用于高速摄影变象管的软X射线光电阴极

光阴极由衬底(包括介质阴极的导电基底)和光电发射膜构成。采用了聚丙烯、Formvar和Paylene三种有机薄膜作阴极衬底。建立了这些薄膜的制备技术。用一台自制的软X射线单色仪在277—7469ev光子能量范围内测量了这些薄膜的透过率。 研究了CsI、CsBr、Au和MgF₂四种光电阴极的光电发射特性和光电发射与阴极厚度的关系,找出了最佳阴极厚度。用软X射线单色仪在277—7469ev光子能量范围内测量了最佳厚度阴极的绝对量子效率,四种阴极最大值分别为4.50、2.90、0.25和0.12。我们还在同一阴极衬底上分区制备了四种阴极,在变象管荧光屏上比较其亮度,结果和测量的一致。 用LAB5型表面分析仪对CsI和Au阴极的光电子初能量分布作了测量,CsI阴极光电子初能量分布半高宽远小于Au。因此CsI是适用于高速摄影变象管比较理想的软X射线光电阴极。     

Efficient immobilization of silver nanoparticles on metal substrates through various thiol molecules to utilize a gap mode in surface enhanced Raman scattering

To utilize a gap mode in surface enhanced Raman scattering, we elucidated the interaction between adsorbed species and Ag nanoparticles (AgNPs). Various thiol molecules such as normal alkanethiols, thiols with a phenyl, cyclohexane or naphthalene ring on Ag films immobilized AgNPs through van der Waals force, and electrostatic interaction. Immobilized AgNPs provided enormous Raman enhancement by a factor of 10⁷–10¹⁰ for thiol molecules at a nanogap, in consistent with that anticipated by finite difference time domain calculations. Only alkanethiols with a tert-methyl group and those with a carboxylic group did not immobilize any AgNPs probably owing to steric hindrance. A gap mode is relevant for a variety of metals even with large damping like Pt and Fe, indicating a crucial role of electric multipoles in AgNPs generated by a localized surface plasmon and induced mirror images in metal substrates for markedly enhanced electric field at a nanogap.     

Wet-chemical treatment and electronic interface properties of silicon solar cell substrates

On textured n-type silicon substrates for solar cell manufacturing, the relation between light trapping behavior, structural imperfections, energetic distribution of interface state densities and interface recombination losses were investigated by applying surface sensitive techniques. The field-modulated surface photovoltage (SPV), in-situ photoluminescence (PL) measurements, total hemispherical UV-NIR-reflectance measurements and electron microscopy (SEM) were employed to yield detailed information on the influence of wet-chemical treatments on preparation induced micro-roughness and electronic properties of polished and textured silicon substrates. It was shown that isotropic as well as anisotropic etching of light trapping structures result in high surface micro-roughness and density of interface states. Removing damaged surface layers in the nm range by wet-chemical treatments, the density of these states and the related interface recombination loss can be reduced. In-situ PL measurements were applied to optimise HF-treatment times aimed at undamaged, oxide-free and hydrogen-terminated substrate surfaces as starting material for subsequent solar cell preparations.      

Thin film substrates from the Raman spectroscopy point of view

We have investigated ten standard single crystal substrates of complex oxides on the account of their applicability in the Raman spectroscopy‐based thin film research. In this study, we suggest a spectra normalization procedure that utilizes a comparison of the substrate's Raman spectra to those of well‐established Raman reference materials. We demonstrate that MgO, LaGaO₃, (LaAlO₃)_0.3(Sr₂AlTaO₆)_0.7 (LSAT), DyScO₃, YAlO₃, and LaAlO₃ can be of potential use for Raman‐based thin film research. At the same time TiO₂ (rutile), NdGaO₃, SrLaAlO₄, and SrTiO₃ single crystals exhibit multiple phonon modes accompanied by strong Raman background that substantially hinder Raman‐based thin film experiments. Copyright © 2014 John Wiley & Sons, Ltd.     

Permeability spectra of Co2Z hexaferrite compacts produced via a modified aqueous co-precipitation technique

Co₂Z hexaferrite materials possess intrinsically high permeability, zero field ferromagnetic resonance values (∼1 GHz), and have their magnetic orientation in the plane perpendicular to the c-axis. These characteristics make these materials practical for applications in low to mid ultra-high frequency and L-band microwave device designs. Due to the relatively large size of elements operating within these bands, it has become important to produce large amounts of Co₂Z type hexaferrite materials. A modified co-precipitation method has been proposed to produce scalable quantities of high quality Co₂Z hexaferrite particles, at ∼24 g/L. These particles have been thoroughly characterized by vibrating sample magnetometry (VSM) and X-ray diffraction (XRD) with regard to phase purity and magnetic properties. After formation and subsequent ball milling, to achieve single domain particles on the order of 0.5–2 um, particles were oriented and pressed into compacts inside a rotating field to ensure magnetization in plane. Samples then underwent VSM, XRD, and scanning electron microscopy to determine the orientation effect. In addition, the complex permittivity and permeability of these samples were measured as a function of applied field and processing conditions. The results show strong orientation in these compacts making them practical for a variety of device applications.     

New Chromogenic Substrates for Rapid Determination of Collagenase Activity

Abstract

Cowhide collagen insolubilized by formaldehyde treatment was grafted with chlorotriazine dyes in order to obtain chromogenic substrates for rapid determination of collagenases. The cross-linking degree and the dyeing procedure were chosen as to permit a maximal sensitivity of the method. Collagenolytic activity was estimated by colorimetric measurement of the coloured soluble split products liberated in supernatant as a result of the enzyme action on the insoluble dyed substrate. Some precision parameters were calculated (cv=6.62%) and proved a satisfactory reproducibility of the method.     

Analytical Separations of Schiff Base Chelates by Reverse Phase Hplc on a 10 Micron C-18 Bonded Silica Subtrate

Abstract

Reverse phase partition chromatography on a 10 micron silica-bonded octadecyl hydrocarbon substrate is applied to the separation of neutral tetradentate chelates of copper (II), nickel (II) and palladium (II) with a range of non-fluorinated and fluorinated beta-ketoamine and salicylaldimine ligands. Variation of retention and resolution with respect to changes in ligand structure and metal chelated is investigated using acetonitrile, methanol and water solvent systems. Detection limits (254 nm) and linearity ranges of response are indicated.     

Nanostructured gold surfaces as reproducible substrates for surface‐enhanced Raman spectroscopy

Raman spectroscopy is a common tool for the qualitative and quantitative chemical analysis of molecules. Although the unique identification of molecules is possible via their vibrational lines, high concentrations (mmol/l) are needed for their nonresonant excitation owing to their low scattering cross section. The intensity of the Raman spectra is amplified by the use of the surface‐enhanced Raman scattering (SERS) technique. While the use of silver sols results only in a limited reproducibility of the Raman line intensities, lithographically designed, nanostructured gold surfaces used as SERS‐active substrates should, in principle, combine the high sensitivity with better reproducibility. For this purpose, we have produced gratings of gold dots on Si(001) surfaces by means of electron beam lithography. Qualitative and quantitative investigations of crystal violet (CV) performed using nanostructured surfaces give high reproducibility and enhancement of the Raman lines. The substrates are reusable after cleaning; all results presented could be obtained from a single SERS substrate. For the experiments very low laser powers were used. Copyright © 2006 John Wiley & Sons, Ltd.     

A low-temperature X-ray diffraction study of the Cu2ZnSnSe4 thin films

Low-temperature XRD measurements were performed to confirm the phase composition and structural parameters of the electrochemically deposited Cu₂ZnSnSe₄ thin films on flexible metal substrates.