Momentum Transfer Cross Sections Research Articles

Calculations of positron scattering from F, F2, HF, and various fluorocarbons

Abstract Single center convergent close-coupling (CCC) calculations have been completed for positron scattering from atomic fluorine. Total, electron-loss, positronium-formation, direct ionization, momentum transfer, elastic, bound-state excitation, and stopping power cross sections have been determined for energies between threshold and 5000 eV. Past calculations for this scattering system exist only for elastic and momentum-transfer cross sections. For high energies, good agreement is found between current and past results. At low energies, however, large differences are found between the current calculations and previous results. The atomic fluorine results are then used in a modified independent atom approach to calculate cross sections for positron scattering on F2, HF, CF4, C2F6, C3F6, C3F8, and C6F6. The current molecular results are typically higher than previous positron experiments across the calculated energy range, however, these experiments were not corrected for the forward angle scattering effect and likely underestimate the true result. Good agreement is found between the current positron results and previous electron experiments and calculations at high energies.

Cross sections for electron scattering from atomic gallium

Abstract The relativistic convergent close-coupling method is applied to calculate cross sections for electron scattering on atomic gallium.
The integrated and momentum-transfer cross sections for elastic scattering are presented from the 4s 24p 4P1/2,3/2 electronic states for incident energies between 0.03 eV and 1000 eV. 
Integrated excitation cross sections are also presented from these initial states to the 4s 24[d,f], 4s 25[s,p,d], 4s 26[s,p] and 4s 27s manifolds, as well as cross sections for excitation of the 4s 24p 4P1/2 state to the 4s 24p 4P3/2 state. 
Estimates were presented for the total single ionisation cross section and total cross section for scattering on gallium in the 4P1/2,3/2 states, including direct ionisation from the 4p, 4s and 3d electrons, and excitation−autoionisation contributions from 4s and 3d electrons.
The estimated total single ionisation cross section was found to agree well with existing experimental data.

A semiempirical model for low energy electron–atom transport cross sections: The case of noble gases

A semiempirical approach to describe low energy electron–atom transport cross sections of easy implementation and reproduction is presented. The heart of the model is an energy independent two-parameter potential that was adjusted to reproduce the accurate total cross sections for He, Ne, Ar and Kr, measured with a threshold photoelectron source technique from meV up to 20 eV. Once the potential was conceived, the model was validated by comparing the values obtained for the calculated scattering lengths and phase shifts with the respective quantities previously reported in the literature. We close the article by presenting the momentum transfer and viscosity cross sections. Good agreement is found when compared to the similar data obtained from swarm experiments, from phase shifts according to differential cross section measurements and to the cross sections reported by sophisticated ab initio relativistic many-body calculations. Tables for the phase shifts and cross sections are provided for direct use and applications.

Elastic cross section data for precursor molecules used in low-temperature plasmas: Sn(CH3)4 and Ga(CH3)3

Tetramethyltin [Sn(CH3)4] and trimethylgallium [Ga(CH3)3] are important source molecules of Sn and Ga atoms which are used in manufacturing techniques involving low-temperature plasmas. Accurate numerical modeling of plasma environments requires a comprehensive set of electron scattering cross sections by these precursor molecules. Here, we report the elastic integral, differential, and momentum transfer cross sections for electron collisions with Sn(CH3)4 and Ga(CH3)3 for energies ranging from 0 to 30 eV. Our calculations were carried out with the Schwinger multichannel method implemented with pseudopotentials and considered two levels of approximation in our calculations, namely static-exchange and static-exchange plus polarization. We identified three shape resonances for Sn(CH3)4 and one clear low-lying resonance for Ga(CH3)3. The low-energy behavior of the s-wave cross section and eigenphase was investigated and, for both molecules, we found evidence of a Ramsauer–Townsend (RT) minimum and a virtual state. Our results indicate that negative differential conductivity would occur in a gas composed of Sn(CH3)4. On the other hand, this effect would be suppressed in a gas of Ga(CH3)3 due to an overlap between the position of the RT minimum and the shape resonance in the momentum-transfer cross section.

Elastic Electron Scattering from Be, Mg, and Ca

We present a comprehensive set of theoretical results for differential, integrated, and momentum transfer cross sections for the elastic scattering of electrons by beryllium, magnesium, and calcium at energies below 1 keV. In addition, we provide Sherman function values for elastic electron scattering from calcium in the same energy range. This study extends the application of our method of calculations, already employed for barium and strontium, to all stable alkaline-earth-metal atoms. Our semi-empirical approach to treating target polarization has produced in our earlier work a satisfactory agreement with experimental values and precise theoretical results such as convergent close-coupling calculations for barium. The present data are expected to be of similar high accuracy, based on our previous success in similar calculations for barium and all inert gases.

Transport cross sections and collision integrals for N(4S)–O(3P) and N(4S)–O(1D) interactions in high-temperature air plasmas

Collisions between nitrogen (N) and oxygen (O) play a crucial role in determining transport coefficients in high-temperature atmospheres of Earth and planetary. In this study, the momentum transfer, viscosity, third-moment, and fourth-moment transport cross sections for the N(4S)–O(3P) and N(4S)–O(1D) interactions are reported in the collision energy range of 10−6–10 Hartree based on the classical and semiclassical methods. The new and accurate potential energy curves for N–O interactions, which are used to provide the input for calculations of the cross sections, are calculated based on the state-of-the-art ab initio method. The classical and semiclassical collision integrals are provided at 300–50 000 K, and the results support the calculation of transport coefficients in a third-order approximation. In particular, the collision data for the N(4S)–O(1D) interaction based on ab initio points are reported for the first time. The calculated transport cross sections and collision integrals are helpful for studies of modeling the high-temperature air plasmas.

Predicting differential cross sections of electron scattering from N2 using DCMe method

The e + N2 scattering system is usually a typical testing model in electron scattering from molecule. The accurate resonant and the non-resonant differential cross sections (DCSs), integral cross sections (ICSs) and momentum transfer cross sections (MTCSs) of electron scattering from N2 molecule are studied using limited experimental DCSs and the difference converging method for electron scattering (DCMe) proposed in our previous work. The DCMe results well represent those known experimental data and obtain all unknown ones at given energies. It supplies a theoretical alternative to correctly predict the DCSs those may be experimentally unknown or hard to have quantum mechanically. This study shows that.

Positron scattering from structurally related biomolecules.

We report the integral elastic, momentum transfer, and inelastic (positronium formation and ionisation) cross sections for positron scattering from structurally related molecules. The molecules chosen for the current investigation are formamide, formylphosphine, formic acid, N-methylformamide, acetone, acetic acid, and formaldehyde. The cross sections were calculated using the optical potential approach and the complex scattering potential-ionisation contribution method for impact energies between 1 and 5 keV. A sizable repository of data is now available for positron scattering from various atoms and molecules; however, data on the impact of positrons on current targets is still scarce and fragmented. While most cross sections are the first of their kind, we analyze our total cross sections (TCSs) with the previous literature available, which has become attractive to researchers trying to model the tracks of charged particles in matter. TCSs have recently seen a resurgence in popularity thanks to their utility in specifying the mean-free path between the collisions of such simulations. We find good qualitative convergence between experimental and theoretical results below and above the positronium formation threshold. However, around the threshold region, a significant discrepancy is encountered, which can be accounted for due to the experiment's lack of forward angle scattering effect discrimination. This level of agreement evolves to become quantitative at intermediate and higher energies.

Positron and Electron Impact Elastic Scattering by Atomic Beryllium

Theoretical results for positron and electron elastic scattering from beryllium atom at incident energies ranging from the first inelastic threshold to 200 eVare presented. Elastic, total, momentum transfer, and differential cross sections are computed using both the first order distorted wave Born approximation andthe optical potential approaches utilizing a complex potential. We have shown that our data agree fairly well with the available data and provided the details of thePhysics in case of discrepancies. This study demonstrates the importance of accurate atomic elastic scattering cross sections.

First Observation of Neutral Bremsstrahlung Electroluminescence in Liquid Argon.

A recent discovery of additional mechanism of electroluminescence (EL) in noble gases due to the neutral bremsstrahlung (NBrS) effect led to a prediction that NBrS EL should be present in noble liquids as well. A theoretical model of NBrS EL in noble liquids was developed accordingly in the frameworks of Cohen-Lekner and Atrazhev. In this work, we confirm this prediction: For the first time, visible-range EL has been observed in liquid argon at electric fields reaching 90 kV/cm, using gas electron multiplier (GEM) and thick GEM structures. Absolute light yields of the EL were measured and found to be in excellent agreement with the theory, provided that the momentum-transfer cross section of electron scattering is used for calculation of the NBrS cross section (instead of the energy-transfer one).

Low-Energy Electron Scattering from Pyrrole and Its Isomers.

Low-energy electron scattering from pyrrole and its isomers, such as 2-H pyrrole, cyclopropanecarbonitrile, and Z-2 butenenitrile, is explored in detail in this article. The electron interaction with the target molecules was studied through R-matrix theory. We have used minimal STO-3G and advanced DZP basis sets on a fine energy grid from 0.1 to 12 eV electron energy in the calculation. The properties of the STO-3G and DZP-based targets, such as their ionization energy, polarizability, dipole moment, rotational constant, principal moment of inertia, ground-state energy, and orbital energies, were investigated and compared to previously reported data. The elastic and inelastic channels showed the appearance of shape and Feshbach resonances for pyrrole and its isomers. The ultralow-energy region resonance was observed for Z-2 butenenitrile at 0.47 eV. With STO-3G and DZP basis sets, we estimated elastic, excitation, and momentum-transfer cross sections. The differential cross section for the present polar molecules was studied at 5 eV. The dissociative electron attachment channel for pyrrole and its isomers was studied for the pyrrolide anion. The data presented here will be helpful in astrophysical, astrochemical, atmospheric, and low-energy plasma modeling due to the presence of pyrrole and its isomers and the pyrrolide anion in the celestial bodies. The estimated data are also helpful in the biomedical field, radiation therapy, and pharmaceuticals.

Electron Impact Cross Sections and Transport Studies of C3F6O

Electron impact scattering from C3F6O is studied in this work. The R-matrix method was used for the calculations of elastic, momentum transfer, and excitation cross sections. The attachment cross section was obtained through a parametric estimator based on the R-matrix outputs. The Binary-Encounter-Bethe (BEB) method was used for computing the ionization cross section. The obtained cross section set was used for the transport studies using the BOLSIG+ code, which is a two-term Boltzmann equation solver. The present calculation was performed for steady-state Townsend experimental conditions for E/N, covering a range of 100–1000 Td. The critical dielectric strength of pure C3F6O was found to be 475 Td, which is much greater than that of SF6 (355 Td). The effect of the addition of different buffer gases, such as CO2, N2, and O2, was also examined. For the C3F6O–CO2, C3F6O–N2, and C3F6O–O2 mixtures with 65%, 55%, and 60% C3F6O, respectively, the critical dielectric strength was determined to be essentially the same as that of pure SF6. The presence of synergism was confirmed for these gas mixtures. We further derived the Paschen curve using a fitting method with the transport parameters as the basic inputs. The minimum breakdown voltage of C3F6O accounted for only 55% of that of SF6. The buffer gas mixture improved the condition; however, the performance of CO2 and O2 mixtures was not satisfactory. The addition of N2 as the buffer gas significantly improved the breakdown property of the gas. The mixture of ≥99% of N2 or ≤1% of C3F6O gave a better breakdown characteristic than SF6. Any proportion ≥90% of N2 or ≤10% of C3F6O was suitable in the higher pressure ranges. The present work demonstrates the potential of C3F6O as a substitute gas for SF6 with a negligible environmental threat.

Low energy electron induced chemistry for e-bromine molecule scattering

The present study focuses on electron collision with bromine molecule, employing ab-initio scattering calculations. Using the R-matrix method, we calculated elastic and inelastic cross-sections using two different scattering models: static exchange with polarization and close-coupling. Our findings reveal total three low energy resonances for e-Br2 scattering which are primarily formed through transient negative ions. This observation is supported by dissociative electron attachment cross-section analysis, potential energy curves, and molecular orbital diagrams. Out of these three, first is at zero-energy, the electron attachment is recognized as shape-resonance and further two π* resonances as core-excited resonances. Present computation becomes more important as many cross-sections are reported as bench mark results in absence of any reported data. For instance: elastic, differential, momentum transfer, excitation and total cross-section. Comparing our results with sparse existing literature, we find good agreement.

Differential cross sections for the N(4S)-H(2S), N(4S)-H[formula omitted] and N[formula omitted](3P)-H(2S) elastic collisions

The differential cross sections for the N(4S)-H(2S), N(4S)-H+ and N+(3P)-H(2S) elastic collisions were calculated and reported in the energy range of 10−4–3.7 hartree for the studies of transport properties of ionized gases with the Boltzmann equation.They were verified by comparison with the integrated and momentum-transfer cross sections. The importance of appropriate grid of angles and possibility of neglecting the smallest phase shifts are discussed.

Temperature-Dependent Functions of the Electron–Neutral Momentum Transfer Collision Cross Sections of Selected Combustion Plasma Species

The collision cross sections (CCS), momentum transfer cross sections (MTCS), or scattering cross sections (SCS) of an electron–neutral pair are important components for computing the electric conductivity of a plasma gas. Larger collision cross sections for electrons moving freely within neutral particles (molecules or atoms) cause more scattering of these electrons by the neutral particles, which leads to degraded electron mobility, and thus reduced electric conductivity of the plasma gas that consists of electrons, neutral particles, and ions. The present work aimed to identify the level of disagreement between four different methods for describing how electron–neutral collision cross sections vary when they are treated as a function of electron temperature alone. These four methods are based on data or models previously reported in the literature. The analysis covered six selected gaseous species that are relevant to combustion plasma, which are as follows: carbon monoxide (CO), carbon dioxide (CO2), molecular hydrogen (H2), water vapor (H2O), potassium vapor (K), and molecular oxygen (O2). The temperature dependence of the collision cross sections for these species was investigated in the range from 2000 K to 3000 K, which is suitable for both conventional air–fuel combustion and elevated-temperature oxygen–fuel (oxy-fuel) combustion. The findings of the present study suggest that linear functions are enough to describe the variations in the collision cross sections of the considered species in the temperature range of interest for combustion plasma. Also, the values of the coefficient of variation (defined as the sample standard deviation divided by the mean) in the collision cross sections using the four methods were approximately 27% for CO, 42% for CO2, 13% for H2, 39% for H2O, 44% for K, and 19% for O2. The information provided herein can assist in simulating magnetohydrodynamic (MHD) power generators using computational fluid dynamics (CFD) models for combustion plasma flows.

Theoretical investigations of positron collisions with phosphorus-containing compounds

A theoretical investigation of positron scattering from phosphorus-containing compounds (viz., PH3, P2H4, PCl3, PF3, PBr3, POF3, POCl3, and H2PO4) is reported in this article. The quantum mechanical potential scattering approach is utilized to calculate integral elastic, excitation, momentum transfer, direct ionization, positronium formation, total ionization, inelastic, differential, and total cross sections on a fine energy grid from 1 to 5000 eV. The ionization contribution in the inelastic scattering is estimated using the complex scattering potential-ionization contribution technique. Prior research on positron collisions with these targets is scarce; as a result, the purpose of this study is to make up, at least in part, for this deficiency in cross-section data. In addition to being pertinent to positron transport analyses, such as Monte Carlo methods, the current results should be useful to benchmark the accuracy and validity of positron molecule collision computations and, more significantly, to compare these calculations with related electron scattering outcomes. Furthermore, the calculated cross sections of PH3 are compared with NH3 and other phosphorus-containing compounds. The analysis makes it abundantly evident that the atoms on the periphery of a molecule have a substantially larger impact on the scattering process than the central atom. To analyze the scattering dynamics of positrons and their anti-particle electrons, a comparative study of cross sections of H2PO4 and H2SO4 is also presented. For most of these targets, positron calculations are carried out for the first time.

Collisions of low- to intermediate-energy electrons with acetonitrile

A systematic investigation was carried out on the elastic scattering of low- to intermediate-energy electrons ( = 0.1–1000 eV eV) by acetonitrile (CH3CN). We calculated differential (DCS), integral (ICS), momentum-transfer (MTCS), and total absorption cross sections from 0.1 to 1000 eV energy range using an absorption-effects-implemented ePolyScat-E3 suite of codes, which applies the Schwinger variational method combined with the Padé-approximants technique. Also, the screen-corrected independent atom model was used to compute DCSs, ICSs, and MTCSs from 10–1000 eV impact energies. Present results are compared to other theoretical and experimental data when available. In general, our DCS and MTCS results show a good agreement with available data, however, the ICSs and the resonance features exhibit fair accordance. Our results show two shape-resonance structures: one at about 3.4 eV and a second at about 7 eV. They are labeled as and , and comprise the and scattering channels, respectively.

Neutral Bremsstrahlung Electroluminescence in Noble Liquids Revisited

Recent discovery of neutral bremsstrahlung (NBrS) mechanism of electroluminescence (EL) in noble gases in two-phase detectors for dark matter searches has led to a prediction that NBrS EL should be present in noble liquids as well. A rigorous theory of NBrS EL in noble liquids was developed accordingly in the framework of Cohen–Leckner and Atrazhev formalism. It has been recently followed by the first experimental observation of NBrS EL in liquid argon, which however deviates significantly from the previous theory. Given these results, we revise previous theoretical calculations of EL NBrS in noble liquids to be consistent with experiment. In particular, NBrS EL yield and spectra were calculated in this work for argon, krypton, and xenon with momentum-transfer cross section for electron scattering (instead of energy-transfer one) being used for calculation of NBrS cross section. The results for light noble liquids, helium and neon, are also reexamined.

Theoretical process for the investigation of dielectric characteristics of F3NO as an alternative gas for SF6

To examine the possibility of using a gas molecule as an SF6 alternative gas, the insulation properties of the molecule must be estimated. In this work, we present a theoretical approach to calculate geometry parameters, electron scattering cross sections, and transport properties of nitrogen fluoride oxide (F3NO), which we have selected as an alternative to SF6. The molecular minimum structure of F3NO was optimized using the ɷB97X-D functional combined with the aug-cc-pVTZ basis set. Using this initial geometry obtained by the molecular structure calculation, the R-matrix calculation was done to obtain the elastic and momentum transfer cross section. The BE-f method was used for electronic excitation cross section. For the ionization cross section, the binary encounter Bethe method was used. From the calculated cross section data, the electron transport coefficients and reaction coefficients were calculated by solving the two-term approximated Boltzmann equation to investigate the discharge and insulation characteristics.

Partial EEDF analysis and electron diagnostics of atmospheric-pressure argon and argon–helium DBD plasma

Partial arbitrary electron energy distribution function (EEDF) results for cold atmospheric-pressure plasma are reported. The EEDF is obtained using the visible bremsstrahlung inversion (VBI) method. This machine learning method requires only optical emission spectroscopy (OES) measurement and a momentum transfer cross section to determine a partial EEDF. Numerical EEDF of a pure-argon dielectric barrier discharge dataset with changing peak-to-peak voltage and a helium–argon discharge with changing mixture ratio are reported. Resemblance between the numerical EEDF and a two-temperature Maxwell distribution is observed and a simplified three-point numerical EEDF is obtained. The electron temperature and relative electron number density for the bulk and high-energy electron populations are measured. The bulk electron temperature was consistently 0.3 eV. For pure argon, the high-energy electron temperature decreased exponentially from 3 to 2.2 eV with increasing peak-to-peak voltage from 3.6 to 6.3 kV. For the helium–argon dataset, the high-energy electron temperature decreased linearly from 4.2 to 2.2 eV with increasing argon fraction 25%–100%. From an OES measurement, the arbitrary EEDF can be observed by utilization of the VBI method. Based on this numerical EEDF, appropriate assumptions can be applied to simplify the quantification of electron diagnostics.