Intracavity laser absorption spectroscopy and cavity ring-down spectroscopy in low-pressure flames

Intracavity laser absorption spectroscopy (ICLAS) and cavity ring-down spectroscopy (CRDS) have been used for measurement of the NH₂-radical spectrum near 643 nm. NH₂ was obtained in low-pressure methane/air flat flames doped with minor amounts of ammonia (as low as 0.023%). The NH₂ concentration was measured both by CRDS and ICLAS in the same conditions. This enables us to compare the practical sensitivity of the two methods. Both methods were also used for measurements in a sooting acetylene/air flame (ϕ = 2.6). The comparative advantages of the methods and their complementarities are discussed.     

Detection of atomic oxygen in flames by absorption spectroscopy

The absolute concentration of atomic oxygen in an atmospheric pressure hydrogen/air flame has been measured using Intracavity Laser Spectroscopy (ICLS) based on a dye laser pumped by an argon-ion laser. Absorptions at the highly forbidden transitions at 630.030 nm and 636.380 nm were observed at an equivalent optical length of up to 10 km. The relatively low intensity of the dye laser avoids photochemical interferences that are inherent to some other methods for detecting atomic oxygen. The detection sensitivity is about 6 × 10¹⁴ atom/cm³ and can be improved with better flame and laser stabilization.     

In situ characterization of liquid network structures at high pressure and temperature using X-ray absorption spectroscopy coupled with the Paris-Edinburgh press

ABSTRACT

We review recent progress in studying structural properties of liquids using X-ray absorption spectroscopy coupled with the Paris-Edinburgh press at third-generation synchrotron facilities. This experimental method allows for detecting subtle changes in atomic arrangements of melts over a wide pressure–temperature range. It has been also employed to monitor variations of the local coordination environment of diluted species contained in glasses, liquids and crystalline phases as a function of the pressure and temperature. Such information is of great importance for gaining deeper insights into the physico-chemical properties of liquids at extreme condition, including the understanding of such phenomena as liquid–liquid phase transitions, viscosity drops and various transport properties of geological melts. Here, we describe the experimental approach and discuss its potential in structural characterization on selected scientific highlights. Finally, the current ongoing instrumental developments and future scientific opportunities are discussed.     

X-ray absorption spectroscopy and high pressure

Abstract

The difficulties of the adaptation of high pressure to x-ray absorption are presented. The advantages of the energy-dispersive geometry are discussed as well as the future improvements expected with the new synchrotron radiation sources.

Presented at the IUCr Workshop on ‘Synchrotron Radiation Instrumentation for High Pressure Crystallography’, Daresbury Laboratory 20-21 July 1991     

Evidence of SiO at the Si-oxide interface by surface soft X-ray absorption near edge spectroscopy

Using synchrotron radiation a new surface sensitive spectroscopy has been applied to determine the local structure of the first surface oxide layer formed on the Si(111) surface. The Surface Soft X-ray Absorption (SSXA) spectra have been measured. From the analysis of the X-ray Absorption Near Edge Structures (XANES) we have extracted structural information. We have first determined that bulk amorphous SiO has a characteristic microsopic structure, which cannot be described by the random alloy or microcrystalline (Si + SiO₂) mixture models. The oxide layer formed on the Si(111) surface by ground-state molecular excitation in ultra high vacuum at temperatures (～700°C) approaching the oxide dissociation point has this unique SiO local structure. Such SiO layer not formed at room temperature is expected to be present in the SiSiO₂ interface grown at high temperature. An electronic transition to empty states at the SiSiO₂ interface has been observed.     

Characterization of surfaces by soft X-ray spectroscopy

Soft X-ray spectroscopy has important capabilities for investigating the surface region of metals and alloys. By calibrating the changes in the soft X-ray emission bands from both the metal and the oxygen, it is possible to determine the oxide thickness, the degree of oxidation, the element in the alloy with which the oxygen has combined, the relative amounts of alloying elements in the surface oxide, and the oxide state of a substrate metal that has a protective coating. For Ti-6Al-4V alloys there was an increase in surface oxygen after prebond treatment which was due to a change in the degree of oxidation rather than in oxide thickness, and the oxygen was combined with the titanium in the surface oxide. The oxygen K intensity distribution, from aluminum that was given a surface chromate treatment, showed that the oxygen is combined with the chromium. In Fe-Cr alloys there is an increase in the amount of chromium combined with oxygen relative to bulk chromium with decreasing chromium content. The oxide surface of steel with a 50 Å metal protective coating was reduced when the oxide of the protective metal coating had a heat formation greater than that of the iron oxide.     

Intracavity laser absorption spectroscopy of sooting acetylene/air flames

Intracavity laser absorption spectroscopy (ICLAS) is used to measure the absolute concentration profiles of HCO and C₂ in low-pressure acetylene/oxygen/nitrogen flames with equivalence ratios ϕ=0.8, 1.0, 1.5, 2.0 and 2.5. The flames with ϕ=2.0 and 2.5 are soot-producing, with light extinction reaching 0.1% per pass in the flame with ϕ=2.5. This strong broadband extinction does not affect the sensitivity of ICLAS, however. The temperature profiles of the flames were measured using laser-induced fluorescence of the OH radicals. For C₂ concentration measurements, the (0–2) vibronic transition of the Swan band is used. The lines of this transition are located close to the HCO lines, making it possible to measure the two radical concentrations simultaneously. The C₂ concentration is highest in the ϕ=1.5 flame, and lower in the lean and heavily sooted ϕ=2.5 flames. PACS  33.20.Kf; 33.70.Fd; 42.60.Da     

基于时分复用技术的吸收光谱气体温度在线测量研究

可调谐半导体激光吸收光谱技术是一种具有高灵敏度、高选择性的非接触式气体在线测量技术。通过直接扫描多条H2O特征谱线并结合最小二乘算法实现对开放环境气体温度的在线测量。利用HITRAN光谱数据库详细讨论了边界效应对气体温度浓度测量的影响,计算结果表明,扫描多特征谱线并结合最小二乘算法可有效减小边界效应对开放环境气体温度测量的影响。实验中采用时分复用技术同时扫描了7 444.36,7 185.60,7 182.95和7 447.48cm-1四条H2O特征谱线,对管式炉573～973K范围内不同工况下的气体温度进行了测量。吸收光谱测量结果与热电偶信号的最大温差小于52.4K,温度测量最大相对误差为6.8%。     

In situ X-ray absorption fine structure detection of reversible photoinduced anisotropy in amorphous selenium

Photoinduced anisotropy in amorphous selenium ( a-Se) has been studied by in situ x-ray absorption fine structure spectroscopy. It is found that upon irradiation with linearly polarized light the chainlike fragments in a-Se are oriented with their c-axis perpendicular to the polarization plane of the inducing light. This chain orientation is reversible, correlates with optical anisotropy, and acts as a prelude to photoinduced anisotropic crystallization. This optically controlled reorientation of molecular fragments in a solid can be a basis for future novel devices.     

Multiphoton emissions in laser-assisted soft X-ray absorption

Cross sections of soft X-ray absorption accompanied by laser multiphoton absorptions or emissions are calculated, showing that under the usual choice of the relevant parameters the stimulated multiphoton emissions by the ejected electrons prevail considerably over the absorptions.     

In situ diffuse reflectance IR spectroscopy and X‐ray absorption spectroscopy for fast catalytic processes

A new instrument for synchronous in situ investigations of catalytic materials by IR and X‐ray absorption spectroscopies was designed and built at the X18A beamline of the National Synchrotron Light Source of Brookhaven National Laboratory. It provides analytical tools for solving structural, electronic and kinetic problems in catalysis science by two complementary methods. Among the features attractive for catalysis research are the broad range of catalytically active elements that can be investigated (starting with Ni and beyond), the wide range of reaction conditions (temperatures up to 873 K, various reactive gases) and time scales (starting from tens of seconds). The results of several representative experiments that illustrate the attractive capabilities of the new set‐up are discussed.     

Bromine metallization studied by X-ray absorption spectroscopy

The experimental data carried out by M?ssbauer and magnetic resonances investigations of the structural phase transitions in K₂ZnCl₄ crystals are discussed by a simple electrostatic model, calculating, the lattice contributions to the local electric potential V(r), electric field intensity E(r) and electric field gradient tensor, (r) and taking into account both the fractional electric point charges and rigid lattice approximations. The validity of the model is proved by a good fit of the computing results and experimental data of quadrupole splitting parameters at K sites obtained by ³⁹K-NMR methods in high temperature incommensurate phase ( Pnam symmetry). The experimental results obtained by M?ssbauer and EPR methods in commensurate phase (Pna2₁ symmetry) of iron and copper doped K₂ZnCl₄ crystals are explained by relaxing the rigid lattice approximation. The insertion of probe ions appear to be done on not-exactly-Zn²⁺ site. Received 3 February 1999 and Received in final form 4 May 1999     

In situ X-ray photoelectron spectroscopy study of the oxidation of CuGaSe2

The thermal and native oxidation of CuGaSe₂ thin films was studied by in situ X-ray photoelectron spectroscopy (XPS). The special design of the XPS chamber allowed to measure XP-spectra under oxidizing gas atmospheres at pressures of up to 5 mbar (in situ) or in ultra high vacuum (UHV). During thermal oxidation, the formation of predominantly Ga₂O₃ and some amount of SeO₂ were observed, but no copper oxides could be detected in the near surface region of the thin films. The same oxides were found after native oxidation in air under ambient conditions. Only after long term native oxidation for longer than 4 months Cu(OH)₂ was detected. An additional sodium oxide compound formed at the thin film surface, Na_xO and Na₂CO₃ after thermal and native oxidation, respectively. The amount of these sodium oxide compounds depends on the Na content on the as prepared surface. The formation of SeO₂ under humid conditions at 100 °C was found to depend on the surface composition of the thin film.     

Photoacoustic X-ray absorption fine-structure spectroscopy of the NiK-edge

The X-ray absorption in a 5 m thick Ni foil for energies from 8.2 keV to 8.8 keV was measured by the photoacoustic method using a gas-microphone-cell. Results are presented for both photoacoustic amplitude and phase as a function of incident photon energy. The absorption fine structure above the NiK-edge is clearly resolved. The data are compared with a simple theory for the signal generation, and discrepancies are explained by discussing the various energy dissipation channels following the X-ray absorption.     

X-ray absorption spectroscopy studies in supercritical aqueous solutions

ABSTRACT

The past two decades have witnessed significant advances in the application of X-ray absorption spectroscopy (XAS) to the study of supercritical aqueous fluids. The data obtained using in situ XAS have provided insights into the stability and the structure of metal complexes that are fundamental to understanding natural and industrial hydrothermal processes. Important recent advances using XAS can be attributed to the use of new high temperature and pressure autoclaves designed specifically for the analysis of fluids at extreme temperatures and pressures, improved techniques for the acquisition of X-ray absorption spectra and molecular-level computational modelling used in association with XAS analysis. High-brilliance light sources have not only provided new opportunities for XAS investigations of supercritical fluids, but have also revealed the effects of beam-induced radiolysis of the same fluids. The advent of energy-dispersive and rapid-acquisition XAS holds promise for future studies of beam-induced radiolysis and of the kinetics associated with the formation of metal complexes in high-temperature fluids.     

Local structure of Fe-doped In 2 O 3 films investigated by X-ray absorption fine structure spectroscopy

$(\mathrm{In}_{1-x}\mathrm{Fe}_{x})_{2}\mathrm{O}_{3}$ $(x=0.07, 0.09, 0.16, 0.22, 0.31)$ films were deposited on Si (100) substrates by RF-magnetron sputtering technique. The influence of Fe doping on the local structure of films was investigated by X-ray absorption spectroscopy (XAS) at Fe K-edge and L-edge. For the $(\mathrm{In}_{1-x}\mathrm{Fe}_{x})_{2}\mathrm{O}_{3}$ films with $x=0.07, 0.09 \mbox{ and } 0.16$ , Fe ions dissolve into $\mathrm{In}_{2}\mathrm{O}_{3}$ and substitute for $\mathrm{In}^{3+}$ sites with a mixed-valence state ( $\mathrm{Fe}^{2+}/\mathrm{Fe}^{3+}$ ) of Fe ions. However, a secondary phase of Fe metal clusters is formed in the $(\mathrm{In}_{1-x}\mathrm{Fe}_{x})_{2}\mathrm{O}_{3}$ films with $x=0.22 \mbox{ and } 0.31$ . The qualitative analyses of Fe-K edge extended X-ray absorption fine structure (EXAFS) reveal that the Fe–O bond length shortens and the corresponding Debye–Waller factor ( $\sigma^{2}$ ) increases with the increase of Fe concentration, indicating the relaxation of oxygen environment of Fe ions upon substitution. The anomalously large structural disorder and very short Fe–O distance are also observed in the films with high Fe concentration. Linear combination fittings at Fe L-edge further confirm the coexistence of $\mathrm{Fe}^{2+}$ and $\mathrm{Fe}^{3+}$ with a ratio of ${\sim}3:2$ ( $\mathrm{Fe}^{2+}: \mathrm{Fe}^{3+}$ ) for the $(\mathrm{In}_{1-x}\mathrm{Fe}_{x})_{2}\mathrm{O}_{3}$ film with $x=0.16$ . However, a significant fraction ( ${\sim}40~\mbox{at\%}$ ) of the Fe metal clusters is found in the $(\mathrm{In}_{1-x}\mathrm{Fe}_{x})_{2}\mathrm{O}_{3}$ film with $x=0.31$ .     

X-ray absorption spectroscopy study of pulsed-laser-evaporated amorphous carbon films

Amorphous carbon (a-C) films obtained by pulsed-laser ablation of graphite have been investigated by X-ray Absorption Spectroscopy (XAS). The onset of 1s ^* transitions in the films lies in the gap between the ^* and ^* bands in graphite and very close to the absorption edge of diamond, indicating a high content ofsp ³ hybridization. A sharp feature at this onset is observed and assigned to a core exciton insp ³-hybridized disordered C atoms. Its shift of 0.5 eV with respect to the core exciton in diamond is probably due to a higher localization of the excited electron induced by disorder. A small peak coming from C–H bonds at the surface is observed and its intensity inereases with the amount ofsp ³-hybridized atoms in the sample. This can be easily explained by associating a higher amount of dangling bonds at the surface to a highersp ³ content. Polarization-dependent XAS measurements show that the angular distribution of these C–H bonds has a mean value close to the normal to the surface.     

Picosecond time-resolved X-ray absorption spectroscopy of ultrafast aluminum plasmas

We have used point-projection K-shell absorption spectroscopy to infer the ionization and recombination dynamics of transient aluminum plasmas. Two femtosecond beams of the 100 TW laser at the LULI facility were used to produce an aluminum plasma on a thin aluminum foil (83 or 50 nm), and a picosecond x-ray backlighter source. The short-pulse backlighter probed the aluminum plasma at different times by adjusting the delay between the two femtosecond driving beams. Absorption x-ray spectra at early times are characteristic of a dense and rather homogeneous plasma. Collisional-radiative atomic physics coupled with hydrodynamic simulations reproduce fairly well the measured average ionization as a function of time.