Kinetic analysis of the ionization ratio effects on a three‐species plasma

In partially ionized plasmas, the energy transferred to electrically charged species by the electromagnetic field can be partly channelized to the population of neutrals, due to interspecies collisional processes. Depending on the relative density of neutrals, these effects may govern the collective plasma dynamics by drastically modifying particle dynamics and energy‐transport processes with respect to the fully ionized plasma‐approximation models. In this work, the influence of the ionization ratio r_i on a partially ionized plasma is analysed by means of a three‐species one‐dimensional kinetic model to compute transient and steady state velocity‐dependent distribution functions. The conservative collision operators accounting for charge–charge and charge–neutral interactions allow studying several plasma scenarios with the same entire number of particles per unit of volume but for an increasing r_i parameter, in the presence of a modulated signal‐like electric field. For a sequence of plasma scenarios of fixed r_i, ranging from typical weakly ionized to highly ionized plasma values r_i ～ 10^?7–10^?4, the mass species flows are examined. These flows behave linearly with respect to r_i up to a value r_i ? 10^?5 from which the quasi‐linear dependence is critically altered. The convection–diffusion equations are solved with the semianalytical Propagator Integral Method, which behaves well to deal with conservative operators, density, and field discontinuities, allowing for the use of collision terms of disparate time and spatial characteristic scales. The results can be relevant to a wide class of plasma systems and to analyse the ionization ratio effects on transport coefficients.     

Synthesis of Self‐Stabilized Poly(N‐(3‐Amidino)‐Aniline) Particles and their CO2‐Responsive Properties

Novel CO₂‐responsive conductive polymer particles based on poly(N‐(3‐amidino)‐aniline) (or PNAAN) are reported in this work. A CO₂‐responsive N‐(3‐amidino)‐aniline (NAAN) monomer is firstly synthesized with the pendant amidine group at the meta‐position of aniline (AN) and subsequently polymerized into the PNAAN polymer by chemical oxidation. Self‐assembly of PNAAN in turn forms the polymer particles. In the strong or weak acid media, the amidine group protonates into cationic amidinium and self‐stabilizes the PNAAN particles without the use of any stabilizers. The reaction media are found to affect the polymerization rate and self‐assembly of particles, and hence the size and size distribution of the resultant particles. The particles synthesized in strong basic media show CO₂‐responsvie properties since the H⁺ released by dissolved CO₂ (dCO₂) can protonate the amidine group into hydrophilic amidinium group and result in swelling of the PNAAN particles. Zeta‐potential measurements show the reversible change of particle surface charges in the presence and absence of dCO₂. Dynamic light scattering (DLS) measurements show the particle size linearly changed with dCO₂ concentration in the range of 5 × 10^?4 and 2.5 × 10^?2 atm. This is the first reported CO₂‐responsive polyaniline (PANI) particles for dCO₂ sensing or reversible fixation of CO₂.     

Hot electron plasmas trapped in helical magnetic surfaces

Experimental studies on nonneutral (pure electron) plasmas of finite temperature, trapped in helical closed magnetic surfaces have been conducted. The helical electron plasmas are produced with thermal electrons launched from the outside of the last closed flux surface (LCFS). About 150 μs after the electron injection, the plasmas reach equilibrium state. Around the LCFS, a steep gradient of plasma space potential φ _s is formed. The corresponding radial electric field is about 2.5 kV/m. On the other hand, around the magnetic axis of helical magnetic surfaces, φ _s is almost constant, indicating that there are little electrons there. The volume-averaged electron density is on the order of 10¹³ m^–3, smaller than the Brillouin density limit. The confinement time seems to be limited by a disruptive instability, and is so far about 1.5 ms.      

超短超强激光与稀薄等离子体相互作用中后孤立子的观测

开展了超短超强激光与稀薄等离子体相互作用实验,在实验中采用等离子体单色成像法观测等离子体发光图像,捕捉到了近乎对称的环形等离子体发光结构. 在对实验结果进行分析并与理论预言进行比较后确认这是由激光-等离子体相互作用形成的后孤立子云外围的高密度等离子体壳层发光所致. 同时通过对等离子体通道的观测还发现,孤立子的形成对超短超强激光在稀薄等离子体中的传输产生了非常大的影响. 关键词： 超短超强激光 稀薄等离子体 单色成像 后孤立子     

Collective Dust‐Dust Attraction in Strong Magnetic Field

It is shown that the collective dust‐dust attraction is enhanced by strong magnetic fields larger then the critical magnetic field determined be the condition that the Lorentz force acting on ions is larger than the friction of ions on dust grains related with the dust drag. It is demonstrated that with an increase of the magnetic field the deepness of the attraction potential well is increased in all directions to the magnetic field, that the distance of the minimum of the potential well along the magnetic filed (in both directions) is changed only slightly while the distance of the minimum of the attraction potential well is substantially decreased for directions perpendicular to the magnetic field. This means that the structures formed by attraction forces such as plasma crystals will be compressed perpendicular to the magnetic field (inter‐dust distance becomes smaller) and that the melting transition temperature should increased with an increase of the strength of the magnetic field. Numerical results are presented for dependence of the attraction potential well on the ratio of the strength of the magnetic field to the critical magnetic field strength, on the parameter P = n_dZ_d/n_i (n_d and n_i being the dust and ion densities respectively) and on the temperature ratio τ = T_i/T_e (T_e and T_i being the electron and ion temperatures respectively). (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Facile Synthesis of Gd(OH)3‐Doped Fe3O4 Nanoparticles for Dual‐Mode T1‐ and T2‐Weighted Magnetic Resonance Imaging Applications

The facile hydrothermal synthesis of polyethyleneimine (PEI)‐coated iron oxide (Fe₃O₄) nanoparticles (NPs) doped with Gd(OH)₃ (Fe₃O₄‐Gd(OH)₃‐PEI NPs) for dual mode T₁‐ and T₂‐weighted magnetic resonance (MR) imaging applications is reported. In this approach, Fe₃O₄‐Gd(OH)₃‐PEI NPs are synthesized via a hydrothermal method in the presence of branched PEI and Gd(III) ions. The PEI coating onto the particle surfaces enables further modification of poly(ethylene glycol) (PEG) in order to render the particles with good water dispersibility and improved biocompatibility. The formed Fe₃O₄‐Gd(OH)₃‐PEI‐PEG NPs have a Gd/Fe molar ratio of 0.25:1 and a mean particle size of 14.4 nm and display a relatively high r₂ (151.37 × 10^?3m ^?1 s^?1) and r₁ (5.63 × 10^?3m ^?1 s^?1) relaxivity, affording their uses as a unique contrast agent for T₁‐ and T₂‐weighted MR imaging of rat livers after mesenteric vein injection of the particles and the mouse liver after intravenous injection of the particles, respectively. The developed Fe₃O₄‐Gd(OH)₃‐PEI‐PEG NPs may hold great promise to be used as a contrast agent for dual mode T₁‐ and T₂‐weighted self‐confirmation MR imaging of different biological systems.     

Generalized Linear Mixing Rule for Classical Coulomb Mixtures

It is shown that the Coulomb energy U of fully ionized ionic mixture can be written as a sum over partial contributions of ion species j: U = T Σ_j N_ju (Γ_j, y_j) (generalized linear mixing rule). In contrast to the traditional linear mixing rule U_LM = T Σ_j N_ju_OCP(Γ_j), applicable for strong coupling, the partial contribution function u depends not only on Γ_j, but on an additional parameter y_j = (r_D/r_D^OCP)² also. Here r_D and r_DOCP are Debye radiuses in the mixture and in the one component plasma at coupling parameter Γ_j, correspondingly. The parameter y_j does not depend on a specific composition of the mixture, but on the Debye radius r_D only, making function u (Γ_j, y_j) universal. The generalized linear mixing rule can be applied at any coupling parameter, if ionic mixture is not crystallized. It reproduces results of the Debye‐Hückel theory at weak coupling and traditional linear mixing rule at strong coupling. It can be easily applied to the complicated mixtures, composed of a large number of ion species. Since y_j is temperature independent, the Coulomb contribution to Helmholtz free energy of the mixture can also be presented in a form of generalized linear mixing rule (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Modification of the Xe 4d giant resonance by the C60 shell in molecular Xe@C60

It is demonstrated that in photoabsorption of the 4d ¹⁰ subshell of a Xe atom in molecular Xe@C₆₀, the 4d giant resonance that characterizes the isolated Xe atom is distorted significantly. The reflection of photoelectron waves by the C₆₀ shell leads to profound oscillations in the photoionization cross section such that the Xe giant resonance is transformed into four strong peaks. Similarly, the angular anisotropy parameters, both dipole and nondipole, are also modified. The method of calculation is based on the approximation of the C₆₀ shell by an infinitely thin bubble potential that leaves the sum rule for the 4d-electrons almost unaffected, but noticeably modifies the dipole polarizability of the 4d-shell. The text was submitted by the authors in English.     

Relaxation times for establishing steady state populations in optically thin helium plasmas

Population densities of HeI and HeII excited states are calculated from a collisional radiative model for non-LTE optically thin helium plasmas. Effect of direct ionisation-excitation of HeI to HeII states on the population density of HeII states is shown. Relaxation times for HeI states calculated from the CR model is reported forT _e from 3 to 18 eV andn _e from 10⁹ to 10¹⁶ cm⁻³. Part of a research project supported by the Department of Atomic Energy.     

纳秒激光诱导铜等离子体中原子激发态5s′~4D_(7/2)的瞬态特性研究

利用时间分辨光谱技术,研究了激光诱导Cu等离子体中激发态5s′4D7/2的形成及其辐射跃迁的瞬态特性.结果表明:在激发态5s′4D7/2原子的制备过程中,电子离子复合、粒子间碰撞机理在不同时刻分别起主导作用.激光峰值到达金属表面后500ns期间,粒子间的剧烈碰撞作用使得激发态5s′4D7/2主要通过向低能态4p′4F9o/2跃迁来转移能量.500ns以后,激发态5s′4D7/2通过以相同的概率辐射CuI465.11nm和CuI529.25nm特征谱线向低能态4p′4F9o/2和4p′4D7o/2转移能量.     

在氢和氘中寻找正的单电荷重粒子

在电磁分离器上用测量粒子荷质比的方法,在氢和氘样品中寻找正的单电荷重粒子。实验中用吸收法排除杂质本底。用特制的薄窗正比计数管记录单个粒子,并且测量粒子的能量。实验扫描了质量从65到220质子质量的重质量区域。扫描的结果给出:天然水中正的单电荷重粒子浓度的上限,在质量65到148质子质量范围内及148到220质子质量范围内,分别小于2×10^-17重粒子/氢原子及5×10^-17重粒子/氢原子。     

Determination of N and O – Atom and N2(A) Metastable Molecule Densities in the Afterglows of N2 and N2‐O2 Microwave Discharges

Early afterglows of N₂ and N₂‐O₂ flowing microwave discharges are characterized by optical emission spectroscopy. The N and O atom and N₂(A) metastable molecule densities are determined by optical emission spectroscopy after calibration by NO titration for N‐atoms and measurements of NO and N₂ band intensities for O‐atoms and N₂(A) metastable molecules. By using N₂ tanks with 50 and 10 ppm impurity, it is determined in the afterglow an O‐ atom impurity of 150‐200 ppm. Variations of the N and O‐atom and N₂(A) metastable molecule densities are obtained in the early afterglow of N₂–(9·10^–5–3·10^–3)O₂ gas mixtures. (© 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

TiO基态 (X 3 Δr) 的势能函数与光谱常数

应用群论及原子分子反应静力学方法推导了TiO分子基态(X³Δ_r)的离解极限.采用不同的计算方法,包括密度泛函B3LYP,B3P86,BP86,B3PW91和MP2,MP4方法,结合不同基组计算了TiO分子基态的平衡核间距、能量和振动频率.研究表明,使用B3LYP方法,对O原子使用6-311+G基组,Ti原子使用6-311+ +G^**基组时计算得到的平衡几何结构、分子离解能和谐振频率与实验值符合得最好.使用优选出的方法和基组对T 关键词： TiO 势能函数 光谱常数 密度泛函理论     

Fine-structure effects in relativistic calculations of the static polarizability of the helium atom

We use the relativistic configuration-interaction method and the model potential method to calculate the scalar and tensor components of the dipole polarizabilities for the excited states 1s3p ³ P ₀ and 1s3p ³ P ₂ of the helium atom. The calculations of the reduced matrix elements for the resonant terms in the spectral expansion of the polarizabilities are derived using two-electron basis functions of the relativistic Hamiltonian of the atom, a Hamiltonian that incorporates the Coulomb and Breit electron-electron interactions. We formulate a new approach to determining the parameters of the Fuss model potential. Finally, we show that the polarizability values are sensitive to the choice of the wave functions used in the calculations. Zh. éksp. Teor. Fiz. 115, 494–504 (February 1999)     

Bound States in Coulomb Systems ‐ Old Problems and New Solutions

We analyze the quantum statistical treatment of bound states in Hydrogen considered as a system of electrons and protons. Within this physical picture we calculate analytically isotherms of pressure for Hydrogen in a broad density region and compare to some results from the chemical picture. Our study is restricted to the range of intermediate temperatures 10⁴K < T < 10⁵K and not too high densities n < 10²⁴ protons per cm³, the formation of molecules is neglected. First we resume in detail the two transitions along isotherms: (i) formation of bound states occurring by increasing the density from low to moderate values, (ii) the destruction of bound states in the high density region, modelled here by Pauli‐Fock effects. Avoiding chemical models we will show, why bound states according to a discrete part of the spectra occur only in a valley in the T‐p plane. First we study virial expansions in the canonical ensemble and then in the grand canonical ensemble. We show that in fugacity representations the population of bound states saturates at higher density and that a combination of both representations provides quickly converging equations of state. In the case of degenerate systems we calculated first the density‐dependent energy levels, and find the pressure in Hartree‐Fock‐Wigner approximation showing the prominent role of Pauli blocking and Fock effects in the selfenergy (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

利用原子芯片上Z形磁阱囚禁中性87Rb原子

利用解析和数值方法计算了Z形磁阱的囚禁势，发现当囚禁中心和芯片表面距离较远时(该距离和Z形线中部导线的一半长度相差不超过一个量级)，势阱的深度不能近似表示成偏置磁场B_y对应的能量，而要减去囚禁中心的势能高度；而增加B_y进行磁阱压缩到一定值时，势阱深度反而会下降.此外介绍了原子芯片的制作方法，以及利用原子芯片上Z形磁阱囚禁中性⁸⁷Rb原子的实验装置和实验过程.最终有2×10⁶个⁸⁷Rb原子被转移到Z形磁阱中.     

Complex-scaling treatment for high-lying doubly excited resonances for screened Coulomb helium atom

This work presents an investigation on the doubly excited ¹S ^e autoionizing states of screened helium atom lying below the n = 4 threshold of the He⁺ ion. The potential generated in this system is represented by a Yukawa type potential. We have employed complex-coordinate rotation method, as it is a powerful scheme to study high lying resonances. Hylleraas type wave function is used to consider the correlation effect between all the charged particles. Our resonance parameters for the resonances lying below the He⁺ (n = 2) threshold agree well with those of the existing calculations by using the stabilization method. Resonances associated with higher thresholds are new calculations. All the present results are well converged with basis length N = 444.     

On the Theory of Hydrogen Atom Ionization by Ultra‐Short Electromagnetic Pulses

An investigation of the probability of hydrogen atom ionization by ultra‐short electromagnetic pulses is carried out in the frame of perturbation theory We consider the case when the electric field strength amplitude E₀ in a pulse by two orders lower than characteristic atomic field strength E_a (E_a ? 5.1 · 10⁹ V/cm). A detailed investigation of the dependence of the probabilities on the pulse duration was performed for Gaussian pulse shapes. In the case where the carrier frequency of the Gaussian pulse is larger than the atomic ionization potential, the probability goes to the standard limit of perturbation per unit time. At the same pulse durations, the probabilities for carrier frequencies less than the ionization potential go to zero. The frequency dependence of the ionization probability becomes equal to the standard threshold dependence with increasing pulse duration time. A comparison between the ionization effects caused by wavelet pulses without carrier frequency and Gaussian pulses with carrier frequency shows that the same ionization probability values are achieved when the pulse carrier frequency is detuned by about 20% from the ionization threshold. (© 2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Substitution and proton doping effect on SrZrO3 behaviour: high‐pressure Raman study

The high‐pressure Raman studies of pure, Yb‐modified, protonated and non‐protonated SrZrO₃ dense ceramics were performed between 0.1 and 40 GPa using a diamond anvil cell. Lanthanide‐modified, protonated SrZrO₃ perovskites are potential materials for electrolytic membrane in fuel cells and electrolysers working at medium temperature. The comparison of the Raman spectra shows important differences in the pressure behaviour between the pure and Yb‐modified SrZrO₃ ceramics. SrZrO₃ exhibits a rigid structure without any structural modification, whereas for both SrZr_0.93 Yb_0.07 O_2.965 and SrZr_0.93 Yb_0.07 O_2.962 H_0.003 a sequence of structural modifications at 10, 20 and 35 GPa is revealed. The character of these structural modifications is very similar to that observed as a function of the temperature (orthorhombic Pnma 750 °C → pseudo‐tetragonal Imma 840 °C → tetragonal I4/mcm 1070 °C → cubic Pm3m), which suggests that they can be considered as the phase transitions. Despite the low level of proton content (0.3% mole/mole), significant difference between protonated and non‐protonated compounds is observed for the 700–750 cm⁻¹ doublet assigned to the Zr O octahedron stretching mode, perturbed by an oxygen atom vacancy and/or neighbouring Yb ion. The location of proton is discussed. Copyright © 2011 John Wiley & Sons, Ltd.     

The transition from bulk to nano as a phase transition

It is demonstrated that the chemical potential of bosons trapped in a harmonic potential shows a discontinuity as a function of the number of particles in the system. In the model used, it is shown that if the number of particles is of the order of 10⁶ or greater, bulk-like behaviour is exhibited by the system. This translates to a ratio of V/V_c>10⁶ for bulk behaviour, where V is the crystallite volume of the experimental sample and V_c is the volume of the unit cell. Several experimental results covering a wide range of physical phenomena that corroborate the fact that such a number-induced phase transition indeed exists are presented.