Thin copper films by plasma CVD using copper-hexafluoro-acetylacetonate

Thin copper films are produced by plasma-enhanced chemical vapour deposition (PECVD) using copper-hexafluoro-acetylacetonate (CF₃-CO-CH=C(O)-CF₃)₂Cu in argon-hydrogen mixtures. Film qualities depend on power density, gas flow, and substrate temperature. ESCA spectra show no Cu-F bonds in the films.     

Wei Hua’s four-parameter potential: Comments and computation of molecular constants αe and εeXe

The value of adjustable parameterC in the four-parameter potentialU(r) =D _e [(1 - exp[-b(r -r _e)])/(1 -C exp[-b(r -r _e)])]² has been expressed in terms of molecular parameters and its significance has been brought out. The potential so constructed, withC derived from the molecular parameters, has been applied to ten electronic states in addition to the states studied by Wei Hua. Average mean deviation for these 25 states has been found to be 3.47 as compared to 6.93, 6.95 and 9.72 obtained from Levine, Varshni and Morse potentials, respectively. Also Dunham’s method has been used to express rotation-vibration interaction constant (α_e) and anharmonicity constant (ω_ex_e) in terms ofC and other molecular constants. These relations have been employed to determine these quantities for 37 electronic states. For α_e, the average mean deviation is 7.2% compared to 19.7% for Lippincott’s potential which is known to be the best to predict these values. Average mean deviation for (ω_ex_e) turns out to be 17.4% which is almost the same as found from Lippincott’s potential function.     

Nonequilibrium Ionization by Vibrationally Excited Molecules in Supersonic Flows

The results of experimental investigations on thermal nonequilibrium ionization in CO₂: N₂: He mixtures are presented. Measurements of electron density, n_e, in vibrationally excited nitrogen were made in a supersonic flow with different CO₂ contents as well as in a CO₂: N₂: He = 1 : 5 : 4 mixture laser gas. The mixtures were heated in a shock tube and expanded through a supersonic nozzle. Furthermore, supersonic mixing of N₂ and CO₂ + He was used in some experiments. The measured values of n_e in the plenum chamber and in the supersonic nozzle are reported, and the processes responsible for nonequilibrium ionization in a laser-active medium are discussed.     

The fast and slow rotation approximations for the description of the kinetics of triplet radical quenching and electron spin polarization

The specific features of the mechanisms and kinetics of generation of net chemically induced dynamic electron polarization (CIDEP) in triplet radical quenching (TRQ) in liquids is analysed in detail. The problem reduces to the analysis of fairly strong non-adiabatic transitions between states of the triplet radical spin Hamiltonian which are known to determine CIDEP generation in TRQ. The analysis is performed in two limits of fast and slow rotation of the triplet molecule using the previously developed method of treatment for non-adiabatic transitions. The method made it possible to derive analytical formulas for the CIDEP generation probability P _e and rate K _e, and for the TRQ probability P _q and rate K _q in the case of relatively strong quenching. It is shown that the dependence of K _e on the relative diffusion coefficient D _r is of bell shape and cannot be described correctly by the usually applied relation K _e = K _q P _e.     

Effective thermal conductivity of granulated two-phase systems at interstitial air pressures

Considering the htermal conduction through molecular collisions an expression for the effective thermal conductivityλ _e of loose and granular two-phase materials at different interstitial air pressure has been derived. The dependence ofλ _e on pore and particle sizes, characteristic pressure and radiative heat transfer is also discussed. Calculated values ofλ _e of glass beads and loose building materials are compared with reported results.     

Abnormal characteristics of binary molecular clusters in DMSO–ethanol mixtures under external electric fields

For the nonlinearly phenomena on the dielectric properties of dimethyl sulfoxide (DMSO)–ethanol mixtures under a low intensity microwave field, we propose a conjecture that there exist some abnormal molecular clusters. To interpret the mechanism of abnormal phenomena and confirm our conjecture about the existence of abnormal molecular clusters, an in-depth investigation about the structure evolutions of (DMSO)_m(C₂H₅OH)_n (m = 0–4; n = 0–4; m + n ≤ 4) molecular clusters induced by external electric fields has been given by using density functional theory. The results show that there exist some binary molecular clusters with large cluster radii in mixtures, and some of them are unstable under exposure of electric fields. It implies that the existence of certain abnormal molecular clusters in DMSO-ethanol mixtures results in their abnormality of dielectric properties.     

Coupled cluster calculations for the interstellar molecule HC3NH+

An accurate equilibrium structure has been established for the linear interstellar molecular cation HC₃NH⁺: r _1e(CH) = 1.0703Å, R _1e(C₍₁₎C₍₂₎) = 1.2097 Å, R _2e(C₍₂₎C₍₃₎) = 1.3509Å, R _3e(C₍₃₎N) = 1.1448 Å and r _2e(NH) = 1.0079Å. Ground-state rotational constants for less abundant isotopomers are predicted with an uncertainty of about 0.02 MHz. The equilibrium dipole moment of HC₃NH⁺ is calculated to be 1.61 D.     

Materials parameters and ion-induced track formation

ABSTRACT

The role of various materials parameters in track formation is discussed. Experimental information is utilized showing a direct quantitative relationship in different solids between the melting points T_m and the ion-induced track radii R_e without involving other materials parameters. It is shown for Θ?=?T_m???T_ir (T_ir – irradiation temperature) that Θ～exp{?R_e²/w²} for S_e/N?=?constant, where S_e and N are the electronic stopping power and the number density of atoms and w?=?4.5?nm. The validity of this universal-type relation is demonstrated for 14 different insulators including LiNbO₃ and BaFe₁₂O₁₉. It is shown that the thermal diffusivity D, the heat of fusion L the band gap energy E_g and the absorption radius α_e of the electron distribution must not affect the track sizes as this would not be coherent with this identical behavior. Original reports on LiNbO₃ and BaFe₁₂O₁₉ with opposite conclusions are critically analyzed. It is shown that an arbitrary value of the ion energy was used in the analysis that modified substantially the results leading to an undue justification of the contribution of L and E_g in apparent agreement with the experimental data.     

Rotational Analysis of the 1–4 Band of the B 2Σ+–X 2Σ+ System of 14C16O+

ABSTRACT

High-resolution emission spectrum of the 1–4 band of the B ²Σ⁺–X ²Σ⁺ transition of ¹⁴C¹⁶O⁺ was observed for the first time by conventional emission spectroscopy. The band spectrum was excited in a water-cooled Geissler lamp filled with commercial gaseous carbon monoxide enriched in about 80% of the radiocarbon ¹⁴C. A rotational analysis has been carried out and obtained molecular constants have been merged with previously published data for the B ²Σ⁺–A ²Π_i and A ²Π_i–X ²Σ⁺ transitions. The principal equilibrium constants for the ground X ²Σ⁺ state obtained from this work are ω_e = 2121.7726(98), ω_e x _e = 13.9055(27), B _e = 1.815290(30), α_e = 1.6594(33) × 10^?2, and γ_e = ? 0.377(73) × 10^?4 cm^?1. Also, presently known experimental equilibrium molecular constants of the X ²Σ⁺ states of the CO⁺ isotopic molecules are summarized and isotopic dependence of the B _e and ω _e constants is discussed.     

Photo-Production of Muons

The total cross-section for the photo-production of muons in the reaction γ + e^? → μ^? + v_e + v_μ is calculated. The dependence of the total cross-section on the incident photon energy is explicitly shown.     

Utilization of rotational and vibrational temperatures for plasma diagnostics of high-pressure discharges

In the spectra of high-pressure discharges excited in molecular gases, very intensive molecular spectral bands may usually be observed. We may determine the rotational and vibrational temperatures without difficulty, however, the rotational and vibrational temperatures (T _r, T_v) do not offen equal to the temperature of neutral gas (T ₀) or to that of electrons (T _e). If the collision cross sections of electronic, atomic, and molecular excitation (deexcitation) are known, we may then calculate the dependence of the rotational and vibrational temperatures onT _e,T ₀,N _e and the pressure of the gas. The calculations have been performed for pure N₂ and for an Ar-N₂ mixture at atmospheric pressure. The computed graphs make it possible to determine some of the values 4T _e,T ₀,N _e if the temperaturesT _r andT _v are known.The author wishes to extend his thanks to Prof. V. Truneek for valuable comments and to Mr. A. Struka for the preparation of the diagrams.     

Theoretical study of the SrLi+ molecular ion: structural,electronic and dipolar properties

ABSTRACT

The structural and electronic properties of (SrLi)⁺ molecular ion have been determined by the use of ab initio approaches. Potential energy curves (PECs) with their spectroscopic constants (R_e, D_e, ω_e, T_e, B_e and ω_eχ_e) have been calculated. Also, the vibrational properties and the electric dipole moments, either permanent (PDM) or transition (TDM) ones, have been investigated and analysed. Large Gaussian basis sets, the full valence configuration interaction (FCI) and the formalism of non-empirical pseudo-potential including the two approaches, effective core potential (ECP) and core polarisation potential (CPP), are analysed. Therefore, (SrLi)⁺ is considered as a two effective electrons system. Numerous excited states of symmetries ^1,3Σ⁺, ^1,3Π and ^1,3Δ dissociating below the ionic limit Sr²⁺Li^? have been investigated. This study shows interesting behaviours around the avoided crossing related to charge transfer involving important processes in physics and astrophysics such as dynamics, pre-dissociation and inelastic transitions.     

Proton shielding function for hydrogen chloride

For a diatomic molecule the nuclear shielding constant σ(ξ) of either nucleus can be expanded as a power series in the relative displacement from equilibrium ξ. Thus the nuclear shielding function is

where ξ=(r-r _e)/r _e with r the actual bond length and r _e the equilibrium bond length. The σ_e ⁽ⁱ⁾ are molecular parameters. By experimental observation of the temperature dependence of the proton magnetic shielding of hydrogen chloride gas it is possible, after allowing for intermolecular effects, to obtain the values σ_e ⁽⁰⁾=32·48 (±0·33) p.p.m. and σ_e ⁽¹⁾=-100 (±24) p.p.m. for the coefficients of the proton shielding function. Using this data it is possible to show that the isotope shift between H³⁷Cl and H³⁵Cl is about 0·001 p.p.m. By a comparison with earlier results for molecular hydrogen it would appear that in some instances differences in vibrational and rotational averaging may alter chemical shifts between different compounds by amounts considerably larger than the experimental error in chemical shift measurement.     

The emission spectrum of the diatomic radical, phosphorus selenide

The emission spectrum of the PSe radical is reported for the first time. Seventy-eight reddegraded bands in the region 4000–6500 Å have been measured and assigned to the A²Π-X²Π transition of PSe. Isotope shifts observed for some bandheads have been utilized in deriving the vibrational numbering. The molecular constants have been determined as (in units of cm⁻¹): ω′ = 406.9, ω′_eχ′_e = 1.3, ω″ = 556.9, ω″_eχ″_e = 1.3, and T_e = 19477.3 for the ²Π_1/2 states; and ω′_e = 402.4, ω′_eχ′_e = 1.5, ω″_e = 556.8, ω″_eχ″_e = 1.6, and T_e = 19178.0 for the ²Π_3/2 states.     

Dynamics of photosensitized singlet oxygen generation and photophysical characteristics of chlorin <Emphasis Type="Italic">e</Emphasis><Subscript>6</Subscript> in photolon ointment

We have used luminescence and absorption spectroscopy to study the dynamics of photosensitized singlet oxygen generation and the photophysical characteristics of chlorin e ₆ in Photolon ointment. We have shown that dimethylsulfoxide and polyethylene glycol 400, in concentrations comparable with their content in the ointment form of the drug Photolon, do not lead to appreciable changes in the spectral characteristics of chlorin e ₆. Substantial changes in the photophysical characteristics of the photosensitizer are observed at significantly higher concentrations of the excipients in the ointment. We have shown that in buffer solution, chlorin e ₆ forms a complex with polyethylene glycol 1500. For the first time, we have detected luminescence of singlet oxygen from the surface of biological tissue treated with Photolon ointment.     

VUV emission model of REB-heated plasma

VUV emission model of a hygrogen plasma with oxygen impurity (T _e=tens of eV,n _e 10¹⁴–10¹⁶ cm^–3,ⁿimp=1–3 % n_e) is constructed in order to judge different possibilities of plasma diagnostics (especiallyT _e measurements) in the REBEX experiments. Two sets of calculations based on the nonstationary corona model are performed: time dependent continuous and line spectra in the range 5 eV—5 keV in the constantT _e approximation (discussion ofT _e measurements by the filter-method) and time dependent intensities of selected spectral lines (2s-2p type) of ionsO ²⁺–O⁵⁺ at variableT _e (including plasma heating by REB and radiative cooling). A possibility of plasma energy content determination from radiation losses is shown.We would like to acknowledge many helpful discussions with dr. P. unka; we thank also dr. J. Ullschmied for comparing our results with diamagnetic measurements.     

Linear operators in Clifford algebras

We consider the real vector space structure of the algebra of linear endomorphisms of a finite-dimensional real Clifford algebra (2, 4, 5, 6, 7, 8). A basis of that space is constructed in terms of the operators M _{eI, eJ} defined by xe _I · x · e _J , where the e _I are the generators of the Clifford algebra and I is a multi-index (3, 7).In particular, it is shown that the family (M _{eI, eJ} ) is exactly a basis in the even case.     

An Efficient Spectroscopic Control — Technique of the Parameters of Thermic Plasmas Produced under the Condition of a Variable Current

The spectroscopic diagnostics has been carried out as an example for an argon plasma from Maecker-Shumaker type electric arc supplied by periodic variable current. It is shown that the time-dependent runs of intensity of the plasma light may be determined using an ordinary oscilloscope. We have stated that the electron concentration N_e in the plasma is the most sensitive quantity to the current pulsations. In the percentage, N_e variations at the arc axis are approximately the same as the current ones.     

Cosmological Post-Newtonian Expansions to Arbitrary Order

We prove the existence of a large class of one parameter families of solutions to the Einstein-Euler equations that depend on the singular parameter e = v_T/c{\epsilon=v_T/c} (0 < e < e₀){(0< \epsilon < \epsilon_0)}, where c is the speed of light, and v _T is a typical speed of the gravitating fluid. These solutions are shown to exist on a common spacetime slab M @ [0,T)×\mathbb T³{M\cong [0,T)\times \mathbb {T}^3}, and converge as e\searrow 0{\epsilon \searrow 0} to a solution of the cosmological Poisson-Euler equations of Newtonian gravity. Moreover, we establish that these solutions can be expanded in the parameter e{\epsilon} to any specified order with expansion coefficients that satisfy e{\epsilon}-independent (nonlocal) symmetric hyperbolic equations.