聚丁二炔Langmuir—BLodgett薄膜的光声谱研究（Ⅱ）光谱综合分析和荧 …

本文用光声谱结合光吸收谱,荧光光谱等对在工业上在潜在应用前景的聚十炔（ｐｏｌｙｄｉａｃｅｔｙｌｅｎｅ,ＰＤＡ）Ｌａｎｇｍｕｉｒ－Ｂｌｏｄｇｅｔｔ（ＬＢ）薄膜进行了研究。     

含氟光敏单体液晶光控取向膜的光谱研究

制备了含氟光敏单体材料六氟戊二醇双肉桂酸酯,实验发现该材料在线性偏振紫外光辐照下可发生定向光交联反应.通过紫外可见光谱与红外光谱分析,表明光交联类型为[2 2]环加成反应.用原子力显微镜对单体光聚后形成的聚合物取向膜表面进行扫描,未观察到明显的各向异性分布现象.实验测得取向膜诱导液晶分子平行排列,取向效果均一,薄膜预倾角为1°～2°.     

用光强衰减方法测量交联型聚氨基甲酸酯的交联温度

提出了用导波光学方法测量交联型聚合物材料的交联温度。即在对聚合物薄膜处理时,利用光波导的衰减全反射光谱中导模峰对聚合物材料的折射率敏感的特性,来测量聚合物材料参量。研究了交联型聚氨基甲酸酯材料在升温过程中薄膜折射率的变化。实验结果发现,温度相关的折射率dn/dT会发生不连续变化。整个dn/dT曲线有两个交叉点,这两个交叉点之间的温度范围就是聚合物材料的交联温度范围。第一个和第二个交叉点的温度分别被称之为材料的开始交联温度和完全交联温度。测得的交联型聚氨基甲酸酯材料的交联温度即最佳极化温度范围为85～122℃。通过对不同极化条件(是指开始极化的温度在测得的交联温度范围中变化)下聚氨基甲酸酯材料电光系数的测量验证了交联温度测量结果的准确性。     

有机混合薄膜中的Foerster能量转移

通过掺杂不同的染料有机电致发光器件可以得到不同颜色的光发射。掺杂小分子有机材料苝酸四甲酯perylene-3，4，9，10-tetracarboxvlicacid(TMEP)到蓝色发光聚合物poly(N—vinyl—carbazole)聚乙烯基咔唑(PVK)，得到了很好的绿光发射。TEMP掺杂质量分数为0．01时，295．5nm激发波长的荧光光谱可以明显观察到在420nm处PVK和530nm处TEMP的发射峰值；当TMEP掺杂质量分数达到0．05～0．10之间，器件的电致发光光谱和荧光光谱发射峰几乎完全被TEMP的绿光所占据。光谱的转移归因于从聚合物PVK到小分子有机材料TMEP的Foerster能量转移。荧光光谱中随着TMEP掺杂浓度的的增大发射峰值有明显的红移，这种现象被归因于在TMEP高浓度掺杂情况下激基缔合物的形成。激基缔合物的形成从TMEP在薄膜状态下与溶液状态下的荧光光谱的比较中得到证实。     

新型极化聚合物薄膜电光调制器研究

用对硝基偶氮苯类为侧链的键合型聚合物，采用高温电晕极化的方法制作电光薄膜，设计并构造极化聚合物薄膜电光调制器。当通光方向和极化方向平行并且垂直于极化聚合物薄膜的表面时，利用法布里-帕罗（F-P）腔中多光束干涉，可以把通过的光由位相调制转化为强度调制，有利于电光调制器的小型化和高速封装。用这种聚合物薄膜电光调制器测量了锢锡氧化物共面波导上的电信号，并对系统的工作原理进行了分析。实验结果表明，薄膜调制器具有线性电光效应；当F-P腔的精细因子为20（为1.3μm的光），调制电场为1V/μm时，研制的极化聚合物电光调制器的调制深度可达到0.01%。     

新型萘酰亚胺类硫氰酸根离子荧光探针的合成及应用

设计合成了一个萘酰亚胺类SCN^-离子探针NNN,其合成方法简单,条件温和。能够在水溶液中专一识别SCN^-离子,检测浓度最小可以达到20 μmol/L,随着SCN^-离子的加入,化合物NNN吸收光谱蓝移了60 nm,从黄色变为无色,这种明显的颜色变化,有利于可视观察。通过双波长比例变化,可以实现SCN^-离子20 μmol/L~0.8 mmol/L范围内的定量检测。SCN^-离子能够猝灭化合物NNN的荧光,荧光强度前后变化明显,荧光量子产率由原来的0.33减弱到0.02。通过荧光光谱和吸收光谱两种手段实现对SCN^-的检测,选择性好,灵敏度较高。     

导电聚合物P3MT的光调制反射谱

本文报道了导电聚合物光调制反射光谱的研究工作。实验观察到聚三甲基噻吩的带间跃迁和与双极化子态有关的跃迁,并且观察了谱结构随掺杂浓度、温度以及调制光强度的变化。实验结果证明,光子能量大于禁带宽度E_g的光可在聚合物分子链中诱导产生双极化子。虽然双极化子可以由光诱导产生,也可以由杂质诱导产生,但它本身是不依赖于诱导方式的聚合物分子链的本征元激发态。荷电的双极化子可受离化杂质的库仑吸引,产生钉扎效应,并使禁闭参数变大。 关键词：     

快重离子辐照聚酰亚胺潜径迹的电子能损效应

快重离子辐照聚合物材料时，由于密集电离激发在其路径上产生几纳米直径的潜径迹，径迹形貌受离子种类、离子能量等多种因素的影响.为了研究电子能损对径迹形成所起的作用，利用1.158GeV 的Fe⁵⁶离子和 1.755GeV Xe¹³⁶离子在室温真空环境下辐照叠层聚酰亚胺(PI)薄膜，结合傅里叶转换红外光谱(FTIR)分析技术对辐照引起的化学变化进行了测量.聚酰亚胺官能团的降解及炔基的生成是离子辐照聚合物的主要特征，在注量1×10¹¹到6×10¹²/cm²范围及较宽的电子能损(dE/dX)_e范围 (Fe⁵⁶ 离子：2.2 到 5.2 keV/nm， Xe¹³⁶ 离子：8.6 到 11.3 keV/nm)对官能团的断键率及炔基生成率进行了研究. 红外结果显示在实验涉及的能损范围都有炔基生成，应用径迹饱和模型对实验结果进行拟合，不同能损下的平均损伤径迹半径及炔基生成径迹半径被得到，通过热峰模型对实验结果拟合，给出了离子在聚酰亚胺中产生潜径迹的能损阈值，实验给出的径迹形貌的电子能损效应曲线与热峰模型预言走势基本一致. 关键词： 离子辐照 潜径迹 红外光谱 热峰模型     

有机混合薄膜中的Frster能量转移

通过掺杂不同的染料有机电致发光器件可以得到不同颜色的光发射。掺杂小分子有机材料苝酸四甲酯perylene- 3,4,9,10 -tetracarboxylicacid(TMEP)到蓝色发光聚合物poly(N -vinyl carbazole)聚乙烯基咔唑(PVK),得到了很好的绿光发射。TEMP掺杂质量分数为0.01时,295. 5nm激发波长的荧光光谱可以明显观察到在420 nm处PVK和530 nm处TEMP的发射峰值;当TMEP掺杂质量分数达到0.050.10之间,器件的电致发光光谱和荧光光谱发射峰几乎完全被TEMP的绿光所占据。光谱的转移归因于从聚合物PVK到小分子有机材料TMEP的F -rster能量转移。荧光光谱中随着TMEP掺杂浓度的的增大发射峰值有明显的红移,这种现象被归因于在TMEP高浓度掺杂情况下激基缔合物的形成。激基缔合物的形成从TMEP在薄膜状态下与溶液状态下的荧光光谱的比较中得到证实。     

有机混合薄膜中的F(o)rster能量转移

通过掺杂不同的染料有机电致发光器件可以得到不同颜色的光发射。掺杂小分子有机材料?p酸四甲酯perylene-3,4,9,10-tetracarboxylicacid(TMEP)到蓝色发光聚合物poly(N-vinyl-carbazole)聚乙烯基咔唑(PVK),得到了很好的绿光发射。TEMP掺杂质量分数为0.01时,295. 5nm激发波长的荧光光谱可以明显观察到在420 nm处PVK和530 nm处TEMP的发射峰值;当TMEP掺杂质量分数达到0.05～0.10之间,器件的电致发光光谱和荧光光谱发射峰几乎完全被TEMP的绿光所占据。光谱的转移归因于从聚合物PVK到小分子有机材料TMEP的Forster能量转移。荧光光谱中随着TMEP掺杂浓度的的增大发射峰值有明显的红移,这种现象被归因于在TMEP高浓度掺杂情况下激基缔合物的形成。激基缔合物的形成从TMEP在薄膜状态下与溶液状态下的荧光光谱的比较中得到证实。     

Effect of metal salts in the optical properties of polydiacetylenes

Films of polydiacetylene (PDA)-containing polyesters with metal salts of Zn, Eu and Gd were prepared. Ultraviolet-visible (UV-VIS) absorption and photoluminescent (PL) spectra indicated that the presence of the metal salts induced a small shift of their maxima to higher and lower energies, respectively. PDAs films with an ester group in allylic position to the conjugated system presented two emission bands. The higher energy emission band was assigned to carbonyl emission and the lower energy emission band to self-trapped excitons (STE). Indeed, the inclusion of metal salts incremented the intensity relation between the higher and lower emission energy bands. On the other hand, Raman spectroscopy measurements performed in PDAs films derived of pentyn-1-ol indicated that the metal salts induced a slight statistical shift in the triple and double bond signals to higher energies. In this way, the intensity variations and band shifts detected by Raman, UV-VIS and PL spectroscopies showed that the presence of metal salts could have a remarkable influence on the energy levels of these PDAs. Nonlinear optical (NLO) third harmonic generation (THG) measurements were performed in order to verify this affirmation as well as the cubic NLO performance of these materials.     

Structural Properties of Thin Films Obtained by Magnetron Sputtering of Polydiacetylene

Physics of the Solid State - Films obtained by radio-frequency sputtering of monocrystalline polydiacetylene (PDA) are under study. The structure is studied by Raman spectroscopy, transmission...     

Surface modification of cobalt-chromium-tungsten-nickel alloy using octadecyltrichlorosilanes

Cobalt-chromium (Co-Cr) alloys have been extensively used for medical implants because of their excellent mechanical properties, corrosion resistance, and biocompatibility. This first time study reports the formation and stability of self-assembled monolayers (SAMs) on a Co-Cr-W-Ni alloy. SAMs of octadecyltrichlorosilanes (OTS) were coated on sputtered Co-Cr-W-Ni alloy thin film and bulk Co-Cr-W-Ni alloy. OTS SAM coated alloy specimens were characterized using contact angle goniometry, Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM). Contact angle analysis and FTIR suggested that ordered monolayers were coated on both sputtered and bulk alloy. XPS suggested the selective dissolution of cobalt from the alloy during the formation of OTS SAM. The bonding between the alloy and the OTS SAM was mainly attributed to Si-O-Cr and Si-O-W covalent bonds and a smaller contribution from Si-O-Co bonds. AFM images showed the distribution of islands of monolayers coated on the alloy. The height of monolayers in majority of the islands was closer to the theoretical length of fully extended OTS molecules oriented perpendicular to the surface. The stability of OTS SAM was investigated in tris-buffered saline at 37 °C for up to 7 days. Contact angle, FTIR, and XPS collectively confirmed that the monolayers remain ordered and bound to the alloy surface under this condition. This study shows that Co-Cr alloys can be surface modified using SAMs for potential biomedical applications.     

聚丁二炔Langmuir—Blodgett薄膜的光声谱研究：（Ⅰ）结构表征与光声？…

本在用Ｘ－射线小角衍射聚合与转载先后次序不同的ＰＤＡ ＬＢ膜进行结构表征的基础上,不同厚度的ＰＤＡ ＬＢ膜的光声新斩波频率效应说明,随着ＰＤＡ ＬＢ膜厚度增加,ＬＢ膜的热学性质逐渐明显。此外,还探讨了如何从ＰＤＡ ＬＢ膜的光声谱求得光声吸收系数问题,本的研究结果表明,光声谱技术是研究ＬＢ膜热学特性的有效手段。     

聚丁二炔Langmuir-Blodgett薄膜的光声谱研究(Ⅰ)结构表征与光声吸收系数

本文在用Ｘ－射线小角衍射对聚合与转载先后次序不同的ＰＤＡＬＢ膜进行结构表征的基础上,不同厚度ＰＤＡＬＢ膜的光声斩波频率效应说明,随着ＰＤＡＬＢ膜厚度增加,ＬＢ膜的热学性质逐渐明显。此外,还探讨了如何从ＰＤＡＬＢ膜的光声谱求得光声吸收系数问题,本文的研究结果表明,光声谱技术是研究ＬＢ膜热学特性的有效手段。     

The role of surface oxidation on luminescence degradation of porous silicon

This study reports a comparative analysis on time dependent degradation of photoluminescence (PL) spectra of porous silicon (PS) during dark-aging (DA) and photo-aging (PA). Fourier Transform Infrared (FTIR) spectroscopy studies have been performed to get an insight on possible chemical changes in the PS surface. It has been found that SiH_x bonds decrease progressively while SiO_x bonds increase. FTIR and PL measurements revealed presence of blue shifts in the PL spectra during the aging stages (PA and DA). While the PL intensity of dark aged PS shows a decrease during the first 3 weeks and an increase afterwards, the PL intensity decreases continuously for photo-aged PS. The change in the PL spectra has been investigated by overlapping of two different PL bands which are reflective of oxidation of PS surface and size of Si naonocrystallites. A possible bond configuration model about the oxidation of PS surface has also been proposed. The results are interpreted in terms of quantum size effects in PS and the influence of the surface composition.     

聚丁二炔Langmuir-Blodgett薄膜的光声谱研究(Ⅱ) 光谱综合分析和荧光量子效率

本文用光声谱（ｐｈｏｔｏａｃｏｕｓｔｉｃｓｐｅｃｔｒｏｓｃｏｐｙ,ＰＡＳ）结合光吸收谱、荧光光谱等对在工业上有潜在应用前景的聚丁二炔（ｐｏｌｙｄｉａｃｅｔｙｌｅｎｅ,ＰＤＡ）Ｌａｎｇｍｕｉｒ－Ｂｌｏｄｇｅｔ（ＬＢ）薄膜进行了研究。对经不同气体环境处理的ＰＤＡＬＢ膜的紫外－可见光声谱、光吸收谱和荧光光谱的综合分析表明,ＰＤＡＬＢ膜的激发态弛豫过程中激子和极化子形成的元激发性质。此外,还讨论了ＰＤＡＬＢ膜的荧光量子效率。本文的研究结果表明,用光声谱研究ＬＢ膜,可以获取仅用其他光谱得不到的信息。     

The Electronic Structure and Spectra of Triphenylamines Functionalized by Phenylethynyl Groups

We study the features of the electronic structure and the IR, UV, and visible spectra of a series of triphenylamines substituted with phenylethynyl groups. The analysis is performed at the level of the density functional theory (DFT) and its nonstationary version in comparison with the experimental data of IR and electron spectroscopy. It is shown that, in the excited state, there is a change in the alternation of single, double, and triple bonds in accordance with the character of bonding and antibonding in the lowest vacant molecular orbital. The gradual introduction of additional phenylethynyl groups does not cause frequency shifts in the IR spectra of the molecules under study, but significantly affects the intensity of the corresponding IR bands. A similar effect is also observed in the electronic-absorption spectra of these compounds. This can be used for optical tuning of triphenylamines as promising materials for organic light-emitting diodes and solar cells.     

Mechanistic comparison of pulse laser induced phase separation of particulates from cellulose paper at 213 nm and 532 nm

The laser-induced phase separation of charcoal particles on additive-free cotton linters cellulose paper was investigated by electron and optical microscopy, colorimetry, and diffuse reflectance FT-IR. The fibre bundles were vaporised in depth of several 10 μm above destruction fluence thresholds using visible 532 nm radiation. This is in contrast to mid-ultraviolet 213 nm radiation, where only the top fibre bundles were modified and partially evaporated. The colorimetric lightness results generally represented the cleaning status, whereas the colorimetric yellowing data represented irreversible chemical and/or photochemical changes. Charcoal-contaminated paper treated with visible and mid-ultraviolet radiation exhibited yellowing, whereas uncontaminated did not. This suggests that the electron-rich plasma generated by the evaporation of the particles heats the adjacent substrate and also excludes oxygen. Mid-ultraviolet, in contrast to visible radiation, shows particle removal always accompanied by paper destruction. IR spectroscopy results suggest cross-linking by ether bonds near the destruction threshold, but do not prove the formation of oxidation products and double bonds as the basis of the yellowing. A “cleaning window” between the cleaning threshold (0.1 J/cm²) and the paper destruction threshold (2.9 J/cm²) with a pulse number of 2 is provided by visible 532 nm laser treatment.