Anomalous proximity effect in an inhomogeneous disordered superconductor

By combining very low temperature scanning tunneling microscopy and spectroscopy on a TiN film we have observed a nonuniform state comprising of superconducting (S) and normal (N) areas. The local density of states displays a spatial dependence between S and N different from the usual proximity effect. We conclude that mesoscopic fluctuations might play a major role in accordance with recent theories describing superconductor-normal-metal quantum transition.     

Neutron-detected tomography of impurity-seeded superfluid helium

We describe a neutron radiography technique that can be used to map the distribution of 3He impurities in liquid 4He, providing direct and quantitative access to underlying transport processes. Images reflecting finite normal- and superfluid-component 4He velocity fields are presented.     

Limit of spin squeezing in finite-temperature Bose-Einstein condensates

We show that, at finite temperature, the maximum spin squeezing achievable using interactions in Bose-Einstein condensates has a finite limit when the atom number N→∞ at fixed density and interaction strength. We calculate the limit of the squeezing parameter for a spatially homogeneous system and show that it is bounded from above by the initial noncondensed fraction.     

Proton affinity ladder for uridine and analogs: influence of the hydroxyl group on the sugar ring conformation

A ladder of relative proton affinities (PA) for a series of modified uridines (e.g. araU, ddU, 5BrU, 5BrdU and 5IU) was established from competitive dissociations of proton-bound heterodimers using Cooks and co-workers' kinetic method. The studied heterodimers are constituted of a modified nucleoside and either an amino acid or a nucleoside with known PA value. These non-covalent heterodimers were prepared under electrospray conditions to be selected and dissociated into the ion-trap analyzer. These results allowed our PA ladder of uridine and deoxyuridine analogs substituted at the C-5 position in the uracil ring to be extended. From this scale, it was showed that the substitution of hydrogen atom at the C-2' position in the sugar ring by a hydroxyl group involves a decrease of about 7 kJ mol(-1). The experimental values for U, 5MeU, dU, 5MedU, ddU and araU are consistent with those obtained by DFT calculations (B3P86/6-31+G//B3LYP/6-31G(.)). Several neutral and protonated conformations of these compounds were considered, in particular the ring conformation of furanose and the orientation of the base with respect to the sugar ring. These calculated results showed the influence of sugar substituent on the conformation of the neutral form of theses nucleosides. However, the most stable protonated structure is the same for all the studied nucleosides except for araU, where the position of the anti 2'-OH group imposes a specific conformation.     

Determination of mixing time by colourimetric diagnosis—Application to a new mixing system

A method for determining mixing times in a transparent stirred vessel for highly viscous fluids has been developed. The method involves a chemical decolourization with two acid-base indicators and a colourimetric diagnosis of digital images, deduced from a video captured during the mixing process. The advantages of the method developed are:(1) there is no disturbance of the fluid flow, and (2) measuring and determination of the degree of homogeneity is relatively effortless and cheap since it requires only a standard colour camera and commercial software for digital image analysis. This paper describes protocols for carrying this method out. In addition, examples of experimental results obtained for a standard impeller (of the helical ribbon agitator type) and a new piece of mixing equipment are given and discussed.     

Heating of thin foils with a relativistic-intensity short-pulse laser

K-shell x-ray spectroscopy of sub-100 nm Al foils irradiated by high contrast, spatially uniform, 150 fs, Ilambda (2)=2 x 10(18) W microm(2)/cm(2), laser pulses is obtained with 500 fs time resolution. Two distinct phases occur: At /=500 fs the resonance transitions dominate. Initial satellites arise from a large area, high density, low temperature (approximately 100 eV) plasma created by fast electrons. Thus, contrary to predictions, a short, high intensity laser incident on a thin foil does not create a uniform, hot dense plasma.     

Ultralow emittance, multi-MeV proton beams from a laser virtual-cathode plasma accelerator

The laminarity of high-current multi-MeV proton beams produced by irradiating thin metallic foils with ultraintense lasers has been measured. For proton energies >10 MeV, the transverse and longitudinal emittance are, respectively, <0.004 mm mrad and <10(-4) eV s, i.e., at least 100-fold and may be as much as 10(4)-fold better than conventional accelerator beams. The fast acceleration being electrostatic from an initially cold surface, only collisions with the accelerating fast electrons appear to limit the beam laminarity. The ion beam source size is measured to be <15 microm (FWHM) for proton energies >10 MeV.     

Parity conservation and polarization of differential cross sections in complex-forming chemical reactions

For complex-forming chemical reactions, such as atom-diatom insertion reactions, quantum scattering and quantum statistical calculations usually predict sharp forward/backward peaks in the Differential Cross Sections (DCS). Conversely, the corresponding classical calculations are unable to reproduce these peaks. We show here that the basic reason for such an intriguing failure is that parity conservation is ignored in classical mechanics. A by-product of the analysis is a simple parity-restoring approximation that might significantly increase the ability of classical mechanics to describe DCSs over the whole angular range for the title processes.