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Multidimensional reactions present various channels that can exhibit very different dynamics and give products of varying subsequent reactivity. Here, we present a combination of experiment and theory to reveal the dynamics of hydrogen abstraction by OH radical at primary and secondary sites in n-butane at a collision energy of 8 kcal/mol. Crossed molecular beam slice imaging experiments unequivocally probe the secondary abstraction channel showing backward angular distributions with mild energy release to product translation, which are accurately captured by trajectory calculations using a specific-reaction-parameter Hamiltonian. Experiments containing both reaction channels indicate a less marked backward character in the angular distribution, whose origin is shown by trajectory calculations to appear as an evolution toward more sideways scattering from the secondary to primary channel. While the two channels have markedly different angular distributions, their energy release is largely comparable, showing ample energy release into the water product. The synergistic combination of crossed-beam imaging and trajectories opens the door to detailed reaction-dynamics studies of chemical reactions with ever-increasing complexity. [ABSTRACT FROM AUTHOR]

We have developed an apparatus capable of performing intrabeam and near-copropagating beam scattering experiments at collision energies from room temperature to below 1 K where interesting quantum phenomena can be observed. A detailed description of the major components of the apparatus, single and dual molecular beam valves, high speed chopper, and the discharge source, is presented. With the intrabeam scattering setup, a novel dual-slit chopper permits collision energies down to millikelvins with a collision energy spread of 20%. With the near-copropagating beam configuration, state-to-state differential cross sections for rotationally inelastic collisions of highly vibrationally excited NO molecules with Ar have been measured at broadly tunable energies documenting the versatility of the instrument. Future applications in stereodynamics and cold state-to-state collisions of vibrationally excited polyatomic molecules are briefly discussed. [ABSTRACT FROM AUTHOR]

We present the first crossed beam scattering experiment using a Zeeman decelerated molecular beam. The narrow velocity spreads of Zeeman decelerated NO (X2Π3/2, j = 3/2) radicals result in high-resolution scattering images, thereby fully resolving quantum diffraction oscillations in the angular scattering distribution for inelastic NO–Ne collisions and product-pair correlations in the radial scattering distribution for inelastic NO–O2 collisions. These measurements demonstrate similar resolution and sensitivity as in experiments using Stark decelerators, opening up possibilities for controlled and low-energy scattering experiments using chemically relevant species such as H and O atoms, O2 molecules, or NH radicals. [ABSTRACT FROM AUTHOR]

At the CERN-ISOLDE radioactive ion beam facility, thick targets are irradiated using a beam of 1.4-GeV protons. One of ISOLDE's key features is the large choice of ion source types and target materials available, enabling us to select the ideal combination for optimal intensity and purity of the isotopes requested by ISOLDE users. The ever-increasing demands in terms of isotope production yield, beam purity, and overall reliability of the employed systems are driving the continuous development efforts. Over the past few years, CERN has invested heavily in facilities and infrastructure that facilitate ongoing developments required for ISOLDE. A dedicated offline laboratory (Offline 2) has been recently equipped with high repetition rate nanosecond tunable lasers required for scheme development and developments of specialized laser ion source types such as VADLIS, LIST and PI-LIST. Moreover, it hosts a twin setup of the ISOLDE RFQ cooler and buncher (ISCOOL), which is envisaged to be used for studies of molecular beam creation and breakup, as well as the development of improved RFQ services and operational modes. For material development, particularly for nanostructured materials, the new nano laboratory has just been commissioned and will enable the production and development of nano actinide targets for ISOLDE. In this contribution we describe the infrastructure required for target and ion source developments, highlight recent efforts and experimental results on both target material development and ion source development, and provide an outlook on what to expect in the near future. [ABSTRACT FROM AUTHOR]

Precision spectroscopy of simple, calculable molecules has become an important tool to compare experiments with theory in an effort to test our understanding of the fundamental laws of physics. For this purpose, we have measured the E F 1 Σ g + (v ′ = 0 , N ′ = 0) ← X 1 Σ g + (v ″ = 0 , N ″ = 0) transition frequency of molecular deuterium ( D 2 ) with unprecedented accuracy. We use Ramsey-Comb spectroscopy at deep-ultraviolet wavelengths (201 nm) with a two-photon, Doppler-free interrogation scheme. The resulting transition frequency is f = 2 , 981 , 779 , 227 , 578 (19) kHz. The 1-σ uncertainty of 19 kHz represents an improvement of more than two orders of magnitude compared to the best previous measurement. In this paper, we give an extensive description of our methods and the experimental apparatus that we employed. Particular attention is given to aspects that we recently improved, such as the frequency comb laser system, the method of signal recording, and the cryogenic D 2 molecular beam apparatus. In combination with future measurements of the ionisation energy of the EF state, our measurement paves the way for an improved determination of the ground state ionisation and dissociation energy of molecular deuterium. [ABSTRACT FROM AUTHOR]

Nitric oxide (NO) molecules travelling in pulsed supersonic beams have been laser photoexcited to long-lived Rydberg states in series converging to the lowest lying, v + = 0 , and first excited, v + = 1 , vibrational states in the ground electronic state of NO + . After excitation, the molecules were decelerated in the travelling electric traps of a chip-based Rydberg–Stark decelerator. Deceleration to rest in the laboratory-fixed frame of reference allowed subsequent electrostatic trapping before in situ detection by pulsed electric field ionisation. The decay rates of the molecules from the traps were measured for states with principal quantum numbers between 32 and 48. Comparison of the corresponding trap decay time constants, ranging from 245 to 400 μ s for states with v + = 1 , with those recorded for molecules in states with v + = 0 , allowed bounds to be placed on the vibrational autoionisation rates of the ℓ-mixed Stark states prepared in the experiments of < 60 Hz. [ABSTRACT FROM AUTHOR]

Cryogenic buffer gas beams are central to many cold molecule experiments. Here, we use absorption and fluorescence spectroscopy to directly compare molecular beams of AlF, CaF, MgF and YbF molecules, produced by chemical reaction of laser ablated atoms with fluorine rich reagents. The beam brightness for AlF is measured as 2 × 10 12 molecules per steradian per pulse in a single rotational state, comparable to an Al atomic beam produced in the same setup. The CaF, MgF and YbF beams show an order of magnitude lower brightness than AlF and far below the brightness of Ca and Yb beams. The addition of either NF 3 or SF 6 to the cell extinguishes the Al atomic beam, but has a minimal effect on the Ca and Yb beams. NF 3 reacts more efficiently than SF 6 , as a significantly lower flow rate is required to maximise the molecule production, which is particularly beneficial for long-term stability of the AlF beam. We use NO as a proxy for the reactant gas as it can be optically detected. We demonstrate that a cold, rotationally pure NO beam can be generated by laser desorption, thereby gaining insight into the dynamics of the reactant gas inside the buffer gas cell. [ABSTRACT FROM AUTHOR]

Experimental and theoretical assessments of phonon and optical characteristics are methodically accomplished for comprehending the vibrational, structural, and electronic behavior of InP1−xSbx/n-InAs samples grown by Gas-Source Molecular Beam Epitaxy. While the polarization-dependent Raman scattering measurements revealed InP-like doublet covering optical modes ( ω L O I n P ~ 350 cm−1, ω T O I n P ~ 304 cm−1) and phonons activated by disorders and impurities, a single unresolved InSb-like broadband is detected near ~195 cm−1. In InP1−xSbx, although no local vibrational (InSb:P; x → 1) and gap modes (InP:Sb; x → 0) are observed, the Raman line shapes exhibited large separation between the optical phonons of its binary counterparts, showing features similar to the phonon density of states, confirming "two-mode-behavior". Despite the earlier suggestions of large miscibility gaps in InP1−xSbx epilayers for x between 0.02 and 0.97, our photoluminescence (PL) results of energy gaps insinuated achieving high-quality single-phase epilayers with x ~ 0.3 in the miscibility gap. Complete sets of model dielectric functions (MDFs) are obtained for simulating the optical constants of binary InP, InSb, and ternary InP1−xSbx alloys in the photon energy (0 ≤ E ≤ 6 eV) region. Detailed MDF analyses of refractive indices, extinction coefficients, absorption and reflectance spectra have exhibited results in good agreement with the spectroscopic ellipsometry data. For InP0.67Sb0.33 alloy, our calculated lowest energy bandgap E0 ~ 0.46 eV has validated the existing first-principles calculation and PL data. We feel that our results on Raman scattering, PL measurements, and simulations of optical constants provide valuable information for the vibrational and optical traits of InP1−xSbx/n-InAs epilayers and can be extended to many other technologically important materials. [ABSTRACT FROM AUTHOR]

In the case of molecular beam epitaxy (MBE), the Mg acceptors are electrically active in the as‐grown material and a priori no additional annealing procedure is necessary. However, there are still some peculiarities in the electrical properties of ammonia‐process grown GaN:Mg and some annealing effect can be observed. Additionally, the character of weak temperature dependence in the vicinity of room temperature suggests that to describe the conduction process an additional conduction channel not related to the free carriers in the valence band must be taken into account. For these reasons, this article presents the results of low‐temperature resistivity and Hall Effect studies of Mg‐doped, ammonia‐process‐grown GaN. The studied samples are grown on low‐temperature buffers of GaN deposited on a sapphire substrate. High‐temperature annealing process (≈800 K) is carried out for all of them. The temperature dependences of the electrical transport properties before and after the annealing procedure are especially investigated at temperatures ranging from 10 up to 300 K. It is found that the low temperatures transport properties are sensitive to the annealing procedure and to describe the observed effects the hopping phenomena must be taken into account. [ABSTRACT FROM AUTHOR]

Engineering flow systems operating under low pressures and/or at the micro/nano scale generally include a physically adsorbed gas layer next to the surface. In this paper, we develop a scattering kernel that accounts for the effect of adsorption, arising from van der Waals interactions, on the dynamics of molecules impinging on solid smooth surfaces. In the limit of low bulk density, surface adsorption becomes negligible and the scattering kernel recovers consistently the Cercignani–Lampis model, which best describes molecular collisions with a clean, smooth surface. In the limit of high bulk density, a dense adsorbed molecular layer forms next to the surface and its presence is picked up by the Maxwell model with complete diffuse reflection, which better captures the multiple collisions suffered by molecules. A weight coefficient based on the Langmuir adsorption isotherm is incorporated into the modelling to handle the transition between these two limiting conditions of low and high densities. The proposed model is validated against high-fidelity molecular dynamics simulations that are performed for a variety of gas–surface combinations and adsorbed molecular layers with different densities. It is shown that the proposed model very well captures the scattering patterns of beams of gas molecules at different velocities impinging on surfaces, as well as momentum and energy accommodation coefficients in the entire range of explored conditions. [ABSTRACT FROM AUTHOR]

The interplay between solute‐solvent and solvent‐solvent interactions plays an essential role in solvation dynamics that has important effects on the mechanism and dynamics of chemical reactions in solution. In this study, the rearrangement of the hydration shell induced by photoionization of a solute molecule is probed in a state‐ and isomer‐specific manner by resonant multiphoton ionization detected IR spectroscopy of the prototypical 4‐aminobenzonitrile−(H2O)2 cluster produced in a molecular beam. IR spectra reveal that the water molecules form a cyclic solvent network around the CN group in the initial neutral state (S0). Different from the singly‐hydrated cluster, in which either the CN or the NH2 group is hydrated, hydration of the NH2 group is not observed in the dihydrated cluster. IR spectra obtained after ionizing the solute molecule into the cation ground state (D0) exhibit features ascribed to both NH‐bound and CN‐bound isomers, indicating that water molecules migrate from the CN to the NH site upon ionization with a yield depending on the ionization excess energy. Analysis of the IR spectra as a function of the excess energy shows that migration produces two different NH2 solvated structures, namely (i) the most stable structure in which both N−H bonds are singly hydrated and (ii) the second most stable isomer in which one of the N−H bonds is hydrated by a H‐bonded (H2O)2 dimer. The product branching ratio of the two isomers depends on the excess energy. The role of the water‐water interaction in the hydration rearrangement is discussed based on the potential energy landscape. Solvation dynamics plays an important role in reaction mechanisms in the condensed phase, where not only solute‐solvent solvation but also solvent‐solvent interactions have a significant influence on the dynamics. Thus, the investigation of solvation dynamics at the molecular level substantially contributes to our understanding of the reaction mechanism. In this study, the dihydrated cluster of 4ABN was utilized as a model for the first solvation layer to elucidate solvent motions induced by ionization of the solute and the role of W−W interactions for the solvent relaxation. [ABSTRACT FROM AUTHOR]

The functionalization of inorganic surfaces by organic functional molecules is a viable and promising method towards the realization of novel classes of biosensing devices. The proper comprehension of the chemical properties of the interface, as well as of the number of active binding sites for bioreceptor molecules are characteristics that will determine the interaction of the sensor with the analyte, and thus its final efficiency. We present a new and reliable surface functionalization route based on supersonic molecular beam deposition (SuMBD) using 2,6-naphthalene dicarboxylic acid as a bi-functional molecular linker on the chemically inert silicon nitride surface to further allow for stable and homogeneous attachment of biomolecules. The kinetically activated binding of the molecular layer to silicon nitride and the growth as a function of deposition time was studied by X-ray photoelectron spectroscopy, and the properties of films with different thicknesses were investigated by optical and vibrational spectroscopies. After subsequent attachment of a biological probe, fluorescence analysis was used to estimate the molecular layer's surface density. The successful functionalization of silicon nitride surface via SuMBD and the detailed growth and interface analysis paves the way for reliably attaching bioreceptor molecules onto the silicon nitride surface. [ABSTRACT FROM AUTHOR]

ISOLDE's Offline 2 laboratory has been upgraded to facilitate development for the production and study of molecular ion beams. New gas injection systems have been implemented for both molecular formation in the ion source and in the radio-frequency quadrupole ion trap used for beam preparation. MagneToF detectors and time-resolved single ion counting data acquisition have been implemented for low intensity beams and studies of laser-atom or laser-molecule interactions. We present a study of the formation and ionization of BaF + using the upgraded facility. • ISOLDE's Offline 2 mass separator facility has been upgraded for studies of molecular ion beams. • High-power laser light interacts with molecules to ionize and dissociate. • Barium and barium fluoride ions are ionized using laser light at 355 nm. [ABSTRACT FROM AUTHOR]

The use of radioactive molecules for fundamental physics research is a developing interdisciplinary field limited dominantly by their scarce availability. In this work, radioactive molecular ion beams containing actinide nuclei extracted from uranium carbide targets are produced via the Isotope Separation On-Line technique at the CERN-ISOLDE facility. Two methods of molecular beam production are studied: extraction of molecular ion beams from the ion source, and formation of molecular ions from the mass-separated ion beam in a gas-filled radio-frequency quadrupole ion trap. Ion currents of U + , UO 1−3 +, UC 1−3 +, UF 1−4 +, UF 1,2 O 1,2 + are reported. Metastable tantalum and uranium fluoride molecular ions are identified. Formation of UO 1−3 +, U(OH) 1−3 +, UC 1−3 +, UF 1,2 O 1,2 + from mass-separated beams of U + , UF 1,2 + with residual gas is observed in the ion trap. The effect of trapping time on molecular formation is presented. [ABSTRACT FROM AUTHOR]

Linear gas stopping cells have been used for nearly two decades to slow down projectile fragments at the National Superconducting Cyclotron Laboratory, now the Facility for Rare Isotope Beams, for experiments with low-energy and reaccelerated beams. In order to efficiently stop and rapidly extract light to medium-mass fast ions, a cyclotron gas-stopper has been constructed. It uses a cyclotron-type magnet and a helium-gas filled stopping chamber to slow down the injected beam. RF ion guides transport the stopped ions to the center of the magnet and axially through the bore before acceleration to < 60 keV. Following successful offline tests, the cyclotron stopper was moved to an experimental vault and connected to a new momentum–compression beam line. Beam transport to and into the cyclotron stopper was tested with stable beams. Using 46K fragments, the first successful stopping and extraction of a high-energy beam with the cyclotron stopper was demonstrated. [ABSTRACT FROM AUTHOR]

The under-construction FRIB-EDM 3 -instrument was designed to study polar radioactive molecules (such as RaF) in transparent cryogenic solids by laser spectroscopy. The instrument is divided into a frontend- and a backend section. The frontend accepts an aqueous sample from isotope harvesting and provides a mass-separated molecular ion beam in an ultra-high vacuum environment. In the backend, the ions are guided into alkali-metal vapor and the resulting neutrals are co-deposited in a solid argon matrix to perform laser spectroscopy. This work addresses the frontend of the instrument. The efficient ionization of harvested radioisotopes from aqueous samples is achieved with a spray-ionization method. Subsequently, the molecular ion beam is analyzed by mass-to-charge ratio by a quadrupole mass filter. To verify the feasibility of the approach, numerical simulations with the COMSOL and SIMION packages have been conducted. While the former was applied to study transport in ion funnels, the latter was used to investigate ion beam transmission through the lower pressure sections. Following promising simulation results, a first experimental setup is under construction. [ABSTRACT FROM AUTHOR]

The work is devoted to the development of a new experimental method for entering controlled disturbances with a given frequency-wave structure into a supersonic boundary layer. Experimental data on the formation of disturbances from two pulsed sources (pulsed glow discharge) in the laminar flat-plate boundary layer at the Mach number equal to 2 are given. The experiments were carried out in the T-325 wind tunnel of ITAM SB RAS. The localized sources were spaced out at the same distance from the leading edge of the plate at 6 mm from each other spanwise. Flow pulsations were measured using a hot-wire probe of constant temperature anemometer, the signal was recorded synchronously with ignition of the discharges. This made it possible to distinguish the pulsations from the discharges against the background of random uncontrolled "natural" pulsations of the boundary layer. The spatial-temporal and frequency-wave structure of the generated disturbances from a single or two discharges, operating synchronously or with a time delay, are analyzed. It is found that the maximum difference in the structure of disturbances from one and two sources is observed in the central region, while at the side boundaries of the disturbances, the pulsations are close in all considered cases. In the wave spectra of disturbances from two discharges, nodes and antinodes are formed. Their position is determined by the distance between the sources and the time delay in their operation. [ABSTRACT FROM AUTHOR]

With the capability of quantitative identifying surface species and measuring desorption kinetics, temperature-programmed desorption (TPD) is widely used in heterogeneous catalysis and surface science fields. Minimum gas load during adsorption, fast substrate replacement, and comprehensive temperature control are of great significance for efficient and high quality TPD experiments. Unfortunately, these requirements usually cannot be met at the same time for the existing apparatuses in surface science. In order to increase the universality, a TPD spectrometer combining minimum gas load, fast substrate replacement, and comprehensive temperature control in our laboratory has been built. By using an automatically controlled microcapillary array-based effusive molecular beam gas doser, optimizing the thermal contact at the sample stage, using liquid nitrogen transfer line and designing thermocouple connection, controllable and reproducible molecule adsorption, minimum gas load, fast substrate replacement, rapid cooling, accurate temperature measuring and excellent linear heating are achieved simultaneously. Capabilities of the TPD spectrometer, for example, determination of desorption energy and desorption order, quantitative measurements of surface species and binding sites, and investigation of surface photochemical reactions, are demonstrated by measuring the desorption of water from highly oriented pyrolytic graphite and TiO2(110) and photocatalyzed oxidation of methoxy anions on TiO2(110). The apparatus described here will contribute effectively to the high throughput measurements. [ABSTRACT FROM AUTHOR]

As the crucial dimension (CD) of logic circuits continues to shrink, the photoresist metrics, including resolution, line edge roughness, and sensitivity, are faced with significant challenges. Photoresists are indispensable in the integrated circuit manufacturing industry, and specifically in achieving smaller critical dimensions. In this study, the effects of two categories of photosensitive compounds on lithography performance are explored, through a series of sulfonium salt‐based photoacid generators (PAGs) with diverse reactivity and photodegradable nucleophiles (PDNs) with varying nucleophilicity. The detailed characterization and exposure experiments suggest that the reactive alterations of different PAGs are mostly associated with the amount of phenyl composed of cations in PAGs. The "PDN first, PAG second" strategy, which employs a combination of low reactivity PAG and high reactivity PDN and involves PDN decomposition first and PAG decomposition second in the electron beam lithography process, achieves high sensitivity (100–270 µC cm−2), high resolution (25 nm 1:1 line/space, L/S), and low line edge roughness (LER ≤ 3.3 nm) stripes. This approach outperforms conventional formulations and may provide a potentially effective and useful strategy to improve electron beam photoresists. [ABSTRACT FROM AUTHOR]

The backward differential formulas of order 3-5 (BDF3-5) are applied to simulate the molecular beam epitaxial (MBE) model with slop selection. The fully implicit BDF3-5 schemes are uniquely solvable under an estimated time-step requirement. We prove that the schemes conserve the modified discrete energy dissipation laws by utilizing the discrete gradient structures of BDF3-5 formulas. Furthermore, we present a new convolution inequality to handle the nonlinear term for the error estimate. More importantly, the L 2 norm convergence analysis of the BDF3-5 schemes are proved rigorously without the assumption of Lipschitz boundedness. Numerical examples are shown to verify the efficiency and the accuracy of the developed schemes. [ABSTRACT FROM AUTHOR]

Tpx3Cam is a newly developed time-stamped camera. With the ability to record the arrival time and position of each event simultaneously, it becomes a powerful tool in atomic and molecular research. As an inherent weakness, the time-walk effect resulting in a deviation in the arrival time is a major obstacle in improving the experimental resolution and reconstruction of momentum along the time-of-flight. We developed an analytic expression to describe and correct the time-walk effect, which is independent of different fragments once the parameters of the spectrometer, the microchannel plate (MCP), the phosphor screen, and the Tpx3Cam, such as voltages on the spectrometer and MCP, are fixed. With the time-walk correction, 3D momentum distributions of N+ and N2+ from the N2 molecule's Coulomb explosion were well extracted, paving a way for filming molecular dynamics in three dimensions with time-stamped velocity map imaging. Simultaneously, a denoising method based on data filtering is presented for Tpx3Cam. [ABSTRACT FROM AUTHOR]

This study proposes the design of modular structural geopolymer concrete elements incorporating decommissioned flexible flowlines. To evaluate and assess the feasibility of the proposed modular structural elements, this study aims to investigate its feasibility from the perspectives of sustainability including cost analysis, circular economy (CE) analysis and CO2 emission estimate. Moreover, a series of numerical analyses using finite element modelling (FEM) is conducted to provide insight into the mechanical behaviour of such modular columns and beams. Apart from the cost-saving, CE and social impact benefits of the proposed elements, the results indicate that modular structural elements incorporating flowline have shown very high axial, shear and flexural capacities, which make them suitable to be used in high-rising buildings, bridges, etc. The proposed elements can be a solution to decommission and reuse the flexible flowline on a large scale in construction. [ABSTRACT FROM AUTHOR]

We propose and demonstrate an approach permitting direct imaging of the spatial distribution of gas-surface reaction products with <60 μm lateral spatial resolution using a velocity filtered ion imaging technique. We demonstrate direct imaging of the density of hydrogen deuteride (HD) molecules desorbed from a patterned platinum (Pt) thin film exposed to molecular beams of hydrogen (H2) and deuterium (D2). Resonance enhanced multiphoton absorption was performed with a 2 + 1 scheme through the E,F state using a nanosecond UV laser at ∼201 nm. The generated cations of HD, D2, and H2 were velocity filtered and accelerated with ion imaging optics toward a multichannel plate and phosphor screen. To reduce the significant image blur caused by the translational energy of the parent molecules, a grounded pinhole with 50 μm diameter is placed at the velocity-mapped imaging plane of the ion optics, which velocity-filters the ions that form the image of the near-surface origination plane, improving the ion imaging resolution by a factor of ∼10. The instrument demonstrates the capability to directly image catalytic output in the gas phase in the near-surface region with tens of micrometers of spatial resolution simultaneously with mass and molecular velocity resolution. [ABSTRACT FROM AUTHOR]

In various applications such as plant mines or mechanical systems, machines in operation generate significant vibrations which are transmitted from the foundation to the surrounding environment and precision instruments. In order to minimize these vibrations, they must be either isolated, absorbed, or damped. The current study investigates the effects of an oil damper, passive vibration isolator, and absorbers (single and double) on the vibration frequency of a composite beam made of Al6061 (with 90% weight fraction) and SiC (with 10% weight fraction) produced through the stir casting process. Experimental analysis was conducted on the fabricated composite beam to investigate the frequencies of the fundamental vibration modes under hinged-hinged, fixed-free, and fixed-hinged boundary conditions. Results indicate that the absorber, damper, and isolator have a significant effect in reducing the amplitude of vibrations, resulting in lower frequencies compared to the main frequency. Furthermore, as the number of holes in the beam increases, the frequencies decrease due to a decrease in stiffness. The frequencies are higher for fixed-free end conditions without holes compared to other conditions. The oil damper was found to be more effective in reducing vibrations compared to absorbers and isolators. [ABSTRACT FROM AUTHOR]

The results of numerical study of relaxation processes in oxygen at high temperatures are presented. Collisions of particles (atoms and molecules) are described by the molecular dynamics methods based on trajectory calculations within the framework of classical mechanics. A complex of programs for calculating the relaxation processes in mixtures of high-temperature gases involving internal modes that describe rotational and vibrational motions in molecules and molecular dissociation and atomic recombination in the presence of a third body is described. The relaxation process is described with reference to variation in the parameters in a mixture of atomic and molecular oxygen with various initial temperatures of the translational and internal modes. The results of calculations of the structure of shock wave in oxygen with the maximum translational temperature on the front higher than 5000–11 000 K are given. The results obtained are compared with experimental data. [ABSTRACT FROM AUTHOR]

Gas chromatography–mass spectrometry (GC–MS) with Cold EI is based on interfacing GC and MS with supersonic molecular beams (SMBs) along with electron ionization of vibrationally cold sample compounds in SMB in a fly‐through ion source (hence the name Cold EI). Cold EI improves all the central performance aspects of GC–MS, and in this paper, we focus on its improvement of signal‐to‐noise ratio (S/N) and limits of detection (LODs). We found that the harder the compound for analysis with standard EI, the greater the Cold EI gain in S/N and LOD. The lower LOD and higher S/N of Cold EI emerge from a few reasons: (a) similar ionization yield as standard EI, (b) enhanced abundance of molecular ions, (c) elimination of vacuum background noise, (d) elimination of ion source‐related peak tailing and degradation, (e) ability to lower the elution temperatures via the use of high column flow rates, and (f) greater range of thermally labile and low‐volatility compounds that can be analyzed. We demonstrate the superior S/N and lower LOD of Cold EI versus standard EI in a range of compounds, from the simple‐to‐analyze octafluoronaphthalene all the way to reserpine and an organo‐metallic compound that cannot be analyzed by standard EI. These compounds include methyl stearate, cholesterol, n‐C32H66, large polycyclic aromatic hydrocarbons, dioctyl phthalates, diundecyl phthalate, pentachlorophenol, benzidine, lambda‐cyhalothrin, and methidathion. The significantly lower Cold EI LODs that can be over 1000 times better than in standard EI further result in far superior response linearity and greater measurement dynamic range. [ABSTRACT FROM AUTHOR]

A narrow-pulsed and velocity-controlled molecular beam system is constructed by using a high-speed chopper and a temperature adjustable pulsed valve. The duration of the hydrogen molecular beam pulse is reduced to approximately 6.3 µs and characterized using resonance-enhanced multiphoton ionization (REMPI) at a distance of ~193 mm downstream from the nozzle. To precisely determine the velocity of the hydrogen molecules, a pump-probe technique combining stimulated Raman pumping and REMPI is employed at a fixed distance (193 mm) with nanosecond lasers. By adjusting the temperature of the pulsed valve, the velocity of the hydrogen beam varies continuously from 1290 m/s to 3550 m/s. The system exhibits potential for multiple applications in the field of chemical reaction dynamics, including its potential to integrate with ion traps and surface scattering experiments. [ABSTRACT FROM AUTHOR]

In a previous report, 25 Å periodic metal–insulator transitions dependent on the thickness of CaRuO3 ultrathin films were discovered. Compared to the conventional size effect caused by quantum wells, the rate of change is a few billions of times greater at low temperatures. Although the electrical resistivity of insulating state differs by several orders with the film thickness, the enhancement trigger was not clarified. In this study, it is clarified that the magnitude of the extraordinary size effect varies with the element supply ratio owing to precise control of the molecular beam rates of calcium and ruthenium. The supplied calcium over ruthenium ratio Ca/Ru = 1.2–1.8 during CaRuO3 deposition results in a stoichiometric ratio of Ca:Ru = 1:1 on the CaRuO3 films. Calcium‐rich elemental supply conditions result in large electrical resistivity variations. Electrical resistivity oscillations with periods of T = 23.4 and 26.3 Å are observed for the growth conditions of Ca/Ru = 1.2 and 1.6, respectively. Furthermore, a flat surface with a roughness of ≈2 Å is required to observe the size effect. Thus, the insulation of an extraordinary size effect is enhanced in CaRuO3 ultrathin films grown under the condition of calcium‐rich Ca/Ru ≈ 1.6. [ABSTRACT FROM AUTHOR]

In order to promote the engineering applications of carbon- and glass-fiber-reinforced epoxy hybrid rods, it is necessary to fully understand its long-term hygrothermal durability. In the present study, the water absorption behaviors of a hybrid rod in a water immersion environment are studied experimentally, the degradation rules of the mechanical properties are obtained, and establishing a life prediction model is attempted. The water absorption of the hybrid rod confirms to the classical Fick's diffusion model, and the water absorption concentration is determined by radial position, immersion temperature, and immersion time. In addition, the radial position of water molecules diffused into the rod is positively correlated with the diffusion concentration. The short-beam shear strength of the hybrid rod decreased significantly after 360 days of exposure; this is because water molecules interact with the polymer through hydrogen bonds to produce bound water during the immersion process, leading to resin matrix hydrolysis and plasticization, as well as interfacial debonding. In addition, the ingression of water molecules caused degradation in the viscoelastic behavior of the resin matrix in hybrid rods. The glass transition temperature of hybrid rods decreased by 17.4% after exposure at 80 °C for 360 days. The Arrhenius equation was used calculate the long-term life of short-beam shear strength in the actual service temperature based on the time–temperature equivalence theory. The stable strength retention for SBSS was found to be 69.38%, which is a useful durability design parameter for hybrid rods in civil engineering structures. [ABSTRACT FROM AUTHOR]

A new proof is presented of a theorem of L. Gurvits [LANL Unclassified Technical Report (2001), LAUR–01–2030], which states that the cone of positive block-Toeplitz matrices with matrix entries has no entangled elements. The proof of the Gurvits separation theorem is achieved by making use of the structure of the operator system dual of the operator system C(S^1)^{(n)} of n\times n Toeplitz matrices over the complex field, and by determining precisely the structure of the generators of the extremal rays of the positive cones of the operator systems C(S^1)^{(n)}\otimes _{\text {min}}\mathcal {B}(\mathcal {H}) and C(S^1)_{(n)}\otimes _{\text {min}}\mathcal {B}(\mathcal {H}), where \mathcal {H} is an arbitrary Hilbert space and C(S^1)_{(n)} is the operator system dual of C(S^1)^{(n)}. Our approach also has the advantage of providing some new information concerning positive Toeplitz matrices whose entries are from \mathcal {B}(\mathcal {H}) when \mathcal {H} has infinite dimension. In particular, we prove that normal positive linear maps \psi on \mathcal {B}(\mathcal {H}) are partially completely positive in the sense that \psi ^{(n)}(x) is positive whenever x is a positive n\times n Toeplitz matrix with entries from \mathcal {B}(\mathcal {H}). We also establish a certain factorisation theorem for positive Toeplitz matrices (of operators), showing an equivalence between the Gurvits approach to separation and an earlier approach of T. Ando [Acta Sci. Math. (Szeged) 31 (1970), pp. 319–334] to universality. [ABSTRACT FROM AUTHOR]

We describe the design, characterization, and application of a simple, highly collimated, and compact atomic/molecular beam source. This source is based on a segmented capillary design, constructed using a syringe needle. Angular width measurements and free molecular flow simulations show that the segmented structure effectively suppresses atoms traveling in off-axis directions, resulting in a narrow beam of Helium atoms having a width of 7 mrad (full width half maximum). We demonstrate an application of this source by using it for monitoring real-time changes in surface coverage on a clean Cu(110) surface exposed to oxygen by measuring the specular reflectivity of the Helium beam generated using this source. [ABSTRACT FROM AUTHOR]

• Influence of Sb/Se ratio of Sb 2 Se 3 films were investigated. • Sb 2 Se 3 films with different compositions fabricated by CMBD method from separate sources of Sb and Se. • The Se content in the solid phase is directly proportional to the Se content in the vapour phase during the growth process. • Sb 2 Se 3 thin films with micro-sized crystal grains exhibit (hk 1) preferential orientation at the stoichiometric composition. Sb x Se y thin-films were obtained by chemical-molecular beam deposition (CMBD) on soda-lime glass from Sb and Se precursors. By the precise control of the Sb/Se ratio, Sb 2 Se 3 thin films with stoichiometric composition were successfully obtained. The elemental and phase composition, as well as the crystal structure of Sb x Se y thin-films, were studied by energy-dispersive X-ray microanalysis, X-ray diffraction, Raman spectroscopy, scanning electron microscopy and atomic force microscopy. The optical bandgap of the films was determined from the absorption spectra acquired by a spectrophotometer. The physical properties of Sb x Se y thin films with different compositions were investigated. [ABSTRACT FROM AUTHOR]

In this work, the heterojunction ZnTe/ZnMnTe/GaAs has been fabricated using the molecular beam epitaxially (MBE) technique. The electric complex impedance has been used to characterize the as-prepared junction at different illumination powers in a wide range of frequencies. It was found that the impedance of the studied junction has the highest value at the darkest point and then decreases with the increase in the applied frequency, illumination power, or both of them. The Cole–Cole diagram showed two relaxation processes for the studied junction for illumination power larger than 10 mWcm−2. Only one relaxation process has been observed for illumination powers greater than 10 mWcm−2. The dielectric relaxation time showed an increase with the increase of the illumination power. Accordingly, the prepared heterojunction can be suggested for use as a photo-sensor and/or photo-switch applications. [ABSTRACT FROM AUTHOR]

We report the use of suboxide molecular-beam epitaxy (S-MBE) to grow β-Ga2O3 at a growth rate of ∼1 µm/h with control of the silicon doping concentration from 5 × 1016 to 1019 cm−3. In S-MBE, pre-oxidized gallium in the form of a molecular beam that is 99.98% Ga2O, i.e., gallium suboxide, is supplied. Directly supplying Ga2O to the growth surface bypasses the rate-limiting first step of the two-step reaction mechanism involved in the growth of β-Ga2O3 by conventional MBE. As a result, a growth rate of ∼1 µm/h is readily achieved at a relatively low growth temperature (Tsub ≈ 525 °C), resulting in films with high structural perfection and smooth surfaces (rms roughness of <2 nm on ∼1 µm thick films). Silicon-containing oxide sources (SiO and SiO2) producing an SiO suboxide molecular beam are used to dope the β-Ga2O3 layers. Temperature-dependent Hall effect measurements on a 1 µm thick film with a mobile carrier concentration of 2.7 × 1017 cm−3 reveal a room-temperature mobility of 124 cm2 V−1 s−1 that increases to 627 cm2 V−1 s−1 at 76 K; the silicon dopants are found to exhibit an activation energy of 27 meV. We also demonstrate working metal–semiconductor field-effect transistors made from these silicon-doped β-Ga2O3 films grown by S-MBE at growth rates of ∼1 µm/h. [ABSTRACT FROM AUTHOR]

This study presents velocity-resolved desorption experiments of recombinatively-desorbing oxygen from Ag (111). We combine molecular beam techniques, ion imaging, and temperature-programmed desorption to obtain translational energy distributions of desorbing O2. Molecular beams of NO2 are used to prepare a p (4 × 4)-O adlayer on the silver crystal. The translational energy distributions of O2 are shifted towards hyperthermal energies indicating desorption from an intermediate activated molecular chemisorption state.

The radionuclides 43Sc, 44g/mSc, and 47Sc can be produced cost-effectively in sufficient yield for medical research and applications by irradiating natTi and natV target materials with protons. Maximizing the production yield of the therapeutic 47Sc in the highest cross section energy range of 24–70 MeV results in the co-production of long-lived, high-γ-ray-energy 46Sc and 48Sc contaminants if one does not use enriched target materials. Mass separation can be used to obtain high molar activity and isotopically pure Sc radionuclides from natural target materials; however, suitable operational conditions to obtain relevant activity released from irradiated natTi and natV have not yet been established at CERN-MEDICIS and ISOLDE. The objective of this work was to develop target units for the production, release, and purification of Sc radionuclides by mass separation as well as to investigate target materials for the mass separation that are compatible with high-yield Sc radionuclide production in the 9–70 MeV proton energy range. In this study, the in-target production yield obtained at MEDICIS with 1.4 GeV protons is compared with the production yield that can be reached with commercially available cyclotrons. The thick-target materials were irradiated at MEDICIS and comprised of metallic natTi, natV metallic foils, and natTiC pellets. The produced radionuclides were subsequently released, ionized, and extracted from various target and ion source units and mass separated. Mono-atomic Sc laser and molecule ionization with forced-electron-beam-induced arc-discharge ion sources were investigated. Sc radionuclide production in thick natTi and natV targets at MEDICIS is equivalent to low- to medium-energy cyclotron-irradiated targets at medically relevant yields, furthermore benefiting from the mass separation possibility. A two-step laser resonance ionization scheme was used to obtain mono-atomic Sc ion beams. Sc radionuclide release from irradiated target units most effectively could be promoted by volatile scandium fluoride formation. Thus, isotopically pure 44g/mSc, 46Sc, and 47Sc were obtained as mono-atomic and molecular ScF 2+ ion beams and collected for the first time at CERN-MEDICIS. Among all the investigated target materials, natTiC is the most suitable target material for Sc mass separation as molecular halide beams, due to high possible operating temperatures and sustained release.

The photodissociation of O3 at 266 nm has been studied using velocity mapped ion imaging. We report temperature-dependent vector correlations for the O2(a1Δg, v = 0, j = 18–20) fragments at molecular beam temperatures of 70 K, 115 K, and 170 K. Both the fragment spatial anisotropy and the v-j correlations are found to be increasingly depolarized with increasing beam temperature. At all temperatures, the v-j correlations for the j = 19 state were shown to be reduced compared to those of j = 18 and 20, while no such odd/even rotational state difference was observed for the spatial anisotropy, consistent with previous measurements. We find that temperature-dependent differences in the populations and v-j correlations between the odd and even rotational states can be explained by a Λ-doublet propensity model. Although symmetry conservation should lead to formation of only the A′ Λ-doublet component, and only even rotational states, out-of-plane rotation of the parent molecule breaks the planar symmetry and permits the formation of the A″ Λ-doublet component and odd rotational states. A simple classical model to treat the effect of parent rotation on the v-j correlation and the odd/even rotational population alternation reproduces both the current measurements and previously reported rotational distributions, suggesting that the "odd" behavior originates from a Λ-doublet propensity, and not from a mass independent curve crossing effect, as previously proposed. [ABSTRACT FROM AUTHOR]

The Langmuir-Hinshelwood barrier (ELH) and the pre-exponential factor (νLH) for CO oxidation have been measured at high temperatures on hexagonal arrays of Pd clusters supported on an ultrathin alumina film on Ni3Al (111). The Pd clusters have a sharp size distribution, and the mean sizes are 174 ± 13, 360 ± 19, and 768 ± 28 atoms. ELH and νLH are determined from the initial reaction rate of a CO molecular beam with a saturation layer of adsorbed oxygen on the Pd clusters measured at different temperatures [493 ≤ T(K) ≤ 613]. The largest particles (3.5 nm) give values of ELH and νLH similar to those measured on Pd (111) [T. Engel and G. Ertl, J. Chem. Phys. 69, 1267 (1978)]. However, smaller particles (2.7 and 2.1 nm) show very different behaviors. The origin of this size effect is discussed in terms of variation of the electronic structure and of the atomic structure of the Pd clusters. [ABSTRACT FROM AUTHOR]

This study focuses on the relationship among defects, annealing temperatures, and solar cell properties in the molecular beam epitaxy-grown GaInNAsSb solar cells. Samples with an n-i-p double heterostructure were annealed at various temperatures from 650 to 850 °C, and the dynamics of deep-level defects were analyzed. A significant improvement was obtained between 750 and 800 °C due to suppression of both the traps and the nonradiative recombination centers. They were distinguished using the DC bias dependence of admittance spectra and were reconfirmed from the electroluminescence and quantum efficiency spectroscopy studies. [ABSTRACT FROM AUTHOR]

The reaction dynamics of methanol and water on Si(001) were investigated by means of molecular beam techniques. The initial sticking probability s0 was determined as a function of the kinetic energy of the incoming molecules, Ekin, and surface temperature, Ts. For both, methanol and water, a nonactivated reactional channel was observed; the dynamics were found to be determined by the reaction into the datively bonded intermediate state. A low conversion barrier was deduced for the conversion from this intermediate into the final state. It is attributed to the reaction mechanism, which proceeds via proton transfer from the OH-group of the datively bonded molecules to a Si surface atom. Despite this low conversion barrier, adsorption into the intermediate and further reaction via proton transfer were found to be largely decoupled. [ABSTRACT FROM AUTHOR]

β-Ga2O3 thin films were grown on the substrates of sapphire, GaN, and single crystals of β-Ga2O3, using plasma-assisted molecular beam epitaxy. By varying deposition conditions, pure-phase epitaxial β-Ga2O3 thin films were obtained, and the crystal quality of the as-grown films was optimized. A systematic characterization and a detailed analysis were performed on the films, including the nucleation process, surface morphology, crystal quality, thermal stability, as well as electrical and optical properties. Optical absorption was investigated using photothermal deflection spectroscopy, which provides detailed information about sub-gap optical absorption. Photocurrent measurements indicated a pronounced persistent photo-conductivity of β-Ga2O3. A blue-UV emission with an energy of 3–3.5 eV was observed by cathodoluminescence spectroscopy. The Fermi level position of the as-grown film was determined based on temperature-dependent electrical conductivity measurements. It is proposed that oxygen vacancies in the film form a defect band at around E c -0.8 eV that pins the Fermi level and is related to the observed photocurrent and cathodoluminescence characteristics. [ABSTRACT FROM AUTHOR]

We report on calculations—using the LEVEL and BCONT programs by Le Roy, the latter of which is a version modified by B. McGeehan—of the dependence of the radiative lifetime of the Na2 sodium dimer 41 Σ g + shelf-state on the initial vibrational and rotational level for corresponding quantum numbers of 0 ≤ v ≤ 75 and 0 ≤ J ≤ 90, respectively. We also present experimental lifetime values for 43 < v < 64, averaged over J = 19 and 21, obtained by a delayed pump-probe method using a previously described molecular beam and time-of-flight apparatus. Our calculated results are based on all possible dipole allowed transitions (to the 21 Σ u + , 1(B)1 Π u , and 1(A)1 Σ u + electronic states) terminating into bound as well as free final states. The shelf of the initial electronic state is a consequence of configuration interaction with the lowest Na+–Na− ion-pair potential and occurs, for the rotationless molecule, at the vibrational level v = 52. From the 41 Σ g + vibrational ground state to the shelf, the calculated lifetimes increase monotonically by a factor of about 3.8. Beyond around v = 52, depending on rotational excitation, the lifetimes decrease, settling to a value intermediate to the maximum and the minimum at v = 0. Within error bars and in the range available, our experimental data are compatible with these findings. In addition, our calculations reveal unusual and pronounced oscillatory variation of the lifetime with rotational quantum numbers for fixed vibrational levels above—but not below—the shelf. We discuss our findings in terms of the appropriate transition dipole moments and wavefunctions and provide a detailed comparison to recent lifetime calculations of sodium dimer ion-pair states [Sanli et al., J. Chem. Phys. 143, 104304 (2015)]. [ABSTRACT FROM AUTHOR]

Nanobowls represent vital molecular building blocks of end-capped nanotubes and fullerenes detected in combustion systems and in deep space such as toward the planetary nebula TC-1, but their fundamental formation mechanisms have remained elusive. By merging molecular beam experiments with electronic structure calculations, we reveal a complex chain of reactions initiated through the gas-phase preparation of benzocorannulene (C24H12) via ring annulation of the corannulenyl radical (C20H9•) by vinylacetylene (C4H4) as identified isomer-selectively in situ via photoionization efficiency curves and photoion mass-selected threshold photoelectron spectra. In silico studies provided compelling evidence that the benzannulation mechanism can be expanded to pentabenzocorannulene (C40H20) followed by successive cyclodehydrogenation to the C40 nanobowl (C40H10) – a fundamental building block of buckminsterfullerene (C60). This high-temperature pathway opens up isomer-selective routes to nanobowls via resonantly stabilized free-radical intermediates and ring annulation in circumstellar envelopes of carbon stars and planetary nebulae as their descendants eventually altering our insights of the complex chemistry of carbon in our Galaxy. Nanobowls represent building blocks of fullerenes and nanotubes as detected in combustion systems and deep space, but their formation mechanisms in these environments have remained elusive. Here, the authors explore the gas-phase formation of benzocorannulene and beyond to the C40 nanobowl. [ABSTRACT FROM AUTHOR]

We introduce an effective and flexible high vacuum interface to probe the liquid phase with photoelectron photoion coincidence (liq-PEPICO) spectroscopy at the vacuum ultraviolet (VUV) beamline of the Swiss Light Source. The interface comprises a high-temperature sheath gas-driven vaporizer, which initially produces aerosols. The particles evaporate and form a molecular beam, which is skimmed and ionized by VUV radiation. The molecular beam is characterized using ion velocity map imaging, and the vaporization parameters of the liq-PEPICO source have been optimized to improve the detection sensitivity. Time-of-flight mass spectra and photoion mass-selected threshold photoelectron spectra (ms-TPES) were recorded for an ethanolic solution of 4-propylguaiacol, vanillin, and 4-hydroxybenzaldehyde (1 g/l of each). The ground state ms-TPES band of vanillin reproduces the reference, room-temperature spectrum well. The ms-TPES for 4-propylguaiacol and 4-hydroxybenzaldehyde are reported for the first time. Vertical ionization energies obtained by equation-of-motion calculations reproduce the photoelectron spectral features. We also investigated the aldol condensation dynamics of benzaldehyde with acetone using liq-PEPICO. Our direct sampling approach, thus, enables probing reactions at ambient pressure during classical synthesis procedures and microfluidic chip devices. [ABSTRACT FROM AUTHOR]

The absolute densities of O and O 3 in the effluent of a kINPen, an atmospheric pressure plasma jet, are determined by molecular beam mass spectrometry. A nitrogen gas curtain surrounding the effluent provides a stable environment and prevents interactions with the ambient air. Both He and Ar were used as feed gas with admixtures of O 2 up to 1%. Measurements are performed at discharge voltages from 1600 to 3000 V pp and at distances from 5.5 to 10.5 mm from the nozzle of the gas shielding device to the orifice of the mass spectrometer. The measured O atom densities are in the order of 1 × 10 14 cm - 3 to 2 × 10 15 cm - 3 , whereas the O 3 molecule densities are in the order of 1 × 10 14 cm - 3 to 5 × 10 14 cm - 3 , respectively, when operated in argon the plasma generates higher densities of reactive species. Additionally, a novel molecular beam chopper design with linear movement has been successfully tested in the mass spectromerty setup as an alternative to a rotating chopper. [ABSTRACT FROM AUTHOR]

Radiation triggers cell death events through signaling proteins, but the combined mechanism of these events is unexplored The Wnt canonical pathway, on the other hand, is essential for cell regeneration and cell fate determination. The relationship between the Wnt pathway's response to radiation and its role in radiotoxicity is overlooked, even though it is a critical molecular control of the cell. The Wnt pathway has been predicted to have radioprotective properties in some reports, but the overall mechanism is unknown. We intend to investigate how this combined cascade works throughout the radiation process and its significance over radiotoxicity. Thirty adult mice were irradiated with electron beam radiation, and 5 served as controls. Mice were sacrificed after 24 h and 30 days of irradiation. We assessed DNA damage studies, oxidative stress parameters, mRNA profiles, protein level (liver, kidney, spleen, and germ cells), sperm viability, and motility. The mRNA profile helps to understand how the combined cascade of the Wnt pathway and NHEJ work together during radiation to combat oxidative response and cell survival. The quantitative examination of mRNA uncovers unique critical changes in all mRNA levels in all cases, particularly in germ cells. Recuperation was likewise seen in post-30 day's radiation in the liver, spleen, and kidney followed by oxidative stress parameters, however not in germ cells. It proposes that reproductive physiology is exceptionally sensitive to radiation, even at the molecular level. It also suggests the suppression of Lef1/Axin2 could be the main reason for the permanent failure of the sperm function process. Post-irradiation likewise influences the morphology of sperm. The decrease in mRNA levels of Lef1, Axin2, Survivin, Ku70, and XRCC6 levels suggests radiation inhibits the Wnt canonical pathway and failure in DNA repair mechanisms in a coupled manner. An increase in Bax, Bcl2, and caspase3 suggests apoptosis activation followed by the decreased expression of enzymatic antioxidants. Controlled several interlinked such as the Wnt canonical pathway, NHEJ pathway, and intrinsic apoptotic pathway execute when the whole body is exposed to radiation. These pathways decide the cell fate whether it will survive or will go to apoptosis which may further be used in a study to counterpart and better comprehend medication focus on radiation treatment (1) Electron beam radiation penetrates inside the cell leading to the production of free radicals, (2) which further produces ROS, RNS, and lipid peroxidation. (3) To counteract with ROS and RNS, SOD, Cat, and iNOS produce to scavenge free radicals. (4) Wnt3a, a natural activator of the Wnt canonical pathway binds to the Fz receptor and starts Wnt canonical pathway for cell proliferation and survival from radiation. (1) Electron beam radiation also cause DSB which further activates (5) NHEJ pathway for DNA repair. (1) Electron beam initiate the intrinsic apoptotic pathway (6) which leads to cell death. Survivin a candidate molecule of (4) Wnt canonical pathway inhibit the action of the intrinsic apoptotic pathway by inhibiting caspase 3 which rescue cell from apoptosis. [ABSTRACT FROM AUTHOR]

26 Lin, Z., Simeone, D.M., Anderson, M.A., Brand, R.E., Xie, X., Shedden, K.A., Ruffin, M.T., and Lubman, D.M. Use of non-porous reversed-phase high-performance liquid chromatography for protein profiling and isolation of proteins induced by temperature variations for Siberian permafrost bacteria with identification by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and capillary electrophoresis-electrospray ionization mass spectrometry. 46 Nie, S., Yin, H., Tan, Z., Anderson, M.A., Ruffin, M.T., Simeone, D.M., and Lubman, D.M. 76 Zhu, J., He, J., Liu, Y., Simeone, D.M., and Lubman, D.M. [Extracted from the article]

Airborne quantum key distribution (QKD) that can synergize with terrestrial networks and quantum satellite nodes is expected to provide flexible and relay links for the large-scale integrated communication network. However, the photon transmission rate would be randomly reduced, owing to the random distributed boundary layer that surrounding to the surface of the aircraft when the flight speed larger than Mach 0.3. Here, we investigate the airborne QKD performance with the BL effects. Furthermore, we take experimental data of supersonic BL into the model and compare the airborne QKD performance under different conditions. Simulation results show that, owing to the complex small-scale turbulence structures in the supersonic boundary layer, the deflection angle and correspondingly drifted offset of the beam varied obviously and randomly, and the distribution probability of photons are redistributed. And the subsonic and supersonic boundary layer would decrease ~35.8% and ~62.5% of the secure key rate respectively. Our work provides a theoretical guidance towards a possible realization of high-speed airborne QKD. [ABSTRACT FROM AUTHOR]