Secondary ion yields produced by keV atomic and polyatomic ion impacts on a self-assembled monolayer surface

A suite of keV polyatomic or 'cluster' projectiles was used to bombard unoxidized and oxidized self-assembled monolayer surfaces. Negative secondary ion yields, collected at the limit of single ion impacts, were measured and compared for both molecular and fragment ions. In contrast to targets that are orders of magnitude thicker than the penetration range of the primary ions, secondary ion yields from polyatomic projectile impacts on self-assembled monolayers show little to no enhancement when compared with monatomic projectiles at the same velocity. This unusual trend is most likely due to the structural arrangement and bonding characteristics of the monolayer molecules with the Au(111). Copyright 1999 John Wiley & Sons, Ltd.     

Composition of particles emitted at largep T and medium angles inpp,dd, andαα collisions at the CERN intersecting storage rings

The relative yields of kaons and protons compared with the yield of pions at highp _T and polar angles θ away from 90° (in the range from 10° to 45°) are presented forpp, dd, and αα interactions at a centre-of-mass energy \(\sqrt {s_{NN} } = 31\) GeV per nucleon-nucleon collision. The measured particle ratios depend on the atomic mass numberA of the beam particles and on θ. TheA dependence of the ratios becomes stronger for largerp _T and is more pronounced at smaller polar angles.     

Spin-dependent shot noise of inelastic transport through molecular quantum dots

Here we present a theoretical analysis of the effect of inelastic electron scattering on spin-dependent transport characteristics (conductance, current–voltage dependence, magnetoresistance, shot noise spectrum, Fano factor) for magnetic nanojunction. Such device is composed of molecular quantum dot (with discrete energy levels) connected to ferromagnetic electrodes (treated within the wide-band approximation), where molecular vibrations are modeled as dispersionless phonons. Non-perturbative computational scheme, used in this work, is based on the Green's function theory within the framework of mapping technique (GFT–MT), which transforms the many-body electron–phonon interaction problem into a single-electron multi-channel scattering problem. The consequence of the localized electron–phonon coupling is polaron formation. It is shown that polaron shift and additional peaks in the transmission function completely change the shape of considered transport characteristics.     

Decoherence in elastic and polaronic transport via discrete quantum states

In this work we study the effect of decoherence on elastic and polaronic transport via discrete quantum states. Calculations are performed with the help of a nonperturbative computational scheme, based on Green’s function theory within the framework of polaron transformation (GFT-PT), where the many-body electron-phonon interaction problem is mapped exactly into a single-electron multi-channel scattering problem. In particular, the influence of dephasing and relaxation processes on the shape of the electrical current and shot noise curves is discussed in detail under linear and nonlinear transport conditions.     

Os(VIII)-catalysed oxidation of sulfides by sodium salt of N-chlorobenzenesulfonamide

Catalytic activity of Os(VIII) in the oxidation of some twenty organic sulfides with sodium salt of N-chlorobenzenesulfonamide (CAB) has been investigated in alkaline (pH8.7) t-butanol–water (1:1 v/v) medium. Significant retarding influence of [OH⁻] on the reactivity is exhibited. The catalysed reaction is strongly accelerated in the presence of Hg(II). Imperfections are observed in the linear Hammett relationship in the case of –NO₂ substituents.     

Conformal geometry of foliations

In this article, we begin a systematic study of conformal properties of codimension-1 foliations. We first define and study local conformal invariants. A case of particular interest is that of harmonic foliations of the plane. Then we study existence of totally umbilical and “Dupin” foliations on compact 3-manifolds of constant curvature.      

Caesium and hydrated lead chlorates studied by35Cl NQR spectroscopy

Molecular dynamics of caesium and lead chlorates (hydrated form) has been studied by³⁵Cl nuclear quadrupole resonance (NQR) spectroscopy. The occurrence of only one resonance line for the two compounds in the whole temperature range studied testifies to the crystallographically equivalent positions of their molecules in elementary cells. The relaxation processes in the two chlorates have been found to be analogous to those in the other chlorates not undergoing phase transitions. Analysis of the temperature dependence of the spin-lattice relaxation time has indicated that at low temperatures the dominant relaxation mechanism consists of torsion vibrations (ClO₃⁻ anion libration), whereas at 260 K the hindered rotation of the chlorate ion about the threefold axis sets on and its activation energy is 50.0 kJ/mol. The temperature dependence of the resonance frequency for the two chlorates studied is best described by the Brown model extended over the low-temperature range, which indicates large anharmonicity of the vibrations.