Dynamics of the infinite-range ising spin glass

The Glauber dynamics of an Ising spin glass with infinite-range interactions and additional static field, h, is investigated near the freezing temperature, T_f. We obtain critical slowing down at and below the de Almeida-Thouless instability line, h_c(T), to order (1?T/T_f)³ with algebraic decay of the spin correlations ～t^?ν, where $\text{ν=}\text{1}\text{2}$ at T_f and $\text{ν≤}\text{1}\text{2}$ for T<T_f.     

Electrical fluctuations in normal metal point-contacts

The low-frequency electrical fluctuations are measured for point-contacts of Cu, Ag, and Au, the contact diameter being less than the electron mean free path. The $\text{1}\text{?}$ spectral density and a nonmonotonic (oscillating) dependence of r.m.s. noise voltage, V_N, on the d.c. bias, eV, are found. The positions of minima in the V_N(eV) curves are in certain connection with the characteristic phonon energies of metals studied. The phenomenon is attributed to the coherent phonon emission by hot electrons moving along the contact axis.     

Polarization dependent reflectivity and optical constants of single crystal rutile RuO2 in the range 0.5 to 9.5 eV

We have measured the near-normal incidence reflectivity of single crystal RuO₂ (rutile) for $\text{E}$ 6 $\text{c}$-axis and $\text{E}$ ⊥ $\text{c}$-axis at room temperature in the photon energy range 0.5 – 9.5 eV. From a Kramers-Kronig analysis of the reflectivity we have obtained the spectral dependence of the real, ?₁(ω), and imaginary, ?₂(ω), parts of the complex dielectric constant. Comparison with recent band structure and density of states calculations and past experimental studies of related solids has enabled us to gain further insight into the nature of the oxygen $\text{p}$-electrons and metal $\text{d}$-electrons in this material.     

Semiconductor-metal transition in doped (CH)x: Thermoelectric power

Thermoelectric power studies of polyacetylene have been carried out as a function of dopant concentration and temperature. The thermopower of pure trans-(CH)_x is large $\text{(S =}\text{+850 μ V}\text{°K}\text{)}$ and positive consistent with p-type material. With iodine doping, (CHI_y)_x, the thermopower remains positive over the full range of concentration 0 < y < 0.22. The semiconductor-metal transition is clearly observed at n_c ? 3 mole %; S falls dramatically from $\text{S =}\text{+850 μ V}\text{°K}$ at y = 0.003 to $\text{S =}\text{+30 μ V}\text{°K}$ at y = 0.03. At higher concentrations, S remains nearly constant saturating at $\text{+18 μ V}\text{°K}$ in the heavily doped metallic polymer. Temperature dependences are consistent with metallic behavior at the highest dopant concentrations and hopping transport in the undoped and lightly doped polymer.     

On the order of levels in charmonium

We prove a theorem concerning the energies of the 2S and 3D states in a potential $\text{V(r) =}\text{?g}{}^2\text{r}\text{+ V}{}_{\mathrm{<mtext>c</mtext>}}\text{(r)}$, where V_c is a non-singular confining potential. If $\text{(}\text{d}\text{d}\text{r)}{}^3\text{(r}{}^2\text{V}{}_{\mathrm{<mtext>c</mtext>}}\text{)}$ is positive, then the 3D state lies above the 2S state, provided

$\text{d}\text{d}\text{r}\text{1}\text{r}\text{d}\text{d}\text{r}\text{2V}{}_{\mathrm{<mtext>c</mtext>}}\text{+r}\text{d}\text{V}{}_{\mathrm{<mtext>c</mtext>}}\text{d}\text{r}\text{< 0, ?}{}_{\mathrm{r}}\text{>0.}$

For V_c = r^α, this corresponds to 0 < α < 2.     

A non-coulombic effective power-law potential for the heavy quarkoniums

An effective power-law potential of the form V(r) = 6.08 r^0.106?6.41 is found to describe satisfactorily the gross features of the mass spectra and the leptonic width ratios of the c$\text{c}$ and b$\text{b}$ systems in a flavour-independent manner.     

Field dependence of a.c. Electroluminescence in ZnS: Mn,Cu, Cl film panels

Electroluminescent (EL) film panels of ZnS: Mn, Cu, Cl operated by a.c. electric field are studied at room temperature. The emission spectrum consists of a single peak at 590 nm. The EL emittance B varies with frequency f of the applied a.c. electric field as B = B_s ? B_m exp ? f/f_c where B_s, B_m and f_c are constants. This equation indicates that B approaches a saturation value B_s when f?f_c and a linear relation between B and f when f?f_c. At a fixed frequency f, B is found to depend on the applied voltage V as B = A exp [-G/F + V^{$\text{1}\text{2}$})] where A, G and F are constants. This formula is valid at all stages of the operating life of the film panel.     

Effects of composition on the upper critical field of V-Ga

Measurements of the temperature dependence of the upper critical field, H_c2(T), for a series of V_100?xGa_x materials are presented for 20.5 ≤ × ≤ 29.6. Fits of the data to conventional theory for a paramagnetically limited, dirty, type II superconductor show: 1) a maximum in T_c and H_c2(0) for x ? 25; 2) a constant ( for x ≤ 25; 3) a slowly increasing value of λ_so with increasing x up to x ～ 25; and 4) good agreement with stoichiometric ordered and thermally disordered V₃Ga. Above $\text{x ? 25}$ broader transitions are observed. For x = 25, T_c = 15.3 K, (, λ_so = 0.3 and H_c2(0) = 23.4 tesla. The effects of inclusion of strong-coupling in the theory are discussed briefly.     

The pair distributions and the osmotic coefficient in anomalous electrolytes up to concentrations c≈ 1 mol/1

The osmotic coefficient of anomalous electrolytes up to concentrations c ≈ 1 mol/l is explained by the pair distributions $\text{n(r) =}\text{exp}\text{[-β(}\text{V}{}_{\mathrm{c}}\text{(r) + V(}{}^{\mathrm{hs}}\text{)(r) + V}{}_1\text{(r))]}$. Here $\text{V}$_c(r) is a screened Coulomb potential, V(^hs)(r) a hard sphere potential and V₁(r) = ?A/r⁶ a short range attractive potential. For the contact distances R₊₊, R_?? and R_+? of the hard sphere potentials between ions with the same sign of their charges (++,??) and ions of opposite charges (+?) the relations R₊₊ = R_?? = R and R_+? = q₁R with 0 < q₁ < 1 are assumed. In contrast to a previous paper the parameter q₁ takes a fixed value q₁ ≈ 0,8. The constant A is determined by the fraction q₂ defined by A/R⁶ = q₂(Z²e²/DR) where the positive integer Z is the charge number of the ions and D the dielectric constant of the solvent. The numerical calculation of the osmotic coefficient of 1-1-valent hydrous electrolytes in the range of temperature 273 K ? T ? 293 K shows that the anomalous electrolytes are described by fractions q₂ in the range 0,25 ? q₂ ? 0,5 if the contact distances R are in the range $\text{3}\text{A}\text{?}\text{? R ? 7}\text{A}\text{?}$.     

Energy levels of interstitial manganese in silicon

Interstitial manganese in silicon can exist in four charge states which imply single acceptor and double donor behaviour. The corresponding level scheme with the acceptor level ($\text{Mn}{}^{\mathrm{<mtext>?</mtext><mtext>0</mtext>}}$) at E_c-0.13eV, the first donor level ($\text{Mn}{}^{\mathrm{<mtext>0</mtext><mtext>+</mtext>}}$) at E_c?0.45eV and the second donor level (Mn^+/++) at E_v+0.30eV is established through EPR-controlled Hall measurements. Another deep donor level at E_c?0.54eV is produced by the donor acceptor pair (MnB) whereas a more shallow one around E_c-0.28eV was already attributed to a Mn₄-cluster.     

One-dimensional magnetism in N2H6FeF5,

A new Fe(III) fluoride N₂H₆FeF₅ has been investigated by magnetic susceptibility measurements and Mössbauer resonance. It has a one-dimensional magnetic behaviour. The intrachain exchange integral ($\text{J}\text{k}\text{= -10.2}\text{K}$) has been determined by fitting the χ^-1 = f(T) curve and the ratio between the inter- and intrachain exchange integrals evaluated with Oguchi's formula. Below T_N = 9 K, N₂H₆FeF₅ shows a long range three-dimensional anti-ferromagnetic ordering.     

Positive cones in enveloping algebras

The concept of strong ordering on enveloping algebras of finite-dimensional Lie algebras is introduced and studied as a generalization of the corresponding notion for the commutative polynomial algebra. A linear functional f on an enveloping algebra $\text{E}$ (G) is called strongly positive if f(x) ? 0 for all x ? $\text{E}$(G) which are mapped on positive operators for all G-integrable irreducible representations of $\text{E}$(G). We prove that for each real connected Lie group G ≠ R₁ there are positive, not strongly positive, linear functionals on $\text{E}$(G). A non-commutative problem of moments is defined. It has a solution iff the corresponding linear functional is strongly positive.     

Exact saturation and degeneracy of isospin bounds and zeros trajectories in pion-nucleon scattering: D. B. Ion. Joint Institute for Nuclear Research,Dubna, Moscow,P. O. Box 79, U.S.S.R.

By exploiting the analogy between the classical equation of heat conduction and the Bloch equation, the canonical density matrix is calculated exactly for noninteracting electrons in a finite step model of a metal surface. This result is then used to calculate the spatial variation of the electron density ?(z) as a function of distance z from the planar metal surface. In particular an expansion in inverse powers of $\text{V}{}^{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}$ and V, V being the step height, is derived. The low-order terms are used to compute the electron density at the surface of Al metal: There is good agreement with a full numerical evaluation. Finally, in the limit $\text{V}\text{E}{}_{\mathrm{f}}\text{→ ∞}$, E_f being the Fermi energy, the change in the shape and size of the exchange (Fermi) hole surrounding an electron is studied as the electron moves into the vicinity of a metal surface. The anisotropy of the Fermi hole is large and the implications for one-body potential theory are briefly discussed.     

A small parameter in the 1Nc expansion and narrowness of hadronic resonances

The dynamical basis for the validity of the $\text{1}\text{N}{}_{\mathrm{c}}$ expansion is investigated in the context of QCD in 1 + 1 dimensions. This is carried out by studying the first non-leading corrections in $\text{1}\text{N}{}_{\mathrm{c}}$ to the mass operator in the space of physical states. The correction to the real part of the mass operator has a direct implication for the convergence of the $\text{1}\text{N}{}_{\mathrm{c}}$ expansion, since a small effective parameter is identified, where its smallness depends on the dynamical circumstances in a known way. The generated imaginary part of the mass operator provides us with an insight concerning the question of the narrowness of hadronic resonances. In order to have a more realistic contact with our world, we include also effects due to the flavor symmetry group SU(N_f). This allows us to understand better the validity and usefulness of the notions of resonance dominance and (smooth) Regge behavior. We also discuss the expansion with $\text{N}{}_{\mathrm{f}}\text{N}{}_{\mathrm{c}}$ fixed and compare the results with those obtained from Dual Resonance Model. It is remarked that a nonuniformity exists between the limits N_c → ∞, N_f = fixed and N_c → ∞, $\text{N}{}_{\mathrm{f}}\text{N}{}_{\mathrm{c}}\text{=}\text{fixed}$, which may affect physical quantities.     

A Mössbauer study of amorphous Fe40Ni40B20

Amorphous Fe₄₀Ni₄₀B₂₀ (VITROVAC 0040) alloy has been investigated using ⁵⁷Fe Mössbauer Spectroscopy. The Curie temperature T_c is found to be well defined and is 695 ± 1 K. The quadrupole splitting just above T_c is 0.64 mm sec^?1. The crystallization temperature is 698 ± 2 K, close to but definitely above T_c. The average hyperfine field H_eff(T) of the glassy state shows a temperature dependence of $\text{H}{}_{\mathrm{<mtext>eff</mtext>}}\text{(0)[1 ? B}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}\text{(T/T}{}_{\mathrm{c}}\text{)}{}^{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}\text{? C}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}\text{(T/T}{}_{\mathrm{c}}\text{)}{}^{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}\text{? …]}$ indicative of the existence of spin wave excitations. The values of $\text{B}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}$ and $\text{C}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}$ are found to be 0.40 and 0.06, respectively, for T/T_c ? 0.72. At temperatures close to T_c, H_eff(T) varies as (1 ? T/T_c)^β where β is one of the critical exponents and its value is found to be 0.29 ± 0.02.     

Deviations from statistical site occupancy in substituted RE2Co17

A neutron diffraction study of polycrystalline Y₂(Co_0.31Fe_0.69)_19.2 in the R$\text{3}$m phase shows the existence of a non-statistical distribution of Fe on the transition metal sites. Fe prefers the 6c sites but avoids the 18f sites. The preferential occupation in 1:5 and 2:17 compounds is shown to be determined by the nearest neighbour number and separation. The influence of the phenomenon upon the cell parameters and magnetic anisotropy is commented upon.     

Pulsed excitation of luminescence in dihydrated oxalic acid

Luminescence has been excited by an a.c. electric field in oxalic acid dihydrate at temperatures 273, 283 and 293 K. The voltage and frequency dependence of the emitted light flux has been studied. The brightness (B) has been observed to increase with voltage (V_rms) and frequency (v). The relation b = b₀ exp(-b/V^{$\text{1}\text{2}$_rms)} describes the voltage dependence of brightness quite accurately at frequencies greater than 500 Hz. The brightness wave forms at different voltages and frequencies of the applied field have also been studied. One primary and one secondary peak have been observed in each half cycle of the applied sinusoidal voltage.     

Core-level reflectance spectroscopy of germanium by means of synchrotron radiation

Reflectance spectra due to 3d core-levels of Ge have been measured in the photon-energy region from 29 to 38 eV by means of synchrotron radiation. Second-energy-derivative spectra have newly shown pairs of doublet structures with energy separation of the Ge $\text{3d}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}\text{?}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}$ core-level splitting. The observed doublet structures are assigned to the transitions from the $\text{3d}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}$ and $\text{3d}{}_{\mathrm{<mtext>3</mtext><mtext>2</mtext>}}$ core-levels to the flat regions of the conduction band around the particular symmetry points of Δ₆^c and L(₃^c(L₆^c, L_4,5^c).