大非线性相移下光学非线性Z扫描特性的研究

采用高斯分解法(GD)对大非线性相移下的Z扫描特性进行了分析，通过对数值算法的优化，将GD推广到对脉冲入射激光下大非线性相移下的Z扫描理论分析.对不同条件下大非线性相移Z扫描曲线峰谷结构的比较，发现在大非线性相移的情况下，Z扫描曲线的峰和谷随透过光阑或入射光强变化表现出某些新的特性.随着透过光阑孔径的增加，Z扫描曲线峰的变化要明显快于谷的变化，而且在谷明显存在的情况下，峰很快消失.采用皮秒脉冲激光下的纯二硫化碳实验对理论结果加以验证，实验结果和理论分析相一致.我们的分析结果对大非线性相移下Z扫描测量有一定的指导性意义，避免在大非线性相移下对Z扫描结果产生错误的分析. 关键词： 大非线性相移 高斯分解法 Z扫描     

Synthesis and characterization of poly(arylene ether)s containing 6‐(4‐hydroxyphenyl)pyridazin‐3(2H)‐one or 6‐(4‐hydroxyphenyl)pyridazine moieties

A series of novel soluble pyridazinone‐ or pyridazine‐containing poly(arylene ether)s were prepared by a polycondensation reaction. The pyridazinone monomer, 6‐(4‐hydroxyphenyl)pyridazin‐3(2H)‐one ( 1 ), was synthesized from the corresponding acetophenone and glyoxylic acid in a simple one‐pot reaction. The pyridazinone monomer was successfully copolymerized with bisphenol A (BPA) or 1,2‐dihydro‐4‐(4‐hydroxyphenyl)phthalazin‐1(2H)‐one (DHPZ) and bis(4‐fluorophenyl)sulfone to form high‐molecular‐weight polymers. The copolymers had inherent viscosities of 0.5–0.9 dL/g. The glass‐transition temperatures (T_g's) of the copolymers synthesized with BPA increased with increasing content of the pyridazinone monomer. The T_g's of the copolymers synthesized from DHPZ with different pyridazinone contents were similar to those of the two homopolymers. The homopolymers showed T_g's from 202 to 291 °C by differential scanning calorimetry. The 5% weight loss temperatures in nitrogen measured by thermogravimetric analysis were in the range of 411–500 °C. 4‐(6‐Chloropyridazin‐3‐yl)phenol ( 2 ) was synthesized from 1 via a simple one‐pot reaction. 2 was copolymerized with 4,4′‐isopropylidenediphenol and bis(4‐fluorophenyl)sulfone to form high‐T_g polymers. The copolymers with less than 80 mol % pyridazinone or chloropyridazine monomers were soluble in chlorinated solvents such as chloroform. The copolymers with higher pyridazinone contents and homopolymers were not soluble in chlorinated solvents but were still soluble in dipolar aprotic solvents such as N‐methylpyrrolidinone. The soluble polymers could be cast into flexible films from solution. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3328–3335, 2006     

LB膜中螺吡喃材料的光学性质研究

利用ＬＢ技术制备螺吡喃有序分子膜，研究了气液界面上螺吡喃材料在不同成份和不同ｐＨ值亚相时的成膜行为，着重研究了螺吡喃在ＬＢ膜这个特殊介质环境中不同于溶液的光致变色机理和光学性质     

双参数变形玻色湮没算符高次幂的本征态及其量子统计性质

本文构造了双参数变形玻色湮没算符高次幂a^'k(k≥3)的k个正交归一木征态的数学结构,发现它们能构成一个完备的Hilbert空间,并且讨论了它们的量子统计性质.     

Bi-1212相和Bi-1222相铜氧化合物的合成和超导电性

对名义组份为(Bi_(1-x),M_x)Sr_2YCu_2O_y(x=0.6—0.7)的样品,当M=Cd,Ni和Zn时合成了Bi-1212相材料,实验发现Cd占据Bi位,可以稳定单BiO层,高压氧下退火,在32K出现超导转变,而Zn和Ni进入CuO平面,占据Cu位,破坏了材料的超导电性。用Cd稳定单BiO层还能够合成Bi-1222相化合物,它的固溶范围比Bi-1212大,对这一现像进行了结构上的分析。在不同氧压退火处理下的Bi-1222相样品,电阻随氧压增大而变小,但在4.2K以上未观察到超导转变。 关键词：