Low frequency surface waves in the presence of an external high frequency electric field

The problem of surface sound propagation in the presence of external high frequency dipole electric field is investigated using Vlasov-Poisson equations. The structure of the electric field of these surface waves is also determined. It has been found that the ion sound waves that exist in the presence of external high frequency waves are true surface waves while those without the external field are quasi-surface waves as the former waves decay within one wavelength away from the surface.     

Photodetachment of H^- in a Static Electric Field near a Surface

The photodetachment of H^- in a static electric field near a surface is investigated based on the closed orbit theory. It is found the distance between the ion and the surface modulates the cross section of photodetachment. For an elastic surface perpendicular to electric field, the detachment spectrum displays a staircase structure, in contrast with the smooth oscillation when only the electric field exists.     

氢负离子在均匀电场和金属面附近的光剥离研究

利用闭合轨道理论,计算了氢负离子在均匀电场和金属面附近的光剥离截面.结果表明,在均匀电场的基础上加上金属面之后,在电离阈附近氢负离子的光剥离截面发生了很大的变化,和仅有均匀电场存在时的光剥离截面相比,截面的振荡幅度增大,振荡频率减小.并且在电场强度相同时,随着金属面与氢负离子距离的不断增大,光剥离截面振荡的幅度不断减小,振荡的频率不断增大,当金属面和氢负离子的距离增大到一定值时,金属面的影响消失,氢负离子的光剥离截面趋近于只有电场存在时的情况.这一结果对于研究负离子体系在界面附近的光剥离问题具有一定的参考价值.     

Magnetic field effect in photodetachment from negative ion in electric field near metal surface

Based on the closed-orbit theory, the magnetic field effect in the photodetachment of negative ion in the electric field near a metal surface is studied for the first time. The results show that the magnetic field can produce a significant effect on the photodetachment of negative ion near a metal surface. Besides the closed orbits previously found by Du et al. for the H in the electric field near a metal surface (J. Phys. B 43 035002 (2010)), some additional closed orbits are produced due to the effect of magnetic field. For a given ion-surface distance and an electric field strength, the cross section depends sensitively on the magnetic field strength. As the magnetic field strength is very small, its influence can be neglected. With the increase of the magnetic field strength, the number of the closed orbits increases greatly and the oscillation in the cross section becomes much more complex. Therefore we can control the photodetachment cross section of the negative ion by changing the magnetic field strength. We hope that our results may guide future experimental studies for the photodetachment process of negative ion in the presence of external fields and surfaces.     

Photodetachment of negative ion in a gradient electric field near a metal surface

Based on closed-orbit theory, the photodetachment of H in a gradient electric field near a metal surface is studied. It is demonstrated that the gradient electric field has a significant influence on the photodetachment of negative ions near a metal surface. With the increase of the gradient of the electric field, the oscillation in the photodetachment cross section becomes strengthened. Besides, in contrast to the photodetachment of H near a metal surface in a uniform electric field, the oscillating amplitude and the oscillating region in the cross section of a gradient electric field also become enlarged. Therefore, we can use the gradient electric field to control the photodetachment of negative ions near a metal surface. We hope that our results will be useful for understanding the photodetachment of negative ions in the vicinity of surfaces, cavities, and ion traps.     

Generation of an extraction electric field in an electromembrane ion source

A mechanism of generating an extraction field in an ion source in which a polymer track membrane with nanodimensional channels is used as an environment-vacuum interface is considered. A high electric field necessary for the effective extraction of ions from a liquid on the membrane surface into the gas phase is maintained by charging the vacuum surface of the membrane. Charging is provided by oppositely charged secondary ions resulting from the disintegration of primary cluster ions on the extraction electrode. A decrease in the source current observed when the vacuum surface discharges counts in favor of this mechanism. The extracted ion energy distribution in the neighborhood of the extraction zone is obtained by the retarding potential method. Various aspects of ion beam formation in the membrane ion source are discussed.     

Field surface ionization of nanosized molecular complexes

The changes in the parameters of the temperature dependences of field surface ionization ion currents upon an increase in the electric field strength at the emitter surface is estimated for systems in which the ions under investigation are the end product of dissociation of multimolecular complexes with a large number of degrees of freedom. Expressions for the maxima on the temperature dependence of ion currents of field surface ionization are derived. The sizes of molecular nanocomplexes formed on the emitter surface are estimated and their thermodynamic stability is analyzed.     

Simulations of plasma formation in the cathode sheath of an efficient excimer lamp

Based on the available experimental data and computer simulations, analytical approximations of the quantities characterizing electron multiplication in the cathode sheath are proposed. The critical electric field is found above which runaway electrons are observed. Using the approximations proposed, the dependences of the plasma parameters (the electron and ion densities and currents and the electric field strength) on the distance from the cathode are analyzed. Simple formulas for the total current, the cathode sheath thickness, and the cathode potential drop as functions of the electric field on the cathode surface are derived.     

Cold emission of negative ions from porous graphite

The electric field strength in the near-wall layers of thermonuclear facilities can be sufficient for the emission of negative ions from the surface of plasma facing materials. The mass spectra of negative ions from MPG-8 porous graphite at electric field strengths up to 4 × 10⁶ V/m and the surface composition of the target have been studied by ion scattering spectroscopy. The dependence of the mass composition of negative ion emission and residual gas on the sample’s temperature has been measured and a correlation between the intensity of negative hydrogen-ion emission and the desorption of water has been established. The temperature dependence of the emission of negative ions and clusters of carbon and hydrocarbon is in qualitative agreement with the chemical erosion of graphite.     

Surface Planar Ion Chip for Linear Radio-Frequency Paul Traps

We propose a surface planar ion chip which forms a linear radio frequency Paul ion trap. The electrodes reside in the two planes of a chip, and the trap axis is located above the chip surface. Its electric field and potential distribution are similar to the standard linear radio frequency Paul ion trap. This ion trap geometry may be greatly meaningful for quantum information processing.     

Electron and ion emission from liquid metal surfaces

The application of positive or negative electric fields to small-area liquid metal surfaces leads to very high brightness DC ion or pulsed electron emission. The stabilization of a cone-shaped structure by the balance of electrostatic and surface tensions forces is described. Electron and ion emission occurs by field emission and field evaporation mechanisms     

Ag-BaO薄膜在电场作用下的可见——近红外波段光学吸收特性

对超额Ba激活的Ag-BaO复合薄膜在外加垂直表面电场作用下的光学吸收特性进行了测量.结果显示,薄膜在可见—近红外光波段存在两个吸收峰,其中近红外光区的吸收峰强度随垂直表面电场的作用而降低.理论分析表明,可见光区的主吸收峰源于埋藏在BaO半导体中的Ag超微粒子的表面等离激元共振吸收;近红外光区的次吸收峰则由BaO半导体基质中杂质能级的光吸收引起,杂质能级的产生与超额Ba在BaO晶体中造成的氧缺位有关.在外加垂直表面电场作用下,BaO基质中的杂质发生电离,并导致杂质能级上束缚电子浓度减小,表现为薄膜在与杂质 关键词： 光吸收 金属超微粒子半导体复合薄膜 表面等离激元 杂质能级     

Calculations of field ionization in the field ion microscope

The ionization of a gas atom as it occurs in the field ion microscope is discussed. A wide range of values for the electric field intensity at the metal surface are considered in calculating the ionization occurring both far away from and close to the tip. Ionization distribution curves are calculated and electric fields strengths are determined at points where the distributions peak. Calculations of ionization zone widths and best image conditions are made and a new interpretation of best image conditions is considered. A new field calibration method is suggested.     

Track-membrane-based interface for field evaporation of ions from polar solutions in the diffusion-drift regime

The possibility of realization of barrier-free field evaporation regime for ions from polar solutions in the conditions when the flux of ions from the liquid is limited by their diffusion and drift from the bulk to the surface is considered. The strength of the electric field extracting ions is estimated by simulating electric fields in an ion source with a track membrane as the interface with allowance for the sizes of channels in the membrane and their density. It is shown that when time-dependent electric fields are used, the regime of barrier-free field evaporation can be realized with an appropriate choice of geometrical parameters of the membrane.     

Field extraction of ions from liquid solutions with the use of polymer track membranes

The general principles of the electric field assisted ion evaporation in the membrane ion source are considered. In the ion source, the liquid sample under investigation is placed in narrow channels of a polymer track membrane, which separates the liquid sample at atmospheric pressure from the vacuum chamber. Stability of the liquid at strong electric fields is provided by a choice of the diameters of channels and the liquid–polymer contact angle. The electric charge on the vacuum–polymer interface is of great importance for creation of the strong electric field near the liquid–vacuum interface. Such a conclusion is made from the computations of the electric field in the framework of the model developed. The mechanism of the electric field assisted evaporation of ions is discussed to explain the observed mass spectra for the ions extracted from liquid.     

Photodetachment microscopy of a hydrogen negative ion in an electric field near a metal surface

According to the semi-classical theory, we study the photodetachment microscopy of H- in the electric field near a metal surface. During the photodetachment, the electron is photo-detached by a laser and the electron is drawn toward a position-sensitive detector. The electron flux distribution is measured as a function of position. Two classical paths lead the ion to any point in the classically allowed region on the detector, and waves traveling along these paths produce an interference pattern. If the metal surface perpendicular to the electric field is added, we find that the interference pattern is related not only to the electron energy and the electric-field strength, but also to the ion-surface distance. In addition, the laser polarization also has a great influence on the electron flux distribution. We present calculations predicting the interference pattern that may be seen in experiment. We hope that our study can provide a new understanding of the electron flux distribution of negative ions in an external field and surface, and can guide future experimental research on negative ion photo-detachment microscopy.     

电场辅助溶解法实现玻璃表面金纳米粒子的形貌控制

贵金属纳米粒子由于其非常独特的光学特性和表面活性, 在光子学、 催化和生物标识等方面都有非常重要的应用. 采用离子溅射和后续热处理相结合的方法在玻璃表面形成了尺寸大约为60-80 nm的单分散的球形金纳米粒子. 在适当的温度条件下, 采用步进式增加的强直流电场, 实现了金纳米粒子的电场辅助溶解过程. 在玻璃表面的不同颜色区域, 初始球形的金纳米粒子溶解成月蚀状形貌. 结合不同颜色区域内金纳米粒子的表面等离子体共振吸收性质和扫描电镜照片, 研究了实验条件对金纳米粒子性质的影响. 结合电场辅助溶解实验过程中的电流-电压特性, 分析了金纳米粒子在强直流电场辅助下溶解的物理过程: 金粒子中动出的电子向阳极的隧穿过程作为开始, 随后是金阳离子向玻璃基体中的传输过程和阴极提供的电子与带有正电荷的金粒子相结合的过程. 详细讨论了电场辅助溶解法实现金纳米粒子形貌控制的物理机制.     

Field ion and field desorption mass spectrometry of inorganic compounds

The review on recent developments in field ionization mass spectrometry of inorganic compounds concerns the different mechanisms of ion formation at surfaces and under the influence of extremely high electric fields, field dependent chemical reactivity at surfaces and ion desorption from surfaces for mass spectrometric analysis. Applications in various areas are discussed, where this method has been used to identify surface compounds or to study kinetic phenomena at interfaces.     

Theory of surface dynamic variation during the high-temperature field evaporation

We consider the heated surface of a metallic tip to which a strong electric field is applied. At temperatures activating surface self-diffusion, crystalline outgrowths and microprotrusions arise on the surface. The latter generate ion fluxes, i.e., act as sources of high-temperature field evaporation, when a positive potential is applied to the emitter. The existence conditions for the microprotrusions on the emitter surface are discussed. It is shown that their stability is provided by the balance between three atomic fluxes: diffusion from the top of the tip, diffusion toward the top, and field evaporation from the top. Different ways of providing such a balance are discussed. In a desorption-type field ion microscope, the microprotrusions and evaporating ions are visualized as bright spots. These spots execute random motion and, at the same time, exhibit ordered cyclic displacements: the microprotrusions first form dotted rings along the developed faces of the crystalline emitter, and then these rings quickly collapse toward the center of the face. A quantitative theory of these cyclic processes is developed for the first time. It explains why the rings “calm down” before collapse and why subsequent collapse develops in an avalanchelike manner. The electric field distribution over the surface in the presence of an outgrowth is calculated, and diffusion fluxes at different stages of its growth and dissolution are analyzed. The calculation shows that the outgrowth heights are relatively small and their slopes are rather smooth.