X射线激光Nd薄膜靶表面氧化特性研究

 利用石英晶体振荡技术测量了不同环境中稀土元素Nd薄膜靶表面氧化速率,用俄歇电子能谱,扫描电镜,X射线衍射,X射线光电子能谱分析了Nd薄膜表面氧化过程,发现保存环境对靶的表面氧化行为有重要影响。空气中水分是引起Nd快速氧化的关键因素。表面氧化层为团聚状的非晶结构,氧化物与金属的体各比较小可能是引起Nd薄膜较易氧化的原因。Nd薄膜靶表面覆盖有一层氢氧化物,其厚度按保存在真空、干燥空气和潮湿空气环境而依次递增。     

基于压电探测判定激光支持燃烧波和爆轰波的点燃阈值

为了获得激光支持燃烧波和爆轰波的点燃阈值,采用压电探测器检测波长为1 064 nm的Nd:YAG激光作用在铝靶表面所产生的应变和冲压。从实验结果观察到压电信号的变化分为3个阶段,分别为光热弹性应变阶段、等离子体增强耦合阶段和激光支持爆轰波对靶表面的压力阶段,并从理论上研究了这3个阶段的激光与靶材料相互作用的机理,从而可以从压电信号是否发生跃变判断出激光支持燃烧波和激光支持爆轰波的点燃阈值,与其它方法所得到结果基本吻合。     

基于压电探测判定激光支持燃烧波和爆轰波的点燃阈值

为了获得激光支持燃烧波和爆轰波的点燃阈值,采用压电探测器检测波长为1 064nm的Nd:YAG激光作用在铝靶表面所产生的应变和冲压。从实验结果观察到压电信号的变化分为3个阶段,分别为光热弹性应变阶段、等离子体增强耦合阶段和激光支持爆轰波对靶表面的压力阶段,并从理论上研究了这3个阶段的激光与靶材料相互作用的机理,从而可以从压电信号是否发生跃变判断出激光支持燃烧波和激光支持爆轰波的点燃阈值,与其它方法所得到结果基本吻合。     

激光诱导荧光光谱分析法研究(Ⅶ)——SM-DBM-TOPO-农乳-100体系的发光机理及应用

以Nd:YAG激光器为激发光源、硅增强靶型光学多道分析仪作检测器并与IBM PC/XT微机联机进行数据的分析处理,研究了DBM,TOPO和Sm-DBM-TOPO在非离子表面活性剂农乳-100存在下的吸光特性和激光诱导发光特性,提出该体系的发光机理和能量传递机制。不经分离,直接用于高纯稀土氧化物中痕量钐的测定,获得了满意的结果。     

空气中激光等离子体冲击波的传输特性研究

根据球形对称冲击波在自由空间中传播的约束条件,提出了空气中激光等离子体冲击波在中远场的传播公式.并用探针式超声换能器实测了能量为10-110mJ、脉宽为15ns、波长为106μm的Nd∶YAG激光作用于铝靶表面产生的等离子体空气冲击波,用此公式计算的结果与实验数据符合得很好 关键词：     

激光烧蚀金属靶诱导靶电势效应的机理研究

利用Nd∶YAG脉冲激光烧蚀Cu靶材,实验研究了不同激光能量下等离子体诱导靶上电势的演变规律.结果表明：靶上电势信号呈现显著的双峰结构,第一个峰出现在激光烧蚀开始之后约20 ns,持续时间仅约50 ns；而第二个峰出现约35 μs之后,持续时间达到了上百微秒.通过对实验结果的详细分析可知靶上电势信号的产生是激光等离子体荷电效应引起的,并提出了等离子体对金属靶的静电感应、电荷复合-转移效应机制,解释了靶上电势信号的演变规律.     

掺溴聚苯乙烯平面调制箔靶的制备及测量

 平面调制靶是ICF分解实验中的重要用靶。介绍了在过去工作的基础上掺溴聚苯乙烯平面调制箔靶的制备工艺,研究旋转涂覆和流延工艺对靶的表面起伏图形转移的影响,采用SEM观察薄膜表面起伏图形的形貌,对掺杂溴的含量进行测量和控制,以台阶仪测量靶的表面粗糙度。     

激光脉冲波形对烧蚀Si靶表面温度的影响

利用双温方程对激光烧蚀Si靶的过程进行了数值模拟,并结合合适的初始条件和边界条件,研究了在飞秒、皮秒激光作用下,脉冲波形(矩形、梯形、三角形和高斯形)对Si靶表面载流子和晶格温度分布的影响。结果表明:激光功率密度是影响载流子温升的主要因素,矩形脉冲激光烧蚀Si靶表面载流子的峰值温度最高,而高斯分布的脉冲引起靶面载流子峰值温度最低。可见,激光脉冲波形对Si靶表面载流子的温度分布具有重要影响。所得结果可为制备高质量的薄膜提供理论依据。     

强激光与高密度气体相互作用中电子和离子加速的数值模拟

在现有的一维粒子模拟程序的基础上发展了带光电离和碰撞电离及蒙特卡罗两体碰撞的模拟程序(1D PIC-MCC). 用此程序模拟研究了短脉冲激光与He气靶相互作用时电子和离子的加速过程. 研究表明当强激光与过临界密度的微米厚度的平面靶相互作用时，靶前表面物质将被激光脉冲前沿迅速离化；新生的电子被激光场有质动力加速成为高能电子，这些电子穿入到靶内，通过电子碰撞电离离化靶内物质；一部分高能电子穿透靶后，会在靶的后表面形成强的电荷分离场，该场迅速离化靶后表面物质，同时使得后表面离子得到加速. 部分穿透靶的超热电子将被电荷分离场重新拉回靶内，在靶的前后表面振荡. 一些振荡电子在此过程中得到电荷分离场加速，离开前表面，在前表面也形成电荷分离场，使前表面离子得到加速. 关键词： 激光等离子体 光电离和碰撞电离 电子加速 离子加速     

高增益Nd∶YAG板条中的放大自发辐射抑制技术

分析了Nd∶YAG板条中产生强烈放大自发辐射(ASE)的原因,开展了抑制高增益激光板条中ASE的理论和实验研究。抽运光占空比为8%,峰值抽运功率为21.38kW,波长为1064nm连续探测光的注入光强为4 W/cm~2,在Nd∶YAG板条上、下表面镀制普通倏逝膜和多层复合膜时探测光功率的放大倍率分别为1.82和1.92,Nd∶YAG板条总储能增大了4.6%。实验结果表明:通过对Nd∶YAG板条上、下表面镀制多层复合膜,可在一定程度上抑制板条内的ASE效应,增大激光板条的总储能。     

稠苯芳杂环及其烷基质子化学位移的计算

本文提出了予测稠苯芳杂环及其烷基链上质子化学位移的计算方法。 将稠苯芳杂环化合物用凯库勒式表示,计算式为为需考虑的苯环内的乙烯基效应。σ_mi,ci为各苯环的环流效应。σ_1,Hc为各芳杂环的屏蔽效应,对杂环上质子它就是该单独芳杂环上相应质子的δ值,对苯环上质子要将它分解为各结构因素的效应,即:σ_1,He=(1/2)^d-1δ_x=y(或σ_z)+σ_c-c·σ_m,H. σ_x-y与σ_z为杂原子或其基团的屏蔽效应,σ_c=c为存在于芳杂环中的乙烯基的效应,σ_m,Hc为芳杂环的环流效应,d为对不同质子所考虑的键数。有取代基时需考虑取代基的效应。计算环上烷基质子的公式为:δ=σ_p,CH3+ασ_c,CH3+βσ_t,CH3+σ_l,G σ_l,G为稠苯芳杂环基的某级效应。     

Structural phase transitions at clean and metal-covered Si(111) surfaces investigated by RHEED spot analysis

Structural phase transitions between various kinds of superlattice structures formed on a Si(111) surface have been investigated by spot analysis of reflection high-energy electron diffraction (RHEED). Reversible transitions induced by temperature changes and irreversible ones induced by metal depositions were observed. Detailed discussions on the dynamics of the phase transitions are made by quantitative analyses of integrated spot intensity and profile. For a phase transition of 7′7  1′1 structures on a clean Si(111) surface, a hysteresis with temperature difference of 5°C. between in heating and cooling processes was found in the spot intensity change, indicating a first-order transition. Hysteresis was hardly recognized, on the other hand, for transitions of Au-induced superstructures (5×2-Au or ×-Au)  1×1-Au. The spot profiles were found to be broadened during the transition of Si(111)-×-Au  1×1-Au, which was a signature of a continuous transition, while the profiles remained unchanged during the transitions of the 7×7  1×1 and 5×2-Au  1×1-Au phases. Structural conversions induced by In adsorption on the Si(111) surface kept at constant temperatures were also analyzed. The conversions at room temperature were totally dependent on the initial substrate surface structures; the 7×7 surface did not show any structural conversion with In adsorption, while the ×-In surface successively converted to a 2×2 and a × phase with coverage increase. The structural transitions at elevated temperatures were sensitively dependent on the temperatures. Sequences of transitions among the 7×7, 4×1, ×, 1×, and ×4 were quantitatively revealed as changes in RHEED spot intensity.     

ErP5O14非晶玻璃的红外量子剪裁

研究了Er_1.0P₅O₁₄铒非晶玻璃的红外量子剪裁现象. 从吸收谱和激发光谱的计算比较中肯定了Er_1.0P₅O₁₄非晶 玻璃的1537.0 nm红外荧光为多光子量子剪裁荧光. 从Er_1.0P₅O₁₄非晶玻璃的可见和红外荧光发射光谱中发现激发²H_11/2, ⁴G_11/2和⁴G_9/2能级所导致的⁴I_13/2→⁴I_15/2量子剪裁红外荧光很强;基于自发辐射速率、无辐射弛豫速率和能量传递速率等参数的计算,对其量子剪裁机理进行了分析.发现起源于基态的强下转换能量传递{²H_11/2→⁴I_9/2,⁴I_15/2→⁴I_13/2},{⁴G_11/2→⁴I_13/2, ⁴I_15/2→²H_11/2},{⁴G_9/2→⁴F_7/2,⁴I_15/2→⁴I_13/2}和{⁴G_9/2→⁴I_13/2, ⁴I_15/2→²H_11/2}是导致Er_1.0P₅O₁₄非晶玻璃具有强的三光子和四光子量子剪裁红外荧光的原因.研究结果对改善太阳能电池效率有一定意义.     

1-forms over the moduli space of irreducible connections defined by the spectrum of Dirac operators

Let (P) be the moduli space of irreducible connections of a G-principal bundle P over a closed Riemannian spin manifold M. Let D_A be the Dirac operator of M coupled to a connection A of P and f a smooth function on M. We consider a smooth variation A(u) of A with tangent vector ω and denote T_ω:= (D_A(u)−f) (u=0. The coefficients of the asymptotic expansion of trace (T_ω · e^-t(D_A−f)2) near t=0 define 1-forms a^(k)_f, K=0, 1, 2, … on (P). In this paper we calculate aa⁽⁰⁾_f, a⁽¹⁾_f, a⁽²⁾_f and study some of their properties. For instance using the 1-form a⁽²⁾_f for suitable functions f we obtain a foliation of codimension 5 of the space of G-instantons of S⁴.     

Phase formation and magnetic properties of Nd2Fe14B-type Nd16Co76B8−xCx alloys and their hydrides

An attempt is made to synthesize Nd₂Co₁₄C compound by mechanical alloying Nd₁₆Co₇₆B_8−xC_x (0x8) alloys and subsequent annealing. Phase formation and magnetic properties of Nd₂Fe₁₄B-type Nd₁₆Co₇₆B_8−xC_x alloys and their hydrides are investigated. The Nd₂Co₁₄(B,C) phase with Nd₂Fe₁₄B-type structure is formed for Nd₁₆Co₇₆B_8−xC_x (0x7) alloys, while NdCo₇C_δ phase with TbCu₇-type structure is observed in Nd₁₆Co₇₆C₈ alloy. The lattice parameter c of the Nd₂Co₁₄(B,C) phase decreases with increasing the carbon content. A limit volume of the unit cell to form the Nd₂Fe₁₄B-type structure is estimated to be 0.870 nm³. The spin-reorientation temperature T_SR increases with increasing the carbon content, due to an enhancement of magnetocrystalline anisotropy caused by carbon substitution for boron. After hydrogenation, the lattice expansion is observed for Nd₁₆Co₇₆B_8−xC_x (0x7) alloys. The spin-reorientation temperature of Nd₁₆Co₇₆B_8−xC_xH_y (0x7) is much lower than that of the host alloys. Some structural and magnetic properties of hypothetic Nd₂Co₁₄C and Nd₂Co₁₄CH_y compounds are estimated by extrapolation.