小液滴撞击壁面传热特性数值分析

小液滴撞击壁面现象在喷雾冷却等领域都有广泛应用.为研究小液滴(微米)撞击热壁面(非沸腾区)传热过程,建立了二维液滴撞壁瞬态模型,并采用相场方法对小液滴换热过程中对流热通量和导热热通量的大小进行了对比.研究结果表明:液滴撞击壁面初期形成“冷斑”,有利于小液滴与壁面的传热;小液滴撞击壁面过程中热通量峰值存在于三相接触点附近,数量级在105—106 W/m²;小液滴撞击壁面过程中受壁面浸润性和液滴尺寸对传导热通量的影响较为显著,而速度和液滴尺寸对对流热通量的影响较为显著;大多数情况下,小液滴撞击壁面传导热通量数量级在103—105 W/m²,对流热通量数量级在104—106 W/m²,对流热通量大于传导热通量,在整个换热过程中占据主导地位.     

Dependence on substrate topography of growth of nanosized dendritic structures in an electron-beam-induced deposition process

Nanometer-sized W-dendrites are fabricated on Al₂O₃ substrates with an electron-beam-induced deposition process. Dependence of growth of nanodendrite on surface topography is investigated with transmission electron microscopy. It is confirmed that the nanodendrite grows on convex surfaces but not around a hole on a substrate. These are attributed to different distribution of charges on surfaces with different topographies during electron beam irradiation when charges are produced on the surface due to emission of second electrons. The charges accumulate on convex surface and do not distribute around a hole. Therefore, the nanodendrite grows on the former and not on the latter.     

有限温度奇异夸克物质

本文简要介绍了近年来有限温度下奇异夸克物质的研究,包括早期宇宙中大块奇异夸克物质的研究;基于ＭＩＴ袋模型的ｓｔｒａｎｇｅｌｅｔ研究,以及运用质量密度相关模型对奇异夸克物质的研究,最后简略评述了关于奇异夸克物质性质的近期研究进展     

Interaction of water with stepped Co(0001): how is it different from flat Co(0001)?

The adsorption and dissociation of water monomer and dimer on stepped Co(0001) surface were studied by means of first-principles calculations. Present results indicate that the adsorption strength of water is greatly enhanced by the presence of step, while the activity of water monomer dissociation does not exhibit a noticeable improvement. Nevertheless, water dimer partial dissociation on stepped Co(0001) is more active than on flat Co(0001), and the promotion of oxygen atom on O–H bond cleavage of H₂O is more prominent on stepped surface than on flat Co(0001). The findings reveal the importance of low coordinated surface atoms on metallic catalysts and the vital role of surface rippling on water dissociation. Together with previous reports, the activity of water dissociation on cobalt-based catalytic surfaces depends dominantly on O-containing species like oxygen atom, H₂O or hydroxyl.     

PNL分子在正、负电性纳米银上的吸附取向

制备了两种不同电性的纳米银粒子的脉体,发现当邻菲罗啉分子分别吸附在这两种纳米银上时,其表面增强喇曼谱有明显的不同.在正电性纳米银上,面外弯曲模式受到增强,而在负电性纳米银上,面内伸缩模式受到增强,通过分析增强谱的差异表明,分子在这两种不同电性胶态纳米银表面上可能分别以平躺及站立方式吸附.     

伪随机序列投影三维测量中的快速子序列匹配

提出了一种适用于伪随机序列投影三维测量技术的子序列匹配快速算法.首先根据源序列的内容及子串长度构造由多层子表组成的表格;然后根据子序列的内容,从首字符开始从左到右,依次从首层表格开始向下查找;最后得到子序列在源序列中的位置.即根据首字符在首层表格中查到对应的第二层表格地址,再在第二层表格中根据第二个字符,查找第三层表格地址.以此类推,查出最后一层表格的地址.在最后一层表格中,根据末字符查找到该子序列在源序列中的位置.给出了理论分析并进行了实验验证,结果表明,在目前主流的计算机上,对于典型场景采用查表法的子序列匹配速度较常用算法快60倍以上.     

Understanding formation of molecular rotor array on Au(111) surface

The motion of single molecules on surfaces plays an important role in nanoscale engineering and bottom-up construction of complex devices at single molecular scale. In this article, we review the recent progress on single molecular rotors self-assembled on Au(111) surfaces. We focus on the motion of single phthalocyanine molecules on the reconstructed Au(111) surface based on the most recent results obtained by scanning tunneling microscopy (STM). An ordered array of single molecular rotors with large scale is self-assembled on Au(111) surface. Combined with first principle calculations, the mechanism of the surface-supported molecular rotor is investigated. Based on these results, phthalocyanine molecules on Au (111) are a promising candidate system for the development of adaptive molecular device structures.     

Triangular Invariants, Three-Point Functions and Particle Stability on the de Sitter Universe

We study a class of three-point functions on the de Sitter universe and on the asymptotic cone. A blending of geometrical ideas and analytic methods is used to compute some remarkable integrals, on the basis of a generalized star-triangle identity living on the cone and on the complex de Sitter manifold. We discuss an application of the general results to the study of the stability of scalar particles on the de Sitter universe.     

EAST 4.6GHz ���Ӳ�����ˮ��ṹ������Ż�

设计了EAST 4.6GHz低杂波器件的一系列主动水冷冷却结构,阐述了直波导、波导弯头、天线单元的水冷结构设计,并使用有限元模拟软件ANSYS计算了这些部件的发热和对流冷却,计算并展示了部件上的温度分布二环结构变形。通过计算,优化直波导单面水冷结构为双面水冷。计算结果表明,立弯波导弯头的水冷结构明显好于侧弯弯头。原天线单元前端温度分布集中,热应力很大,不符合实验要求。优化后的天线单元前端的温升和热变形可以达到LHCD实验要求。     

颗粒物质中静摩擦力与接触面形状有关

用实验方法研究了探测棒在颗粒物质中受到的最大静摩擦力与棒截面形状的关系.观测到圆棒受到的最大静摩擦力最大,方棒次之,扁棒最小.根据力的传递原理,分析棒形状对颗粒物质内部力链传递的影响,计算结果与实验基本吻合.     

C---H bond activation of formate on clean and K-covered Ru(001): a theoretical study

An extended Hückel (EH) study is performed on the clusters representing a formate adsorbed on Ru(001) and on in order to investigate the effect of potassium on the selectivity of decomposition of formate on Ru(001). The adsorption geometry and the VSIP (valence state ionization potential) values of EH parameters are determined from ab initio calculations on small clusters. The EH calculation reproduces well the site preference of formate on each surface suggested from experiments. The C---H bond of formate, which is our focus in this study, is calculated to be almost the same on the two surfaces when the molecular plane of formate is perpendicular to the surface; but when the plane is tilted from the surface normal and thus the C---H bond approaches the surface, the C---H bond is weakened to a much higher extent on clean Ru(001) than on K-covered Ru(001). This is in good agreement with the experimental result that the presence of potassium changes the reaction pathway of the decomposition of formate on Ru(001) by suppressing C---H bond cleavage.     

重离子碰撞中的同位旋效应

根据近年来利用同位旋相关输运理论在中能重离子碰撞同位旋效应研究方面的成果 ,并结合国际上在该问题上的进展 ,综合介绍和分析了中能重离子碰撞中的多重碎裂、原子核阻止和前平衡发射中子-质子比的同位旋效应及其随入射道条件:入射能量、碰撞参数、碰撞系统的质量 ,特别是随中子-质子比的演化过程.讨论了利用以上物理观测量在提取同位旋非对称核物质状态方程知识方面的可能性 ,并对其发展进行了展望. Based on the achievements for the intermediate energy heavy ion collision in our recent work and the progresses in the world, the isospin effects and the dependence of the entrance channel conditions on them in the intermediate energy heavy ion collisions were introduced, analysed and commended. From the calculation results by using isospin dependence quantum molecular dynamics, it is clear to see that the nuclear stopping power strongly depends on the in medium isospin dependence...     

有限温度奇异夸克物质

本文简要介绍了近年来有限温度下奇异夸克物质的研究,包括早期宇宙中大块奇异夸克物质的研究;基于ＭＩＴ袋模型的ｓｔｒａｎｇｅｌｅｔ研究,以及运用质量密度相关模型对奇异夸克物质的研究,最后简略评述了关于奇异夸克物质性质的近期研究进展     

NH_x(x=1～3)在金属Ir表面吸附与解离的第一性原理研究

采用密度泛函理论,在slab模型下,研究了NH_x(x=1~3)在Ir(100)、Ir(111)和Ir(110)表面上的最稳定吸附位置、几何构型以及逐步脱氢分解过程,计算了相应的吸附能和活化能.计算结果表明,在Ir(100)、Ir(111)面上,NH_3是以C_3轴垂直吸附在顶位,在Ir(110)上,NH_3是以N-Ir键与表面成68.6°吸附在顶位,且吸附能依赖于表面的结构而不同,相比而言,NH_3更容易吸附在开放表面Ir(100)、Ir(110)面上,说明NH_3在这些表面的吸附具有结构敏感性.NH_(x(x=1~3))的分解,在Ir(100),NH_3的吸附与分解存在竞争,在Ir(110)面NH_3最容易分解,在Ir(111)面NH_3是分子性吸附,不能分解.NH_2、NH在三个表面均能够分解,在Ir(110)面活化能均较高.     

LEFT-INVARIANT PSEUDO-EINSTEIN METRICS ON LIE GROUPS

In this article, we focus on left-invariant pseudo-Einstein metrics on Lie groups. To begin with, we give some examples of pseudo-Einstein metrics on Lie groups. Also we calculate the Levi-civita connection, and then Ricci tensor associated with left-invariant pseudo-Riemannian metrics on the unimodular Lie groups of dimension three. Furthermore, we show that the left-invariant pseudo-Einstein metric on SL(2) is unique up to a constant. At last, we study the left-invariant pseudo-Riemannian metrics on compact Lie groups and classify the pseudo-Einstein metrics on the low-dimensional compact Lie groups.     

Calculation of geometries and chemisorption energies of adatoms on simple metals

We report results of calculations with a formalism that in principle applies quite generally for chemisorption on a real metallic substrate. Including the substrate structure within perturbation theory on a self-consistent jellium-plus-adatom calculation, we have computed the dependence of the binding energy of an adatom on the surface geometry. Specifically, in the case of hydrogen on Al, our model calculation predicts that the stable positions are bridge configurations on the (100) and (110) surfaces and atop positions on the (111) surface, and that they have almost the same heats of chemisorption (1.8–2.0 eV). For geometrical reasons the bridge configuration seems to be a reasonable result while the atop result for the (111) surface is more uncertain. Thus, chemisorption of H on Al should require predissociation of the H₂ gas. In addition, the predicted values for hydrogen desorption imply that measurements on H on Al surfaces should be performed at low temperatures to avoid desorption. Results for H on a jellium of Na density indicates that hydrogen should be absorbed in rather than adsorbed on Na metal.     

B、N、S掺杂石墨烯表面质子吸附的第一性原理研究

表面吸附是石墨烯中质子(H~+)输运的基础步骤.本文基于第一性原理计算研究了B、N、S掺杂对石墨烯表面H~+吸附行为的影响.结果表明,B、N、S掺杂对石墨烯的晶体结构、内聚能及电子性质有重要影响,且影响程度与掺杂元素的性质密切相关,进而导致对石墨烯表面H~+吸附行为产生不同程度的影响.从吸附能的观点看,N、B、S掺杂对石墨烯表面H~+的吸附有利.研究结果对石墨烯在氢贮存、氢同位素分离、燃料电池等领域的应用具有重要的指导意义.     

Piperidine adsorption on two different silver electrodes: A combined surface enhanced Raman spectroscopy and density functional theory study

The surface enhanced Raman scattering (SERS) spectra of piperidine in silver colloid solution, on roughened silver electrode and on roughened silver electrode modified with silver nanoparticles were studied, and the high-quality SERS spectra of piperidine on roughened silver electrode modified with silver nanoparticles were obtained for the first time. Surface selection rules derived from the EM enhancement model were employed to deduce piperidine orientations on the different surfaces. On the basis of this, two models of piperidine adsorbed on the surface of the silver nanoparticles were built, and DFT-B3PW91/LanL2dz was applied to calculate the Raman frequencies. It proves that, at higher potential values, the piperidine is perpendicularly standing on the roughened silver electrode surface though its lone-electron pair, but in silver colloid solution and on the silver nanoparticles modified silver electrode the piperidine molecular lies flat on the silver surface. In the meantime, the potential dependent SERS of piperidine on the modified electrode were studied.     

On the Lie Group of Projective Canonical Transformations

The transformation properties of the projective canonical group are considered. It is shown that the group acts transitiv on functions defined on configuration space but not transitiv on those defined on the phase space. We prove moreover that this group is the largest finite-dimensional Lie group of point transformations determined on the configuration space.     

Surface charge dynamics studied by the temporal evolution of the corona charging current

The decay of surface charges deposited on the dielectric material by the partial discharge (PD) activity has a great impact on the repetition of partial discharges. In this work, the effect of dielectric placed on the surface of ground electrode in a needle-plane configuration on the discharge activity was investigated, with the application of a periodic negative step voltage. The charge decay mechanisms on a corona charged dielectric surface were investigated based on a comparison between experiments and a FEM-based numerical model. The comparison indicates that the surface charges may decay due to different mechanisms depending on the applied stress.