Solving the initial condition of the string relaxation equation of the string model for glass transition:part-I

The string model for the glass transition can quantitatively describe the universal a-relaxation in glassformers, including the average relaxation time, the distribution function of the relaxation time, and the relaxation strength as functions of temperature. The string relaxation equation （SRE） of the model, at high enough temperatures, simplifies to the well-known single particle mean-field Debye relaxation equation, and at low enough temperatures to the well-known Rouse-Zimm relaxation equation that describes the relaxation dynamics of linear macromolecules. However, its initial condition, necessary to the further model predictions of glassy dynamics, has not been solved. In this paper, the special initial condition （SIC） of the SRE, i.e. for straight strings and the dielectric spectrum technique that is one of the most common methods to measure the glassy dynamics, was solved exactly. It should be expected that the obtained SIC would benefit the solution of the general initial condition of the SRE of the string model, i.e. for stochastically spatially eonfigurating strings, as will be described in separate publications.

Solving the initial condition of the string relaxation equation of the string model for glass transition:part-Ⅱ

The string model for the glass transition can quantitatively describe the universal a-relaxation in glassformers. The string relaxation equation （SRE） of the model simplifies the well-known Debye and Rouse-Zimm relaxation equations at high and low enough temperatures, respectively. However, its initial condition, necessary to the further model predictions of glassy dynamics, has not been solved. In this paper, the general initial condition of the SRE for stochastically spatially configurative strings is solved exactly based on the obtained special initial condition of the SRE for straight strings in a previous paper （J. L. Zhang et al. 2010 Chin. Phys. B 19, 056403）.

Thermodynamic and Kinetic Analysis of Low-temperature Thermal Reduction of Graphene Oxide

The thermodynamic state and kinetic process of low-temperature deoxygenation reaction of graphene oxide(GO) have been investigated for better understanding on the reduction mechanism by using Differential Scanning Calorimetry(DSC), Thermogravimetry-Mass Spectrometry(TG-MS), and X-ray Photoelectron Spectroscopy(XPS). It is found that the thermal reduction reaction of GO is exothermic with degassing of CO_2, CO and H_2O. Graphene is thermodynamically more stable than GO. The deoxygenation reaction of GO is kinetically controlled and the activation energy for GO is calculated to be 167 k J/mol(1.73 e V/atom).

Structure and Transport Properties in CMR Materials of La_((1-x)2/3)Ca_(1/3)MnO_3 with Rare Earth Vacancies

Samples of manganese oxides La（1-x）2/3Ca1/3MnO3（x 〈 0.10） with Lavacancy were prepared by standard solid-state reaction method. All the samples are single phase, with orthorhombic symmetry （Pnma ）, analyzed by XRD and with Rietveld Refinement. The effect of different La-site vacancies concentration on electronic transport of La（1-x）2/3Ca1/3MnO3 was investigated. The insulator-metal transition temperature （about 267 K） nearly remains unchanged with the increase of vacancy concentration, which indicates that small La-vacancy does not destroy the double exchange interaction. But the electronic resistance increases and MR value decreases with La-vacancy content x 〉 0.04. The maximum of the MR value （8 T） is about 220% at transition temperature （TMI）.

Conversion Efficiency Enhancement of Multi-crystalline Si Solar Cells by Using a Micro-structured Junction

A new approach for enhancing the conversion efficiency of solar cells is proposed. A surface with columnar structures is employed on the fabrication of multi-crystalline silicon solar cells, for increasing the collection probability of photon-generated minority carriers in the cells. For comparison, three types of surfaces （planar surface, surfaces with columns of 12μm in radius and columns of 9 μm in radius, respectively） are used. It is demonstrated that the cells with columnar structured surfaces have better spectral response and higher efficiencies than the cells with planar surface, while the cells with columns of 9 μm in radius show better spectral response than the cells with columns of 12 μm in radius. However, the cells with columns of 12 μm exhibit higher efficiencies than the cells with columns of 9 μm in radius for their difference in fill factors. Moreover, the effect of the columnar structured surface on the minority carrier collection efficiency is verified with wafers of different minority carrier lifetimes （0.5 μs and 1.0 μs）. This work may significantly consider its potential in the manufacturing of highefficiency solar cells at low cost by using low quality materials.

Detailed assessment of homology detection using different substitution matrices

Homology detection plays a key role in bioinformatics, whereas substitution matrix is one of the most important components in homology detec- tion. Thus, besides the improvement of alignment algorithms, another effective way to enhance the accuracy of homology detection is to use proper substitution matrices or even construct new matrices. A study on the features of various matrices and on the comparison of the performances between differ- ent matrices in homology detection enable us to choose the most proper or optimal matrix for some specific applications. In this paper, by taking BLOSUM matrices as an example, some detailed features of matrices in homology detection are stud- ied by calculating the distributions of numbers of recognized proteins over different sequence identities and sequence lengths. Our results clearly showed that different matrices have different preferences and abilities to the recognition of remote homologous proteins. Furthermore, detailed features of the vari- ous matrices can be used to improve the accuracy of homology detection.

Microstructural stability of NiO-containing spin valves annealed at room temperature

Microstructure of NiO-containing Co/Cu/Co spin valves （CCC-SV） annealed at room temperature for nearly four years has been studied by synchrotron radiation X-ray diffraction. With the annealing time expanding, the thickness of each sub-layer remains nearly unchanged while the interface roughness varies obviously compared with that of samples without annealing. The roughness at the interface of NiO/Co decreases with the annealing time increasing for both of the samples with NiO layer on the top （TSV） and under the bottom （BSV） of CCC-SV. On the other hand, the roughness at Co/Cu interface increases with the annealing time expanding for BSV while it decreases for TSV. These results indicate that the structure of TSV is more stable than that of BSV.

High resolution X-ray diffraction investigation of epitaxially grown SrTiO_3 thin films by laser-MBE

SrTiO3 thin films are epitaxially grown on DyScO3, LaAlO3 substrates with/without buffer layers of DyScO3 and SrRuO3 using laser-MBE. X-ray diffraction methods, such as high resolution X-ray diffraction, grazing incident X-ray diffraction, and reciprocal space mapping are used to investigate the lattice structure, dislocation density, in-plane lattice strain distribution along film thickness. From the measurement results, the effects of substrate on film lattice quality and microstructure are discussed.

Reversible optical control of the metal-insulator transition across the epitaxial heterointerface of a VO_(2)/Nb:TiO_(2) junction

Optical control of exotic properties in strongly correlated electron materials is very attractive owing to their potential applications in optical and electronic devices.Herein,we demonstrate a vertical heterojunction made of a correlated electron oxide thin film VO_(2) and a conductive 0.05 wt% Nb-doped TiO_(2) single crystal,whose metal-insulator transition(MIT)across the nanoscale heterointerface can be efficiently modulated by visible light irradiation.The magnitude of the MIT decreases from ~350 in the dark state to ~7 in the illuminated state,obeying a power law with respect to the light power density.The junction resistance is switched in a reversible and synchronous manner by turning light on and off.The optical tunability of it is also exponentially proportional to the light power density,and a 320-fold on/off ratio is achieved with an irradiance of 65.6 mW cm^(-2) below the MIT temperature.While the VO_(2) thin film is metallic above the MIT temperature,the optical tunability is remarkably weakened,with a one-fold change remaining under light illumination.These results are co-attributed to a net reduction(~15 meV)in the apparent barrier height and the photocarrier-injection-induced metallization of the VO_(2) heterointerface through a photovoltaic effect,which is induced by deep defect level transition upon the visible light irradiance at low temperature.Additionally,the optical tunability is minimal,resulting from the quite weak modulation of the already metallic band structure in the Schottky-type junction above the MIT temperature.This work enables a remotely optical scheme to manipulate the MIT,implying potential uncooled photodetection and photoswitch applications.

A spin-less particle on a rotating curved surface in Minkowski space

In Minkowski space M,we derive the effective Schrodinger equation describing a spin-less particle confined to a rotating curved surface S.Using the thin-layer quantization formalism to constrain the particle on we obtain the relativity-corrected geometric potential V_(g)’,and a novel effective potential V(g) related to both the Gaussian curvature and the geodesic curvature of the rotating surface.The Coriolis effect and the centrifugal potential also appear in the equation.Subsequently,we apply the surface Schrodinger equation to a rotating cylinder,sphere and toms surfaces,in which we find that the interplays between the rotation and surface geometry can contribute to the energy spectrum based on the potentials they offer.

Electron mass enhancement and magnetic phase separation near the Mott transition in double-layer ruthenates

We present a detailed investigation of the specific heat of Ca3（Ru1-xMx）2O7 （M = Ti, Fe, Mn） single crystals. Depending on the dopant and doping level, three distinct regions are present： a quasi- two-dimensional metallic state with antiferromagnetic （AFM） order formed by ferromagnetic bilayers （AFM-b）, a Mott insulating state with G-type AFM order （G-AFM）, and a localized state with a mixed AFM-b and G-AFM phase. Our specific heat data provide deep insights into the Mort transitions induced by Ti and Mn doping. We observed not only an anomalous large mass enhancement, but also an additional term in the specific heat, i.e., C ∝ T2, in the localized region. The C ∝ T2 term is most likely due to long-wavelength excitations with both FM and AFM components. A decrease in the Debye temperature is observed in the G-type AFM region, indicating lattice softening associated with the Mott transition.