Electronic Stopping Power for 0.05--10MeV Protons in a Group of Organic Materials

Electronic stopping powers for 0. 05-10 MeV protons in a group of organic materials are systematically calculated. The calculations are based on Ashley＇s dielectric model, and an evaluation approach of optical energy loss function is incorporated into Ashley＇s model because no experimental optical data are available for most of the organic materials under consideration. The Barkas-effect correction and Bloch correction are included. The proton stopping powers for the considered organic materials except for mylar in the energy range from 0.05 to 10 MeV are presented for the first time. The results may be useful for studies of various radiation effects in these materials and for space research.     

Detailed Characteristics of Expansion Velocity of Si from Laser Ablated SiC

Optical emission of plasma is used to investigate the characteristics of dynamics distribution in the plume gen- erated by ablation of a SiC sample using Nd：YAG laser. The plume expansion dynamics is characterized by time-of-flight measurement. We find that the profiles of Si （I） （390.55 nm） split into two components and the Si （1I） （634. 71 nm） spectra show two distinct expansion dynamics regions. The time-of-flight measurement of Si（ll） （634. 71 nm） under different laser irradianee conditions, from 0.236 G W/cm^2 to 1.667 G W/cm^2, are presented and discussed.     

Energetics of carbon and nitrogen impurities and their interactions with vacancy in vanadium

We studied the energetic behaviors of interstitial and substitution carbon(C)/nitrogen(N) impurities as well as their interactions with the vacancy in vanadium by first-principles simulations. Both C and N impurities prefer the octahedral site(O-site). N exhibits a lower formation energy than C. Due to the hybridization between vanadium-d and N/C-p, the N-p states are located at the energy from-6.00 e V to-5.00 e V, which is much deeper than that from-5.00 e V to-3.00 e V for the C-p states. Two impurities in bulk vanadium, C–C, C–N, and N–N can be paired up at the two neighboring Osites along the 111 direction and the binding energies of the pairs are 0.227 e V, 0.162 e V, and 0.201 e V, respectively.Further, we find that both C and N do not prefer to stay at the vacancy center and its vicinity, but occupy the O-site off the vacancy in the interstitial lattice in vanadium. The possible physical mechanism is that C/N in the O-site tends to form a carbide/nitride-like structure with its neighboring vanadium atoms, leading to the formation of the strong C/N–vanadium bonding containing a covalent component.     

纳米固体材料的性能与界面微观结构

综述了纳米陶瓷ＴｉＯ２和纳米金属Ａｇ的力学性能，以及纳米离子导体ＣａＦ２和ＰｂＦ２等的离子导电性能，结合其界面微观结构特征，对上述纳米固体材料的优异性能进行了初步解释     

Single-Walled Carbon Nanotubes Acting as Controllable Transport Channels

The motion and equilibrium distribution of water molecules adsorbed inside neutral and negatively charged singlewalled carbon nanotubes (SWNTs) have been studied using molecular dynamics simulations (MDSs) at room temperature based on CHARMM (Chemistry at HARvard Molecular Mechanics) potential parameters. We find that water molecules have a conspicuous electropism phenomenon and regular tubule patterns inside and outside the charged tube wall. The analyses of the motion behaviour of water molecules in the radial and axial directions show that by charging the SWNT, the adsorption efficiency is greatly enhanced, and the electric field produced by the charged SWNTs prevents water molecules from flowing out of the nanotube. However, water molecules can travel through the neutral SWNT in a fluctuating manner. This indicates that by electrically charging and uncharging the SWNTs, one can control the adsorption and transport behaviour of polar molecules in SWNTs for using as a stable storage medium or long transport channels. The transport velocity can be tailored by changing the charge on the SWNTs, which may have a further application as modulatable transport channels.     

Energetic Evolution of Single-Crystalline ZnO Nanowires and Nanotubes

We report the formation energies of wurtzite zinc oxide （w-ZnO） nanowires （NWs） and nanotubes （NTs） with faceted morphologies, and show that hexagonal NWs （h-NWs） are energetically advantageous over the NWs with rhombic （r-）, squared （s-）, and triangular （t-） cross sections. The formation energies of h-NWs are proportional to the inverse of wire radius, whereas those of single-crystalline NTs are proportional to the inverse of wall thickness, irrespectively to tube radius. A simple model is presented to interpret these features.     

Self-Organized Micro-Columns and Nano-Spheres Generated by Pulsed Laser Ablation of Ti/A1 Alloy in Water

Dense arrays of micro-columns are formed on the surface of Ti-AI alloy by cumulative nanosecond pulsed laser ablation in water. The fabric-like structure characterized by Ti-A1 nano-spheres absorbed on micro-duster in liquid is most likely responsible for the occurrence of laser micro-etching and localized melting, resulting in continuous deepening of micro-holes and the formation of micro-columns. Laser induced plasma spectroscopy is carried out to reveal the effect of micro-columns on subsequent pulse laser ablation. The intensity of spectral lines from Ti ions by additional laser ablation of the modified spot is higher than that created over a smooth surface. These results suggest that the micro-columns lead to an enhanced absorption of the following laser energy. The proposed results and relevant discussions are of importance for the development of light-trapping coatings on a metal surface.     

Monte Carlo Simulation on Energy Deposition of Low-Energy Electrons in Liquid Water

A Monte Carlo approach to simulate the transport and energy deposition of low energy electrons (E0≤10keV) in liquid water is presented. The elastic scattering of electrons is described by Mott cross section, which is derived from the relativistic wave equation of Dirac. The inelastic scattering model of electrons is based on the dielectric response theory with exchange effect included. A new method of sampling various inelastic scattering events is proposed in the simulation. Using the approach stated, the spatial distribution of inelastic scattering events and energy deposition of electrons in liquid water are computed and the results are compared with other theoretical studies.     

透镜到靶材的距离对脉冲激光诱导等离子体的影响机理研究

采用高功率抽运调Q激光器分别在真空和空气中烧蚀Ti-Al合金靶材激发等离子体,研究了在不同气体压强下透镜到靶材的距离对等离子体参数的影响机理对于焦距为111mm的聚焦透镜,当透镜到靶材距离小于透镜焦距时,随着距离逐渐接近焦距,真空和空气中电子温度、电子密度和谱线强度均逐渐增强.当透镜到靶材距离大于透镜焦距时,真空中,电子温度和电子密度仍然继续升高,而谱线强度却变化不大.空气中,等离子体参数却有不同的演化特性:等离子体的电子温度、电子密度和谱线强度在透镜到靶材距离为107 mm时达到最大值,当距离继续增大时,均呈现出迅速下降的趋势,当透镜到靶材距离大于112mm时,电子温度和电子密度又有明显上升,特征谱线强度却大幅下降.     

纳米离子导体在流体静压力下的复阻抗谱研究

 用惰性气体蒸发和真空原位加压方法制备了具有清洁界面的平均粒度16 nm的纳米固体CaF₂，并在0.1~2 400 MPa范围不同的静水压下用100 kHz~100 Hz内70种频率，精确测量了纳米CaF₂的复平面阻抗谱。分别给出纳米CaF₂离子电导率和相对介电常数随流体静压力的变化规律。最后的讨论指出：离子迁移通遭受压后的变化（大于、等于或小于最佳值）是影响离子电导率-压力曲线的主要因素；界面层空间电荷极化是造成纳米CaF₂相对介电常数较大的原因，由此界面效应可理解介电常数-压力曲线。