光学材料折射率和色散的高精度测量技术研究

本文探讨了在一般精度的测角仪器上达到高精度测量折射率和色散的新原理和新方法,这些新原理和方法包括:光学角规补偿法测色散、直角照射法、自准封闭式最小偏向角法。通过实际大量的测量工作证明在1″测角仪(测角精度为3″)和测微望远镜上,上述原理方法都可以达到△n~±3×10~(-6),△(n_λ_1-n_λ_2)~±2×10~(-6)的精度。     

微楔形镜加工技术研究

微楔形镜的加工不能像平行平面元件那样,采用大块抛光,切片分割的办法。针对零件尺寸小、精度要求高的特点,研究了加工过程中的粘结上盘、面形精度控制和楔形角检测等技术,设计了吸附式粘结上盘和楔形角测量等专用装置,应用于尺寸为3×3×1mm(6°)的Nd∶YVO4(掺钕钒酸钇)晶体批量生产中,提高了零件的面形精度和加工可靠性。测试结果表明:面形精度优于λ/10(λ=632.8nm),表面光洁度达0/0级,楔形角合格率达98%以上。     

多程放大系统光学元件静态波前畸变研究

 通过研究光学元件静态波前畸变对多程放大系统光传输的影响，给出了满足聚焦光斑要求的均方根梯度值以及光学元件加工误差的最大允容值。加工误差的峰谷值不超过λ/3、均方根值不超过0.079λ,相位梯度的峰谷值不超过0.033λ/cm、相位梯度均方根不超过0.007λ/cm。通过光传输模拟程序校验了波前畸变的相干叠加和非相干叠加规律。     

低对称性非线性光学晶体硼酸铋(BIBO)的1064nm三倍频性质

采用高温溶液法成功生长出高光学质量的硼酸铋 (BIBO)晶体 ,尺寸达到 2 4mm× 19mm× 35mm ,质量为4 8g。对BIBO晶体进行了定向 ,并测量了该晶体的主轴折射率。讨论了BIBO晶体的 10 6 4nm三倍频性质 ,包括相位匹配角、有效非线性光学系数deff、容限角、走离角等。结果表明 ,BIBO晶体的最佳三倍频方向为 (137.7°,130°) ,其有效非线性光学系数值达到 3.6 0 pm/V ,属I类相位匹配。就主平面内的相位匹配方向而言 ,(14 6 .4°,90°)具有最大的有效非线性光学系数值 ,为 3.16pm/V。在 10 6 4nm的腔外三倍频实验中 ,(14 6 .4° ,90°)BIBO晶体的转换效率达到 39.5 % ,角度容限半宽为 0 .2 2mrad·cm ,该数值与 0 .175mrad·cm的计算值基本符合。由于(33.6°,90°)BIBO晶体的有效非线性光学系数较小 (0 .31pm/V) ,其三倍频转换效率小于 5 %。     

光折变晶体钛酸钡锶电荷传输参数的测量

报道用两波耦合技术测量光折变晶体钛酸钡锶(Ba_(1-x)Sr_xTiO-3,BST)的电荷传输参数φμτ在激光波长λ=515nm和光功率密度I—1W/cm~2下测得光折变响应时间为0.5sec.考虑到BST晶体吸收系数的光强相关性,修改了光栅形成率的函数变量,得到BST晶体的暗电导σ_a和电荷传输参数φμτ的拟合值分别为1.0×10~(-11)(Ωcm)~(-1)和2.8×10~(-10)cm~2/V.     

掺Tm钒酸钇的光学性能

钒酸钇(YVO4)晶体有高的激光损伤阈值和高的激光输出斜率效率,也有很好的机械性能和化学稳定性.从测量TmYVO4晶体的吸收谱入手,考虑该晶体的各向异性效应,拟合出Tm3+的光学强度参量,进一步得到了振子强度f,辐射跃迁速率A和积分发射截面Σ等光学参量.在350-2500nm范围内,YVO4晶体基质的吸收很小,而Tm3+在YVO4晶体中发光能力很强;特有的是蓝光1D2→3F4(约为454nm)跃迁有极大的振子强度(38×10-6)和积分发射截面(33×10-18cm),有利于实现短波长的激光输出.     

用Judd-Ofelt理论计算TmP5O14晶体中Tm3+的光谱参数

根据Judd-Ofelt理论,测得了Tm3+ 在TmP5O14晶体中的强度参数分别为Q2=:1.50×10-20cm2,Q4=1.51×10-20cm2,Q6=0.916×10-20cm2,计算的振子强度Pcal.与实验值Pexp.符合较好,平均根方误差为2.60×10-7。求得Qλ后,计算了J多重激发态之间的振子强度,自发辐射跃迁速率,辐射寿命和荧光分支出,与YAlO3:Tm3+,YAG:Tm3+、Y2O3:Tm3+等晶体和掺Tm3+玻璃的光谱参数进行了比较,并就3H4→3H6,3F4→3H5,1D2→3H4和1G4→3H4的跃迁进行了对比和讨论。观察到Tm3+在不同介质中的Pexp.与强度参数的总和∑τλ=τ2+τ4+τ6存在Pexp=α∑τλ+b的关系。     

菲的无保护性介质流体室温磷光性质研究

在无任何保护性介质存在下,以Na2SO3作化学除氧剂,KI为重原子微扰剂,菲即能产生强而稳定的流体室温磷光发射.激光和发射波长λex/λem为283/482,504nm,不同有机溶剂存在对其磷光发射的性质有不同影响.1%乙腈存在时,菲浓度在8.0×10-7～6.0×10-6mol*L-1和6.0×10-6～4.0×10-5mol*L-1范围内分别与磷光发射强度呈良好的线性关系,检出限为2.6×10-8mol*L-1.     

(Tb,Dy)Fe_2金属间化合物的巨大磁致伸缩

一、引言 在铁磁金属和合金中,Ni,Fe-Co,Fe-Ni,Fe-Al等合金都是较好的磁致伸缩材料。它们的纵向饱和磁致伸缩都不过10~(-6)。最常使用的纯Ni的λ_s 仅约—35 ×1O~(-6)。 1971年Clark等报道,稀土-铁Laves相化合物在室温下尚有极大的磁致伸缩值。例如Tb-Fe_2在25KOe下,磁致伸缩高达λ_(11)～1750×10~(-6),约为Ni的五十倍。这类材料可能在高功率换能器及声路器件方面有重要应用。     

大口径光学元件磁流变加工驻留时间求解算法

为了解决大口径光学元件磁流变高精度加工问题,基于矩阵运算模型,提出了SBB(Subspace Barzilai and Borwein)最小非负二乘与自适应Tikhonov正则化相结合的驻留时间快速求解方法。同时,在一次收敛中采用双去除函数优化螺旋线轨迹下光学元件的加工,保证中心区域与全口径面形精度一致。仿真表明该算法与常用Lawson-Hanson最小非负二乘法相比,计算精度一致且求解效率大幅提高。对Φ600mm以彗差为主的光学表面模拟加工,峰谷(PV)值和均方根(RMS)值从初始的2.712λ与0.461λ中心区域全局一致收敛到0.306λ和0.0199λ(λ=632.8nm)。因此,提出的算法能够在有效保证面形收敛精度的同时快速获得稳定可靠的驻留时间分布,为磁流变抛光应用于大口径光学元件提供有力支持。     

用于光纤电流传感器的掺Bi稀土铁石榴石单晶生长与磁光性能

用熔盐法生长了两种Bi替代的高法拉第旋转、温度稳定的稀土铁石榴石磁光单晶Bi-HoYbIG和Bi-GdYIG,测试分析了其在近红外波段的磁光性能及其温度特性。Ho3-z-y,YbyiBixFe512(x＝1.03,y=1.20)单晶的比法拉第旋转角为-891°/cm(λ=1.31μm)和-767°/cm(λ＝1.55μm),Y3-z-yGdyBixFe5O12(x=0.46,y=0.24)单晶的值为－1067°／cm(λ=1.31μm)和-882°／cm(λ=1.55μm),两者都比纯YIG晶体高出许多。而且这两种晶体的法拉第旋转角随温度变化较小,在250～400K范围内,其温度灵敏度S分别为4. 60×10-4／K和4. 20×10-4/K。分析表明,Bi的掺入能大大提高晶体的法拉第旋转角,而yb3+、Gd3+等离子的掺入可以有效降低Bi3+替代磁光单晶的法拉第旋转的温度灵敏性,Bi-HoYbiG和Bi-GdYIG等磁光晶体非常适合作为高灵敏度、温度稳定的光纤电流传感器中的法拉第转子材料。     

Interaction between parallel polymer fibers insonificated by ultrasound of low/mild intensity: an analytical theory and experiments

The purpose of this article is to develop a simple mathematical model to address some bioeffects which may be caused by a static attractive force between two long neighboring parallel thin fibers (for example, a pair of collagen bundles of connective tissue) when they are insonificated by a continuous (CW) traveling plane ultrasound (US) under the condition that the fiber length (L)?the distance between them (h) and h?the wavelength of US (λ). The theory predicts that there is an attractive force between these fibers when they are exposed to the CW US with an intensity of a magnitude of 100mW/cm(2). The relationship between the relative approaching velocity of the fibers and the acoustic pressure amplitude can be calculated using the theory. An experiment was performed to verify the theoretical predictions. A plastic test chamber (diameter × height=6mm × 3.5mm) with a cap made of a sound-absorbing material and filled full with distilled water was placed on a microscope stage. A polymer fiber pair of 100μm diameter (d) and 4mm length (L) were immersed in water and aligned parallel in a plane which is normal to the US propagation direction. They floated at the central area of the chamber and h ≤10d. A 25mm diameter, 1MHz quartz crystal was used as an ultrasound source as well as the bottom of the test chamber. The quartz crystal was gold-coated on both sides, but a 5mm diameter center was left transparent (electrode free) to enable optical observation via a microscope. The maximum acoustic intensity, I(max), of the CW wave generated by the source was set at 300mW/cm(2); the corresponding acoustic pressure amplitude was 100kPa. The magnitude of the average approaching velocity of the fiber pair due to the attractive force was found in agreement with that predicted by the theory.     

EPR, optical absorption and superposition model study of Fe³(+) doped strontium nitrate single crystals

Electron paramagnetic resonance (EPR) study of Fe3(+) ions doped strontium nitrate (SN) single crystals is performed at liquid nitrogen temperature and at X band frequency. The spin Hamiltonian (SH) parameters are determined from the resonance lines observed at different angular rotations. The crystal field parameters (CFPs) are evaluated using superposition model of Newman. The Zeeman g-factor and zero-field splitting parameters (ZFSPs) of Fe3(+) ion in SN (truncated SH considered) are: g=1.9989 ± 0.002 and ∣D∣=(338 ± 5) × 10?? cm?1, ∣E∣=(10 ± 5)× 10?? cm?1, a=(458 ± 5)× 10?? cm?1, respectively. The Fe3(+) ion enters the lattice substitutionally replacing the Sr2(+) sites of cubic symmetry. The local site symmetry of Fe3(+) ion in the crystal is orthorhombic (lower than that of the host). The optical absorption study of the crystal is also done at room temperature in the wavelength range 195-925 nm. The energy values of different orbital levels are determined. The observed bands are assigned as transitions from the (6)A?(g)(S) ground state to various excited states of Fe3(+) ion in a cubic crystal field approximation. The observed band positions are fitted with four parameters, the Racah interelectronic repulsion parameters (B and C), the cubic crystal field splitting parameter (Dq) and the Trees correction (α) yielding: B=934, C=2059, Dq=1450, and α=90 (in cm?1). On the basis of EPR and optical data, the nature of metal-ligand bonding in this crystal is discussed. The ZFSPs are also determined theoretically using microscopic SH theory based on perturbation theory and CFPs, B(kq) obtained from superposition model. The values of ZFSPs thus obtained are ∣D∣=(340 ± 5) × 10?? cm?1 and ∣E∣=(15 ± 5) × 10?? cm?1.     

八元瓜环诱导菲、芴的室温磷光研究

以八元瓜环为诱导剂、碘化钾作重原子微扰剂,在亚硫酸钠除氧下,实现了菲、芴的室温磷光发射。在该体系中菲、芴的最大激发和发射波长分别为282和509 nm,276和518 nm,磷光寿命分别为1.82和3.68 ms。在最佳实验条件下,菲在1.0×10-7～1.5×10-6mol·L-1,1.5×10-6～1.0×10-5 mol·L-1和芴在8.0×10-7～8.0×10-6mol·L-1的浓度范围内分别与其磷光强度呈良好的线性关系,检出限分别为4.8×10-9和8.0×10-9 mol·L-1。     

High Power All-Solid-State Nd: YVO_4 laser and its intracavity SHG

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Cs(6DJ)+Cs(6S1/2)非弹性碰撞转移截面的测定

在9×1014～2.1×1015cm-3 Cs密度范围内,利用脉冲激光双光子激发Cs(6S1/2)到Cs(6D5/2)态,使用原子荧光光谱方法,通过三能级模型的速率方程分析,由对直接荧光和转移荧光的时间积分强度的测量,得到6D5/2→6D3/2精细结构转移截面为(2.1±0.4)×10-14cm2,而6D3/2态向6D以外态的转移截面为(1.6±0.4)×10-14cm2,它应是过程Cs(6 D3/2)+Cs(6S)→Cs(6P)+Cs(6P),6D3/2→7P3/2和6D3/2→7 P1/2碰撞转移截面之和.第二个实验可以得到6 D3/2→7P3/2和6D3/2→7 P1/2的碰撞转移截面.在1×1012～6×1012cm-3的低密度Cs蒸气中,激光双光子激发6S至6D3/2或6D5/2态,测量6DJ→6PJ'与7PJ"→6S1/2的时间积分荧光强度比,得到6D3/2→7P1/2与6D5/2→7R3/2的碰撞转移截面分别为(7.6±2.4)×10-15cm2与(1.6±0.5)×10-15cm2.由此得到碰撞能量合并的逆过程即[Cs(6D3/2)+Cs(6S1/2)→Cs(6P)+Cs(6P)]的转移截面为(1.3±0.4)×10-14cm2.     

Z箍缩等离子体均匀色散晶体光谱成像

为了诊断Z箍缩等离子体X射线相关信息,利用自聚焦和均匀色散原理,研制了一种新型的均匀色散弯晶谱仪。晶体分析器采用-石英（1010）,布拉格角为43.4~72.7,利用有效面积为10 mm50 mm的X射线胶片接收光谱信号,实验在中国工程物理研究院阳加速器装置上进行,摄谱元件获得了Z箍缩铝丝阵等离子体的类H及类He谱线。实验结果表明:谱线分布遵循均匀色散条件,所研制均匀色散弯晶谱仪线色散率为-116.198 mm/nm,与理论值-120 mm/nm的相对误差为3.168%,能够用于Z箍缩等离子体X射线的光谱学研究。     

RP-HPLC同时测定白花檵木花中的槲皮素和山奈酚

建立用反相高效液相色谱法同时测定白花檵木花中槲皮素和山奈酚含量的方法。采用Eclipse XDB-C18色谱柱(4.6mm×250mm,5μm);柱温:25℃;流动相为乙腈-0.4%磷酸水溶液(35:65,V/V);流速为1.0mL·min-1;检测波长为360nm。槲皮素在1.08×10-3—1.08×10-1μg·μL-1的范围内具有良好的线性关系(r=0.9999),平均回收率97.23%,RSD为1.26%;山奈酚在1.04×10-3—1.04×10-1μg.μL-1的范围内具有良好的线性关系(r=0.9999),平均回收率99.78%,RSD为0.46%。方法简便、准确、可靠,可作为白花檵木花中槲皮素和山奈酚的定量分析方法。