Yb~(3+)和Er~(3+)共掺杂氟硼酸盐玻璃材料光学跃迁及红外到可见上转换

利用 J-O理论和吸收光谱实验数据计算了 Er3 +掺杂的氟硼酸盐玻璃材料的光学跃迁参数 ,从而得到了一些能级间跃迁的振子强度、跃迁几率、分支比、及寿命等数据。在室温下观察到了在 970 nm LD激发下红色和绿色上转换发光 ,讨论了红色上转换发光强度与 LD电流的关系。     

An azo-isomerization-induced Freedericksz transition of a nematic liquid crystal

We observed an azo-isomerization-induced Freedericksz transition of the 5CB liquid crystal doped with 1% double-azo. In experiment, we found that the Freedericksz transition threshold occurred at optical intensity level of 0.3 mW/mm² for the 12.5 μm-thickness planar alignment doped 5CB, which is four orders of magnitude lower as that for the pure 5CB. Using optical phase retardation, we measured the relations between the Freedericksz transition threshold and the pump beam polarization. The maximum twist angle of liquid crystal molecules under different pump beam intensity is given. The experiment indicated that trans–cis isomerization plays an important role in the decrease of the Freedericksz transition threshold.     

在线单模光纤偏振控制器研究

利用Ｐｏｉｎｃａｒｅ球理论首次全面分析了在线全光纤偏振控制器。结果发现该偏振器可以有八种不同路径，实现任意偏振态之间的转化，最后通过实验验证了其工作性能。     

2，5─哌嗪二酮与α，β─不饱和醛反应研究

综合运用了多种波谱学方法及化学手段确证并归属了２，５－哌嗪二酮与α，β－不饱和醛在超声波分散金属钾及双季铵盐作用下反应产物的立体化学与核磁共振信号，为研究这个反应提供了有用的信息．     

漂移管中相对论电子束引导的匹配条件

本文介绍了对连续型相对论电子束的两种引导及箍缩方法:磁场引导和离子通道的静电引导。在线性引导力的假定下,求得了单磁场引导、单静电引导以及同时使用磁场和电场的混合引导的这三种情况下的匹配条件的解析结果。解析公式表明。在混合引导情况下,为了使电子束匹配,当电子束的中和因子线性增加时,相应的引导磁场不是线性地减小。而是抛物线形地减小。本文还使用了模拟束片内电子横向运动的LGERKB编码,通过对N_0个束内电子的模拟计算,求得了电子束包络。电子束的均方根发射度、典型电子轨道、失配和匹配情况下的束内电子相空间分布(相图)及其演变过程等大量资料。线性模拟结果与解析分析结果完全一致。     

Low-temperature heat capacities and standard molar enthalpy of formation of N-methylnorephedrine C11H17NO（s）

This paper reports that low-temperature heat capacities of N-methylnorephedrine C11H17NO（s） have been measured by a precision automated adiabatic calorimeter over the temperature range from T=78K to T=400K. A solid to liquid phase transition of the compound was found in the heat capacity curve in the temperature range of T=342-364 K. The peak temperature, molar enthalpy and entropy of fusion of the substance were determined. The experimental values of the molar heat capacities in the temperature regions of T=78-342 K and T=364-400 K were fitted to two poly- nomial equations of heat capacities with the reduced temperatures by least squares method. The smoothed molar heat capacities and thermodynamic functions of N-methylnorephedrine C11H17NO（s） relative to the standard refer- ence temperature 298.15 K were calculated based on the fitted polynomials and tabulated with an interval of 5 K. The constant-volume energy of combustion of the compound at T=298.15 K was measured by means of an isoperibol precision oxygen-bomb combustion calorimeter. The standard molar enthalpy of combustion of the sample was calculated. The standard molar enthalpy of formation of the compound was determined from the combustion enthalpy and other auxiliary thermodynamic data through a Hess thermochemical cycle.     

Electromagnetic tunneling through conjugated single-negative metamaterial pairs and double-positive layer with high-magnetic fields

We show that resonant tunneling of electromagnetic （EM） fields can occur through a six-layer structure con- sisting of two pairs of bilayer slabs： one＇being an epsilon-negative layer and the other being a mu-negative layer with a double-positive （DPS） medium and air. This type of tunneling is accompanied by high-magnetic field. The Poynting vector distributions and the material dissipation are studied. Our results demonstrate that the EM field in the structure is controlled flexibly by single-negative media and DPS slab. Therefore, this structure has potential applications in wireless energy transfer.     

Relationship Between Total Surface Tension of Monomer and Its Homopolymer

The surface and interfacial properties of polymers are important for their applications. In one of our previous articles, we discussed the relationship between the dispersive surface tension component and the density and molecular weight of solvents and polymers to seek a simple and easy method to estimate the rationality of surface tension results of polymers. We found that for 30 organic solvents and 12 polymers, there was a good relationship between the dispersive surface tension and the experiential parameter 1/ρ² M ^0.2 _w . In this article, the existence of the squared density term is simply deduced from the general molecular interaction energy equation and is proved with four pairs of polymer/monomer; these are polystyrene/styrene, polyisoprene/isoprene, polymethyl methacrylate/methyl methacrylate, and polyvinyl acetate/vinyl acetate.     

Damping Properties of Blends Based on EVM

The mechanical and damping properties of blends of ethylene-vinyl acetate rubber (VA content >40% wt) (EVM)/ethylene-propylene-diene copolymer (EPDM) and EVM/nitrile butadiene rubber (NBR), both with 1.4 phr BIPB (bis (tert-butyl peroxy isopropyl) benzene) as curing agent, were investigated by dynamic mechanical analysis (DMA). The effect of added polyvinyl chloride (PVC), amido donor N-cyclohexyl-2-benzothiazole sulfonamide (CZ), and dicumyl peroxide (DCP) as a substitute curing agent, on the damping and mechanical properties of both rubber blends were studied. The results showed that in EVM/EPDM/PVC blends, EPDM was immiscible with EVM and could not expand the damping range of EVM at low temperature. PVC was miscible with EVM and dramatically improved the damping property of EVM at high temperature while keeping good mechanical performance. In EVM/NBR/PVC blends, PVC was partially miscible with EVM/NBR blends and remarkably widened the effective damping temperature range (EDTR) from 41.1°C for EVM/NBR to 62.4°C. Curing agents BIPB and DCP had a similar influence on EVM/EPDM blends. DCP, however, dramatically raised the height of tan δ peak of EVM/NBR = 80/20 and expanded its EDTR to 64.9°C. CZ had no obvious influence on the EVM/EPDM blends cured with BIPB. However, a small content of CZ enlarged the tan δ peak of EVM/NBR = 80/20 in both height and width, but at the cost of a deterioration of mechanical performance.     

Photoluminescence study of the annihilation process of donor-bound excitons in ZnO： observation of quantum mechanical interference

We report a photoluminescence observation of the coupling of donor-bound excitons and longitudinal optical phonons in high-quality ZnO crystals at 5 K. The first-order phonon Stockes line of donor-bound excitons exhibits a distinct asymmetric line shape with a clear dip at its higher energy side, suggesting that quantum mechanical interference occurs during the annihilation of donor-bound excitons. The donor binding energy is determined to be 49.3 meV from spectral featural.