for given time delays in the front edge of the plasma while at 5 and 10 mbar the whole plasma edge is perturbed. Rayleigh–Taylor instability is proposed as an explanation to this observed effect. A time integrated emission spectroscopy diagnostic has been also used to identify plasma species. A plasma emission spectrum shows the presence of Zn⁺, Zn and O emission lines both in vacuum and in O₂ atmosphere. As the distance from the target surface increases the Zn⁺ emission line disappears.     

Classification of singly ionized iron emission lines in the 160–250 nm wavelength region from Grimm-type glow discharge plasma

In order to investigate the emission behavior of singly ionized iron lines excited by a Grimm-type glow discharge plasma, we have compiled a wavelength table of the lines in the 160–250 nm region. Three different plasma gases (argon, neon, and argon-helium mixed gas) have been employed to compare the relative intensities of the ionic iron lines. It is found that the emission intensities of some line groups which appear in the wavelength range of less than 190 nm are especially dependent on the nature of the plasma gas employed. These excitations can be principally explained from charge transfer collisions between iron atoms and plasma gas ions.     

Dynamics of the dissociation of thes-tetrazine dication produced by one photon excitation of the neutral molecule

¹³C isotope separation by multiphoton dissociation of CHClF₂ was studied by a continuous-discharge CO₂ laserQ-switched at 8 kHz. This laser can easily emit two or more wavelengths with good spatial and temporal overlap. The best irradiation results were obtained by the line pair 9P16 + 9P28. After optimizing also the pressures of CHClF₂ and of buffer gases (He and Ar), the energy density and the gas speed, the process is now much less nonlinear than in previous experiments with a single wavelength. Differences to the TEA laser induced process were observed, and generally the pressure influence on yield and selectivity showed a variety of phenomena. They were interpreted in terms of collisional changes of spectra during the laser pulse.     

Local damage of HT-materials by laser irradiation in the SEM

By using a pulsed Nd:YAG laser the high temperature materials zirconium oxide, fine grain graphite and silicon nitride were rapidly irradiated (heating thermal shock) and their damage behavior was investigated. The laser beam parameters at sample surface were detected by a laser beam analyzing system and correlated with the local damage mechanisms of the materials as erosion, crack formation and solid-solid phase transformation. For the investigations image analysis, localized x-ray analysis, and the ion beam slope cutting technique were applied. The temperature field in the material was simulated by using temperature dependent material parameters for different laser beam parameters. The results illustrate both the strong influence of the temporal and spatial laser energy profile and the materials properties to the material damage.Dedicated to Professor Dr. rer. nat. Dr. h.c. Hubertus Nickel on the occasion of his 65th birthday     

Narrow-Linewidth 2 μm All-Fiber Laser Amplifier with a Highly Stable and Precisely Tunable Wavelength for Gas Molecule Absorption in Photonic Crystal Hollow-Core Fibers

In recent years, mid-infrared fiber lasers based on gas-filled photonic crystal hollow-core fibers (HCFs) have attracted enormous attention. They provide a potential method for the generation of high-power mid-infrared emissions, particularly beyond 4 μm. However, there are high requirements of the pump for wavelength stability, tunability, laser linewidth, etc., due to the narrow absorption linewidth of gases. Here, we present the use of a narrow-linewidth, high-power fiber laser with a highly stable and precisely tunable wavelength at 2 μm for gas absorption. It was a master oscillator power-amplifier (MOPA) structure, consisting of a narrow-linewidth fiber seed and two stages of Thulium-doped fiber amplifiers (TDFAs). The seed wavelength was very stable and was precisely tuned from 1971.4 to 1971.8 nm by temperature. Both stages of the amplifiers were forward-pumping, and a maximum output power of 24.8 W was obtained, with a slope efficiency of about 50.5%. The measured laser linewidth was much narrower than the gas absorption linewidth and the wavelength stability was validated by HBr gas absorption in HCFs. If the seed is replaced, this MOPA laser can provide a versatile pump source for mid-infrared fiber gas lasers.     

Effect of magnesium nitrate vaporization on gas temperature in the graphite furnace

The vaporization of magnesium nitrate was observed in longitudinally-heated graphite atomizers, using pyrocoated and Ta-lined tubes and filter furnace, Ar or He as purge gas and 10–200-μg samples. A charge coupled device (CCD) spectrometer and atomic absorption spectrometer were employed to follow the evolution of absorption spectra (200–400 nm), light scattering and emission. Molecular bands of NO and NO₂ were observed below 1000°C. Magnesium atomic absorption at 285.2 nm appeared at approximately 1500°C in all types of furnaces. The intensity and shape of Mg atomization peak indicated a faster vapor release in pyrocoated than in Ta-lined tubes. Light scattering occurred only in the pyrocoated tube with Ar purge gas. At 1500–1800°C it was observed together with Mg absorption using either gas-flow or gas-stop mode. At 2200–2400°C the scattering was persistent with gas-stop mode. Light scattering at low temperature showed maximum intensity near the center of the tube axis. Magnesium emission at 382.9, 383.2 and 383.8 nm was observed simultaneously with Mg absorption only in the pyrocoated tube, using Ar or He purge gas. The emission lines were identified as Mg ³P°–³D triplet having 3.24 eV excitation energy. The emitting species were distributed close to the furnace wall. The emitting layer was thinner in He than in Ar. The experimental data show that a radial thermal gradient occurs in the cross section of the pyrocoated tube contemporaneously to the vaporization of MgO. This behavior is attributed to the reaction of the sample vapor with the graphite on the tube wall. The estimated variation of temperature within the cross section of the tube reaches more than 300–400°C for 10 μg of magnesium nitrate sampled. The increase of gas temperature above the sample originates a corresponding increase of the vaporization rate. Fast vaporization and thermal gradient together cause the spatial condensation of sample vapor that induces the light scattering.     

Ring Size Effects on Multi‐Stimuli Responsive Luminescent Properties of Cyclic Amine Substituted β‐Diketones and Difluoroboron Complexes

Emissive β‐diketones (bdks) and difluoroboron complexes (BF₂bdks) show multi‐stimuli responsive luminescence in both solution and the solid state. A series of bdk ligands and boron coordinated dyes were synthesized with different cyclic amine substituents in the 4‐position to explore ring size effects on various luminescent properties, including solvatochromism, viscochromism, aggregation‐induced emission (AIE), mechanochromic luminescence (ML) and halochromism. Red‐shifted absorption and emission were observed in CH₂Cl₂ for both bdk ligands and boron dyes with increasing substituent ring size. The compounds displayed bathochromic emission in more polar solvents, and higher fluorescence intensity in more viscous media. The AIE compounds exhibited enhanced emission when aggregated. For solid‐state properties, a large emission wavelength shift was shown for the piperidine substituted bdk after melt quenching on weighing paper. Large blue‐shifted emissions were observed in all the boron dye spin cast films after trifluoroacetic acid vapor annealing, and the original emissions were partially recovered after triethylamine vapor treatment.     

Enhancing antireflection property of silicon through direct picosecond laser surface texturing

Crystalline silicon was laser surface textured by picosecond pulsed laser to enhance its antireflection property. The influence of laser scan speed and number of passes in fabricating the uniform surface microtexture were evaluated. Surface texture so generated was investigated and a grid of spherical domes and cavities, with nanoripples in the order of incident laser wavelength spread over it was observed. Reflectivity of bare silicon was greater than 40% and was significantly reduced well below 2% upon laser texturing, over a wavelength range of 400 to 700 nm. Antireflecting surface is an essential requirement for more efficient performance of devices for optical and photovoltaic application.     

Free-standing boron doped CVD diamond films grown on partially stabilized zirconia substrates

Boron doped diamond films have been grown adhered to silicon substrates by chemical vapor deposition using boron containing gases. In this work it was shown that it is possible to grow free-standing boron doped CVD diamond films on partially stabilized zirconia substrates using boron powder as the source for doping. Results from Raman spectroscopy confirmed the boron incorporation with concentration up to ∼10²⁰ cm⁻³. X-ray diffraction and scanning electron microscopy showed that the effect of boron incorporation in the microstructure of the diamond film is negligible. The measurement of the resistivity as a function of temperature confirmed the semiconductor behavior, as expected for p-type diamond.     

Interaction of datolite concentrate with ammonium hydrodifluoride

The interaction of datolite concentrate with ammonium hydrodifluoride were studied. Under heating, ammonium hydrodifluoride fluorinates datolite to form complex fluoroammonium salts of boron, silicon, and impurity metals. The activation energy and rate constants were calculated for the reaction of datolite concentrate with ammonium hydrodifluoride in the range 100–150°C. The composition of the volatiles formed upon the heating of the fluorinated concentrate was studied, the temperature parameters of the evolution of boron and silicon to the gas phase were determined, and a process for separating these elements was proposed.