Recurrence spectra of non—hydrogen Rydberg atoms in paralled electric and magnetic fields

We present a new method for computing the recurrence spectra of n≈40, m=0 lithium Rydberg atoms in strong parallel external electric and magnetic fields. This method is based on an extended closed-orbit theory allowing the computation of the scattering of the electron by the ionic core. We pay particular attention to the scaling properties, which are extremely important for understanding the correspondence between classical and quantum mechanics. The spectra with a constant scaled electric field \tilde F=0.01 and a scaled energy ε=-0.03 are recorded and compared with those of hydrogen obtained by the standard closed-orbit theory. The result shows that the additional strong resonance structures can be interpreted in terms of the core-scattered classical closed orbits.     

Vibrational transition spectra of H2＋ in a strong magnetic field

Vibrational transition spectra of H2+ in an ultra-strong magnetic field are determined. The validity of Born-Oppenheimer approximation is analyzed based on one-center method and B-spline basis sets. It is shown that Born-Oppenheimer approximation is reliable for the investigation on the ground state and low excited states of H2+ subjected to the strong magnetic field. Furthermore, it is found that the vibrational transition spectra from 1σ g , 1π u , and 1δ g states lie in infrared, visible, and ultraviolet ranges with increasing magnetic field strength.     

Short-ranged potential effects on the recurrence spectra of lithium M = 1 atoms in parallel electric and magnetic fields

This paper presents recurrence spectra of highly excited lithium atoms with M = 1 state in parallel electric and magnetic fields at a fixed scaled energy ε = -0.03. Short-ranged potentials including ionic core potential and centrifugal barrier are taken into account. Their effects on the states and photo-absorption spectrum are analysed in detail. This demonstrates that the geometric features of classical orbits are of special importance for modulations of the spectral pattern. Thus the weak polarization as well as the reduction of correlation of electrons induced by short-ranged potentials give rise to the recurrence spectra of lithium M = 1 atoms more compact than that of the M = 0 one, which is in good agreement with the experimental prediction.     

Stereodynamics of the He ＋ D2^＋ → HeD^＋ ＋ D Reaction on the PALMIERI Surface

Using the quasi-classical trajectory method, the product rotational polarization of the ion-molecule reaction He^＋D2^＋ has been calculated at different collision energies on the PALMIERI potential energy surface [Palmieri et al. Mol. Phys. 98 （2000） 1835]. The distribution angle between k and j′, P（Or）, the distribution of the dihedral angle P（Фr）, and the angular distribution of product rotational vectors in the form of polar plots in θr and Фr are calculated. In addition, four polarization-dependent differential cross sections are also presented in the center-of-mass frame, respectively. The results indicate that the rotational polarization of the product HeD^＋ presents different characters for different collision energies. These discrepancies may be ascribed to the different collision energies and constructions of the potential energy surface.     

Influences of Mg^2＋ ion on dopant occupancy and upconversion luminescence of Ho^3＋ ion in LiNbO3 crystal

The effects of a Mg^2＋ ion on the dopant occupancy and upconversion luminescence of a Ho^3＋ ion in LiNbO3 crystal are reported. The birefringence gradient of the crystal is measured to investigate the optical homogeneity. The X-ray powder diffraction spectrum and the upconversion luminescence are used to investigate defect structure and spectroscopic properties of Mg,Ho：LiNbO3. Under 808-nm excitation, blue, red, and very intense yellow-green bands are observed. Based on the energy levels of Ho^3＋ in LiNbO3, and the pump intensity dependence of the observed emission, an excitation scheme is presented. The upconversion emission spectra reveal an enhancement of upconversion intensity when the Mg^2＋ ions are introduced into Ho：LiNbO3. The main upconversion mechanism is discussed in this work.     

Comparative analysis of energy-level splitting of Pr3＋ doped in LiYF4 and LiBiF4 crystals： a complete energy matrix calculation

Based on the combination of Racah's group-theoretical consideration with Slater's wavefunction, a 91 × 91 complete energy matrix is established in tetragonal ligand field D_2d for Pr³⁺ ion. Thus, the Stark energy-levels of Pr³⁺ ions doped separately in LiYF₄ and LiBiF₄ crystals are calculated, and our calculations imply that the complete energy matrix method can be used as an effective tool to calculate the energy-levels of the systems doped by rare earth ions. Besides, the influence of Pr³⁺ on energy-level splitting is investigated, and the similarities and the differences between the two doped crystals are demonstrated in detail by comparing their several pairs of curves and crystal field strength quantities. We see that the energy splitting patterns are similar and the crystal field interaction of LiYF₄:Pr³⁺ is stronger than that of LiBiF₄:Pr³⁺.     

NLO Corrections of HTC∏^0 and ∏＋∏- Pair Production at ILC in TC2 Model

As well known, if the Higgs boson were not observed at LHC, the technicolor model would be the most favorable candidate responsible for the symmetry breaking. To overcome some defects in the previous model, some extended versions have been proposed. In the TC2 model typical signature is existence of heavy HTC and technipion ∏. A direct proof of validity of the model is to produce them at accelerator. Thus we study the production rates of e＋e^- → HTC∏^0 and e＋e^- → ∏＋∏- at ILC in the topcolor-assisted technicolor （TC2） model. In fact, there is a flood of models belonging to new physics, which can result in products with characteristics similar to HTC ＋ ∏ of the TC2 model. Therefore to distinguish this model from others one may need to investigate some details by calculating the cross section to NLO. We indeed find that the NLO corrections are significant, namely the ratio δ ≡（ σNLO - σLO）/σLO in e＋e- →HTC∏^0 exceeds 100% within a plausible parameter space.     

里德堡NO分子在强磁场中的回归谱

利用分子轨道理论,结合一个新的模型势,我们给出了里德堡NO分子中激发态电子所受到的作用势的解析表达式.利用分子的闭合轨道理论和分区自洽的迭代方法,首次从理论上计算了NO分子在强磁场中的回归谱.通过和A.Matzkin等人给出的NO分子在强磁场中的实验谱的比较,表明我们的计算是正确的.     

Semiclassical calculation of the recurrence spectra of He Rydberg atom in perpendicular electric and magnetic fields

Closed orbit theory is a semiclassical technique for explaining the spectra of Rydberg atoms in external fields. By developing the closed orbit theory from two degrees of freedom to three non-separable degrees of freedom, we calculated the recurrence spectra of He Rydberg atom in perpendicular electric and magnetic fields. The closed orbits in the corresponding classical system have also been obtained. Fourier transformed spectra of He atoms have allowed direct comparison between the resonance peaks and the scaled action values of closed orbits, whereas the nonhydrogenic resonance can be explained in terms of the new orbits created by the core scattering. The semiclassical result is in good agreement with the quantum spectra, which suggests that our method is correct.     

垂直电磁场中He原子的吸收谱和回归谱的理论计算

半经典闭合轨道理论已经成功地计算了在外加磁场和平行电磁场中的里德堡原子的回归谱.但对于垂直电磁场中的里德堡原子,理论和计算都变得更为复杂.本文把闭合轨道理论推广到三维情况,采用 B.Hüpper的模型势计算了ε=-0.03,主量子数n≈ 40,m=0下He原子在垂直电磁场中的光吸收谱和回归谱,并和H原子在垂直电磁场中的回归谱作比较,突出了实散射的贡献.计算中应用了离子实散射的分区自洽迭代方法,并考虑到轨道的多次重复和离子实的多次散射效应.这是对闭合轨道理论的验证和进一步推广.     

氢分子在磁场中回归谱的散射矩阵理论研究

利用散射矩阵理论,结合扩展的半经典闭合轨道理论和多通道量子亏损理论,计算了磁场中高里德堡H2分子的回归谱.该方法使用了两个空间散射矩阵来描述里德堡电子的动力学性质,计算中可以包括所有阶的实散射的作用.回归谱的每一个尖峰对应着一条闭合轨道,新的额外峰是由于弹性散射和非弹性散射所引起的通道内和通道间的轨道组合,进一步证明了体系通道间和通道内的散射具有同等的重要性.     

氢分子在磁场中回归谱的散射矩阵理论研究

利用散射矩阵理论，结合扩展的半经典闭合轨道理论和多通道量子亏损理论，计算了磁场中高里德堡H2分子的回归谱．该方法使用了两个空间散射矩阵来描述里德堡电子的动力学性质，计算中可以包括所有阶的实散射的作用．回归谱的每一个尖峰对应着一条闭合轨道，新的额外峰是由于弹性散射和非弹性散射所引起的通道内和通道间的轨道组合，进一步证明了体系通道间和通道内的散射具有同等的重要性．     

强磁场中Rydberg NO分子的回归谱研究

利用分子的闭合轨道理论和多通道量子亏损理论,考虑核的转动影响,计算了Rydberg NO分子在外磁场中的回归谱.研究表明,复杂谱的结构可以用包含分子实散射的闭合轨道理论来解释,不管是同一通道内的弹性散射还是不同通道间的非弹性散射都起着非常重要的作用,尤其是较大标度作用量下,散射作用远大于基本轨道和重复轨道的贡献,很大程度上影响着体系的动力学性质。     

Absorption and Recurrence Spectra of Li Rydberg Atom in Perpendicular Electric and Magnetic Fields

We develop the semi-closed orbit theory from two degrees of freedom to three non-separable degrees of freedom and put forward a new model potential for the Li Rydberg atom, which reduces the study of the system to an effective one-particle problem. Using this model potential and the closed orbit theory for three degrees of freedom, we calculate the recurrence spectra of Li Rydberg atom in perpendicular electric and magnetic fields. The closed orbits in the corresponding classical system have also been obtained. The Fourier transformed spectra of Li atom have allowed direct comparison between the resonance peaks and the scaled action values of closed orbits, whereas the nonhydrogenic resonance can be explained in terms of the new orbits created by the core scattering. Our result is in good agreement with the quantum spectra, which suggests that our calculation is correct.     

Absorption and Recurrence Spectra of Li Rydberg Atom in Perpendicular Electric and Magnetic Fields

We develop the semi-closed orbit theory from two degrees of freedom to three non-separable degrees of freedom and put forward a new model potential for the Li Rydberg atom, which reduces the study of the system to an effective one-particle problem. Using this model potential and the closed orbit theory for three degrees of freedom, we caiculate the recurrence spectra of Li Rydberg atom in perpendicular electric and magnetic fields. The closed orbits in the corresponding classicai system have also been obtained. The Fourier transformed spectra of Li atom have ailowed direct comparison between the resonance peaks and the scaied action values of closed orbits, whereas the nonhydrogenic resonance can be explained in terms of the new orbits created by the core scattering. Our result is in good agreement with the quantum spectra, which suggests that our calculation is correct.     

平行电磁场中He+2的回归谱与闭合轨道的研究

利用半经典闭合轨道理论和分区自洽迭代方法计算了Rydberg态下He⁺₂在平行电磁场中的回归谱与闭合轨道. 为了模拟分子实的散射作用,引入一个包含电子交换势的新势能. 利用这一新势能,结合多通道量子亏损和分子闭合轨道理论,讨论了分子实散射效应对平行电磁场中He⁺₂的回归谱与闭合轨道的影响. 关键词： 回归谱 分子半经典闭合轨道 交换势 实散射