Sputtering of metals at ion-electron irradiation

It has been found that, in contrast to the commonly accepted opinion, simultaneous irradiation by 15-keV Ar⁺ ions and 2.5-keV electrons at temperatures above 0.5T _m (T _m is the melting temperature) induces much larger sputtering of metallic copper, nickel, and steel than irradiation only by Ar⁺ ions. The effect increases with the temperature. At T = 0.7T _m, the sputtering coefficients in the case of ion-electron irradiation are more than twice as large as the sputtering coefficients in the case of irradiation by Ar⁺ ions. The experiments on the sublimation of copper show that the sublimation rate in the case of the heating of a sample by an electron beam is higher than that in the case of heating in an electric vacuum oven. The revealed effects are explained by the electron-induced excitation of adatoms (atoms stuck over the surface, which appear owing to ion bombardment). Excited adatoms have a smaller binding energy with the surface and are sputtered more easily.     

Surface self-diffusion studied by microscopic measurements of crystallite profile evolutions

Dendritic gold crystallites on graphite are heated in ultra high vacuum up to less than 0.5 of the melting point (T_m). Electron microscopy shows that the gold crystallites change their shapes by surface self-diffusion. The dendritic contours round off while the crystallite remains very flat (20 to 40 Å). The increase with time of the radii of dendrite tips is measured statistically. Such an evolution can be described by analogy to the blunting of either metal tips (Nichols and Mullins) or monoatomic cleavage tips (Höche and Bethge). Using this result, a new technique to measure surface self-diffusion coefficients (D) is proposed. Test measurements have shown that this is an interesting, very sensitive method to measure D (down to 10^?13 cm^?2 s^?1) which enables measurements to be made in an unusual low temperature range (0.25 T_m < T < 0.5T_m). In special cases the dendrites are split by the surface self-diffusion which is qualitatively in agreement wih the theory.     

Mechanism of 3He-mediated nuclear spin-lattice relaxation at surfaces

We measured the nuclear spin-lattice relaxation time T₁, of several surface-bound nuclei, ¹H, ¹⁹F, ¹¹B, ¹³C, ²⁹Si, and ²H, immersed in liquid ³He over the temperature range 0.01 K ⩽ T < 1 K. The Larmor frequencies of these nuclei in a 3.39 T field extended from 22 to 144 MHz. All T₁ values were temperature-independent and ranged from a few seconds to several hours, depending on the particular nucleus and the surface geometry of the sample. The results indicate that the coupled relaxation of surface spins is a phenomenon occurring in all solids immersed in ³He and thus provides a general mechanism for obtaining high nuclear polarization in solids, that the relaxation is controlled by direct dipole-dipole interactions between the surface spins and ³He in the first surface layer, that the ³He motion dynamics do not change appreciably from one surface to another, and that measurements of T₁ may thus be useful for determining the structure of surfaces.     

On viscous mechanism for surface diffusion at high temperatures (T/Tm > 0.75) due to formation of a 2D dense fluid on metallic surfaces

Experimental determinations of temperature dependence of surface self-diffusion coefficient of several metals exhibit a strong increase in D_s values and in activation energy for temperatures near the melting point T_m. This variation is illustrated by a bending of the Arrhenius plot of surface self-diffusion coefficients of tungsten, which are obtained experimentally by tip profile variation technique. For T/T_m < 0.75 the apparent activation energy for W is 2.85 eV and the pre-exponential term is equal to 0.24 cm²/s, while for T/T_m > 0.75 we have respectively 5.57 eV and 1.08 × 10⁴ cm²/s. To account for these unexpected variations in the activation energy and diffusivities, the hypothesis that the surface mass transport mechanism changes from individual atomic jumps at low temperatures towards a cooperative motion at temperatures near the bulk melting point, namely a viscous mechanism, is proposed. This model is based on the postulation of the formation of a 2D dense fluid on the metallic surfaces about 75% of the bulk melting temperature. Discussions of existing models on surface diffusion proposed by Rhead, by Bonzel, or by Tsong are given, and a technique to characterize surface viscosity of a 2D dense fluid is suggested.     

Possible mechanism of superconductivity in the CuO-Cu interface

Apparently, a two-dimensional CuO lattice is formed on the surface of copper oxide in the CuO-Cu interface. This lattice consists of Cu²⁺ and O^1? ions, which form a narrow, partially filled two-dimensional band. In this case, local electron pairs (LEPs) can form in the oxygen subsystem as a result of the fulfillment of the Shubin-Vonsovskii conditions. A crude estimate of the formation temperature of LEPs gives T* ～ 10 4 K. At the concentration in the interface layer n～1.6×10²⁰ cm^?3 and the effective mass of carriers m* ～ m _e, the onset temperature of Bose-Einstein condensation may take a value of T _c ～ 1000 K. The estimate obtained for the temperature T _c corresponds to the experimental value by an order of magnitude.     

Comment on “variable range hopping in Si:P at very low temperature” surface conduction in Si:P

The electrical resistivity of doped semiconductor Si:P in the intermediate concentration range was measured under various surface conditions. The surface treatments are shown to have a great influence upon the low temperature electrical conduction, and T^-2-like temperature dependence of resistivity is attributed to the surface layer electrical conduction.     

Brillouin and raman scattering studies of the melting transition in salol

Brillouin and Raman scattering studies of salol from room temperature to within 5 mK of the melting transition at T_m = 40.97°C are reported. Changes in the Brillouin shifts and linewidths were accurately determined by nonlinear least-squares fitting and deconvolution. A marked increase in the deconvoluted Brillouin linewidth (~400%) and a gradual softening (~20%) of the transverse acoustic modes were observed very close to T_m. The increase of the Brillouin linewidths was analyzed by a simple dislocation model assuming the hypersonic attenuation to be proportional to the concentration of thermally generated defects near T_m. The defect formation energy E_D(T) was computed from the temperature-dependent linewidth data, and was found to decrease significantly (~60%) near T_m, suggesting a cooperative effect producing a catastrophic growth of defects which brings about melting by destroying the long range order of the crystal. The conclusion that melting is mediated by a sudden growth of defect concentration near T_m was further strengthened by Raman scattering experiments in which 13 new Raman modes appeared close to T_m. These new modes are believed to be defect activated through breaking of the local symmetry of the crystal. A slight softening of the Raman modes (~5%) was observed close to the melting point.     

Thermodynamics of SU(3) lattice gauge theory

The pressure and the energy density of the SU(3) gauge theory are calculated on lattices with temporal extent N_τ = 4, 6 and 8 and spatial extent N_σ = 16 and 32. The results are then extrapolated to the continuum limit. In the investigated temperature range up to five times T_c we observe a 15% deviation from the ideal gas limit. We also present new results for the critical temperature on lattices with temporal extent N_τ = 8 and 12. At the corresponding critical couplings the string tension is calculated on 32⁴ lattices to fix the temperature scale. An extrapolation to the continuum limit yields T_c/√σ = 0.629(3). We furthermore present results on the electric and magnetic condensates as well as the temperature dependence of the spatial string tension. These observables suggest that the temperature dependent running coupling remains large even at T ≅ 5T_c. For the spatial string tension we find √σ_s/T=0.566(13)g²2(T) with g² (5T_c) ≅ 1.5.     

Surface energies of metals in both liquid and solid states

Although during the last years one has seen a number of systematic studies of the surface energies of metals, the aim and the scientific meaning of this research is to establish a simple and a straightforward theoretical model to calculate accurately the mechanical and the thermodynamic properties of metal surfaces due to their important application in materials processes and in the understanding of a wide range of surface phenomena. Through extensive theoretical calculations of the surface tension of most of the liquid metals, we found that the fraction of broken bonds in liquid metals (f) is constant which is equal to 0.287. Using our estimated f value, the surface tension (γ_m), surface energy (γ_SV), surface excess entropy (−dγ/dT), surface excess enthalpy (H_s), coefficient of thermal expansion (α_m and α_b), sound velocity (c_m) and its temperature coefficient (−dc/dT) have been calculated for more than sixty metals. The results of the calculated quantities agree well with available experimental data.     

Spin correlations in Ni-Mn-Ga

Results of measuring small-angle neutron scattering and neutron depolarization in a Ni_49.1Mn_29.4Ga_21.5 single crystal in the temperature range 15<T<400 K and in the range of magnetic fields 0<H<4.5 kOe are presented. The characteristic temperatures of the alloy were found to be as follows: T _C=373.7 K and the martensite transition temperature T _m=301–310 K. The magnetic critical scattering at T _C and the scattering at T<T _C were adequately described by the relationship I _m=A(q ²+κ²)^?2 (q is the transferred wave vector and R _c=1/κ is the correlation radius), and the temperature dependences of the A and R _c scattering parameters were determined. Left-right asymmetry was observed at 150<T< T _m in the scattering of neutrons polarized along or opposite to the applied field. This asymmetry was due to the inelastic magnetic interaction of neutrons in the sample. The magnetization of the alloy at T _m, critical scattering at T?T _C, anomalies in scattering, and the softening of magnetic excitations at 150 <T<T _m are discussed.     

Void formation in Nickel during high temperature proton irradiation

Pure Ni foils, doped with He from 0 to 28 appm, were irradiated with protons at temperatures in the range 0.3–0.6 T_m (T_m = melting point in °K) and void formation was studied. The influence of He doping, irradiation temperature and alloying were investigated. For constant He content and proton fluence, void number density and swelling are maximum at about 400°C, while the void size increases with temperature. Most voids are octahedral in shape with no sign of truncation. Helium is required to nucleate voids, and lowering the stacking fault energy by alloying suppresses void formation completely. Present results suggest that void nucleation is inhomogeneous. Some implications of these findings are discussed.     

Molecular binding states on clean and oxidized surfaces: SiO(g) + W(clean) and SiO(g) + W(oxidized)

The interactions between a molecular beam of SiO(g) and a clean and an oxidized tungsten surface were examined in the surface temperature range 600 to 1700 K by mass spectrometrically determined sticking probabilities, by flash desorption mass spectrometry (FDMS) and by Auger electron spectroscopy (AES). The sticking probability, S, of SiO has been determined as a function of coverage and of surface temperature for the clean and the oxidized tungsten surface. Over the temperature range studied and at zero coverage S = 1.0 and 0.88 for the clean and oxidized tungsten surfaces respectively. The results are consistent with both FDMS and AES. For coverage up to one monolayer there is one major adsorption state of SiO on the clean tungsten surface. FDMS shows that T_m = constant (T_m is the surface temperature at which the desorption rate is maximum) and that desorption from this state is described by a simple first order desorption process with activation energy, E_d = 85.3 kcal mole^?1 and pre-exponential factor, ν = 2.1 × 10¹⁴ sec^?1. AES shows that the 92 eV peak characteristic of silicon dominates. In contrast on the oxidized tungsten surface, T_m shifts to higher temperatures with increasing coverage. The data indicate a first order desorption process with a coverage dependent activation energy. At low coverage (θ ? 0.14) there is an adsorption state with E_d = 120 kcal mole^?1 and ν = 7.6 × 10¹⁹, while at θ = 1.0, E_d = 141 kcal mole^?1. This variation is interpreted as due to complex formation on the surface. AES shows that on oxidized tungsten, in contrast to clean tungsten, the dominant peaks occur at 64 and 78 eV, and these peaks are characteristic of higher oxidation states of silicon. Thus, it is concluded that SiO exists in different binding states on clean and oxidized tungsten surfaces.     

Surface free energies of solid metals: Estimation from liquid surface tension measurements

An equation is derived on semi-theoretical grounds which expresses the solid-vapour surface free energy as a function of the liquid surface tension and the solid-liquid interfacial free energy. A means of calculating reliable values for the solid-liquid energy is presented, which then allows an accurate estimate of solid surface energy at the melting temperature, T_m, to be made for the large number of elements for which dependable liquid surface tension data exist. A method of estimating surface entropy is presented, and has been used to calculate the energies typical of “average”, high-index surfaces at temperatures ranging from 0 K to T_m. It is felt that this paper describes the most accurate method presently available for the calculation of the surface energy of solids in the absence of direct experimental measurement.     

Microstructural evolution of pure copper during friction-stir welding

The microstructural evolution of pure copper during friction-stir welding was found to be principally influenced by welding temperature. At temperatures below ~0.5 T_m (where T_m is melting point), the microstructure was shown to be essentially determined by continuous recrystallization, leading to significant grain refinement and related material strengthening in the stir zone. In contrast, grain structure development at temperatures above ~0.5 T_m was dominated by discontinuous recrystallization producing a relatively coarse grain structure in the stir zone and giving rise to material softening.     

Anomalous nuclear spin relaxation in liquid 3He4He mixtures

The longitudinal relaxation time, T₁, was measured in liquid ³He⁴He mixtures with molar concentrations of ³He of 0.12, 0.20 and 0.45 under saturated vapor pressure. λ-anomaly was clearly observed in the temperature dependence of T₁.     

Properties of the superconducting state in molecular metallic hydrogen under pressure at 347 GPa

The thermodynamic properties of the superconducting state induced in metallic molecular hydrogen under the influence of pressure 347 GPa were determined. In particular, it has been shown that the critical temperature (T_C) changes in the range from 120 to 90 K for μ^?∈〈0.08,0.15〉, where μ^? is the value of the Coulomb pseudopotential. Next, the energy gap near the temperature of zero Kelvin (2Δ(0)) was calculated. It has been stated, that the dimensionless ratio 2Δ(0)/k_BT_C slightly decreases with the increase of μ^? from 3.98 to 3.84. In the last step, the ratio of effective electron mass (m^?_e) to the bare electron mass (m_e)) was determined. It has been proved that m^?_e/m_e takes its highest value equal to 1.96 for T=T_C.     

Ni-15%Mo合金熔体热物理性质的Monte Carlo模拟

采用EAM势对6×6×6的Ni-15%Mo合金熔体进行Monte Carlo模拟,通过对不同温度下获得的NVT系统的平衡态统计分析得出Ni-15%Mo合金熔体在过冷态和过热态时的热物理性质.通过构造系统生成新表面,表面张力做功使系统能量发生改变,从而得到液态表面张力的模拟结果.Ni-15%Mo合金熔体的表面张力在1500—2000 K的温度范围内,随温度的变化规律为σ=1.918-1.130×10^-3（T-T_m） N/m 关键词： Monte Carlo模拟 表面张力 比热 Ni-15%Mo合金     

Nuclear acoustic resonance of V51 in a single crystal of V3Si above and below the martensitic transformation

The EFG and the Knight shift anisotropy of V⁵¹ in a single crystal of V³Si have been measured both above and below the martensitic transformation temperature T_m, using the nuclear acoustic resonance technique. Deviations of the axial symmetry of the EFG tensor have been found below T_m. The orientation of the tetragonal c axis in the crystal is also given.     

Measurements of surface relaxation time of solid,liquid and adsorbed 3He in porous glasses

The surface relaxation time T_ls has been investigated in solid, liquid and adsorbed ³He in porous glasses for a wide frequency range by using pulsed SQUID-NMR. ALL T_ls agreed with each other and were proportional to the frequency at least at low frequencies. A model is proposed to explain the above results of T_ls.     

Dislocation structure of copper single crystals in high-temperature creep test

It has been shown that in the high-temperature creep test at 0·85 kp mm^?2 and 0·7T _m (T _m is the melting temperature in °K) the dislocation substructure of copper single-slip oriented crystals is formed practically at the early stage of the test. The subsequent changes of substructure consist in the growth of subgrain misorientation and in the transformation of tangled subgrain boundaries into regular dislocation networks. There is a pronounced tendency to the formation of subboundaries in the {111} and {110} planes.