Doppler effect in resonant photoemission from SF6: correlation between Doppler profile and Auger emission anisotropy

Fragmentation of the SF6 molecule upon F 1s excitation has been studied by resonant photoemission. The F atomiclike Auger line exhibits the characteristic Doppler profile that depends on the direction of the photoelectron momentum relative to the polarization vector of the radiation as well as on the photon energy. The measured Doppler profiles are analyzed by the model simulation that takes account of the anisotropy of the Auger emission in the molecular frame. The Auger anisotropy extracted from the data decreases with an increase in the F-SF5 internuclear distance.     

KLL Auger resonant Raman transition in metallic Cu and Ni

High energy resolution KL₂₃L₂₃ Auger spectra of polycrystalline Cu and Ni were measured using photon energies up to about 50 eV above the K-absorption edge and down to 5 eV (Cu KLL) and 4 eV (Ni KLL) below threshold. The spectra show strong satellite structures varying considerably as a function of the photon energy. In the sub-threshold region the linear dispersion of the diagram line energy positions and a distortion of the line shape as a function of photon energy, attributable to the Auger resonant Raman process, is clearly observed, indicating the one-step nature of the Auger emission. These changes in the resonant spectra are interpreted using a simple model based on resonant scattering theory in combination with partial density of states obtained from cluster molecular orbital (DV-Xα) calculations.     

X-ray excited Auger and photoelectron spectra of partially oxidized magnesium surfaces: The observation of abnormal chemical shifts

A comparison of the spectra of metals and their oxides reveals large differences between the chemical shifts in Auger and photoelectron lines. The data for magnesium are discussed in detail. An explanation is proposed which is based upon the difference in polarization energy between the double-hole state produced by the Auger electron emission and the single-hole state which results from the photoelectron emission.     

Tracking the excitation dynamics in the Mn:Ge(111) metallic interface by resonant electron spectroscopy

Resonant photoemission from the valence band of a (√3 × √3)R30° reconstructed Mn:Ge(111) metallic interface has been carefully analyzed with the aim to track the transition from resonant Raman to normal Auger emission. The transition energy has been compared with the Mn 2p binding energy, as well as with the Mn L(3) absorption edge energy. Close similarities emerge with respect to the case of elemental Mn thin films, suggesting that the excitation dynamics is dominated by the electronic properties of Mn 3d states, in spite of the bonding with Ge atoms. The switching from the resonant Raman Auger (RRAS) to the normal Auger regime is found about 2 eV below the Mn L(3) absorption edge. A change of the lineshape due to the transition from an overall N - 1 electron final state (RRAS channel) to an N - 2 electron final state (normal Auger channel) is evidenced by the analysis of the experimental data, which also allowed the ratio to be tracked between charge delocalization and core-hole time scales as the photon energy is tuned across the Mn L(3) edge.     

苝四甲酸二酐薄膜电子结构的同步辐射共振光电子能谱研究

利用基于同步辐射的近边X射线吸收精细结构谱(NEXAFS)和共振光电子谱(RPES)研究了苝四甲酸二酐分子(PTCDA)薄膜的电子结构.碳K边NEXAFS谱中能量小于290 eV的四个峰对应于PTCDA分子不同化学环境碳原子1s电子到未占据分子轨道的共振跃迁.RPES谱中观察到共振光电子发射和共振俄歇电子发射导致的共振峰结构,以及二次谐波激发的碳1s信号.根据电子动能对入射光能量的依赖性分别对三类峰结构进行了归属.同时,发现PTCDA分子轨道共振光电子峰的强度具有光子能量依赖性.这种能量选择性共振增强效应是由于PTCDA分子轨道空间分布差异导致的.共振俄歇峰主要源于高结合能(4.1 eV)分子轨道能级电子参与的退激发过程.明确RPES实验谱图中各个峰结构的起源有助于准确利用基于RPES的芯能级空穴时钟谱技术定量估算有机分子/电极异质界面处电子从分子未占据轨道到电极导带的超快转移时间.     

Charging mechanisms of trapped element-selectively excited nanoparticles exposed to soft x rays

Charging mechanisms of trapped, element-selectively excited free SiO2 nanoparticles by soft x rays are reported. The absolute charge state of the particles is measured and the electron emission probability is derived. Changes in electron emission processes as a function of photon energy and particle charge are obtained from the charging current. This allows us to distinguish contributions from primary photoelectrons, Auger electrons, and secondary electrons. Processes leading to no change in charge state after absorption of x-ray photons are identified. O 1s-excited SiO2 particles of low charge state indicate that the charging current follows the inner-shell absorption. In contrast, highly charged SiO2 nanoparticles are efficiently charged by resonant Auger processes, whereas direct photoemission and normal Auger processes do not contribute to changes in particle charge. These results are discussed in terms of an electrostatic model.     

What are the correct L‐subshell photoionization cross sections for quantitative X‐ray spectroscopy?

For fundamental parameter‐based, quantitative X‐ray fluorescence, X‐ray photoelectron spectroscopy or Auger electron spectroscopy, it is crucial to accurately know the photoionization cross sections (PCS). This atomic probability to absorb the exciting photon and eject a photoelectron, in general, followed by a subsequent decay resulting in the emission of a fluorescence photon or an Auger electron, strongly depends on the electron configuration and photon energy. Two contrary models for the photon energy dependence of the L‐subshell PCS, or the 2s, 2p ½ and 2p 3/2; energy levels, respectively, exist in the literature, and an experimental verification was not available until recently. In this work, the two models for calculating the PCS are discussed, and their influence on quantitative experiments is demonstrated by means of the fluorescence production cross sections for the three L shells. Depending on the excitation conditions, these fluorescence production cross sections and, thus, the derived quantitative results can differ significantly if the wrong PCS model is employed. Copyright © 2016 John Wiley & Sons, Ltd.     

InGaAs/GaAs量子链的光学特性研究

研究了InGaAs/GaAs量子链的稳态和瞬态光谱特性,特别是载流子的动力学过程.实验发现荧光寿命有很强的探测能量依赖关系,荧光寿命随发光能量的增加而减小;实验还发现,当激发功率较小时,荧光寿命随激发功率增大而增大,当激发功率足够大时,荧光寿命趋于饱和.这些结果清楚地表明,在量子链结构中,参与发光的载流子之间存在明显的耦合和输运现象,进一步分析表明,这种输运主要是由于载流子沿量子链方向的耦合造成的.发光的偏振特性研究进一步证实了载流子沿量子链方向输运过程. 关键词： InGaAs/GaAs 量子点 量子链     

Polarization Properties of Quantum-Dot-Based Single Photon Sources

Polarization properties of single photons emitted by optical pumping from a single quantum dot （ QD） are studied by using a four-level system model. The model is capable of explaining the polarization uncertainty observed in single photon emission experiments. It is found that the dependence of photon emission efficiency and polarization visibility on pump power are opposite in general cases. By employing QDs with small size and strong carrier confinement, the photon polarization visibility under high pump power can be improved. In addition, embedding a QD into a well designed microcavity is also found to be favourable, whereas the trade-off between high polarization visibility and multi-photon emission is noted.     

Spin-polarized electrons in collisions of multicharged nitrogen ions with a magnetized Fe(001) surface

We report on the first spin-resolved energy spectra for the emission of electrons during grazing scattering of 150 keV multicharged nitrogen ions from a magnetized Fe(001) surface. A substantial spin polarization for KLL Auger electrons emitted in the final stage of the neutralization sequence during the interaction of multicharged ions with a metal surface is observed. We conclude from our data that the projectile L shell is dominantly populated by electrons from the conduction band of the target. For low energy electrons we find an increase of their spin polarization with an increase of the projectile charge.     

Resonant inelastic scattering of an X-ray photon by a linear molecule

The double differential cross section of resonant inelastic scattering of a linearly polarized X-ray photon by a spatially oriented HF molecule in a gas phase is theoretically described in the energy range of the ionization threshold of the deep molecular orbital 1σ. The effects of radial relaxation of the wave functions of the core and excited scattering states in fields of the formed core vacancies, the vibronic effects, and the effects of Auger and radiative decays of the vacancies are taken into account in the nonrelativistic Hartree-Fock approximation. The results of the calculations are predictive and agree well with the results of the experimental measurements of the Kα emission spectrum of the HF molecule at an incident photon energy of 2 keV, which considerably exceeds the energy of the 1σ ionization threshold.     

Electrodynamic response of a nanosphere placed in a magnetic field

Absorption of electromagnetic radiation by 2D electrons at the surface of a quantum sphere placed in a weak magnetic field is studied. It is shown that at low temperatures, the absorption curve exhibits four resonance peaks observed in the Faraday geometry (photon wave vector parallel to the magnetic field) and six peaks in the Voigt geometry (photon wave vector perpendicular to the magnetic field). In the particular case of the Voigt geometry, where the photon polarization vector is parallel to the magnetic field, the absorption curve exhibits only two resonance peaks. The shape, position, and intensity of the peaks are examined. It is shown that at temperatures close to zero, steps of two types appear in the absorption curve. One type of steps is associated with crossing of the μ-?ω level by the electron energy levels, while steps of the other type arise when electron energy levels cross the chemical potential μ.     

Electronic structure and optic absorption of phosphorene under strain

We studied the electronic structure and optic absorption of phosphorene (monolayer of black phosphorus) under strain. Strain was found to be a powerful tool for the band structure engineering. The in-plane strain in armchair or zigzag direction changes the effective mass components along both directions, while the vertical strain only has significant effect on the effective mass in the armchair direction. The band gap is narrowed by compressive in-plane strain and tensile vertical strain. Under certain strain configurations, the gap is closed and the energy band evolves to the semi-Dirac type: the dispersion is linear in the armchair direction and is gapless quadratic in the zigzag direction. The band-edge optic absorption is completely polarized along the armchair direction, and the polarization rate is reduced when the photon energy increases. Strain not only changes the absorption edge (the smallest photon energy for electron transition), but also the absorption polarization.     

Polarized optical gain and polarization-narrowing of heavily oxidized porous silicon

We report on a polarization-sensitive optical gain in a blue-emitting Si/SiO(2) nanocrystalline system having a high degree of emission polarization memory. This system can show a positive optical gain or optical loss depending on the polarization state of the pump and emitted light. Under optical gain conditions, the degree of polarization of the amplified spontaneous emission increases with the pumping fluence. This effect has been attributed to an increase in the stimulated emission efficiency occurring for the linearly polarized emission component characterized by high photon occupation numbers (stimulating photon flux). This finding is independently supported by other experimental observations. The occurrence of polarization dependent stimulated emission strongly indicates the relevance of morphological effects in light emission from ultrasmall elongated silicon nanostructures.     

Polarization bremsstrahlung in α decay

A mechanism of formation of electromagnetic radiation that accompanies α decay and is associated with the emission of photons by electrons of atomic shells due to the scattering of α particles by these atoms (polarization bremsstrahlung) is proposed. It is shown that, when the photon energy is no higher than the energy of K electrons of an atom, polarization bremsstrahlung makes a significant contribution to the bremsstrahlung in α decay.     

Formation of Ti and TiN ultra-thin films on Si by ion beam sputter deposition

Ultra-thin titanium and titanium nitride films on silicon substrate were obtained by ion beam sputtering of titanium target in vacuum and nitrogen atmosphere, using argon ions with energy of 5 keV and 15 μA target current. Elemental composition and chemical state of obtained films were investigated by X-ray photoelectron spectroscopy with using Mg-Kα X-ray radiation (photon energy 1253.6 eV). It was shown that it is possible to form both ultra-thin titanium films (sputtering in vacuum) and ultra-thin titanium nitride films (sputtering in nitrogen atmosphere) in the same temperature conditions. Photoelectron spectra of samples surface, obtained in different steps of films synthesis, detailed spectra of photoelectron emission from Si 2p, Ti 2p, N 1s core levels and also X-ray photoelectron spectra of Auger electrons emission are presented.     

Monochromatic soft-x-ray-induced reactions of CF2Cl2 adsorbed on Si(111)-7 × 7 studied by continuous-time photon-stimulated desorption spectroscopy near the F(1s) edge

Continuous-time core-level photon-stimulated desorption (PSD) spectroscopy was used to investigate the monochromatic soft x-ray photoreactions of CF(2)Cl(2) adsorbed on Si(111)-7 × 7 near the F(1s) edge (681-704 eV). Sequential F(+) PSD spectra were observed as a function of photon exposure at the CF(2)Cl(2)-covered surface (dose = 2.0 × 10(14) molecules cm(-2), ～0.75 monolayer). The F(+) PSD and total electron yield (TEY) spectra of solid CF(2)Cl(2) near the F(1s) edge were also measured. Both F(+) PSD and TEY spectra depict three features in the energy range of 687-695 eV, and are assigned to the excitations of F(1s) to (13a(1) + 9b(2))[(C-Cl)(?)], (7b(1) + 14a(1))[(C-F)?] antibonding and 5p Rydberg orbitals, respectively. Following the Auger decay process, two holes are created in the C-F bonding orbitals producing the 2h1e final state which results in the F(+) desorption. This PSD mechanism, responsible for the F(+) PSD of solid CF(2)Cl(2), is used to explain the first F(+) PSD spectrum in the sequential F(+) PSD spectra. The variation of spectral shapes in the sequential F(+) PSD spectra shows the consumption of adsorbed CF(2)Cl(2) molecules and the production of surface SiF species as a function of photon exposure. The photolysis cross section of the adsorbed CF(2)Cl(2) molecules by photons with varying energy (681-704 eV) is deduced from the sequential F(+) PSD spectra and found to be ～6.0 × 10(-18) cm(2).     

Polarization fields in the positronium atom undergoing emission or absorption of optical photons

This paper solves the problem of the interaction of an electron and positron via the field of soft and hard photons with emission or absorption of a real photon. The interaction is interpreted as a third-order QED effect in the coordinate representation. The role of intermediate states with positive and negative frequencies is studied. A general expression is derived for the matrix elements of the operator of the effective electron-positron interaction energy for different types of quantum transitions. The expression makes it possible to calculate the probabilities of the corresponding transitions in the nonrelativistic approximation. Electric dipole transitions in the positronium atom accompanied by emission (absorption) of an optical photon are investigated. Two-particle wave functions of the positronium atom are used to introduce the concept of polarization fields inside the positronium atom. It is found that the polarization fields depend on the coordinates and time and on the choice of the pair of states between which a quantum transition with emission or absorption of a photon takes place. Zh. éksp. Teor. Fiz. 113, 471–488 (February 1998)     

多波段相关光子光谱分布与时间相关性测量实验研究

基于相关光子的定标技术能够实现“无标准传递”绝对定标,研究相关光子的光谱辐射特性及时间相关特性对遥感器在宽波段的辐射定标具有重要意义。为满足光电探测器在宽谱段量子效率定标需求,基于相关光子的定标技术有必要从单一波段向更多波段扩展。根据自发参量下转换所满足的相位匹配条件,推导出相关光子在晶体内的非共线角计算公式,通过数值模拟相关光子光谱辐射角度分布规律,优化晶体相位匹配角,使得自发参量下转换产生的相关光子具有宽光谱分布,并且相关光子辐射角度与光谱波长能够一一对应。根据光谱分布数值模拟结果,建立了多波段相关光子的光谱分布和时间相关性测量实验系统,利用该系统测量了四对相关光子的光谱分布、符合计数、相关时间以及偏振特性。其中,测量的光谱分布范围为633~808 nm,最大光谱分布测量偏差为1.51 mm,光谱分布实验测量结果与数值模拟结果符合一致;测量了四对相关光子对的相关时间,最小相关时间为0.32 ns,并在实验中观察到了“符合三峰”现象;相关光子单光子计数及符合计数与泵浦光的偏振方向呈正弦函数关系。实验研究表明,相关光子对具有可见光~近红外宽波段分布、时间相关及偏振特性。论文研究结果在国内外尚属首次报道,该研究结果有望应用于光电探测器在多波段的辐射定标。     

Quantum effects on polarization bremsstrahlung from electron-atom collisions in partially ionized dense hydrogen plasmas

The quantum effects on the polarization bremsstrahlung emission due to the low-energy electron-atom collisions are investigated in partially ionized dense hydrogen plasmas. The impact parameter analysis is employed to describe the motion of the projectile electron in order to investigate the variation of the bremsstrahlung emission spectrum as a function of the impact parameter, de Broglie wave length, Debye length, and radiation photon energy. The results show that the quantum effects strongly suppress the polarization bremsstarhlung emission. It is also found that the polarization bremsstarhlung emission cross section shows the maximum value at the position of the Bohr radius. It is interesting to note that the quantum effects are found to be more important than the screening effects in the polarization bremsstarhlung emission.