Dynamics of molybdenum nano structure formation on the TiO2(1 1 0) surface: A kinetic Monte Carlo approach

The rutile TiO₂(1 1 0) surface is a highly anisotropic surface exhibiting “channels” delimited by oxygen rows. In previous experimental and theoretical DFT works we could identify the molybdenum adsorption sites. They are located inside the channels. Moreover, experimental studies have shown that during subsequent annealing after deposition, special molybdenum nano structures can be formed, especially two monolayer high pyramidal chains of atoms.In order to better understand the dynamics of nano structure formation, we present a kinetic Monte Carlo study on diffusion and adsorption of molybdenum atoms on a TiO₂(1 1 0) surface. A quasi one-dimensional lattice gas model has been used which describes the possible adsorption sites of a Mo atom in a single channel of the surface. The atomic positions of a 1.5 monolayer thick Mo film formed of pyramidal chains define the lattice sites of the model. Thereby the formation of three-dimensional clusters could be studied. Here we have studied the cluster formation as a function of parameters that can be controlled in a growth experiment by physical vapor deposition: deposition and annealing temperature, flux and total amount of deposited Mo. Good qualitative agreement with recent experiments is obtained.     

Mesoscopic resonating valence bond system on a triple dot

We theoretically introduce a mesoscopic pendulum from a triple dot. The pendulum is fastened through a singly occupied dot (spin qubit). Two other strongly capacitively coupled islands form a double-dot charge qubit with one electron in excess oscillating between the two low-energy charge states (1,0) and (0,1). The triple dot is placed between two superconducting leads. Under realistic conditions, the main proximity effect stems from the injection of resonating singlet (valence) bonds on the triple dot. This gives rise to a Josephson current that is charge- and spin-dependent and, as a consequence, exhibits a distinct resonance as a function of the superconducting phase difference.     

Directed and elliptic flow in 197Au+197Au at intermediate energies

Directed and elliptic flow for the ¹⁹⁷Au+¹⁹⁷Au system at incident energies between 40 and 150 MeV per nucleon has been measured using the INDRA 4π multi-detector. For semi-central collisions, the excitation function of elliptic flow shows a transition from in-plane to out-of-plane emission at around 100 MeV per nucleon. The directed flow changes sign at a bombarding energy between 50 and 60 MeV per nucleon and remains negative at lower energies. Molecular dynamics calculations (CHIMERA) indicate sensitivity of the global squeeze-out transition on the σ _NN and demonstrate the importance of angular momentum conservation in transport codes at low energies.     

高阶效应对超短艾里-高斯脉冲相互作用的影响

本文运用分步傅里叶变换,对满足高阶耦合非线性薛定谔方程的超短艾里脉冲与超短高斯脉冲,利用MATLAB数值模拟了在高阶效应下两脉冲相互作用后的演化过程以及时域上的强度变化.获得了负三阶色散效应使超短脉冲相互作用能传输更远距离;正三阶色散效应会减慢超短脉冲相互作用的传输.自陡峭效应通过孤子分裂现象的形式使超短脉冲相互作用产生时域位移.内拉曼效应可以将超短脉冲相互作用的能量由前沿处转移到后沿处.     

Dynamic response of permalloy/Cu/Co magnetoresistive sandwiches

The dynamic response of trilayer magnetoresistive permalloy/Cu/Co films was studied by high-frequency permeability spectra measurements. The resonance frequency is shown to depend on the interlayer copper thickness. This dependence is related to exchange coupling between permalloy and cobalt and the interaction field is estimated using the Landau–Lifschitz–Gilbert model.     

Facile synthesis of SnO2–ZnO core–shell nanowires for enhanced ethanol-sensing performance

The design of core–shell heteronanostructures is powerful tool to control both the gas selectivity and the sensitivity due to their hybrid properties. In this work, the SnO₂–ZnO core–shell nanowires (NWs) were fabricated via two-step process comprising the thermal evaporation of the single crystalline SnO₂ NWs core and the spray-coating of the grainy polycrystalline ZnO shell for enhanced ethanol sensing performance. The as-obtained products were investigated by X-ray diffraction, scanning electron microscopy, and photoluminescence. The ethanol gas-sensing properties of pristine SnO₂ and ZnO–SnO₂ core–shell NW sensors were studied and compared. The gas response to 500 ppm ethanol of the core–shell NW sensor increased to 33.84, which was 12.5-fold higher than that of the pristine SnO₂ NW sensor. The selectivity of the core–shell NW sensor also improved. The response to 100 ppm ethanol was about 14.1, whereas the response to 100 ppm liquefied petroleum gas, NH₃, H₂, and CO was smaller, and ranged from 2.5 to 5.3. This indicates that the core–shell heterostructures have great potential for use as gas sensing materials.     

Design of an insensitive-polarization all-optical switch based on multimode interference structures

This paper presents a new design for an insensitive-polarization all-optical switch using 2 × 2 multimode interference (MMI) couplers. The switching structure can operate at central operating wavelength 1550 nm for both polarizations. A nonlinear directional coupler is used to realize the phase shifter and therefore switching mechanism is obtained. The transfer matrix method and beam propagation method are used to design and optimize the whole device structure.     

磁绝缘传输线电压的初步测量

针对快脉冲直线变压器驱动源装置上的真空磁绝缘传输线（MITL)电压测量的需求,开展了微分型电容分压器和电感分压器的设计、标定和实验。通过不同的电压值、负载阻抗的装置实验中探头输出结果的分析和比较,讨论了测量方法的可行性和适用范围。实验结果表明：微分型电容分压器能够应用于完全磁绝缘状态下的MITL电压测量,但容易受阴极电子发射的影响导致探头输出波形发生畸变。电感分压器受分布电容和电感的影响导致输出信号存在寄生振荡,采用波形重建的方法初步获得了合理的测量结果。     

Possible candidates for discrete gamma rays linking superdeformed and yrast states in an odd nucleus:193Pb

The francium isotopes^200–202Fr were produced in the reaction³⁵Cl+¹⁷⁰Yb using bombarding energies of 4.9–5.3 MeV/nucleon. Fusion products were separated in-flight from the primary beam using a gas-filled recoil separator. An alpha line with the alpha particle energy and half-life of (7468±9) keV and (19 ₋₆ ⁺¹³ ) ms, respectively, was assigned to²⁰⁰Fr. Previously reported decay properties of^201,202Fr were confirmed. Communicated by V. Metag