全固态多波长飞秒脉冲激光系统

利用棱镜对引进频谱空间啁啾来补偿飞秒脉冲激光二次谐波产生中的相位失配,提高了倍频效率建立了一套全固态、多波长(1065nm, 532nm,823.1nm, 402nm)飞秒脉冲激光系统自制的Nd:YVO4激光器输出532nm绿光激光,最高平均功率可达5.6W当用2.5W绿光激光泵浦时,从自制的钛宝石激光器及经BBO倍频可分别输出中心波长为823.1nm和402nm,平均功率300mW和73mW,谱宽32.3nm和5.1nm,脉宽22fs和33.3fs、重复率108MHz的近红外和蓝光激光整个系统具有结构紧凑、倍频效率高、运行稳定的特点.     

SBN:Cr晶体的光折变四波混频相位共轭特性实验研究

从实验上研究了同成分SBN:Cr晶体在He-Ne激光照射下的四波混频相位共轭特性.首先测量了在不同泵浦光与信号光光强比m及不同光束夹角2θ的情况下,晶体的四波混频相位共轭反射率R随泵浦光强比p的变化关系.其次测量了泵浦光束与信号光束耦合方向对SBN:Cr晶体的四波混频相位共轭特性的影响,并就两种不同掺杂浓度的晶体样品进行了对比,所得实验结果与理论分析基本一致.最后,利用SBN:Cr晶体四波混频相位共轭特性进行了图象畸变消除实验.     

二次谐波中大相位失谐下入射啁啾脉冲对相位的影响

讨论了在大相位失谐下,基波为频率啁啾脉冲的二次谐波产生过程,结果表明选取合适的啁啾参量可以使二次谐波的光强提高,但同时会使其波形和相位发生变化.三波相位的畸变主要取决于入射的基波啁啾脉冲,而与相位匹配的失谐量关系不大.     

Squeezing and Quantum Canonical Transformations

In this paper we present an approach to quantum mechanical canonical transformations. Our main result is that time-dependent quantum canonical transformations can always be cast in the form of squeezing operators. We revise the main properties of these operators in regard to its Lie group properties, how two of them can be combined to yield another operator of the same class and how can also be decomposed and fragmented. In the second part of the paper we show how this procedure works extremely well for the time-dependent quantum harmonic oscillator. The issue of the systematic construction of quantum canonical transformations is also discussed along the lines of Dirac, Wigner, and Schwinger ideas and to the more recent work by Lee. The main conclusion is that the classical phase space transformation can be maintained in the operator formalism but the construction of the quantum canonical transformation is not clearly related to the classical generating function of a classical canonical transformation. We hereby propose the much more efficient method given by the squeezing operators. This method has also been proved to be very useful, by one of the authors, in the framework of the dynamical symmetries (Cerveró, J. M. (1999). International Journal of Theoretical Physics 38, 2095–2109).     

三羟甲基甲胺、季戊四醇及其二元体系固-固相变的变温红外光谱研究

利用傅里叶变温红外光谱仪分别测定了三羟甲基甲胺（TAM）、季戊四醇（PE）及其二元体系变温红外谱。实验表明，多元醇分子中羟基吸收峰随温度升高耐发生位移向高波数移动，此结果既能反映多元醇及其二体系固－固相变的温度区间，又与转变热相对应，从而揭示了多元醇及其二元体系固－固相变贮热的机理。     

稀土配合物中重叠峰分离的相分辨光声光谱研究

首次利用相分辨光声光谱法对稀土配合物中不同吸收中心的重叠谱峰进行了分离。在Nd(Trp) 3 Cl3 ·H2 O固态配合物中 (Trp :色氨酸 ) ,30 0～ 4 0 0nm这一波段内由于色氨酸配体强的π π 跃迁吸收 ,Nd3 +的光声峰被掩盖。通过光声谱同相和交相信号可以计算配体光声吸收的位相为 10 6° ,位相改变 90°后就得到仅与Nd3 +相关的光声光谱。相分辨光声光谱法用于谱峰分离时有它独特的优点 ,它不受谱峰形状和重叠程度的限制 ,而仅与不同吸收峰对应的光声位相有关     

Design of an insensitive-polarization all-optical switch based on multimode interference structures

This paper presents a new design for an insensitive-polarization all-optical switch using 2 × 2 multimode interference (MMI) couplers. The switching structure can operate at central operating wavelength 1550 nm for both polarizations. A nonlinear directional coupler is used to realize the phase shifter and therefore switching mechanism is obtained. The transfer matrix method and beam propagation method are used to design and optimize the whole device structure.     

Determination of Paint Solvents by Vapour Phase Fourier Transform Infrared Spectrometry.

A fast procedure has been developed for the direct determination of paint solvents. The method is based on the injection of small volumes of untreated solvent mixtures into a heated Pyrex glass reactor in which the sample is volatilized and introduced by means of a flow of nitrogen into an IR multiple pass gas cell and the spectrum in the mid-IR region is registered as a function of time. Data found for samples are interpolated in calibration graphs obtained by injecting different volumes of pure compounds which constitute the solvent mixture. A methylisobutylketone (MIBK) toluene mixture was used as test system to develop the proposed procedure. The method provides a limit of detection of the order of 1–4 μg, a relative standard deviation of the order of 0.4 to 2% for five independent measurements, and recovery percentage values from 99.8 till 103.6 %. A commercial sample of polyurethane paint solvent has been analysed by the developed procedure.     

Structural Phase Transition and the Dielectric Permittivity of the Model Lipid Bilayer [(CH2)12(NH3)2]CuCl4

Structural phase transitions in the lipid-like bilayer material [(CH₂)₁₂(NH₃)₂]CuCl₄ have been observed using differential thermal scanning. The compound shows an irreversible thermochromic transition at ? 465 K and three reversible transitions at T ₁ = 433 ± 4 K and T ₂ = 411 ± 2 K and T ₃ = 358 K. The transition at 350 K is ascribed to chain melting. The other two correspond to crystalline phase transformation.

Phase (IV) T₃ = 358 ± 2K Phase (III) T₂ = 411 ± 2K Phase (II) T₁ = 433 ± 4K Phase (I)

Dielectric permittivity is studied as a function of temperature in the range 300-440 K and frequency, range (60 Hz-100 kHz). It confirms the observed transitions. The dielectric permittivity reflects rotational and conformational transitions for the compound. The variation of the real part of the conductivity with temperature is thermally activated in the temperature range above 350 K, with frequency-dependent activation energy, the values of activation energy lie in the range of ionic hopping. The dependence of the conductivity on frequency follows the universal power law σ = σ₀ + A(T) ω ^{s ( T )} with 0<s<1. Comparison of this material with other members of the series is discussed