太赫兹半导体探测器研究进展

太赫兹（THz）探测器是THz技术应用的关键器件之一．基于半导体的全固态THz量子阱探测器（THzQWIP）具有探测响应速度快、制作工艺成熟、体积小和易集成等优点．文章简要介绍了THz探测器的分类和特点，重点介绍了THzQWIP的工作原理和研究进展．     

Near-Field and Polarized Evanescent Field Excited Fluorescence of Self-Organized Particle Arrays of Organic Dye

A wetting/dewetting process was utilized to prepare self-organized organic dye particles of micrometer and submicrometer size. Near-field scanning optical microscopy successfully identified near-field excited near-field fluorescence from single particles. The majority of the small particles with diameters around 2 mm or less, however, did not show fluorescence under near-field observation. In contrast, far-field fluorescence, when excited by a polarized evanescent field, was observed, with the intensity depending on the excitation polarization, indicating that molecules' transition moment within dye particles was oriented parallel to the substrate surface. Single particle fluorescence spectrum consistently showed an identical sharp peak with a large redshift, indicating that the particles were composed of identical dye aggregates similar to J-aggregates. These observations suggest that the near-field at the probe tip was polarized parallel to the probe axis. Another observation, that molecules were oriented in a similar direction among adjacent particles, suggests that the dewetting process contributed to the alignment of the molecular direction among adjacent particles, which further proves that the present specimen was formed by a self-organizing mechanism.     

Investigation of the Doughnut Effect in Cy3-Labeled Protein Microarrays using Scanning Near-Field Optical Microscope

We demonstrate the fluorescence mapping of protein microarrays by the technique of scanning near-field optical microscopy (SNOM) and confocal microscopy. Micron sized spots (300 μm) of human Immunoglobulin G (hIgG) protein with and without a Cy3 dye labeling have been fabricated on glass substrates by an immobilization method which makes use of calixcrown derivatives termed Prolinker. We have also tried to probe into the well-known “doughnut effect” observed in fluorescence images of proteins using the SNOM technique. The topographic and fluorescence SNOM images revealed that the number of proteins at the boundary of the spot were more than at the center in the case of the microarray spot which showed brighter luminescence at the edge than at the center in the confocal image.     

Study of the spectrum of CH335C1 between 4250 and 4600 CM?1: thev2+v4 andv4+v5 rovibrational bands

About 2500 lines of CH₃ ³⁵Cl have been assigned. The strong xy Coriolis resonance between thev ₂ andv ₅ modes is quite visible between thev ₄+v ₄ ^±1 perpendicular band, centered around 4383 cm^–1, and thev ₄ ^±1 +v ₅ ^±1 perpendicular component, centered around 4475 cm^–1, with a crossing of upper energy levels allowing the observation of lines which are normally forbidden. Although not yet observed with certainty, because of the great density of lines of the spectrum, thev ₄ ¹ +v ₅ ^±1 parallel component is nevertheless detectable by its effects onv ₂+v ₄ ^±1 which is linked by Coriolis resonance to both components ofv ₄+v ₅. Moreover the spectrum is much complicated by many other resonances with weak bands which occur at level crossings: it is the case ofv ₂+3v ₆ ^±1 , connected tov ₂+v ₄ ^±1 by the well known Darling Dennison resonance which couplesv ₄ ^±1 and 3v ₆ ^±1 , and also ofv ₅ ^±1 +3v ₆ ^±1 connected tov ₄ ^±1 +v ₅ ^±1 by the same resonance; but this last case is complicated by an anharmonic resonance betweenv ₅ ^±1 +3v ₆ ^±1 and 2v ₃+3v ₆ ¹ . Two more perturbations occur on the K=–1 side ofv ₂+v ₄: a weak Coriolis resonance gives rise to one subband ofv ₁+v ₂ at a level crossing withv ₂+v ₄, and thev ₁+v ₅ band (linked of course tov ₁+v ₂ by the Coriolis resonance between thev ₂ andv ₅ modes) is quite visible and perturbs several subbands ofv ₂+v ₄ of high values of K through an anharmonic resonance. Moreover, the complex (3v ₅ ^±1 ,v+2v ₅ ⁰ , 2v ₂+v ₅ ^±1 , 3v ₂,v ₂+2v ₅ ^±2 , 3v ₅ ^±3 ) system of Coriolis-connected bands is linked to the bands studied in the present work by two Fermi resonances: one betweenv ₂+2v ₅ ⁰ andv ₁+v ₂, and the other one betweenv ₁+v ₅ and 3v ₅ ^±1 , whose several subbands have been observed on the low part of the spectrum. The values of all the band centres and of the different coupling constants have been estimated, but all these interactions make the line assignments and the interpretation of the spectrum very difficult.     

聚乙烯单晶的退火效应

用混合晶红外光谱法和ＳＡＸＳ、ＤＳＣ和ＬＡＭ等方法研究了聚乙烯单晶在７５℃、９０℃和１０５℃退火前后的结构变化，发现在９０℃以下和１０５℃以上退火，遵循不同的退火机制     

付里叶变换红外光谱仪的操作参数对光谱的影响

本文以二苯基甲酮的ＫＢｒ压片为标样，在Ｂｒｕｋｅｒ ＩＦＳ １２０ＨＲ付里叶变换红外光谱仪上系统考察了该仪器折一些重要操作参数（光源光栏、切趾函数、扫描速度）对光谱质量（信噪比，分辨率）的影响。从而获得了测样时的优化操作条件。     

近临界水中苯丁烯酮合成新方法

试探了一种以水为反应介质合成本丁烯酮的新方法。在近临界水中，以苯甲醛 和丙酮为原料，在不外加任何催化剂、反应温度为260℃、反应时间为6h的条件下 ，苯丁烯酮的产率可达46．2％。该新方法避免了盐类副产物的产生，省去了常规 方法中反庆后繁琐的中和分离步骤。     

FTS-20E富里叶红外光谱仪数据系统改造

报道了ＦＴＳ－２０Ｆ富里叶红外光谱仪数据系统改造的工作采用ＩＢＭ４８６计算机及新的数据接口取代了陈旧的ＮＯＶＡ４数据系统，文章详细描述了其硬件设计和软件编辑，改造不仅更新了ＦＴＳ－２０Ｅ里叶红外光谱仪，而且还使其达到９０年代的水平。     

氯雷他定的结构分析

氯雷他定是一种高效抗过敏药。采用质谱、红外光谱、核磁共振氢谱、碳谱以及^1H检测的异核多量子相干相关谱等技术，对氯雷他定的分子结构进行了谱图解析。     

Thermal Stability Of Folic Acid in the solid-state

This study attempts to identify the degradative process which folic acid undergoes in the solid-state under thermal stress. In order to facilitate the process, the various pieces of the chemical structure, namely, p-amino benzoic acid, pterin and glutamic acid as both its d- and l-isomers were investigated as separate entities. These structured solid-state pieces were then compared to the composite solid state folic acid degradative curves in order to identify the peaks seen and provide direction for the interpolation of the degradative mechanism. It was observed that none of the structural pieces could be superimposed as assumed earlier and hence an attempt was made to identify the decomposition products using various analytical techniques such as infrared spectroscopy, mass spectroscopy and X-ray diffraction which suggested that the glutamic acid fragment is lost first as evidenced by acid loss and amide enhancement in the IR spectra. The vitamin was ultimately degrading to carbon fragments and that further identification was not necessary. This revised version was published online in August 2006 with corrections to the Cover Date.