Dissociative excitation of HD+, D2+ , and DT+ by electron impact

In the framework of the Multi-Channel Quantum Defect Theory (MQDT), a theoretical study of the dissociative excitation is presented. Numerical results for the dissociative excitation cross sections of HD ⁺, D ₂⁺, and DT ⁺ with electrons of energy between 2 and 12 eV are reported. The contribution of the vibrational continua of the two lowest electronic states as explicit ionization channels has been considered. Within a quasi-diabatic representation of the molecular electronic states, the Born expansion of second order is done in the K-matrix evaluation.     

Li~+,Zn~(2+),Mg~(2+)掺杂Lu_2O_3∶Er~(3+)荧光粉的制备及发光特性

用微波高温固相法合成了Er~(3+)单掺Lu_2O_3,Li~+与Er~(3+)共掺Lu_2O_3及Li~+,Zn~(2+),Mg~(2+)掺杂Lu_2O_3∶Er~(3+)的荧光粉。实验表明金属离子Li~+、Zn~(2+)、Mg~(2+)、Er~(3+)掺杂Lu_2O_3,不影响Lu_2O_3的立方晶相。扫描电子显微镜测量表明,Li~+掺杂可以有效改善粉体的分散性和形貌,Li~+,Zn~(2+),Mg~(2+)共掺杂获得的粉体颗粒分布更加均匀,粒径范围为80～100 nm。379 nm激发下,Li~+与Er~(3+)共掺样品发光较单掺Er~(3+)样品在565 nm处的发光增强了4.5倍,而Li~+、Zn~(2+)、Mg~(2+)与Er~(3+)共掺样品较其发光增强5.3倍。980 nm激发下,Li~+与Er~(3+)共掺样品,Li~+、Zn~(2+)、Mg~(2+)与Er~(3+)共掺样品的发光分别比单掺Er~(3+)样品在565 nm处发光增强23倍与39倍,在662 nm处发光强度分别增强20倍与43倍。379 nm激发下,较单掺Er~(3+)的样品,掺杂Li~+的样品和Li~+,Zn~(2+),Mg~(2+)和Er~(3+)共掺的样品荧光寿命均有所增加,而Zn~(2+)、Er~(3+)共掺及Mg~(2+)、Er~(3+)共掺样品的荧光寿命则有所缩短。     

Ni^2＋：LiNbO3的光学吸收谱和EPR的研究

应用三角晶场中d^2(d^8)电子组态的包括静电相互作用和自旋－轨道耦合相综合利用物强场能量矩阵,采用完全对角化方法,精确地计算了具有C3V对称的Ni^2 :LiNbO3的光学吸收谱和EPR谱。理论结果与实验值符合得很好。     

电子与类铍N3+和O4+离子碰撞激发截面的相对论扭曲波计算

采用全相对论扭曲波方法,系统地计算了类铍N³⁺和 O⁴⁺离子从基态到2s2p和2p² 的各激发态以及从亚稳态到2p²各激发态的电子碰撞激发截面,详细地讨论了靶态的关联效应对激发截面的影响.结果表明：对于2s-2p的单电子激发,在低能碰撞时,靶态的电子关联效应起非常重要的作用,且使得激发截面降低;而高能碰撞时,靶态波函数的描述对连续态波函数的影响比较小,对激发截面影响也比较小.对于2s²-2p²的双电子激发,其中基态2s²¹S₀到J=0的2p²³P₀,¹S₀的激发截面较大,其主要原因是末离子态波函数与基组态波函数的混合,但是其他几个激发的激发截面较小. 关键词： 全相对论扭曲波方法 电子碰撞激发 电子关联效应     

Extrinsic luminescence of BaF2: R 3+ crystals ( R 3+ = La3+, Y3+, Yb3+)

This paper reports on a study of cross-luminescence in barium fluoride crystals doped by a variety of impurities (K⁺, Cd²⁺, Y³⁺, Yb³⁺, La³⁺). It is shown that doping of the crystal with a trivalent impurity gives rise to the formation of an additional cross-luminescence band peaking at 7.5 eV, the intensity of this band increasing with increasing impurity concentration. Original Russian Text ? A.S. Myasnikova, E.A. Radzhabov, A.V. Egranov, 2008, published in Fizika Tverdogo Tela, 2008, Vol. 50, No. 9, pp. 1582–1584.     

Combined analysis of the PFOODR data on the a 3Σ u+ , 23Πg, 23Σ g+ , 33Πg, and 43Σ g+ states of the K2 molecule

The known and new heterogeneous spectral data on the triplet states a ³Σ _u ⁺ , 2³Π_g, 2³Σ _g ⁺ , 3³Π_g, and 4³Σ _g ⁺ of the K₂ dimer are simultaneously fitted. The data published in J. Mol. Spectrosc. 234, 41 (2005) are refined. The new information used in the analysis contains the data on the 2³Σ _g ⁺ state, which have not been considered previously. The range of internuclear distances where the potential function of the lowest triplet state a ³Σ _u ⁺ is defined is extended. Original Russian Text ? V.B. Sovkov, V.S. Ivanov, D. Li, F. Xie, Li Li, 2007, published in Optika i Spektroskopiya, 2007, Vol. 103, No. 5, pp. 747–751.     

Tm^3＋掺杂MFT玻璃材料上转换荧光浓度猝灭的研究

我们制备了Tm3+掺杂的不同浓度的MFT玻璃材料,在650nm激发下观察了Tm3+掺杂的MFT玻璃材料的两个蓝色上转换发光,研究了上转换发光的浓度猝灭。实验结果证明这种材料的蓝色上转换荧光的猝灭浓度达到0.6mol*%,比其他材料中报道的猝灭浓度高3倍。研究了Tm3+离子间的交叉弛豫行为,详细讨论了引起浓度猝灭的原因。     

Electron impact excitation of Fe25+

A three-state close-coupling calculation of the impact excitation of the 2s and 2p states of the hydrogenic ion Fe²⁵⁺ has been performed using the algebraic variational method.     

Charge transfer excitation of the Nd3+, Sm3+, Dy3+, Ho3+, Er3+ and Tm3+ emission in CaGa2S4

The excitation spectra of the Nd³⁺, Sm³⁺, Dy³⁺, Ho³⁺, Er³⁺ and Tm³⁺ emission in the sodium-compensated CaGa₂S₄ host lattice, a sulfide with wide band gap, contain an intense band below the absorption edge. Comparison of the energy of its maximum with thermodynamic data and correlations to Jørgensen's refined spin-pairing theory predictions allow one to ascribe this band to a charge transfer transition ending onto 4f orbitals. The irregular variation within the rare earth series contrasts with the monotonic variation of the absorption edge in stoichiometric rare earth sulfides (e.g. NaLnS₂), associated with interband transitions.     

CaMoO4：Eu3+,Bi3+,Li+红色荧光粉的共沉淀制备与表征

采用共沉淀法合成了红色荧光粉Ca_0.75MoO₄：Eu_0.25³⁺、Ca_0.75MoO₄：Eu_0.25-x³⁺,Bi_x³⁺及Ca_0.5MoO₄：Eu_0.25-2x³⁺, Bi_x³⁺,Li_0.25+x⁺,并采用X射线衍射(XRD)、拉曼光谱,扫描电镜(SEM)和荧光光谱(PL)测定分析了其结构形貌特征及发光性能。结果表明：制备的CaMoO₄：Eu³⁺,Bi³⁺,Li⁺红色荧光粉为白钨矿结构,颗粒尺寸约为0.5~1 μm。掺杂Bi³⁺的Ca_0.75MoO₄：Eu_0.25-x³⁺,Bi_x³⁺的相对发光强度明显高于未掺Bi³⁺的Ca_0.75MoO₄：Eu_0.25³⁺荧光粉。Bi³⁺离子的掺杂将吸收来的能量传递给激活离子Eu³⁺,起到了能量传递的作用。当Bi³⁺掺杂量为x=0.005时,在395 nm激发下,主发射峰在616 nm处的相对发光强度最大,但掺杂浓度过高时会出现浓度猝灭现象。另外,电荷补偿剂的掺入能够解决材料中因同晶取代引起的电荷不平衡的问题,以Li⁺作电荷补偿剂、Eu³⁺和 Bi³⁺共掺合成的Ca_0.5MoO₄：Eu³⁺_0.23,Bi_0.01³⁺,Li⁺_0.26红色荧光粉的发光性能强于Ca_0.75MoO₄：Eu_0.25³⁺、Ca_0.5MoO₄：Eu_0.25³⁺, Li_0.25⁺及Ca_0.75MoO₄：Eu_0.24³⁺,Bi_0.01³⁺。     

Elastic π± + 3He scattering

Differential cross sections have been measured at θ≈20–120° at 50, 100 and 200 MeV. Salient features of the angular distributions are Coulomb interference effects at 50 MeV and clear spin-flip contributions to π^? compared to π⁺ scattering in the angular region of θ≈80° dominated by the πN p-wave minimum. Comparison with optical model calculations account for the data up to 200 MeV while this first-order scattering theory misses conspicuous features of data at 295 MeV.     

Excitation energy of the lowest 2+ and 3− levels in 32Mg and 146Gd

The excitation energy of the lowest 2⁺ and 3^? levels is calculated for neutron rich Mg-isotopes as well as for N=82 isotones. The calculations are made by assuming quadrupole-quadrupole and octupole-octupole forces. The quasiparticle energies and occupation numbers are taken from the energy density method.     

Li+ transport in Li0.40MoO3 studied by pulse NMR

Pulsed ⁷Li NMR relaxation time measurements are reported for the intercalate Li_0.40MoO₃ in the temperature range 200K < T < 460K at 20 MHz. Temperature dependences of T₁ and T₂ indicate translation of Li⁺ with E_A = 23 kJ mol^-1. The data lead to an estimate for the Li⁺ self-diffusion coefficient at 300K of D¹_300K ? 4 x 10^-12 cm² sec^-1.     

Vibrational analysis of the a3Σ+-X1Σ+ and b3Π-X1Σ+ band systems of GeS

Spectra of GeS have been obtained in a chemiluminescent flame produced by the reaction Ge + OCS → GeS + CO. Neither of the known band systems, D¹Π-X¹Σ⁺ and E¹Σ⁺-X¹Σ⁺, was observed, but two new band systems in the regions 350–400 and 420–650 nm were obtained. By comparison with similar systems in isovalent molecules, these were assigned as b³Π₁-X¹Σ⁺ and a³Σ⁺-X¹Σ⁺, respectively. Vibrational assignments were made with the help of the germanium isotope effect and vibrational constants were obtained for the states involved. Approximate Morse potential Franck-Condon factors were computed and were shown to fit the general trend of the intensity distribution for both systems. Addition of active nitrogen to the flame was shown to increase the intensity of the b-X system by an order of magnitude while hardly affecting the a-X system. Constants (in cm^?1) obtained for the two new states are: a³Σ⁺: T_e = 21986.3 ± 2.3, ω_e = 388.9 ± 1.0, ω_ex_e = 1.35 ± 0.11; b³Π₁: T_e = 27192.0 ± 1.8, ω_e = 435.4 ± 1.1, ω_ex_e = 1.68 ± 0.20.     

Ultraviolet and visible upconversion dynamics in Er^3＋：YAlO3 under ^2H11/2 excitation

The luminescence of Er^3＋：YAlO3 in ultraviolet visible and infrared ranges under the 518 nm excitation of the multiples ^2H11/2 have been investigated. Ultraviolet （275 nm and 318 nm）, violet （405 nm and 413 nm） and blue （474 nm） upconversion and infrared downconversion luminescence has been observed. By means of measuring the fluorescence decay curves and using the theory of rate equations, the luminescence kinetics was studied in detail and the processes of energy transfer upconversion （ETU） and excitation state absorption （ESA） were proposed to explain the upconversion phenomena.     

The 1Σ+-X1Σ+ transition of the PN molecule

The recently observed ¹Σ⁺-X¹Σ⁺ transition of the PN molecule (J. Phys. B.13, 2251–2254 (1980)) has been photographed at high dispersion in the 1600–1900-Å region. A rotational analysis is carried out and shows 11 vibrational levels of the new ¹Σ⁺ state. These levels are perturbed and absolute vibrational numbering cannot be determined. Some perturbations can be accounted for by interactions with the A¹Π state. Weakening of lines are explained as accidental predissociations and allow us to discuss the dissociation energies of the X¹Σ⁺ and A¹Π states.     

N2O+离子A2Σ+电子态的光解动力学研究

用一束波长为360.55nm的激光，通过N2O分子的（3+1）共振多光子电离（REMPI）过程制备纯净且布居完全处于X2Π(000)态的母体离子N2O+，然后用另一束波长在275—328nm范围内的可调谐激光将制备的N2O+离子激发至预解离电子态A2Σ+.实验发现，由于解离碎片NO+所具有的一定的反冲速度，其TOF质谱峰明显比N2O+母体宽.通过分析NO+碎片TOF质谱峰形状，得到了解离产物的总平均平动能〈ET〉；通过考察〈ET〉随光解能量的变化，发现光解能量在32000cm-1附近约250cm-1的变化 关键词： N2O+离子A2Σ+态 TOF质谱峰 预解离机理     

White emission from Tm3+/Tb3+/Eu3+ co-doped fluoride zirconate under ultraviolet excitation

We synthesize Tm3+/Tb3+/Eu3+triply-doped ZrF4–BaF2–LaF3–AlF3–NaF(ZBLAN) transparent glass by using a melt-quenching method. Under excitation of 365 nm, the white emission with Commission internationale deL’Eclairage(CIE) coordinates of(0.33, 0.33) is achieved at the Eu3+concentration of 1.1 mol%. The mechanisms for white emission and the energy transfer process of Tb3+→ Eu3+are discussed in terms of the photoluminescence, photoluminescence excitation spectra, and the light emission decay curves. The nature for the Tb3+→ Eu3+energy transfer is described with the aid of an energy level diagram.     

On the inelastic excitation of 2− state of 16O by α particles

The excitation of the unnatural parity state (2^?, 8.87 MeV) of ¹⁶O by inelastic scattering of 40 MeV α particle is investigated microscopically. The two step excitation mechanism via the 3^? state at 6.13 MeV is found to reproduce the magnitude of the measured cross section of the 2^- excitation. The α-nucleon interaction used for the 2^- excitation also reproduces the 3^- excitation.     

The ξ-approximation and the 2− (0.96 MeV β−)2+ transition in 198Au

It is shown that the recent measurement of β-γ(circularly polarized) correlation in ¹⁹⁸Au performed by Hartman and Daniel is inconsistent with a great number of experiments realized previously on the 2^?(0.96 MeV β^?)2⁺ transition. In addition, we have confirmed that this process is qualitatively well described by the ξ-approximation.