MgB_2超导体参量的拟和简化计算

关联长度ξ、临界Cooper对速度、London穿透深度λ以及临界电流密度jc与温度T的变化关系一直是二硼化镁超导体倍受关注的焦点。文中在各向同性的GL理论的框架内对以上参量随温度的变化关系通过计算机进行拟和,得出了数学形式相对简单、物理内涵又比较清晰的数学表达式,达到了对MgB2超导体参量拟和简化计算的目的。     

A Multi‐Thresholding Algorithm for Sizing out of Focus Particles

A methodology is presented that enables efficient acquisition of sufficient droplet information (e.g. diameter and aspect ratio) from images of in and out of focus droplets. The newly developed multi‐threshold algorithm is successfully implemented in the automatic particle/droplet image analysis (PDIA) system. Under the same optical hardware set‐up, and compared to the dual threshold methods [1], the multi‐threshold method increases the measurable/acceptable depth of field (DoF) of particles, especially for the small particles of diameters less than 50 μm (1098 pixels in this optical set‐up). When testing the 70 μm~110 μm and 100 μm~200 μm moving glass spheres, the dual threshold method can only detect 11%~29 % of the particles found by the multi‐threshold method. The multi‐threshold method is also capable of generating the aspect ratios of particles more accurately than dual threshold methods.     

Destabilization of Thiolated Gold Clusters for the Growth of Single‐Crystalline Gold Nanoparticles and Their Self‐Assembly for SERS Detection

Thiolate‐protected gold nanoclusters with high chemical stability are exploited extensively for fundamental research and utility in chosen applications. Here for the first time, the controlled destabilization of extraordinarily stable thiolated gold clusters for the growth of single‐crystalline gold nanoparticles (AuNPs) is demonstrated, which was achieved simply via the oxidation of surface‐protecting thiolates into disulfides by hydrogen peroxide under basic condition. By combining with our experimental observations over the entire destabilization and growth process, the new growth mechanism from clusters to AuNPs is revealed by density functional theory (DFT) calculations. It is found that the size of AuNPs decreases with the increase of hydrogen peroxide concentration due to the generation of more nuclei at the higher hydrogen peroxide concentrations. In addition, the preparation of AuNPs is tuned by changing the concentration of hydrogen peroxide, and they are self‐assembled into microspheres via an evaporation‐mediated process, which can induce strong plasmonic coupling between adjacent AuNPs for ultrasensitive surface‐enhanced Raman scattering detection. The present work demonstrates a facile route to functionalize and engineer AuNPs via controlling the reaction conditions and the ratio of precursors, and thus bring new possibilities for using more clusters as precursors to construct novel nano/microstructures for various applications.     

Raman study of Fano interference in p‐type doped silicon

As the silicon industry continues to push the limits of device dimensions, tools such as Raman spectroscopy are ideal to analyze and characterize the doped silicon channels. The effect of inter‐valence band transitions on the zone center optical phonon in heavily p‐type doped silicon is studied by Raman spectroscopy for a wide range of excitation wavelengths extending from the red (632.8 nm) into the ultra‐violet (325 nm). The asymmetry in the one‐phonon Raman lineshape is attributed to a Fano interference involving the overlap of a continuum of electronic excitations with a discrete phonon state. We identify a transition above and below the one‐dimensional critical point (E = 3.4 eV) in the electronic excitation spectrum of silicon. The relationship between the anisotropic silicon band structure and the penetration depth is discussed in the context of possible device applications. Copyright © 2010 John Wiley & Sons, Ltd.     

Self‐Assembly of Spherical or Rod‐Shaped Magnetic Nanocrystals onto Curved Substrates Governed by the Radius of Curvature

The way the assembly of colloidal nanostructures into heterostructures takes place substantially affects their physicochemical properties and performance. The layer‐by‐layer self‐assembly has shown in this regard a huge ability to drive nanomaterials onto curved substrates. Hindering the clustering to improve the distribution and allocation of nanoparticles on these assemblies can be partially controlled by geometric frustration, herein demonstrated driving magnetic nanocrystals with different morphology onto spherical substrates of tuned curvature.     

Raman spectroscopy of ionic liquids derived from 1‐n‐butyl‐3‐methylimidazolium chloride and niobium chloride or zinc chloride mixtures

Anionic species formed in mixtures of 1‐n‐butyl‐3‐methylimidazolium chloride (BMICl) with different amounts of niobium pentachloride (NbCl₅) or zinc dichloride (ZnCl₂) were investigated by Raman spectroscopy. In the BMICl and NbCl₅ ionic mixtures the presence of the anion NbCl₆⁻ was detected for all compositions (molar fraction, X) and a mixture of this anion and the neutral Nb₂Cl₁₀ in acid ones. Two different anions were observed for basic mixtures of BMICl and ZnCl₂: ZnCl₄²⁻(0 < X < 0.35) and Zn₂Cl₆²⁻(X > 0.3), whereas for acidic ones three species were detected: Zn₂Cl₆²⁻(X < 0.7), Zn₃Cl₈²⁻(X > 0.7) and Zn₄Cl₁₀²⁻(X > 0.7). It has also been observed that in both cases, the formation of larger anions causes a shift of the C H stretching modes to higher wavenumbers as the result of a decrease in the hydrogen bond between Cl and the hydrogens from the cation. Copyright © 2008 John Wiley & Sons, Ltd.     

Optical Chirality from Dark‐Field Illumination of Planar Plasmonic Nanostructures

Dark‐field illumination is shown to make planar chiral nanoparticle arrangements exhibit circular dichroism in extinction, analogous to true chiral scatterers. Single oligomers, consisting rotationally symmetric arrangements of gold nanorods, are experimentally observed to exhibit circular dichrosim at their maximum scattering with strong agreement to numerical simulation. A dipole model is developed to show that this effect is caused by a difference in the projection of a nanorod onto the handed orientation of electric fields created by a circularly polarized dark‐field normally incident on a glass‐air interface. Owing to this geometric origin, the wavelength of the peak chiral response is experimentally shown to shift depending on the separation between nanoparticles. All presented oligomers have physical dimensions less than the operating wavelength, and the applicable extension to closely packed planar arrays of oligomers is demonstrated to amplify the magnitude of circular dichroism. This realization of strong chirality in these oligomers demonstrates a new path to engineer optical chirality from planar devices using dark‐field illumination.     

Preparation and Characterization of the Fluorescent Carbon Dots Derived from the Lithium‐Intercalated Graphite used for Cell Imaging

Zero‐dimensional fluorescent carbon dots (CDs) that are used as a cell‐imaging reagent are prepared by using a simple and effective route employing lithium‐intercalated graphite from lithium‐ion batteries as a carbon source. Under ultrasonic exfoliation, the interlayer space increases, while the layer distortion and remaining lithium of the lithium‐intercalated graphite are utilized to disrupt the graphitic structure and produce the CD suspension. Subsequently, after concentration and purification, the obtained colloidal CD suspension has a fluorescent yield of up to 1.2% and is therefore comparable to the CDs prepared in previous reports. These CD products are water‐soluble, nanosized (approximately 3.5 nm), and biocompatible and can easily enter into HeLa cells to act as a cell‐imaging reagent without any further functionalization. In addition, these CDs do not impose toxicity against HeLa cells and have high photostability with low photobleaching and demonstrate potential applications for bio‐labeling as well as solution state optoelectronics.