Multiple Auger Decay Following Xe+(4p3−1/2)Ionization

The Auger decay for the many-electron Xe+(4p3^?1/2)state is studied in detail,using multistep approaches.It is found that the single Auger decay channels are primarily Coster–Kronig processes,which is in accord with other theoretical and experimental results.The double and triple Auger decays result primarily from cascade processes,i.e.,the sequential two-step and three-step Auger decay,and as such,the contributions from direct processes can be neglected.Level-to-level rates for single,double,and triple decays are obtained,based on which comprehensive Auger electron spectra and ion yields are obtained.Our decay paths and Auger electron spectra are in agreement with the experimental analysis[Hikosaka et al.,Phys.Rev.A 76(2007)032708],and our ion yield ratios(Xe²⁺:Xe³⁺:Xe⁴⁺=4.6:87.0:8.4)are also in line with their values(5.0:86.0:9.0).However,with respect to the ion yield ratios,a discrepancy still remains among the experimental and theoretical results.Taking into account the complexity of Xe’s electronic structure,further,more detailed experiments are still required.     

Subsidiary conditions of the general Gel'fand-Yaglom wave equation based on the representation (1/2,3/2)⊕(−1/2,3/2)⊕(1/2,5/2)⊕(−1/2,5/2)⊕ (1/2,3/2)⊕(−1/2,3/2)

A method is given of obtaining the subsidiary conditions of the second kind of the general Gel'fand-Yaglom wave equation based on the representation (1/2, 3/2)(–1/2, 3/2)(1/2, 5/2)(–1/2, 5/2)(1/2, 3/2)(–1/2, 3/2) and in the presence of an external electromagnetic field by reformulating the wave equation in spinor form. The wave equations accepting these subsidiary conditions form a class defined by a set of simultaneous equations that is not empty.     

新系列超导相TlBaCan-1CunO2n+2.5(n=2,3)的晶体结构和超导电性

本文用粉末烧结法合成了Tl-Ba-Ca-Cu-O体系TlBa₂Ca_n-1Cu_nO_2n+2.5新系列超导相,用粉末衍射法测定了n=2和3的晶体结构,属简单四方单胞,空间群为D_4h¹-P4/mmm,点阵常数a相同,而c值不同,随n值而增大。a=3.847?,c分别为12.73?和15.89?,每单胞含一个化合式单位,阳离子沿四方晶系的(0,0,z)和(1/2,1/2,z)位置交替排列,排列的顺序相同,n=3比n=2依次多增加Ca和Cu及相应的氧离子。TlBa₂Ca_nCu_nO_2n+2.5,n=3时,零电阻超导转变温度T_c(0)=112K;n=2时,T_c(0)=101K,与Tl₂Ba₂Ca_n-1Cu_nO_2n+4型体心四方晶胞超导相不同,TlBa₂Ca_n-1Ca_nO_2n+2.5结构中缺氧类钙钛矿型结构单元[Ba₂Ca_n-1Cu_nO_2n+1]仅被TI-O单层所隔开,当n相同时,Tl-O双隔层的体心四方单胞比Tl-O单层的简单四方单胞的超导转变温度高10K左右,这说明Tl-Ba-Ca-Cu-O体系中超导相的转变温度不仅与类钙钛矿结构单元的[CuO₄]和[CuO₅]的数目有关,而且与Tl-O的隔层数目有关。 关键词：     

Why are the band-like states suppressed in the M3–M4,5M4,5 super Coster–Kronig electron spectrum of Cu metal compared to those in the L3–M4,5M4,5 Auger electron spectrum?

The relative spectral intensity of the band-like two M_4,5-hole state to the atomic-like localized one is much suppressed in the coincidence M₃–M_4,5M_4,5 super Coster–Kronig (sCK) electron spectrum of Cu metal compared to the one in the coincidence L₃–M_4,5M_4,5 Auger electron spectroscopy (AES) spectrum. The M₃-hole lifetime width of Cu metal is calculated by an ab initio atomic many-body theory (the extended relaxed core random phase approximation with exchange). The calculated M₃-hole lifetime width of Cu metal agrees well with the experimental one. The M₃–M_4,5M_4,5 sCK decay width of Cu metal decreases much with delocalization of the two M_4,5 holes in the sCK final state, whereas the Auger decay width is fairly independent of localization and delocalization of the two M_4,5 holes in the Auger final state. Thus, the relative spectral intensity of the band-like state is much suppressed in the coincidence M₃–M_4,5M_4,5 sCK-electron spectrum of Cu metal compared to the one in the coincidence L₃–M_4,5M_4,5 AES spectrum.     

碱金属Li,Na,K,Rb,Cs,Fr的ns2S1/2,np2P1/2,3/2, nd2D3/2,5/2 和nf2F5/2,7/2 里德伯能级理论研究

本文在多通道量子数亏损理论(MQDT)框架下,利用相对论多通道理论(RMCT),分别在冻结实近似、 考虑Δl=-1的偶极极化效应、Δl=+1的偶极极化效应、Δl=± 1的偶极极化效应、伸缩模效应以及同时考虑偶极极化效应和伸缩模效应等不同层次近似下,系统地计算了碱金属Li, Na, K, Rb, Cs和Fr七个里德伯系列的能级,即ns²S_1/2, np²P_1/2, np²P_3/2, nd²D_3/2, nd²D_5/2, nf²F_5/2 和nf²F_7/2.计算结果表明,电子关联效应对碱金属原子的里德伯能级的影响很大.总的来说,偶极极化效应比伸缩模效应重要,而在偶极极化效应中, Δl = + 1的偶极极化效应比Δl = - 1的偶极极化效应重要.但对于Na的ns²S_1/2,(nd²D_3/2,nd²D_5/2)里德伯系列的能级,和Li的(np²P_1/2,np²P_3/2)里德伯系列的能级,是伸缩模效应比较重要.     

Resonant Auger Scattering by Attosecond X-Ray Pulses

As x-ray probe pulses approach the subfemtosecond range, conventional x-ray photoelectron spectroscopy(XPS) is expected to experience a reduction in spectral resolution due to the effects of the pulse broadening.However, in the case of resonant x-ray photoemission, also known as resonant Auger scattering(RAS), the spectroscopic technique maintains spectral resolution when an x-ray pulse is precisely tuned to a core-excited state. We present theoretical simulations of XPS and RAS spectra on a sho...     

合成反铁磁Ni81Fe19/Co90Fe10/Ru/Co90Fe10/Ni81Fe19的研究

采用直流磁控溅射方法制备了一系列的合成反铁磁及以其为自由层的自旋阀.研究发现,在Ni₈₁Fe₁₉与Ru层之间插入适当厚度的Co₉₀Fe₁₀层后,可有效地提高合成反铁磁两磁性层间的反铁磁耦合强度,得到具有饱和场H_s更高、饱和磁化强度M_s更低、热稳定性更好的合成反铁磁.另外,以这种合成反铁磁作自旋阀的自由层时,可有效提高自旋阀的稳定性. 关键词： 合成反铁磁 退火 自旋阀     

The magnetoelectric effect in layered composites Ni0.4Zn0.6Fe2O4—Pb0.95Sr0.05Zr0.53Ti0.47O3

The magnetoelectric effect in two- and three-layered composites based on nickel-zinc ferrite and lead zirconate-titanate was investigated. The value of the magnetoelectric response in layered composites depends largely on the frequency of the alternating magnetic field, the volume ratio of the electric phase forming the composite, and the mechanical interaction between magnetostriction and piezoelectric layers.     

π+π+ and π+π? Colliding in Noncommutative Space

By studying the scattering process of scalar particle pion on the noncommutative scalar quantum electrodynamics, the non-commutative amendment of differential scattering cross-section is found, which is dependent of polar-angle and the results are significantly different from that in the commutative scalar quantum electrodynamics, particularly when cosθ∼±1. The non-commutativity of space is expected to be explored at around Λ_NC∼TeV.     

CO2同位素分子16O12C16O, 16O12C17O, 16O13C17O配分函数研究

本文主要研究了CO2的三种同位素分子16O12C16O , 16O12C17O ,16O13C17O 70 K~6000 K的总内配分函数 (TIPS)。在总内配分函数的计算中, 转动配分函数的计算采用了McDowell的解析式法, 振动配分函数则采用了简谐振动近似(HOA)获得。最后通过将两配分函数乘积近似计算得出TIPS, 并将其70~3000 K的数据和HITRAN04数据进行了比较, 发现所得结果和数据库符合的较好, 且其误差可以近似看成一条直线。并通过对误差的拟合修订了高温区(3000~6000 K)的计算数据, 给出了在高温下的较为准确的TIPS值。     

High-resolution study of the ν1/ν5 and 2ν1/ν1+ν5 P-H stretching bands of PH2D

The P-H stretching bands ν₁/ν₅ and 2ν₁/ν₁+ν₅ were recorded using a Bruker 120 HR interferometer with a resolution of 0.0042 and 0.0088 cm⁻¹, respectively, and analyzed. From the fits 33 and 50, respectively, vibrational, rotational, centrifugal distortion, and resonance interaction parameters were obtained. These reproduce 668 and 497 rovibrational energies of the pairs of states ν₁/ν₅ and 2ν₁/ν₁+ν₅ with experimental accuracies, rms=0.00016 and , respectively. “Local mode” behavior of the PH₂ fragment is established and discussed in detail.     

BaB2O4-K2O和BaB2O4-K2B2O4赝二元系相图的研究

用X射线衍射和差热分析方法研究了BaB₂O₄-K₂O和BaB₂O₄-K₂B₂O₄赝二元系的相平衡关系。BaB₂O₄-K₂B₂O₄属共晶体系,共晶温度为850±3℃,共晶点成分为45mol％K₂O。在Ba 关键词：     

BaO-Li2O-B2O3三元系中BaB2O4-Li2B2O4和BaB2O4-Li2O截面相平衡关系的研究

本文用X射线和差热分析方法对BaO-Li₂O-B₂O₃三元系中的两个截面:BaB₂O₄-Li₂B₂O₄和BaB₂O₄-Li₂O作了研究。在BaB₂O₄-Li₂B₂O₄赝二元系中发现了一个新的化合物4BaB₂O₄·Li₂B₂O₄。化合物在930±3℃由包晶反应形成,并与Li₂B₂O₄形成共晶反应。共晶温度为797±3℃,共晶点组分为79mol％Li₂B₂O₄。在BaB₂O₄-Li₂O截面中也存在化合物4BaB₂O₄·Li₂B₂O₄,其包晶反应温度从930±3℃随Li₂O含量增加下降到908±3℃。在组分60mol％Li₂O处形成另一个新的化合物2BaB₂O₄·3Li₂O。该化合物在630±3℃也是由包晶反应形成,并与Li₂O和Li₂CO₃分别形成共晶反应,共晶温度分别为400±3℃和612±3℃。在BaB₂O₄-Li₂B₂O₄和BaB₂O₄-Li₂O体系中都没有观察到固溶体。用计算机程序分别对化合物4BaB₂O₄·Li₂B₂O₄和2BaB₂O₄·3Li₂O的X射线粉末衍射图案进行了指标化,其结果:4BaB₂O₄·Li₂B₂O₄的空间群为Pmma,a=13.033?,b=14.630?,c=4.247?,每个单胞包含两个化合式单位;2BaB₂O₄·3Li₂O的空间群为Pmmm,a=4.814?,b=9.897?,c=11.523?,每个单胞也含有两个化合式单位。 关键词：     

Measurement of the decayτ? →ρ?ντ

An analysis of the decay ^--0 v has been performed using the ARGUS detector at the DORIS II storage ring. The branching ratio has been determined to be Br(^--0 v =(22.6±0.4±0.9)%. The shape of the ^-0 invariant mass spectrum is found to be in good agreement with the predictions obtained using the conserved vector current (CVC) hypothesis, suggesting that the ^-0 system is produced in aJ ^P=1^– state. An analysis of the measured decay angular distribution of the pions with respect to the flight direction of the ^-0 system demonstrates the vector nature of the coupling at the v vertex. With the assumption of zerov mass thev spin has been shown to be .Supported by the German Bundesministerium für Forschung und Technologie, under contract number 054DO51 P     

La2/3Ca1/3MnO3/Eu2CuO4/La2/3Ca1/3MnO3磁性隧道结的制备与表征

采用磁控溅射，紫外线光刻和离子束刻蚀制备了La_2/3Ca_1/3MnO₃/Eu₂CuO₄/La_2/3Ca_1/3MnO₃磁性隧道结.通过对获得的磁性隧道结的I-V特性测量，发现非线性的I-V特性，显示结样品的隧穿特性.有趣的是发现在电极材料La_2/3Ca_1/3MnO₃的金属-绝缘体转变温度(Tp)以下，I-V曲线出现一个跳变.随着温度降低，开始出现跳变的临界电流增大，但是跳变都发生在同样的电压下～209mV.当电流增大或减小在跳变点附近出现回滞.这一跳变只发生在铁磁金属态，表明这是一个磁性相关联的效应，可能对应一种新的磁性开关过程.虽然，目前对这一现象背后的物理机理还不清楚，但是，这一现象有可能在未来自旋电子学器件方面具有潜在的应用价值. 关键词： 庞磁电阻 磁性隧道结 开关效应     

Auger图示对锰原子共振结构的影响

使用多体微扰理论(many-body perturbation theory, MBPT)计算了锰原子的3p63d54s2→3p53d54s2nd系列里德堡共振结构.在耦合方程方法中考虑了Auger图式,计算表明,Auger图式有效地抑制了3p→nd系列共振结构的发散.     

Li4SiO4-Li3VO4赝二元系和Li4GeO4-Li4SiO4-Li3VO4赝三元系中新的锂离子导体

本文在室温到300℃的温度范围内研究了Li₄SiO₄-Li₃VO₄和Li₄GeO₄-Li₄SiO₄-Li₃VO₄体系中的离子导电性,发现γ_II相固溶体Li_3+xV_1-xSi_xO₄是好的锂离子导体。所研究的成分中Li_3.3V_0.7Si_0.3O₄的离子电导率最高,室温下为1×10^-5Ω^-1·cm^-1,在42—192℃的电导激活能为0.36eV,电子电导率可以忽略,因而这是迄今所发现的最好的锂离子导体之一。粗略确定了Li₄GeO₄-Li₄SiO₄-Li₃VO₄三元系中电导率高的范围,发现在Li_3.5V_0.5Ge_0.5O₄中Si部分取代Ge可以使电导率进一步提高,Li_3.5V_0.5Ge_0.4Si_0.1O₄的室温电导率可达1.3×10^-5Ω^-1·cm^-1,电导激活能为0.40eV。 关键词：     

Temperature effects on exciton–phonon coupling and Auger recombination in CdTe/ZnTe quantum dots

We report the results of experimental studies on temperature-dependent thermal escape and Auger recombination coefficients in CdTe/ZnTe quantum dots. We show that at low temperatures, there is a thermally activated transition between two different states separated by a localization energy of about 15.8 meV, while the primary non-radiative process at high temperatures is thermal escape assisted multi-longitudinal optical (LO) phonons absorption with three phonons. The most striking result is a rapid increase in the Auger coefficient and a reduction in the decay time with increasing temperature above 35 K. These results show that the Auger process is assisted by the participation of phonons with an energy threshold of 34.4 meV and an LO phonon energy of around 19 meV.     

Bi2Pb2V2O10的晶体结构

使用X射线单晶衍射法测定了Bi₂Pb₂V₂O₁₀的结构。该晶体属三斜晶系,空间群为C₁¹-P1,单位晶胞内化学式数Z=1,晶胞参数为:a=7.084(4)?,b=7.278(3)?,c=5.587(3)?,α=111.91(5)°,β=95.01(6)°,γ=108.86(4)°,V=245.70?³,D_x=7.35g/cm³,μ(MoK_α)=678,94cm^-1,F(000)=456。用Patterson函数分析及Forier技术测定了结构,对原子坐标、各向同性及各向异性热参数进行了最小二乘方修正,R=0.079。结构分析表明,Bi₂Pb₂V₂O₁₀的Pb原子与O原子形成八角十二面体,Bi原子与O原子形成六角多面体。两个共棱的Pb—O多面体与两个共棱的Bi—O多面体相连,并沿bc平面无限延伸。讨论了吸收的影响。最后,将Bi₂Pb₂VO₁₀的结构与Pb₂SO₅的结构进行了比较。 关键词：