椭偏光法研究晶体各向异性光学性质——对KNSBN铁电晶体的应用

本文分析了椭偏光法测量各向异性晶体时入射角和起偏角对测量灵敏度的影响,着重讨论了如何选择合适的实验条件以测量低度各向异性(|n₀—n_c|<0.1)晶体的光学性质。利用单波长椭偏仪和多波长椭偏谱仪测量了方解石和KNSBN铁电晶体样品,得到各向异性折射率和消光系数值,与文献有关结果作了比较。对于|n₀—n_c|<0.1的KNSBN铁电晶体,获得了可靠的结果。 关键词：     

光谱型椭偏仪对各向异性液晶层的测量

探讨了利用普通光谱型椭偏仪对各向异性液晶层进行综合性测量的可行性. 并利用法国Jobin Yvon公司的UVISEL SPME(Spectroscopic Phase Modulated Ellipsometer)光谱型椭偏仪测量了光学各向异性液晶层的折射率n_o和n_e及液晶层厚d，进一步利用椭偏仪在透射方式下测量了平行排列液晶层的光延迟特性Δnd，二者取得了很好的一致性，说明利用光谱型椭偏仪可以实现对光学单轴性液晶层及其他材料的测量，测厚精度为纳米量级. 关键词： 光谱型椭偏仪 各向异性 折射率 相位延迟     

教学型椭偏仪测量各向异性单轴晶体光学参数的方法研究

椭偏仪是一种常用的现代光学测量仪器,在物理实验教学中常用于测量各向同性材料的折射率、表面薄膜厚度等光学参数。本文提出一种利用教学型椭偏仪测量各向异性单轴晶体折射率等光学参数的方法。采用多入射角的方法增加系统自由度,建立数值反演模型,获得各向异性单轴晶体光学参数,并实验测量了钒酸钇晶体的折射率等光学参数。使用教学型椭偏仪测量各向异性单轴晶体光学参数,拓展了原有教学仪器的实验范围,有助于激发学生对实验的兴趣。     

光折变晶体中二波耦合光强依赖现象和各向异性热透镜效应

实验发现,掺Ce离子的光折变晶体KNSBN中二波耦合光强依赖现象和各向异性热透镜效应有共生关系.光吸收引起晶体温升乃至引起.光折射率的增加是产生这种现象的主要原因. 关键词：     

用椭偏光谱仪测量不同波长下砷化镓的光学参量

讨论了把单长TP－77型随偏仪改装成椭偏光谱仪的原理，并用改装后的椭偏仪测量多个波长下GaAs的光学参量，测量结果与参考文献的结果符合较好，改进后的实验提高了学生的动手能力，加深了学生对椭偏技术的了解。     

掺杂KNSBN晶体各向异性自衍射的耦合波分析

在晶体光轴垂直于入射面的各向异性实验组态下,对掺杂KNSBN晶体的各向异性自衍射过程进行了理论分析和实验观测,给出了包含空间电荷场前两阶分量作用的各向异性自衍射的耦合波方程及其数值解。理论分析和实验结果都表明各向异性自衍射光来自于两束入射光的共同作用。     

KNSBN掺Cu晶体高反射率自泵浦位相共轭反射镜

利用KNSBN掺Cu晶体实现了自泵浦位相共轭;掺Cu量0.04wt％的晶体自泵浦位相共轭反射率高达65％;测量了自泵浦位相共轭反射率,响应时间和氩离子激光波长的关系。     

对称分子H2+在强短波激光场中高次谐波椭偏率性质的研究

通过数值计算,研究了强短波(400—600 nm)激光场中H₂⁺分子高次谐波辐射的椭偏率性质.研究表明,H₂⁺分子在不同激光强度、不同激光波长、不同核间距及不同取向角下高次谐波的椭偏率性质是不同的;特别是在两中心干涉区,激发态在高次谐波产生中起着重要作用,但在不同取向角下,激发态对谐波椭偏率的影响不同;分析表明,这些不同的影响源于沿平行和垂直于激光偏振方向辐射的高次谐波的相对产量,以及激发态对平行和垂直谐波产量的影响;此外,椭偏率的测量检验了强场近似和平面波近似在强短波激光场中是成立的,并对强短波激光场中分子动力学做了更充分的研究.     

基于棱镜的椭偏法测量液体复折射率

通过引进等腰棱镜,利用椭偏测量技术实现了液体复折射率的精确测量.基于菲涅尔公式及椭偏测量原理,从理论上分析仪器测量得到的椭偏参数与棱镜-液体界面椭偏参数的关系,并讨论了测量液体折射率及吸收系数的精度.使用消光式椭偏仪,测量了水和印度墨水的复折射率,得到了样品的折射率、吸收系数随浓度变化的实验曲线,实验结果与参考文献基本一致.实验表明:棱镜椭圆偏振技术测量液体折射率及吸收系数的精度分别为0.000 4和0.000 3,适合于快速测量.     

薄膜光学常数的椭偏测量

利用光谱型椭偏仪测量了镀在熔石英玻璃基片上的氟化镁薄膜在300～850nm波长范围内的椭偏参数.并利用Levenberg-Marquardt算法.反演出了氟化镁薄膜在该波长范围内的色散曲线.通过与纯氟化镁体材料的色散曲线比较,发现所镀的氟化镁薄膜的折射率略小于体材料的折射率.     

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.