Spectral broadening and electron–photon coupling in III–V infrared detectors of low dimensional quantum confined system

Present work explores the mid-IR photodetection mechanism in III–V quantum confined system in twofold ways. Firstly, it models the extent of spectral linewidth broadening of photo-detector. Secondly, it investigates whether a strong perturbation of light can modulate the electronic bandstructure. Photo-absorption mechanism in the detector correlated to reduced carrier lifetime in ground state leading to homogeneous spectral widening is calculated. Besides, contribution of non-uniform size and composition of quantum dots towards spectral broadening is modeled in order to get the envelop of inhomogeneously broadened photocurrent spectrum. Our model generates photocurrent spectrum with 1.4 μm broadening centered at 3.5 μm at 77 K for a DWELL-IP, which agrees with the experimental result. The calculated photocurrent spectral width of 1.3 μm for GaAs/AlGaAs Quantum Well (QW) centered at 8.31 μm at 77 K also supports experimental data. In addition, our calculation reveals the emergence of a broad resonant peak in the spectrum of QW-IP in far infrared region (20–50 μm) as the photon volume density increases up to 0.1% of carrier density inside the active region. We introduce a hybrid density-of-states for strongly coupled electron–photon system to explain both mid and far IR peak.     

Experimental transition probabilities in the Ar III and Ar IV UV spectra

We present transition probabilities (Einstein's A values) for 38 Ar III (doubly ionized argon) and 14 Ar IV (triply ionized argon) spectral lines from the wavelength interval 240–308 nm. Considered spectral lines are recorded in laboratory pulsed discharge. The relative line intensity ratio procedure has been applied in evaluation of transition probabilities. As a reference for transition probability evaluation we have chosen A value of 241.884 nm spectral line in Ar III spectrum and A value of 280.947 nm in Ar IV spectrum, both obtained theoretically. Careful analysis of experimental and existing theoretical data is conducted in order to deduce uncertainties. Presented Ar III and Ar IV A values are for the first time obtained relying on experimental data.     

Ultra-broad and flat supercontinuum generation in short photonic crystal fiber combined with conventional fibers

In order to gain ultra-broad and flat super-continuum (SC) spectrum, we propose and demonstrate a new scheme. By coupling a train of short pulses with 100 fs width and 16.2 mW average power generated by a mode-locked laser into the scheme – short photonic crystal fiber (PCF) combined with conventional fibers. The SC spectrum has 491 nm bandwidth at −15 dBm below the spectral peak with ±0.5 dBm uniformity 100 nm in only 0.45 m PCF. The spectral bandwidth generated in the scheme increases 292 nm than spectrum generated in the two conventional fibers, and increases 152 nm than spectrum generated in the three convention fibers.     

Fine structure of far infrared spectrum of ethanol in the lowest OH-torsional vibrational trans-state (e0) of ethanol

In this report the spectroscopic results for far infrared Fourier transform spectrum corresponding to the b-type transitions within the lowest lying trans-substrate (e₀) have been presented. The calculated matrix elements connecting various K-levels suggest that ΔK = 1 transitions within the trans- subs-state should be quite strong but the transitions between the trans state to the gauche states would quite week (practically non-existent). This was also concluded by previous studies using microwave and millimeter wave regions (Pearson et al., 1982; Millar, 1995). The assignments were confirmed by direct observations at the spectrum and the agreement between the observed and calculated spectrum using precise energy levels reported by Pearson et al. (1982). All the strong ^RR and some ^RQ branch lines starting from K = 10 ← 9 through K = 24 ← 23 have been identified. State dependent expansion parameters for all the 15 sub-bands have been presented. These parameters can reproduce the experimental wave numbers within experimental uncertainty. An atlas for about 450 transition lines corresponding to transitions within the e₀ torsional–vibrational species has been prepared. To our knowledge this is the first time the high resolution far infra-red spectral region study for ethanol have been performed.     

Visible,near-infrared and infrared optical properties of silica aerogels

Silica aerogel is an excellent thermal insulation material with a low thermal conductivity and a high porosity and has attracted great concern in applications. This paper was to experimentally investigate the optical properties of optically thick silica aerogel in the visible, near-infrared and infrared spectrum region. The fiber-loaded silica aerogel sample was prepared through sol–gel technique and supercritical drying process. Silica fibers were added into the aerogel during the preparation procedure to strength the skeleton of aerogel. As a comparison with the fiber-load silica aerogel, a silica fiber composite sample with the same chemical component and different physical structure was also prepared. A simplified two-flux model neglecting the boundary effect was used to describe the radiation propagation characteristics inside the samples. The spectral normal-hemispherical reflectances, transmittances, and normal emittances of silica aerogel and silica fiber samples were measured and compared in the wavelengths of 0.38–15 μm. Then the spectral optical constants of samples were determined using the experimental data. The spectral absorption and scattering coefficients of silica aerogel were within (0.01 cm⁻¹, 31.0 cm⁻¹) and (1.4 cm⁻¹, 25.8 cm⁻¹). The results showed that the spectrum region where the scattering coefficient is low usually corresponds to a high absorption coefficient. In addition, the total radiation properties of samples were predicted at high temperatures. The analysis of optical properties of silica aerogel is necessary to provide valuable data in applications.     

Remote sensing estimation of Chlorophyll a and suspended sediment concentration in turbid water based on spectral separation

Chlorophyll a and suspended sediment are important indicators of water quality, and remote sensing estimation of them is difficult due to the optical complexity of turbid water. The spectrum above water surface is influenced by phytoplankton, suspended sediment and colored dissolved organic material in water, thus spectral separation is important before estimating one specific component. Based on the field experiment of pond water and Taihu lake, China, this study calculated the Gaussian parameters of Chlorophyll a (Chla) and suspended sediment (SS) through spectral decomposition, and then these parameters were used to separate the mixed spectrum of water samples from pond water and Taihu lake. After spectral separation, the Chla estimation model based on the peak height at 650 nm has high accuracy (R² = 0.78, RMSE = 4.80 mg/m³), better than the band-ratio model; the SS estimation model based on the peak height at 811 nm (R² = 0.82, RMSE = 6.80 mg/L) performs better than the single-band model. Results in this study indicate that spectral separation based on Gaussian parameters is a good method for Chla and SS estimation in turbid lake water.     

Polarized absorption spectra of highly oriented two-dimensional aggregates of tetrachlorobenzimidazolocarbocyanine in thin films

Reaching a control on the mesoscopic morphology and internal molecular arrangement of cyanine aggregates is an important step for realization of devices with tailor-made optical properties. Despite a wealth of research, understanding of the relationship between molecular organization, excitonic states and dynamics of aggregates is still preliminary. To this end, we have employed polarized absorption spectroscopy to investigate the relationship between internal molecular organization and excitonic states of J-aggregates in 1,1′,3,3′tetraethyl-5,5′,6,6′-tetrachlorobenzimidazolocarbocyanine (TTBC) thin films in poly-vinyl alcohol (PVA). Angular dependence of the UV–vis spectra has been measured at 11 different orientations between the electric field polarization and the macroscopic alignment axis. Aggregate spectral response consisted of an asymmetrically split Davydov pair of bands exhibiting opposite polarization: an H-band (505 nm, Lorentzian-like, polarized along the macroscopic film axis) and a J-band (594 nm, one-dimensional J-aggregate like band shape, polarized perpendicular to the macroscopic film axis). The polarized absorption observations were found to be consistent with a herringbone model for which the internal molecular arrangement, the excited state structure and dynamics have recently been detailed by us upon interpretation of isotropic absorption data in ionic aqueous solution.     

Oxygen non-stoichiometry and electrical conductivity of Pr2−xSrxNiO4±δ with x = 0–0.5

Oxygen non-stoichiometry and electrical conductivity of the Pr_2−xSr_xNiO_4±δ series with x = 0.0–0.5 were investigated in Ar/O₂ (pO₂ = 2.5 to 21 000 Pa) within a temperature range of 20–1000 °C. The equilibrium values of oxygen non-stoichiometry and electrical conductivity of these nickelates were determined as functions of temperature and oxygen partial pressure (pO₂). The nickelates with x = 0–0.5 appear to be p-type semiconductors in the investigated temperature and pO₂ ranges. The nickelates with x = 0.3–0.5 show very feebly marked pO₂ dependencies of the conductivity. Pr_1.7Sr_0.3NiO_4±δ shows the anomalies of the conductivity versus oxygen partial pressure which can be related to the orthorhombic–tetragonal crystal structure transformations. The conductivity of the Pr_2−xSr_xNiO_4±δ samples correlates with the average oxidation state of the nickel cations. The samples with x = 0.5 have the highest nickel oxidation state (≈ 2.5+), the highest [Ni³⁺]/[Ni²⁺] ratio close to 1 and show the highest conductivity (≈ 120 S/cm) in the whole pO₂ and temperature ranges investigated.     

An inverse Sturm–Liouville problem with a fractional derivative

In this paper, we numerically investigate an inverse problem of recovering the potential term in a fractional Sturm–Liouville problem from one spectrum. The qualitative behaviors of the eigenvalues and eigenfunctions are discussed, and numerical reconstructions of the potential with a Newton method from finite spectral data are presented. Surprisingly, it allows very satisfactory reconstructions for both smooth and discontinuous potentials, provided that the order α ∈ (1, 2) of fractional derivative is sufficiently away from 2.     

Multispectral pyrometry for surface temperature measurement of oxidized Zircaloy claddings

Non-contact temperature measurement in a nuclear reactor is still a huge challenge because of the numerous constraints to consider, such as the high temperature, the steam atmosphere, and irradiation. A device is currently developed at CEA to study the nuclear fuel claddings behavior during a Loss-of-Coolant Accident. As a first step of development, we designed and tested an optical pyrometry procedure to measure the surface temperature of nuclear fuel claddings without any contact, under air, in the temperature range 700–850 °C. The temperature of Zircaloy-4 cladding samples was retrieved at various temperature levels. We used Multispectral Radiation Thermometry with the hypothesis of a constant emissivity profile in the spectral ranges 1–1.3 µm and 1.45–1.6 µm. To allow for comparisons, a reference temperature was provided by a thermocouple welded on the cladding surface. Because of thermal losses induced by the presence of the thermocouple, a heat transfer simulation was also performed to estimate the bias. We found a good agreement between the pyrometry measurement and the temperature reference, validating the constant emissivity profile hypothesis used in the MRT estimation. The expanded measurement uncertainty (k = 2) of the temperature obtained by the pyrometry method was ±4 °C, for temperatures between 700 and 850 °C. Emissivity values, between 0.86 and 0.91 were obtained.     

Application of hyperspectral imaging for characterization of intramuscular fat distribution in beef

In this study, a hyperspectral imaging system in the spectral region of 400–1000 nm was used for visualization and determination of intramuscular fat concentration in beef samples. Hyperspectral images were acquired for beef samples, and spectral information was then extracted from each single sample from the fat and non-fat regions. The intramuscular fat content was chemically extracted and quantified for the same samples. Chemometrics including analysis of variance (ANOVA) and spectral similarity measures involving spectral angle measure (SAM), and Euclidian distance measure (EDM) were then used to analyze the data. An ANOVA analysis indicates that the two selected spectral variables (e.g., 650.4–736.4 nm) are effective to generate ratio image for visualization of the intramuscular fat distribution in beef. The spectral similarity analysis methods, which is based on the quantifying the spectral similarities by using predetermined endmember spectrum vector, provided comparable results for characterization and detection of intramuscular fat in beef. In term of overall classification accuracy, spectral similarity measure methods outperformed the ratio image of selected bands based on the result of ANOVA analysis. The results demonstrate that proposed technique has a potential for fast and nondestructive determination of intramuscular fat in beef.     

Stark and Frequency Measurements in the FIR Spectrum of H2O2

The submillimeter-wave spectrum of H₂O₂has been recorded by means of a tunable FIR spectrometer. Stark measurements have been performed on three selected transitions in then= 0 state, namely, the 2₂₀–1₁₀(τ = 4 ← 2) at 1 272 297 MHz, the 8₂₆–7₁₆(τ = 1 ← 3) at 882 451 MHz, and the 9₂₈–8₁₈(τ = 1 ← 3) at 962 933 MHz. Accurate values of the transition dipole moments of the molecule have been derived by considering the interaction between the levels involved in the transition and the close near-resonant levels. About 40 new lines, belonging to the^rQ₄and^rQ₅subbranches of the rotational transitions between the lowest torsional states (τ = 1, 2, 3, 4n= 0), have been measured in the 2.8 and 3.4 THz spectral regions and analyzed together with the previously measured millimeter- and submillimeter-wave, as well as IR, transitions.     

Acoustic and optical phonons in EVOH–TiO2 nanocomposite films: Effect of aggregation

Films of an organic–inorganic nanocomposite material formed by a polymeric matrix (ethylene–vinyl alcohol copolymer—EVOH) and nanometric TiO₂ particles (ca. 10 nm) have been obtained with photo-catalytic properties in the elimination of pathogens. Optical spectroscopy experiments have been performed in order to characterize the films and evaluate their properties as a function of TiO₂ doping in the range between 0.25 and 13 wt%. Anatase TiO₂ nanoparticles seem to be well-dispersed up to 2% but aggregation for higher doping originates the two different regimes observed in the acoustic modes as well as in the optical absorption in the visible spectral range.     

Synthesis and growth of sodium bitartrate monohydrate a new organometallic nonlinear optical single crystal

Sodium bitartrate monohydrate (SBTMH) a new organometallic nonlinear optical material, with molecular formula, [C₄H₅NaO₆ · H₂O] has been synthesized at ambient temperature. Spectral, thermal and optical techniques have been employed to characterize the new material. Bulk single crystals of size 13 × 4 × 4 mm³ of SBTMH have been grown by slow cooling method. The unit cell parameters of the grown crystal were determined by single crystal XRD. Functional groups present in the sample were identified by FTIR spectral analysis. Thermal stability of SBTMH was determined using TGA/DTA. The grown crystals exhibit nonlinear properties. The dielectric response of the crystal with varying frequencies was studied. The optical transparency range and the lower cut-off wavelength of the material were identified from the UV–vis–NIR absorption spectrum.     

The role of torsional modes in the electronic absorption spectrum of acetone

The electronic absorption spectrum of acetone is revisited to evaluate the role of hot bands due to low lying torsional modes in the assignment of vibronic transitions. The UV–VUV photoabsorption spectrum of acetone is recorded in the energy region 3.5–11.8 eV at a resolution of ～4 meV at 4 eV and ～10 meV at 10 eV using synchrotron radiation. The absorption spectrum is dominated by richly structured Rydberg series (ns, np and nd) converging to the first ionization potential of acetone at 9.708 eV. Careful consideration of hot band contributions from torsional modes and symmetry selection rules have resulted in an improved set of vibronic assignments as compared to earlier room temperature work. Revised quantum defect values for some of the Rydberg transitions and a few new assignments in the nd series are also reported in this paper.     

In situ Raman spectroscopy of cubic boron nitride to 90 GPa and 800 K

The temperature and pressure dependences of the Raman spectrum of the transverse-optical mode of cubic boron nitride were calibrated for applications to a Raman spectroscopy pressure sensor in optical cells to about 800 K and 90 GPa. A significant deviation from linearity of the pressure dependence is confirmed at pressures above 20 GPa. At ambient temperature, dv/dP slopes are 3.41(7) and 2.04(7) cm⁻¹/GPa at 0 and 90 GPa, respectively. A polynomial expression is used to fit the pressure–temperature dependence of the Raman line. The pressure dependence does not significantly change with temperature, as determined from experiments conducted up to 800 K. At 0 GPa, the dv/dP slope is 3.46(7) cm⁻¹/GPa at 800 K. At pressures above 90 GPa, the Raman spectrum of the transverse-optical mode cannot be observed because of an overlap of the signals of cubic boron nitride and diamond used as the anvils in the high-pressure cell.     

Effect of the surface oxidization and nitridation on the normal spectral emissivity of titanium alloys Ti–6Al–4V at 800–1100 K at a wavelength of 1.5 μm

This work strived to model the effect of surface oxidization and nitridation on the normal spectral emissivity of Ti–6Al–4V alloys at a temperature range of 800–1100 K and a wavelength of 1.5 μm. In experiments, the detector was as close to perpendicular to the surface of the specimens as possible so that only the normal spectral emissivity was measured. Two thermocouples were symmetrically welded near the measuring area for accurate measuring and monitoring of the temperature at the surface of the specimen. The specimens were heated for 6 h at a certain temperature. During this period, the normal spectral emissivity values were measured once every 1 min during the initial 180 min, and once every 2 min thereafter. The measurements were made at certain temperatures from 800 to 1100 K in intervals of 20 K. One strong oscillation in the normal spectral emissivity was observed at each temperature. The oscillations were formed by the interference between the radiation stemming from the oxidization and nitridation layer on the specimen surface and radiation from the substrate. The uncertainty in the normal spectral emissivity caused only by the surface oxidization and nitridation was found to be approximately 9.5–22.8%, and the corresponding uncertainty in the temperature generated only by the surface oxidization and nitridation was approximately 6.9–15.5 K. The model can reproduce well the normal spectral emissivity, including the strong oscillation that occurred during the initial heating period.     

All fiber passively mode locked zirconium-based erbium-doped fiber laser

All passively mode locked erbium-doped fiber laser with a zirconium host is demonstrated. The fiber laser utilizes the Non-Linear Polarization Rotation (NPR) technique with an inexpensive fiber-based Polarization Beam Splitter (PBS) as the mode-locking element. A 2 m crystalline Zirconia–Yttria–Alumino-silicate fiber doped with erbium ions (Zr–Y–Al-EDF) acts as the gain medium and generates an Amplified Spontaneous Emission (ASE) spectrum from 1500 nm to 1650 nm. The generated mode-locked pulses have a spectrum ranging from 1548 nm to more than 1605 nm, as well as a 3-dB bandwidth of 12 nm. The mode-locked pulse train has an average output power level of 17 mW with a calculated peak power of 1.24 kW and energy per pulse of approximately 730 pJ. The spectrum also exhibits a Signal-to-Noise Ratio (SNR) of 50 dB as well as a repetition rate of 23.2 MHz. The system is very stable and shows little power fluctuation, in addition to being repeatable.     

Stabilized flames in hybrid aluminum-methane-air mixtures

A premixed methane–air bunsen-type flame is seeded with micron-sized (d₃₂ = 5.6 μm) atomized aluminum powder over a wide range of solid fuel concentrations. The burning velocities of the resulting two-phase hybrid flame are determined using the total surface area of the inner flame cone and the known volumetric flow rate, and spatially resolved flame spectra are obtained with a spectral scanning system. Flame temperatures are derived through polychromatic fitting of Planck’s law to the continuous part of the spectrum. It is found that an increase in the solid fuel concentration changes the aluminum combustion regime from low temperature oxidation to full-fledged flame front propagation. For stoichiometric methane–air mixtures, the transition occurs in the aluminum concentration range of 140–220 g/m³ and is manifested by the appearance of AlO sub-oxide bands and an increase in the flame temperature to 2500 K. The flame burning velocity is found to decrease only slightly with an increase in aluminum concentration, in contrast to the rapid decrease in flame speed, followed by quenching, that is observed for flames seeded with inert SiC particles. The observed behavior of the burning velocity and flame temperature leads to the conclusion that intense aluminum combustion in a hybrid flame only occurs when the flame front propagating through the aluminum suspension is coupled to the methane–air flame.     

Numerical analysis of a broadband spectrum generated in a standard fiber by noise-like pulses from a passively mode-locked fiber laser

This paper covers a numerical analysis of supercontinuum spectrum generation in a piece of standard fiber by using as the pump noise-like pulses produced by a passively mode-locked fiber laser. An experimental study was also carried out, yielding results that support the numerical results. In the numerical study we estimated that the spectral extension of the generated supercontinuum reaches ~ 1000 nm, and that it presents a high flatness over a region of ~ 220 nm (1630 nm-1850 nm) when we use as the pump noise-like pulses with a wide optical bandwidth (~ 50 nm) and a peak power of ~ 2 kW. Experimentally, the output signal spectrum extends from ~ 1530 nm to at least 1750 nm and presents a high flatness over a region of 1640 nm to 1750 nm for the same value of numerical input power, 1750 nm being the upper limit of the optical spectrum analyzer. The numerical analysis presented here is thus an essential part to overcome the severe limitation in measuring capabilities and to understand the phenomena of supercontinuum generation, which is mainly related to Raman self-frequency shift. Finally, this work demonstrates the potential of noise-like pulses from a passively mode-locked fiber laser for broadband spectrum generation.