A measurement of ∧ and Ξ<Superscript>−</Superscript> polarization in inclusive production by Σ<Superscript>−</Superscript> of 340 GeV/c in C and Cu targetsof 340 GeV/c in C and Cu targets

We have measured the polarization of ∧ and Ξ^? hyperons produced inclusively by a Σ^? beam of 340 GeV/c momentum in nuclear targets, using samples of 9.5 million ∧ decays and 880000 Ξ^? decays. The large statistics allowed a two-dimensional analysis as functions ofx _F andp _t . The polarization w.r.t. the production normal is mainly positive for ∧ and negative for Ξ^?. The positive sign of the ∧ polarization is opposite to predictions. Atp _t >1 Gev/c, the ∧ polarization decreases to zero or even negative values, in sharp contrast to the plateau abovep _t <1 GeV/c observed in inclusive ∧ production by protons. No such effect is observed for the Ξ^? polarization, and its sign is as expected.     

Study of the centrally producedK 1 0 K ± π∓ system at 85 GeV/c

We have analyzed theK ₁ ⁰ K ^± π^? system in the reactions π⁺/pp→π⁺/p(K ₁ ⁰ K ^± π^?)p. A spin-parity analysis of theK ₁ ⁰ K ^± π^? system in the “4C” channel confirms the existence of the 1⁺⁺ E meson which decays mainly throughK ^* \(\bar K\) . The data allow the presence of a 0^?+ wave at a level of 14% of theE/ι signal. The production ofD andE mesons in the channels where theK ₁ ⁰ K ^± π^? system is produced along with a π⁰ or π⁺π^? system is suppressed.     

Wavelength dependence of high-efficiency second-harmonic generation in CdGeAs2

The frequency-doubling performance of CdGeAs₂ as a function of wavelength has been characterised using a representative selection of lines from the 9 and 10 m bands of a single mode TEA CO₂ laser. Results are shown to be in good agreement with theory in which wavelength dependent absorption, most significant for the generated signal, is taken into account.     

Fixed-node diffusion Monte Carlo study of the structures of m-benzyne

Diffusion Monte Carlo (DMC) calculations are performed on the monocyclic and bicyclic forms of m-benzyne, which are the equilibrium structures at the CCSD(T) and CCSD levels of coupled cluster theory. We employed multiconfiguration self-consistent field trial wave functions which are constructed from a carefully selected eight-electrons-in-eight-orbitals complete active space [CAS(8,8)], with configuration state function coefficients that are reoptimized in the presence of a Jastrow factor. The DMC calculations show that the monocyclic structure is lower in energy than the bicyclic structure by 1.9(2) kcal/mole, which is in excellent agreement with the best coupled cluster results.     

Eliminating spin contamination in auxiliary-field quantum Monte Carlo: realistic potential energy curve of F(2)

The use of an approximate reference state wave function mid R:Phi(r) in electronic many-body methods can break the spin symmetry of Born-Oppenheimer spin-independent Hamiltonians. This can result in significant errors, especially when bonds are stretched or broken. A simple spin-projection method is introduced for auxiliary-field quantum Monte Carlo (AFQMC) calculations, which yields spin-contamination-free results, even with a spin-contaminated mid R:Phi(r). The method is applied to the difficult F(2) molecule, which is unbound within unrestricted Hartree-Fock (UHF). With a UHF mid R:Phi(r), spin contamination causes large systematic errors and long equilibration times in AFQMC in the intermediate, bond-breaking region. The spin-projection method eliminates these problems and delivers an accurate potential energy curve from equilibrium to the dissociation limit using the UHF mid R:Phi(r). Realistic potential energy curves are obtained with a cc-pVQZ basis. The calculated spectroscopic constants are in excellent agreement with experiment.     

Auxiliary-field quantum Monte Carlo calculations of molecular systems with a Gaussian basis

We extend the recently introduced phaseless auxiliary-field quantum Monte Carlo (QMC) approach to any single-particle basis and apply it to molecular systems with Gaussian basis sets. QMC methods in general scale favorably with the system size as a low power. A QMC approach with auxiliary fields, in principle, allows an exact solution of the Schrodinger equation in the chosen basis. However, the well-known sign/phase problem causes the statistical noise to increase exponentially. The phaseless method controls this problem by constraining the paths in the auxiliary-field path integrals with an approximate phase condition that depends on a trial wave function. In the present calculations, the trial wave function is a single Slater determinant from a Hartree-Fock calculation. The calculated all-electron total energies show typical systematic errors of no more than a few millihartrees compared to exact results. At equilibrium geometries in the molecules we studied, this accuracy is roughly comparable to that of coupled cluster with single and double excitations and with noniterative triples [CCSD(T)]. For stretched bonds in H(2)O, our method exhibits a better overall accuracy and a more uniform behavior than CCSD(T).     

Neutral transverse momentum spectra in 60 and 200A·GeV16O+nucleus and proton+nucleus reactions

Transverse momentum (p _T) distributions fo inclusive photons and neutral pions at midrapidity are measured with a lead glass calorimeter in 60 and are measured with a lead glass calorimeter in 60 and 200A·Gev¹⁶O+nucleus and and proton+nucleus reactions. Inclusive photon distributions are compared for central and peripheral reactions. The degree of centrality is determined either from the charged particle multiplicity or from the remaining projectile energy in the forward direction. Deviations from a nucleus+nucleus interaction model based upon linear extrapolation from p+p reactions are observed in central¹⁶O+Au data. The variation of theaverage transverse momentum is investigated as function of centrality. The target-mass and energy dependence of π⁰ p _T distributions are presented. For¹⁶O+Au a change of slope in these distributions is observed atp _t ≈0.8 GeV/c compatible with hydrodynamic expansion models.