3D-TOFSIMS characterization of black spots in polymer light emitting diodes

The occurrence and formation of black spots areas in PolyLED devices has been studied by time-of-flight SIMS (TOFSIMS). The composition, shape and position of the black spots is visualised by three-dimensional (3D)-TOFSIMS depth-profiling. It has been established that the formation of non-emissive spots is due to the growth of aluminium oxide clusters at the AlBa/polymer interface. Electron injection in the black spots is lost by the resulting local increase of the resistivity of the cathode.     

采用热处理方法提高MEH-PPV单层聚合物有机发光二极管发光性能的研究

对以MEH－PPV为发光层的单层聚合物有机发光二极管（OLED）器件在最佳条件下进行真空热处理，并用金相显微镜观察施加电压后器件的阴极表面形貌。发现处理后的器件阴极表面的气泡及黑斑明显减少。器件的发光性能显著提高。与未经处理的器件相比，最大相对发光强度提高了一个数量级、启亮电压降低了2．0V，半寿命提高了12．7倍。初步分析表明热处理方法提高器件发光性能的主要原因在于有效地减少了器件在工作过程中由于焦耳热产生的某些气体，从而减少阴极表面气泡及黑斑的出现，另一方面，热处理方法也增强了有机发光层与阴极接触界面的结合力，提高电子注入水平。     

改进型迈克耳孙干涉仪

采用分光梭镜代替迈克耳孙干涉仪中的分束镜和补偿板，不仅消除了杂散光斑，且简化了仪器的结构．     

面阵探测器的像点亚像素定位研究

面阵探测器可直接探测点目标图像的位置，但其定位精度受到探测器分辨率的限制。因此，亚像元精度技术得到了发展。它是利用目标像点的灰度分布特性，通过内插细分算法，确定出像点位置。可将定位精度提高1—2个数量级。本文介绍了几种实现目标像点亚像素定位的内插细分算法。对它们的计算公式、特点进行了分析，并进行了实验验证。     

Multiple polypeptide forms observed in two-dimensional gels of Methylococcus capsulatus (Bath) polypeptides are generated during the separation procedure

We have examined two-dimensional electrophoresis (2-DE) gel maps of polypeptides from the Gram-negative bacterium Methylococcus capsulatus (Bath) and found the same widespread trains of spots as often reported in 2-DE gels of polypeptides of other Gram-negative bacteria. Some of the trains of polypeptides, both from the outer membrane and soluble protein fraction, were shown to be generated during the separation procedure of 2-DE, and not by covalent post-translational modifications. The trains were found to be regenerated when rerunning individual polypeptide spots. The polypeptides analysed giving this type of trains were all found to be classified as stable polypeptides according to the instability index of Guruprasad et al. (Protein Eng. 1990, 4, 155-161). The phenomenon most likely reflects conformational equilibria of polypeptides arising from the experimental conditions used, and is a clear drawback of the standard 2-DE procedure, making the gel picture unnecessarily complex to analyse.     

One site fits both: A model for the ternary complex of folate + NADPH in R67 dihydrofolate reductase, a D2 symmetric enzyme

R67 dihydrofolate reductase (DHFR) is a novel enzyme that confers resistance to the antibiotic trimethoprim. The crystal structure of R67 DHFR displays a toroidal structure with a central active-site pore. This homotetrameric protein exhibits 222 symmetry, with only a few residues from each chain contributing to the active site, so related sites must be used to bind both substrate (dihydrofolate) and cofactor (NADPH) in the productive R67 DHFR?NADPH?dihydrofolate complex. Whereas the site of folate binding has been partially resolved crystallographically, an interesting question remains: how can the highly symmetrical active site also bind and orient NADPH for catalysis? To model this ternary complex, we employed DOCK and SLIDE, two methods for docking flexible ligands into proteins using quite different algorithms. The bound pteridine ring of folate (Fol I) from the crystal structure of R67 DHFR was used as the basis for docking the nicotinamide-ribose-P_i (NMN) moiety of NADPH. NMN was positioned by both DOCK and SLIDE on the opposite side of the pore from Fol I, where it interacts with Fol I at the pore's center. Numerous residues serve dual roles in binding. For example, Gln 67 from both the B and D subunits has several contacts with the pteridine ring, while the same residue from the A and C subunits has several contacts with the nicotinamide ring. The residues involved in dual roles are generally amphipathic, allowing them to make both hydrophobic and hydrophilic contacts with the ligands. The result is a `hot spot' binding surface allowing the same residues to co-optimize the binding of two ligands, and orient them for catalysis.     

Modified silver staining in 2DE improves protein detection even at extremely low sample concentration

The typical concentration of protein loaded varies from 0.13 to 1.40 μg/μL for a classical silver staining method in 2DE gel. Here, we present a simple modified classical silver staining method by modifying the silver impregnation and development reaction steps. This modified method detects the protein spots at extremely low loaded concentrations, ranging from 0.0048 to 0.0480 μg/μL. We recommend this modified silver staining as an excellent method for the limited biological samples used for silver‐stained 2DE analysis. Altogether, the protocol takes close to two days from first dimension separation to second dimension separation, followed by silver staining, scanning, and analysis.     

固定接触界面法向静弹性刚度

基于Hertz接触理论推导了两个微凸体之间互相作用的法向接触静弹性刚度.根据修正后的一个微接触点的平截面积尺寸分布,给出了界面的总法向接触静弹性条件刚度、总条件载荷的解析解.将法向静弹性刚度的解析解嵌入到有限元软件中,获得整机的理论模态.通过实验对解析解进行了定量验证.以机床结合部为研究对象,在理论振型与实验振型一致的...     

Quantification of Polycyclic Aromatic Hydrocarbons in Avian Dried Blood Spots by Ultra-performance Liquid Chromatography with Simple Liquid Extraction and Phospholipid Solid-phase Extraction Preparation

Here, a simple, reliable method for the quantification of the 16 EPA priority polycyclic aromatic hydrocarbons in dried blood spots is outlined using liquid extraction and phospholipid solid-phase sample cleanup coupled with analysis by ultra-performance liquid chromatography with ultraviolet–visible detection. Whole blood spotted on Whatman FTA cards was efficiently quantified by extraction into acidified methanol and passed through a phospholipid solid-phase extraction well plate before injection into a liquid chromatography under reverse-phase conditions. The analyte recoveries in quality control samples ranged from 63.4 to 104.1%, with relative standard deviations from 0.48 to 2.04%. These figures of merit are comparable with measurements in whole blood or serum using similar techniques. The method detection limits were from 45.0?ng·g^?1 for benzo[g,h,i]perylene to 118.7?ng·g^?1 for chrysene, with matrix spike recoveries from 64.3 to 99.4%, demonstrating acceptable sensitivity and low matrix interference. With a simple liquid extraction approach and short 16-min liquid chromatography, the dried blood spots were effectively and rapidly analyzed.     

Controlled preparation of aluminum borate powders for the development of defect-related phosphors for warm white LED lighting

The optimization of the elaboration conditions of a new family of highly emissive white phosphors based on glassy yttrium aluminum borates (g-YAB) compositions is presented. Their preparation from solutions is based on the polymeric precursor method (modified Pechini process), involving non-toxic and low cost precursors. The resulting resins were first dried at moderate temperatures followed by two-step annealing treatments of the obtain powders under controlled atmospheres: a first pyrolysis under nitrogen followed by a calcination under oxygen. This favored the gradual oxidation of organic moieties coming from starting materials, avoiding uncontrolled self-combustion reactions, which generate localized hot spots. This prevented phase segregations and the formation of pyrolytic carbon or carbonates, which are strongly detrimental to the luminescence properties. Thus, coupled chemical analyses and luminescence characterizations showed the high chemical homogeneity of the resulting powders and their intense emissions in the whole visible range. These emissions can be tuned from blue to warm white by adjusting the calcination temperature that is an important advantage for the development of LED devices. We showed that impurities of monovalent and divalent cations act as quenching emission centers for these phosphors. Therefore, by increasing the purity grade, we significantly enhanced the PL emissions leading to high internal quantum yields (80–90%). Finally, cathodoluminescence emissions showed the homogeneous dispersion of emitting centers in the g-YAB matrix.