用空心阴极放电管研究金属原子的光离化过程(Ⅱ)——铀原子的三光子电离测量

本文报道利用自制的Kr-U空心阴极放电管研究测量铀原子的单色三光子和双色三光子共振光电离谱.给出了所测得的12根强的单色三光子电离谱线和19根强的和较强的双色三光子电离谱线.表明了这一装置的优越性.     

强光场中氦原子的ATI谱

提出了一个新的处理强光中基态氦原子阈上电离谱的解析模型。由这个模型算得的基态氦原子阈上电离谱同最近的实验结果作了比较。同时简单地讨论了现在的模型对先前的模型的改进。     

用伪谱方法计算强激光场中一维原子的阈上电离谱

引入非线性空间变换,用伪谱方法求解了一维原子在强激光场中的薛定谔方程,再利用B样条函数和傅立叶级数的线性组合构造原子未微扰的本征函数,计算了一维原子在强激光场中的阈上电离谱,其结果与分裂算符法得到的结果符合得很好.     

用ICE技术观察和测定镁Mg原子3p9d(J=1,3)的自电离谱

用原子束技术—ＩＣＥ分步激发方案—激光共振电离—飞行时间质谱探测离化信号的方法，观察到了原子束中镁Ｍｇ原子３ｐ９ｄ（Ｊ＝１，３）的自电离谱，并对实验结果进行了讨论和分析。     

用ICE技术观察和测定镁Mg原子3p9d（J=1,3）的自由离谱

用原子束技术－－ＩＣＥ分步激发方案－－激光共振电离－－飞行时间质谱探测离化信号的方法，观察到了原子束中镁Ｍｇ原子３ｐ９ｄ（Ｊ＝１，３）的自电离谱，并对实验结果进行了讨论和分析。     

Gd掺杂ZnO纳米线磁耦合性质的第一性原理研究

本文利用基于密度泛函理论的第一性原理方法计算了钆(Gd)掺杂氧化锌(ZnO)纳米线的磁耦合特性. 讨论了两个Gd原子替换ZnO纳米线中不同位置Zn原子的各种可能情况. 计算发现, ZnO中掺杂的Gd原子处于相邻的位置时它们之间的相互作用是铁磁性的, 并且体系的铁磁性可以通过注入合适数目的电子来得到加强. 同时发现Gd掺杂ZnO纳米线后s-f耦合作用变得显著, 使得体系的铁磁性变得更加稳定, 这也是Gd掺杂ZnO纳米线呈现铁磁性的原因. 这些结果为实验上发现的Gd掺杂ZnO纳米线呈铁磁性提供了理论依据.     

稀土元素Gd掺杂BiFeO3的第一性原理研究

采用基于密度泛函理论的局域自旋密度近似加U法（LSDA+U:Hubbard参数）计算了多铁材料BiFeO3铁电相以及稀土元素Gd掺杂BiFeO3材料的能带结构、态密度（DOS）、原子轨道占据数和净电荷分布等,对稀土元素Gd掺杂BiFeO3可能引起的电子结构、介电常数和铁磁性的改变进行了第一性原理研究。计算结果表明：Gd掺杂对材料钙钛矿结构影响不大,BiFeO3铁电性主要来源于Fe原子3d轨道和O原子2p轨道杂化;掺杂Gd后材料中的Fe原子和O原子的共价性减弱,Bi原子和O原子的离子性增强,禁带宽度变窄,绝缘性减弱,铁磁性明显增强;计算得到的光学性质表明材料的静态介电常数有所增加。     

金属样品中铁元素激光共振电离谱的实验研究

本文采用共振激光烧蚀技术研究了钛和铝样品中铁元素的激光共振电离谱,讨论了元素的含量与共振电离谱线强度的关系及基体效应的影响.     

稀土元素Gd掺杂BiFeO3的第一性原理研究

采用基于密度泛函理论的局域自旋密度近似加U法（LSDA+U:Hubbard参数）计算了多铁材料BiFeO3铁电相以及稀土元素Gd掺杂BiFeO3材料的能带结构、态密度（DOS）、原子轨道占据数和净电荷分布等,对稀土元素Gd掺杂BiFeO3可能引起的电子结构、介电常数和铁磁性的改变进行了第一性原理研究。计算结果表明：Gd掺杂对材料钙钛矿结构影响不大,BiFeO3铁电性主要来源于Fe原子3d轨道和O原子2p轨道杂化;掺杂Gd后材料中的Fe原子和O原子的共价性减弱,Bi原子和O原子的离子性增强,禁带宽度变窄,绝缘性减弱,铁磁性明显增强;计算得到的光学性质表明材料的静态介电常数有所增加。     

铀原子单色多光子共振电离

利用Ｎｄ：ＹＡＧ激光泵浦的脉冲染料激光记录了铀原子产以多光子共振电离谱。获得的绝大多数共振属于三光子电离过程，而另外一些共振，我们认为是四光子电离过程。     

强激光场中模型氢原子和真实氢原子的高次谐波与电离特性研究

利用数值方法求解含时薛定谔方程，研究了一维、二维模型氢原子和真实的三维氢原子在强激光场中产生的高次谐波和电离特性.结果表明，在多光子电离区域和过垒电离区域，模型氢原子与真实的氢原子产生的高次谐波和电离概率差别很小；在隧道电离区域，它们产生的高次谐波的平台特征和截止位置相似，电离概率随时间变化的趋势相近，但其数值有明显的差异.对产生这种差异的原因进行了分析. 关键词： 强激光场 高次谐波 电离概率     

Mass Spectrometry,Review of the Basics: Ionization

Abstract: Mass spectrometry (MS) has become an integral tool in life sciences. The first step in MS analysis is ion formation (ionization). Many ionization methods currently exist; electrospray ionization (ESI) and matrix-assisted laser desorption ionization (MALDI) are the most commonly used. ESI relies on the formation of charged droplets releasing ions from the surface (ion evaporation model) or via complete solvent evaporation (charge residual model). MALDI ionization, however, is facilitated via laser energy and the use of a matrix. Despite wide use, ESI cannot efficiently ionize nonpolar compounds. Atmospheric pressure chemical ionization (APCI) and atmospheric pressure photo ionization (APPI) are better suited for such tasks. APPI requires photon energy and a dopant, whereas APCI is similar to chemical ionization. In 2004, ambient MS was introduced in which ionization occurs at the sample in its native form. Desorption electrospray ionization (DESI) and direct analysis in real time (DART) are the most widely used methods. In this mini-review, we provide an overview of the main ionization methods and the mechanisms of ion formation. This article is educational and intended for students/researchers who are not very familiar with MS and would like to learn the basics; it is not for MS experts.     

Time-resolved quantum dynamics of double ionization in strong laser fields

Quantum calculations of a (1+1)-dimensional model for double ionization in strong laser fields are used to trace the time evolution from the ground state through ionization and rescattering to the two-electron escape. The subspace of symmetric escape, a prime characteristic of nonsequential double ionization, remains accessible by a judicious choice of 1D coordinates for the electrons. The time-resolved ionization fluxes show the onset of single and double ionization, the sequence of events during the pulse, and the influences of pulse duration and reveal the relative importance of sequential and nonsequential double ionization, even when ionization takes place during the same field cycle.     

Electron-impact ionization cross-sections and ionization rate coefficients for atoms and ions from scandium to zinc

Using the empirical formula recently proposed, electron-impact ionization cross-sections for single ionization from the ground state are given for free atoms and for nearly all ionization stages from scandium (Z=21) to zinc (Z=30). For these species ionization rate coefficients are given under the assumption of a Maxwellian distribution of the impacting electrons. Multiple ionization, lowering of ionization potential, or collision limit are not taken into account.     

The effects of self-induced resonance in multiphoton ionization

The ionization of atoms in the presence of an intermediate two-photon resonance is considered. The ionization probability and spectral distribution of the ionized electrons are obtained for the case when the resonant is turned on adiabatically. The limiting cases of small and large ionization widths are investigated. At sufficiently large intensities of the resonant field an essential asymmetry in the ionization probability depending on the sign of the two-photon detuning is obtained.     

Development of ionization in nonequilibrium inert-gas plasmas in magnetogasdynamic channels

Effects accompanying the interaction of a flow of preionized inert gas with a magnetic field are studied: selective electron heating, the development of nonequilibrium ionization, and the onset of the ionization instability. Local and average densities and temperatures of the electrons are measured and the average ionization rate is determined. It is found that the average electron density increases as the magnetic induction is raised, in both stable and ionization unstable plasmas. The difference in the rates at which ionization develops in these two states is revealed. The mechanism for the coupling between the average ionization rate in an ionization unstable plasma and the spatial-temporal characteristics of the plasma inhomogeneities is established. Zh. Tekh. Fiz. 69, 56–61 (November 1999)     

Photoelectron angular distributions from two-photon ionization of atoms near ionization threshold

Photoelectron angular distributions(PADs) from two-photon ionization of atoms in linearly polarized strong laser fields are obtained in accordance with the nonperturbative quantum scattering theory.We also study the influence of laser wavelength on PADs.For two-photon ionization very close to the ionization threshold,most of the ionized electrons are vertically ejected to the laser polarization.PADs from twophoton ionization of atoms are determined by the second order generalized phased Bessel function at which the ponderomotive parameter plays a key role.In terms of dependence of PADs on laser wavelength,corresponding variations for the ponderomotive parameter are demonstrated.     

Kinematically complete study of dissociative ionization of by ion impact

We present a kinematically complete study of dissociative ionization of D(2) by 13.6 MeV/u S(15+) ions. The experiment allows us to unravel the competing mechanisms, namely, direct single ionization, autoionization of doubly excited states, ionization excitation, and double ionization, and to analyze the corresponding electron angular distribution from fixed-in-space molecules. The conclusions are supported by theoretical calculations in which the correlated motion of all electrons and nuclei and the interferences between them are described from first principles.     

Determination of three-photon ionization cross sections of xenon atoms from comparison with electron ionization

Multiphoton and electron-impact ionization of a gas-dynamic beam of xenon atoms are compared in order to determine the effective multiphoton ionization cross sections. The three-photon ionization cross section of the xenon atom is determined.     

Numerical simulation of the ionization dynamics of a two-electron quantum system in a femtosecond pulse

The ionization of a simple two-electron model system, viz., the one-dimensional negative hydrogen ion, is investigated using direct numerical integration of the time-dependent Schrödinger equation. The one-and two-electron ionization probabilities as functions of frequency and radiation intensity are obtained. It is shown that two-electron ionization is mediated by both direct and sequential mechanisms. The stabilization of the two-electron system against the ionization process is investigated. The data obtained are compared with calculations performed within the one-dimensional single-particle model of H^?. The photoelectron spectrum is analyzed in the region of parameters corresponding to the single-electron ionization regime.