超导体／半导体界面处的电子相互作用──JOFET器件和Andreev反射

介绍了低维系统物理与器件研究领域内最近兴起的一个十分引人注目的交叉学科课题：超导体／半导体／超导体双异质结结构中电子在超导体／半导体界面处的相互作用行为，包括超导邻近效应（ｐｒｏｘｉｍｉｔｙｅｆｆｅｃｔ）及Ｊｏｓｅｐｈｓｏｎ场效应晶体管（ＪＯＰＥＴ）的探索研究，此外，还讨论了此领域内一个重要物理问题──Ａｎｄｒｅｅｖ反射。     

LaAlO_3/SrTiO_3界面增强光伏效应

探索LaAlO_3/SrTiO_3(LAO/STO)界面产生的新奇物理特性对理解关联电子系统中多自由度耦合和设计功能材料器件具有重要的价值.本文通过脉冲激光沉积方法在SrTiO_3基底上制备了LAO/STO薄膜,研究了正面照射LAO/STO膜面和侧面照射LAO/STO界面时的光伏效应,探讨了LAO/STO界面对光伏效应的影响.研究结果表明,在同样光照能量下侧面照射LAO/STO界面产生的光电压远高于正面照射LAO/STO膜面产生的光电压,说明LAO/STO界面对光伏效应有明显的增强作用.通过偏压调控可以进一步增强照射LAO/STO界面产生的光电压,当偏压为60 V时, LAO/STO样品的位置探测灵敏度达到了36.8 mV/mm.这些研究结果为设计场调控位置敏感探测器等新型光电子器件提供了新的思路.     

液晶在电场和剪切耦合作用下的流变学行为

本文通过理论和实验对液晶 5CB在剪切和电场耦合作用下流变行为进行了研究. 采用液晶连续理论, 建立了包括界面锚定能, 弹性自由能, 介电自由能和流动能在内的系统 Gibbs自由能公式, 通过最小化系统自由能的方法求解液晶在剪切和电场耦合作用下的取向分布及其黏度变化, 从分子基础模型上揭示了液晶在耦合作用下的流变行为、微观机理及其影响规律, 并通过流变测试对此进行验证. 对比分析了理论和试验结果的误差和原因, 发现界面锚定效应对于液晶分子的取向和黏度具有重要影响. 理论和试验结果均表明, 液晶在电场作用下具有明显的电黏效应, 表现出非牛顿流变行为, 其黏度值由剪切和电场的竞争和耦合作用共同决定. 在外电场作用下液晶的黏度可以增加到初始值的 4倍左右, 液晶这种其自身黏度可随着外场 (例如运动速度) 改变的特性在一定的条件下可以自适应地满足不同工况对黏度的要求, 这对实现智能摩擦润滑具有重要的意义. 关键词： 液晶 流变行为 电黏效应 耦合作用     

激波加载初始非均匀气体流场界面不稳定性数值模拟

流体力学界面不稳定性及其后期的界面混合现象,是一种十分复杂的多尺度非线性物理问题,在惯性约束聚变、天体物理以及水中爆炸等领域有着广泛的应用前景,对该问题的研究不仅具有很高的学术价值,而且对促进相关领域的发展具有重要意义.中国工程物理研究院流体物理研究所基于Euler有限体积方法,发展了适用于可压缩多介质黏性流动具有多亚格子尺度模型的大涡模拟程序MVFT,并评估分析了不同亚格子尺度模型对界面不稳定性及界面混合的模拟能力;提出了流场非均匀性对R-M不稳定性影响的问题,并在激波驱动轻重气体双模扰动R-M界面不稳定性实验中成功应用并解读了新的实验现象和规律,在此基础上进而开展了反射激波作用下两种初始非均匀流场界面不稳定性引起的界面混合数值模拟研究,探讨了流场非均匀性对激波反射后强非线性阶段界面不稳定性发展、演化规律的影响,近期还对非均匀流场R-M不稳定性的演化规律、初始流场非均匀性和初始扰动效应及其影响的物理机制进行了分析和研究.      

Fe和Co对Ni2MnGa合金(110)马氏体孪晶界面电子结构的影响

利用密度泛函理论研究了Fe，Co两种合金元素对Ni₂MnGa合金(110)马氏体孪晶界面电子结构的影响. 分别从界面能、偏聚能、磁矩、键序和电子态密度等角度对合金元素在界面处的掺杂效应进行了分析和比较. 计算结果表明，在对界面的钉扎作用上，Co的界面掺杂效应较Fe的掺杂效应强；对于界面磁性的影响，Fe掺杂对界面磁结构的作用比Co掺杂显著. 关键词： 密度泛函理论 孪晶界面 掺杂效应 马氏体     

随机稀释基底上刻蚀模型动力学标度行为的数值模拟研究

表面界面动力学粗化过程是凝聚态物理领域重要的研究内容,为研究基底不完整性对刻蚀模型动力学 标度行为的影响,本文采用Kinetic Monte Carlo(KMC)方法,分析研究了在随机稀释基底上刻蚀模型(Etching model)生长表面的动力学标度行为.研究发现:尽管随机稀释基底的不完整性会对刻蚀表面的动力学 行为产生显著的影响,导致刻蚀表面粗糙度指数和生长指数有明显的增加, 但其仍基本满足原有的动力学标度规律.此外,本文还对刻蚀表面动力学标度指数的有限尺寸效应进行了 分析讨论.     

高精度数控化学抛光技术

高精度光学表面数控化学抛光技术研究是针对强激光光学元件的应用需求，研究光学表面的化学抛光加工机理；基于Marangoni界面效应，采用数控化学抛光技术来实现光学表面面形及微结构形貌的高精度控制；为完成高精度激光光学元件(包括传统意义上的激光光学镜面和新型的静态连续波前校正板等)的制造进行新原理和新手段的探索。     

Fe和Co对Ni2MnGa合金(110)马氏体孪晶界面电子结构的影响

利用密度泛函理论研究了Fe,Co两种合金元素对Ni2MnGa合金(110)马氏体孪晶界面电子结构的影响.分别从界面能、偏聚能、磁矩、键序和电子态密度等角度对合金元素在界面处的掺杂效应进行了分析和比较.计算结果表明,在对界面的钉扎作用上,Co的界面掺杂效应较Fe的掺杂效应强;对于界面磁性的影响,Fe掺杂对界面磁结构的作用比Co掺杂显著.     

几种元素的界面插层对Ta/NiFe/Ta的各向异性磁电阻效应的影响

文章中,通过磁控溅射制备了界面处插入4d,5d元素薄层(包括Ru,Pd,Ag和Au)的Ta/NiFe/Ta多层膜,并对它们的磁输运和磁性以及微结构进行了测试和表征.结果显示,Pd和Pt一样界面效应显著,能有效地提高NiFe薄膜退火前后的AMR比值,并抑制磁性死层.表面能比较小、熔点相对低的插层材料Ag,Au在退火过程中容易通过晶界扩散,强烈破坏其AMR性能.对于熔点高、表面能比较大的插层材料如Ru,磁性死层同样得到了抑制,NiFe薄膜的温度稳定性也可以得到提高.结果表明界面插层从界面电子自旋-轨道散射、界面死层和界面原子扩散等方面深刻影响NiFe薄膜的AMR. 关键词： 各向异性磁电阻 界面效应 原子扩散     

表面科学研究回顾与21世纪发展展望

表面与界面是材料物理、化学性质发生空间突变的二维区域,材料的许多重要物理、化学过程首先发生在表面,同时材料的很多破坏和失效也首先起源于表面和界面。因此,表面是材料与外部环境直接发生联系的窗口,从研究材料表面界面的各种物理化学过程入手最终可以达到改善材料性能的目的。过去１０年中,材料表面科学在促进材料科学基础研究、推动新材料新技术发展中发挥了关键作用。世纪之交乃至下一世纪,表面科学将面临新的挑战和机     

脉冲激光诱导液-固界面反应合成金刚石纳米晶中的结构相变模型

 探讨了脉冲激光诱导液-固界面反应法（PLIR: Pulsed-Iaser Induced Liquid-Solid Interface Reaction ）制备金刚石纳米晶的物理化学机制,提出了金刚石纳米晶的成核机理,即由激光诱导石墨六方结构原子团过渡到石墨菱方结构、然后转变成立方金刚石晶核,以及由石墨六方结构直接转变成六方金刚石结构的相变模型,并讨论了基于液-固界面反应的纳米晶生长动力学,较好地从动力学上解释了合成金刚石纳米晶的物理化学机制。     

Molecular dynamics simulations of PVP kinetic inhibitor in liquid water and hydrate/liquid water systems

The possible effects of PVP (poly(N-vinylpyrrolidone)) on the properties of liquid and water in clathrate hydrate has been investigated using NVT molecular dynamics simulations. A model for a monomer of the PVP polymer is immersed in three systems, liquid water, a unit cell of a hydrate in liquid water with a hydrate former and a third system where some of the liquid water molecules of this last system are replaced by a PVP monomer. Both molecular dynamics simulation and integral equation theory predict hydrogen bonding between the double bonded oxygen in the PVP ring and hydrogens in water. For the composite system, the PVP monomer has a preference for hydrogen bonding to hydrogens from the water molecules at the surface of the hydrate lattice. The simulations indicate that the PVP monomer tends to orient perpendicular to the hydrate surface. For the model systems in this study PVP may form hydrogen bonds with liquid water through the double bonded oxygen in the ring. When a hydrate crystal is immersed in the liquid water phase this hydrogen bonding is shifted towards the hydrate due to a more favourable Coulomb interaction involving hydrogens from more than one water molecule at the hydrate surface. The PVP monomer has a preference for perpendicular orientation with respect to the hydrate surface. A scheme is suggested for the characterization of kinetic hydrate inhibitors based on molecular dynamics simulations and on three basic properties. In addition to the energy between the active groups of the inhibitor and hydrate water another point of focus is the free energy changes in the interactions between the inhibitor and water as the charges are changed from zero to the original model charges. In particular the difference between this integral for the (hydrate water)–(PVP monomer) interaction and the (liquid water)–(PVP inhibitor) interaction should reflect the driving forces in freezing the inhibitor out from the liquid water phase and onto the hydrate surface. The third property in the characterization scheme is the diffusivities of groups connecting to the hydrate crystal, relative to the diffusivities of the hydrate crystal. Results are presented from simulations where a small cavity with a methane model as a guest is immersed in liquid water with free methane molecules at a temperature of 150K. Changes in structure, diffusivities and energy indicate a tendency towards a more solid–like structurde around the cavity.     

Supercooling molecular hydrogen down through the superfluid transition

Recent calculations by Vorobev and Malyshenko [JETP Lett. 71, 39 (2000)] show that molecular hydrogen may stay liquid and superfluid in strong electric fields of the order of 4x10(7) V/cm. I demonstrate that strong local electric fields of similar magnitude exist beneath a two-dimensional layer of electrons localized in the image potential above the surface of solid hydrogen. Even stronger local fields exist around charged particles (ions or electrons) if the surface or bulk of a solid hydrogen crystal is statically charged. Measurements of the frequency shift of the 1 --> 2 photoresonance transition in the spectrum of a two-dimensional layer of electrons above a positively or negatively charged solid hydrogen surface performed in the temperature range 7-13.8 K support the prediction of electric field induced surface melting. The range of surface charge density necessary to stabilize the liquid phase of molecular hydrogen at the temperature of superfluid transition is estimated.     

聚酰亚胺LB膜上液晶表面锚定的研究

通过测试光延迟研究了聚酰亚胺ＬＢ膜的光学各向异性，分析了在ＬＢ膜成膜过程中成膜分子的流动取向特性，并研究了液晶的表面锚定能，分析了ＬＢ膜上液晶的取向机制．聚酰亚胺ＬＢ膜的链段的取向程度较强摩擦情形的聚酰亚胺表面的链段取向要差．强摩擦的聚酰亚胺会比聚酰亚胺ＬＢ膜具有更好的排列液晶分子的能力．ＬＢ膜的流动取向模式使得聚酰亚胺成膜分子沿拉伸方向形成一定的有序排列，并诱导液晶分子定向排列，液晶和聚合物分子相互作用是液晶表面排列的主要动力 关键词：     

Why are alkali halide surfaces not wetted by their own melt?

Alkali halide (100) crystal surfaces are anomalous, being very poorly wetted by their own melt at the triple point. We present extensive simulations for NaCl, followed by calculations of the solid-vapor, solid-liquid, and liquid-vapor free energies showing that solid NaCl(100) is a nonmelting surface, and that its full behavior can quantitatively be accounted for within a simple Born-Meyer-Huggins-Fumi-Tosi model potential. The incomplete wetting is traced to the conspiracy of three factors: surface anharmonicities stabilizing the solid surface; a large density jump causing bad liquid-solid adhesion; incipient NaCl molecular correlations destabilizing the liquid surface. The latter is pursued in detail, and it is shown that surface short-range charge order acts to raise the surface tension because incipient NaCl molecular formation anomalously reduces the surface entropy of liquid NaCl much below that of solid NaCl(100).     

Effect of surface acoustic waves on activity in heterogeneous catalysis

A synopsis of the recent developments in acoustically influencing and controlling gas-surface interactions is presented. The cleaning effect of ultrasound and its surface activation play an important role for the sonochemical enhancement of reactivity in chemical processes involving solid and liquid phases. So far, there have only been a few studies on the effects of surface acoustic waves on surface chemical reactions under high-vacuum conditions by the application of piezoelectric surface acoustic wave transducers. Very recently, metal films deposited between InterDigital Transducer (IDT) electrodes on a LiNbO₃ substrate have shown a significant inerease in catalytic activity during surface acoustic excitation and Edge-Bonded Transducers (EBT) with a metal single crystal as a substrate have been used to acoustically influence the rate in the oscillatory reaction for CO oxidation. Tunable narrowband surface acoustic excitation is anticipated to be an efficient route to control catalytic processes, and in our work this approach is being used to investigate the physical basis of this process.     

双轴向列相液晶的表面能

利用双轴向列相液晶表面能对指向矢和序参量矩阵的旋转不变性,构造了与指向矢^a,^b,^c对易取向轴^a0,^b0,^c0的偏离有关的表面能Fs(a,b,c),以及与序参量矩阵有关的表面能Fs(Q),并得到两种表达式的等价形式.在Fs(a,b,c)和Fs(Q)中分别有四个和两个独立参量.为讨论上述独立参量的物理意义,假设一液晶分子对表面相互作用的简单模型,将液晶分子沿易取向轴^b0,^c0的双轴性取向看成是受到沿^b0,^c0两相互垂直的平均场作用的结果.为测量表面锚泊系数,考虑了三种简单形变位型,即在外磁 关键词： 液晶 弹性能 表面能     

液晶显示用取向材料聚甲基丙烯酸肉桂酰氧基乙酯的光控取向研究

通过实验研究了光聚合物材料聚甲基丙烯酸肉桂酰氧基乙酯（ＣＥＭＣ）的光化学反应过程, 以及对液晶材料ＬＣ－６７１０Ａ 的取向能力． 通过原子力显微镜（ＡＦＭ）观察了取向层表面在光化学反应前后的变化, 测量了光控取向膜液晶盒中液晶分子的预倾角及单面光控取向扭曲向列液晶显示器（ＴＮＬＣＤ）的电光特性和时间响应特性曲线, 研究了液晶分子排列取向的机理．     

Dynamics of domain-wall motion in ferroelectric liquid crystals in an electric field

The director reorientation in smectic liquid crystals with ferroelectric properties has been considered in the case where the interaction of liquid-crystal molecules with the surface leads to a partial unwinding of the helical structure of the liquid crystal and the reorientation occurs as a result of the domain-wall motion. The dependences of the velocity of domain-wall motion on the electric field strength, electric field variation frequency, boundary conditions, spontaneous polarization, and viscosity of the liquid crystal have been determined. It has been demonstrated that an increase in the electric field variation frequency or the polar part of the anchoring energy and the spontaneous polarization of the liquid crystal at a constant field frequency results in an increase of the velocity of domain-wall motion. As a consequence, the time of the electro-optic response of the liquid crystal in weak electric fields (from 0.4 to 2.0 V/μm) decreases by a factor of more than three.     

Surface-induced ordering in thin uniaxial liquid crystal films

The interface localization transition in thin uniaxial liquid crystal films with competing surface fields has been studied using Metropolis Monte Carlo simulations. The model is constructed from a lattice of continuously orientable interacting spins, and the Hamiltonian contains both bilinear and biquadratic contributions. The biquadratic contribution to the Hamiltonian is familiar from the Lebwohl-Lasher model, and accounts for the particle anisotropy in a liquid crystal. The head-tail asymmetry of the molecules in a uniaxial liquid crystal is taken into account through a bilinear contribution familiar from the classical ferromagnetic Heisenberg model with exchange anisotropy Lambda. The critical temperature T(c), characterizing the interface localization transition within the uniaxial liquid crystal film, depends strongly on the relative magnitudes of the bilinear and biquadratic interactions between the spins. For systems dominated by the biquadratic interaction, T(c) is found to be close to the bulk critical temperature of the system. But as the biquadratic interaction strength is reduced, T(c) departs markedly from the bulk critical temperature of the system.