Wei Hua’s four-parameter potential: Comments and computation of molecular constants αe and εeXe

The value of adjustable parameterC in the four-parameter potentialU(r) =D _e [(1 - exp[-b(r -r _e)])/(1 -C exp[-b(r -r _e)])]² has been expressed in terms of molecular parameters and its significance has been brought out. The potential so constructed, withC derived from the molecular parameters, has been applied to ten electronic states in addition to the states studied by Wei Hua. Average mean deviation for these 25 states has been found to be 3.47 as compared to 6.93, 6.95 and 9.72 obtained from Levine, Varshni and Morse potentials, respectively. Also Dunham’s method has been used to express rotation-vibration interaction constant (α_e) and anharmonicity constant (ω_ex_e) in terms ofC and other molecular constants. These relations have been employed to determine these quantities for 37 electronic states. For α_e, the average mean deviation is 7.2% compared to 19.7% for Lippincott’s potential which is known to be the best to predict these values. Average mean deviation for (ω_ex_e) turns out to be 17.4% which is almost the same as found from Lippincott’s potential function.     

Universal relation between spectroscopic constants

A universal relation between the Sutherland parameter, Δ (= k _e r _e ^/2 /2D _e) and the dimensionless parameter G (= 8ω _e x _e /B _e ), has been established using 40 electronic states, which include ground as well as excited states of polar and non-polar molecules. This relation is used to predict the dissociation energy of four lowest electronic states of S ₂ molecule. The respective values for the states X ³Σ _g ^/− , a ¹Δ _g , b ¹Σ _g ^/+ and B ³Σ _u ^/− turn out to be 36557, 31431, 28247 and 13429 cm⁻¹, and are in good agreement with the experimental values. Furthermore, metastable states a ¹Δ _g and b ¹Σ _g ^/+ of S ₂ are shown to dissociate into ³ P ₁ + ³ P ₁ as against the dissociation of X ³Σ _g ^/− into ³ P ₂ + ³ P ₁. In addition, a relation between Sutherland parameter Δ and internuclear distance r _e , viz., Δ=2.2r _e has been obtained for the ground state of alkali diatomic molecules.     

Large Deviations for the Fermion Point Process Associated with the Exponential Kernel

For the fermion point process on the whole complex plane associated with the exponential kernel , we show the central limit theorem for the random variable ξ(D _r , the number of points inside the ball D _r of radius r, as r → ∞ and we establish the large deviation principle for the random variables {r ⁻²ξ (D _r ), r > 0}.     

Pseudovector heavy quarkonia in e + e −2 collisions

It is shown that BR(χ _b1(1 P)→e ⁺ e ⁻)≃3.3· 10⁻⁷ and BR(χ _c1(1 P)→e ⁺ e ⁻)≃10⁻⁸. This gives realistic possibilities for searching for the production of χ _b1(1 P) and ξ _c1(1 P) states in e ⁺ e ⁻ collisions, even on the present-day colliders, to say nothing of b and c-τ factories. Pis’ma Zh. éksp. Teor. Fiz. 63, No. 8, 569–574 (25 April 1996)     

Intensity distribution in the bands of theD 1Π →X 1Σ+ system of SnO

Relative integrated intensities of the bands of theD ¹Π →X ¹Σ⁺ system of SnO have been measured by the technique of heterochromatic photographic photometry. Using the Rydberg-Klein-Rees Franck-Condon factors andr-centroids, the variation of electronic transition momentR _e with the internuclear separationr is found to beR _e (r)=const. (0.564r−1) in the range of 1.865 A≤r≤2.041A. The relative band strengths are derived. Effective vibrational temperature of the source is found to be 2559 K.     

Comment on: “Universal relation between spectroscopic constants”

Kaur and Mahajan [1] have claimed to derive a universal relation InG = 1.91578(±0.09727) + 0.97111(±0.03809) In Δ between the Sutherland parameter Δ(=ω _er _e ² /2D_e) and the dimensionless parameterG(= 8ω _ex_e/B_e) for the ground as well as excited electronic states of diatomic molecules. Validity of this relation is checked and we find that the relation is not correct. Next, we checked the validity of the relation Δ = 2.2r_e for the alkali group diatomic molecules. This relation is also found not to be correct.     

Hypervirial perturbation theory for eigenenergies for two types of atomic potentials

Eigenenergies are calculated for the potentialsV ₁(r)=−(a/r)[1+(1+br)e^−2br ] andV ₂(r)=−(v/r)[1 −λr(1−Z ⁻¹)(1+λr)⁻¹], using renormalized series technique. Accurate results produced here for various eigenstates agree with those available in the literature.     

Possible molecular states of D*s[`(D)]*sD^{*}_{s}\bar{D}^{*}_{s} system and Y(4140)

The interpretation of Y(4140) as a D^*_s[`(D)]<sup>*</sup><sub>s</sub>D^{*}_{s}\bar{D}^{*}_{s} molecule is studied dynamically in the one boson exchange approach, where σ, η and φ exchange are included. Ten allowed D<sup>*</sup><sub>s</sub>[`(D)]^*_sD^{*}_{s}\bar{D}^{*}_{s} states with low spin parity are considered, and we find that the J ^PC =0⁺⁺, 1⁺⁻, 0⁻⁺, 2⁺⁺ and 1⁻⁻ D^*_s[`(D)]<sup>*</sup><sub>s</sub>D^{*}_{s}\bar{D}^{*}_{s} configurations are most tightly bound. We suggest that the most favorable quantum numbers are J <sup>PC</sup> =0<sup>++</sup> for Y(4140) as a D<sup>*</sup><sub>s</sub>[`(D)]^*_sD^{*}_{s}\bar{D}^{*}_{s} molecule; however, J ^PC =0⁻⁺ and 2⁺⁺ cannot be excluded. We propose to search for the 1⁺⁻ and 1⁻⁻ partners in the J/ψ η and J/ψ η′ final states, which is an important test of the molecular hypothesis of Y(4140) and the reasonability of our model. The 0⁺⁺ B^*_s[`(B)]^*_sB^{*}_{s}\bar{B}^{*}_{s} molecule should be deeply bound; experimental search in the ϒ(1S)φ channel at Tevatron and LHC is suggested.     

Excess 1/f noise in systems with an exponentially wide spectrum of resistances and dual universality of the percolation-like noise exponent

The excess 1/f noise in a random lattice with bond resistances r∼exp(−λx), where x is a random variable and λ≪1, is studied theoretically. It is shown that if the correlation function {δr ²}∼r r ^θ+2, then the relative spectral density of the noise in the system is expressed as C _e∼λ^m exp(−λ(1−p _c)), where p _c is the percolation threshold and m=νd (ν is the critical exponent of the correlation length and d is the dimensionality of the problem). It is hypothesized that the exponent m possesses a dual universality: It is independent of 1) the geometry of the lattice and 2) the θ-mechanism responsible for the generation of the local noise. Numerical modeling in a three-dimensional lattice gives m=52.3 for θ=1 and θ=0, in agreement with the hypothesis. Pis’ma Zh. éksp. Teor. Fiz. 63, No. 8, 614–618 (25 April 1996)     

Cross sections and other parameters ofe − − H2O scattering (E i⩾50 eV)

Our previous theoretical work one ⁻ − H₂O scattering has been modified and extended to intermediate and high energiesE _i. Using the Bethe plot, we compare the present inelastic cross-sections with the experimental ionization cross sections. Total cross-sections are analytically represented asQ _TOT(cm²)=a.(E _ieV) ^−b and the parameters ‘a’ and ‘b’ are discussed for molecules H₂O, NH₃ and CH₄ in the rangeE _i=100–1000eV.     

Bound states and critical behavior of the Yukawa potential

We investigate the bound states of the Yukawa potential V (r)=−λexp(−αr)/r, using different algorithms: solving the Schr?dinger equation numerically and our Monte Carlo Hamiltonian approach. There is a critical α = α_C, above which no bound state exists. We study the relation between α_C and λ for various angular momentum quantum number l, and find in atomic units, α_C(l) = λ[A ₁ exp(−l/B ₁) + A ₂ exp(−l/B ₂)], with A ₁ = 1.020(18), B ₁ = 0.443(14), A ₂ = 0.170(17), and B ₂ = 2.490(180).     

Some new four-parameter potentials and their use in the study of vibrational thermodynamical quantities of diatomic molecules

Three four-parameter potentials,U _I,U _II andU _III have been proposed and their accuracy has been demonstrated by finding the mean square deviation from the true RKR potential curve for 15 electronic states of 12 diatomic molecules. Their percentage average mean square deviations from RKR curve have been found to be 1.45, 1.86 and 2.89, respectively. These compare favourably with the value 2.67 for the recently suggested four-parameter potential of Wei Hua which itself yields better results than the commonly employed three-parameter potentials. The superiority of the new potentials (especially ofU _I andU _II has been further established by using these potentials to calculate the molecular constants α_e and ω_ex_e following Dunham’s method. The corresponding percentage average mean deviations, for α_e, turn out to be 3.75, 5.13 and 15.43 and for ω_ex_e 8.73, 17.23 and 27.49, respectively, against the respective values of 7.97 and 18.88 with Wei Hua’s four-parameter potential. Also included are the values of dissociation energy determined with these potentials and these too corroborate the better performance ofU _I andU _II. The relative worth of various potential functions has been further tested by carrying out numerical study of vibrational partition function (evaluated by sum over states method), entropy and thermal capacity for the ground state of 7 molecules and comparing these with the corresponding findings based on the RKR data.     

An application of hypervirial perturbation theory to calculate energy eigenvalues of the Morse potential for various diatomic molecules

The Schrödinger equation with the potentialV(r)=D[exp(?2β(r?r _e))?2exp(?β(r?r _e))] is treated in the framework of the hypervirial-renormalization parameter scheme. The energy eigenvalues of various eigenstates for different molecules are calculated.     

First measurement of J/ ψ azimuthal anisotropy in PHENIX at forward rapidity in Au + Au collisions at $\sqrt{s_{\mathit{NN}}}=200$ GeV

In this paper, we calculate the decay rates of the D ⁺→D ⁰ e ⁺ ν, D _S ⁺→D ⁰ e ⁺ ν, , D _S ⁺→D ⁺ e ⁻ e ⁺ and B _S ⁰→B ⁰ e ⁻ e ⁺ semileptonic decay processes, in which only the light quarks decay, while the heavy flavors remain unchanged. The branching ratios of these decay processes are calculated with the flavor SU(3) symmetry. The uncertainties are estimated by considering the SU(3) breaking effect. We find that the decay rates are very tiny in the framework of the standard model. We also estimate the sensitivities of the measurements of these rare decays at future experiments, such as BES-III, super-B and LHC-b.     

The structure of the Yang–Mills spectrum for arbitrary simple gauge algebras

The mass spectrum of pure Yang–Mills theory in 3+1 dimensions is discussed for an arbitrary simple gauge algebra within a quasigluon picture. The general structure of the low-lying gluelump and two-quasigluon glueball spectrum is shown to be common to all algebras, while the lightest C=− three-quasigluon glueballs only exist when the gauge algebra is A _r≥2, that is, in particular, \mathfraksu(N 3 3)\mathfrak{su}(N\geq3). Higher-lying C=− glueballs are shown to exist only for the A _r≥2, D_odd−r≥4 and E₆ gauge algebras. The shape of the static energy between adjoint sources is also discussed assuming the Casimir scaling hypothesis and a funnel form; it appears to be gauge-algebra dependent when at least three sources are considered. As a main result, the present framework’s predictions are shown to be consistent with available lattice data in the particular case of an \mathfraksu(N)\mathfrak{su}(N) gauge algebra within ’t Hooft’s large-N limit.     

Directed polymers in a random environment: Some results on fluctuations

We consider a polymer model on ℤ ₊ ^d where to each edgee is associated a random variable v(e). A polymer configuration is represented by a directed pathr and has a weight exp[-β ∑ _e ∈r ν(e)], withβ=1/T the inverse temperature. We extend some rigorous results that have been obtained for the ground state of this model to finite temperatures. In particular we obtain some upper and lower bounds on sample-to-sample free energy fluctuations, and also rigorous scaling inequalities between the exponents describing free energy fluctuations and transversal displacements of polymer configurations     

Quark-Antiquark states and their radiative transitions in terms of the spectral integral equation: Bottomonia

In the framework of the spectral integral equation, we consider the states and their radiative transitions. We reconstruct the interaction on the basis of data for the levels of the bottomonium states with J ^PC = 0⁻⁺, 1⁻⁻, 0⁺⁺, 1⁺⁺, 2⁺⁺ as well as the data for the radiative transitions γ (3S) → _γχbJ(2P) and γ(2S) → _γχbJ(1P) with J = 0, 1, 2. We calculate bottomonium levels with the radial quantum numbers n ≤ 6, their wave functions, and corresponding radiative transitions. The ratios Br[_χbJ(2P) → _γγ(2S)]/Br[_χbJ(2P) → _γγ(1S)] for J = 0, 1, 2 are found to be in agreement with data. We determine the component of the photon wave function using the data for the e ⁺ e ⁻ annihilation, e ⁺ e ⁻ → γ(9460), γ(10 023), γ(10 036), γ(10 580), γ(10 865), γ(11 019), and predict partial widths of the two-photon decays ηb0 → γγ, χb0 → γγ, χb2 → γγ for the radial excitation states below the threshold (n ≤ 3). The text was submitted by the authors in English.     

Enhanced direct <Emphasis Type="Italic">CP</Emphasis> violation and branching ratios in bottom hadron decays

In the framework of factorization we study direct CP violation in the decays of bottom hadrons containing a strange quark or a charm quark, H _b →f ρ ⁰(ω)→f π ⁺ π ⁻ (H _b is the bottom hadron and f is the product hadron) including the effect of ρ–ω mixing. We find that the CP violating asymmetry can be enhanced greatly via the ρ–ω mixing mechanism when the invariant mass of the π ⁺ π ⁻ pair is in the vicinity of the ω resonance. For the processes associated with b→d transitions, e.g. , , B _c ⁻→D ⁻ π ⁺ π ⁻, B _c ⁻→D ^*− π ⁺ π ⁻, Ξ _b ⁰→Λ π ⁺ π ⁻, and Ω _b ⁻→Ξ ⁻ π ⁺ π ⁻, the maximum CP violating asymmetries can reach about −84%, while for the processes associated with b→s transitions, e.g. , , B _c ⁻→D _s ⁻ π ⁺ π ⁻, B _c ⁻→D _s ^*− π ⁺ π ⁻, Ξ _b ⁻→Ξ ⁻ π ⁺ π ⁻, and Ω _b ⁻→Ω ⁻ π ⁺ π ⁻, the CP violating asymmetries can be enhanced to about 95%. Furthermore, taking ρ–ω mixing into account we calculate the b-hadron decay branching ratios. We also discuss the possibility to observe the predicted CP violating asymmetries at the LHC.     

An improved model for band tail states inn-type degenerate semiconductors

Summary Using two screened donor potential energy models and a wave vectork-positionr uncertainty relation, the results of the exponential band tail states, inn-type degenerate semiconductors, obtained in our previous paper, are improved. The second-order cumulant or the correlation functionW (ϱ,E) is expressed as a function of the total donor concentration ϱ and total carrier energyE. Near band edges, the conduction and valence band tails are, respectively, proportional to exp [E/E ₀(ϱ)] and exp [−E/E ₀(ϱ)], whereE ₀(ϱ) is the energy characteristic of the appropriate band tail, in good accordance with those experimentally obtained by Pankove. Far below the conduction band edge, our result of the conduction band tail is proportional to exp [−BE ² exp [A ]], whereA andB are the functions of ϱ, which is reduced to zero more rapidly in comparison with the corresponding result obtained by Halperin and Lax (i.e. exp [−|E| ⁿ , wheren varies between 1/2 and 2). To speed up publication, the authors of this paper have agreed to not receive the proofs for correction.     

The Combined Effect of Connectivity and Dependency Links on Percolation of Networks

Percolation theory is extensively studied in statistical physics and mathematics with applications in diverse fields. However, the research is focused on systems with only one type of links, connectivity links. We review a recently developed mathematical framework for analyzing percolation properties of realistic scenarios of networks having links of two types, connectivity and dependency links. This formalism was applied to study Erdős-Rényi (ER) networks that include also dependency links. For an ER network with average degree [`(k)]\bar{k} that is composed of dependency clusters of size s, the fraction of nodes that belong to the giant component, P <sub>∞</sub>, is given by P<sub>￥</sub>=p<sup>s-1</sup>[1-exp(-[`(k)]pP_￥) ]^sP_{\infty}=p^{s-1}[1-\exp{(-\bar{k}pP_{\infty})} ]^{s} where 1−p is the initial fraction of randomly removed nodes. Here, we apply the formalism to the study of random-regular (RR) networks and find a formula for the size of the giant component in the percolation process: P _∞=p ^s−1(1−r ^k ) ^s where r is the solution of r=p ^s (r ^k−1−1)(1−r ^k )+1, and k is the degree of the nodes. These general results coincide, for s=1, with the known equations for percolation in ER and RR networks respectively without dependency links. In contrast to s=1, where the percolation transition is second order, for s>1 it is of first order. Comparing the percolation behavior of ER and RR networks we find a remarkable difference regarding their resilience. We show, analytically and numerically, that in ER networks with low connectivity degree or large dependency clusters, removal of even a finite number (zero fraction) of the infinite network nodes will trigger a cascade of failures that fragments the whole network. Specifically, for any given s there exists a critical degree value, [`(k)]<sub>min</sub>\bar{k}_{\min}, such that an ER network with [`(k)] ￡ [`(k)]_min\bar{k}\leq \bar{k}_{\min} is unstable and collapse when removing even a single node. This result is in contrast to RR networks where such cascades and full fragmentation can be triggered only by removal of a finite fraction of nodes in the network.