Helical Shell Structures of Ni-A1 Alloy Nanowires and Their Electronic Transport Properties

Six kinds of Ni-A1 alloy nanowires are optimized by means of simulated annealing. The optimized structures show that the Ni-A1 alloy nanowires are helical shell structures that are wound by three atomic strands, which is very similar to the case with pure metallic nanowires. The densities of states （DOS）, transmission function T（ E）, current-voltage （I - V） curves, and the conductance spectra of these alloy nanowires are also investigated. Our results indicate that the conductance spectra depend on the geometric structure properties and the ingredients of the alloy nanowires. We observe and study the nonlinear contribution to the I-V characteristics that are due to the quantum size effect and the impurity effect. The addition of Ni atoms decreases the conductance of the Ni-A1 alloy nanowire because the doping atom Ni change the electronic band structures and the charge density distribution. The interesting statistical results shed light on the physics of quantum transport at the nano-scale.     

Entanglement of Formation for Quantum States

We investigate the entanglement of formation for a class of high-dimensional quantum mixed states. We present a kind of generalized concurrence for a class of high-dimensional quantum pure states such that the entanglement of formation is a monotonically increasing convex function of the generallzed concurrence, from the monotonicity and convexity the entanglement of formafion for a class of high-dimensional mixed states has been calculated analytically,     

Enhanced Efficiency of Polymer： Fullerene Bulk Heterojunction Solar Cells with the Insertion of Thin TiO2 Layer near the LiF/A1 Electrode

The insertion layer of TiO2 between polymer-fullerene blend and LiF/AI electrode is used to enhance the shortcircuit current Isc and fill factor （FF）. The solar cell based on the blend of poly[2-methoxy-5-（2＇-ethylhexyloxy）- 1,4-phenylenevinylene] （MEH-PPV） and C60 with the modifying layer of TiO2 （about 20nm） shows the open- circuit Voc of about 0.62 V, short circuit current Isc of about 2.35 mA/cm^2, filling factor FF of about 0.284, and the power conversion efficiency （PCE） of about 2.4% under monochromatic light （50Onto） photoexcitation of about 17mW/cm^2. Compared to ceils without the TiO2 layer, the power conversion efficiency increases by about 17.5%. Similar effect is also obtained in cells with the undoped MEH-PPV structure of ITO/PEDOT：PASS/MEH- PPV/（TiO2）LiF/AI. The improved solar cell performance can be attributed to enhanced carrier extraction efficiency at the active layer/electrode interfaces when TiO2 is inserted.     

An optical scheme for conditional generation of W state and photon-added coherent state

We propose a simple scheme to generate an arbitrary photon-added coherent state of a travelling optical field by combining an array of degenerate parametric amplifiers and corresponding single-photon detectors. Particularly, when the single-photon-added coherent state is observed by developing the novel technique of Zavatta et al （2004 Science 306 660）, we can simultar/eously obtain the generalized N-qubit W state.     

Single-Proton Pickup Reaction of the Halo Nucleus ^6He on a ^9Be Target at 25 MeV/nucleon

The inclusive differential cross sections of the ^7 Li nucleus in a reaction induced by ^6He on a ^9Be target are measured at an incident energy of 25 MeV/nucleon. Finite-range distorted-wave Born approximation calculations suggest that these ^7 Li particles are formed in a direct single-proton pickup reaction ^9Be（^6He,^7 Li）^8Li. The experimental data can be well reproduced by taking into account of the contributions of both the ground states and the first excited states of ^7Li and ^8Li.     

M元混沌扩频多通道Pattern时延差编码水声通信

Pattern时延差编码水声通信体制利用信息码元的时延值调制信息,他的抗多途扩展干扰能力与码型种类及码型脉宽有关.扩频通信可获得扩频增益,可胜任远程水声通信,但其通信速率低是使用受限的重要原因.提出将扩频通信与Pattern时延差编码水声通信体制相结合,并采用M元扩频、多通道工作方式,构成一种新的适用于水声环境的通信方案,既可获得扩频通信的优良性能,又可提高通信速率.湖试结果验证了本文提出的M元混沌扩频多通道Pattern时延差编码水声通信方案的鲁棒性及可行性.     

基于表面等等离波子的新型Y分支波导

新型高效的纳米光波导器件的研制纳米集成光学的核心技术之一。Y分支波导作为最基本的分光和光路连接元件是纳米光学器件设计与制备的基础。运用时域有限差分(FDTD)法,模拟计算了基于表面等等离波子(SPP)的纳米Y分支波导的传输特性。结果表明,该新型Y分支波导在光通信波段可以实现大角度的分光功能,且在180°分支情况下,传输效率仍高达92.8%以上。另外,该波导还具有导波性能良好、对分叉处间隙缺陷大小不敏感及制作容差较大和器件尺寸在纳米量级等特点。对该新型光波导器件的研究为未来纳米集成光学器件的研制和应用有一定的指导意义。     

Synthesis of photocleavable poly(methyl methacrylate‐block‐d‐lactide) via atom‐transfer radical polymerization and ring‐opening polymerization

The synthesis and characterization of a photocleavable block copolymer containing an ortho‐nitrobenzyl (ONB) linker between poly(methyl methacrylate) and poly(d ‐lactide) blocks is presented here. The block copolymers were synthesized via atom transfer radical polymerization (ATRP) of MMA followed by ring‐opening polymerization (ROP) of d ‐Lactide and ROP of d ‐lactide followed by ATRP of MMA from a difunctional photoresponsive ONB initiator, respectively. The challenges and limitations during synthesis of the photocleavable block copolymers using the difunctional photoresponsive ONB initiator are discussed. The photocleavage of the copolymers occurs under mild conditions by simple irradiation with 302 nm wavelength UV light (Relative intensity at 7.6 cm: 1500 μW/cm²) for several hours. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 4309–4316     

Synthesis and crystallization behavior study of syndiotactic polystyrene‐g‐isotactic polypropylene (sPS‐g‐iPP) graft copolymers

Based on coordination polymerization mechanism only, novel stereoregular graft copolymers with syndiotactic polystyrene main chain and isotactic polypropylene side chain (sPS‐g‐iPP) were synthesized via two steps of catalytic reactions. First, a chain transfer reaction was initiated by a chain transfer complex composed of a styrene derivative, 1,2‐bis(4‐vinylphenyl)ethane, and hydrogen in propylene polymerization mediated by rac‐Me₂Si[2‐Me‐4‐Ph(Ind)]₂ZrCl₂ and MAO, which gave iPP macromonomer bearing a terminal styryl group (iPP‐t‐St). Then the iPP‐t‐St macromonomers of varied molecular mass were engaged in syndiospecific styrene polymerization over a typical mono‐titanocene catalyst (CpTiCl₃/MAO) under different conditions to produce sPS‐g‐iPP graft copolymers of varied structure. With an effective purification process, well‐defined sPS‐g‐iPP copolymers were obtained, which were then subjected to differential scanning calorimetry (DSC) and polarized optical micrograph (POM) studies. The graft copolymers were generally found with dual melting and crystallization temperatures, which were ascribable respectively to the sPS backbone and iPP graft. However, it was revealed that the two segments displayed largely different melting and crystallization behaviors than sPS homopolymer and the precursory iPP‐t‐St macromonomer. Consequently, the graft copolymer exhibited much distinctive crystalline morphologies when compared with their individual components. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011.