Atomically resolved spin-dependent tunneling on the oxygen-terminated Fe3O4(111)

We employ spin-polarized STM to study the spin-dependent tunneling between a magnetite (111) sample and an antiferromagnetic tip through a vacuum barrier at room temperature. Atomic scale STM images show significant magnetic contrast corresponding to variations in the local surface states induced by oxygen vacancies. The estimated variations in tunneling magnetoresistance of 250% suggest that the spin-transport properties are significantly altered locally by the presence of surface defects.     

Modified z-gradient filtering as a mean to obtain phased deuterium autocorrelation 2D NMR spectra in oriented solvents

We describe a modified z-gradient filter scheme specifically designed to obtain pure absorption mode deuterium 2D NMR spectra recorded in oriented solvents. The proposed technique is investigated by analysing the evolution of the density operator for a spin I=1. The method is applied to the recently designed Q-COSY and Q-resolved 2D experiments to simplify the analysis of chiral molecules dissolved in weakly orienting chiral liquid crystals. The efficiency of this z-gradient filtering technique is illustrated using the perdeuterated 1-butanol, a prochiral molecule of average Cs symmetry, dissolved in an organic solution of poly-gamma-benzyl-L-glutamate (PBLG). The experimental results as well as the advantages of the new experiments compared with the previous ones are described and discussed.     

Comparative measurements of loudspeakers in a listening situation

Comparison of loudspeakers is a major concern during design or product selection. There are several standards for the measurement of loudspeaker characteristics, but none of them provides hints for a rigorous comparison between devices. In this study, different ways of evaluating acoustical dissimilarity between loudspeakers were compared. Several methods of signal analysis were used, and for each method a metric evaluating the dissimilarity between two signals was defined. The correlation between the different dissimilarity evaluations over a significant panel of loudspeakers led to identified classes of measurements. A specific aspect of this work is that measurements were performed in a standard listening environment, rather than in an anechoic or reverberant one. It allowed the use of the recorded signals for a simple listening test, providing a perceptual metric which was compared to the acoustical ones. It also allowed the introduction of auditory models in the computation of some acoustical metrics, so defining a new class of measurements which gave results close to the perceptual ones.     

Local foliations and optimal regularity of Einstein spacetimes

We investigate the local regularity of pointed spacetimes, that is, time-oriented Lorentzian manifolds in which a point and a future-oriented, unit timelike vector (an observer) are selected. Our main result covers the class of Einstein vacuum spacetimes. Under curvature and injectivity bounds only, we establish the existence of a local coordinate chart defined in a ball with definite size in which the metric coefficients have optimal regularity. The proof is based on quantitative estimates for, on one hand, a constant mean curvature (CMC) foliation by spacelike hypersurfaces defined locally near the observer and, on the other hand, the metric in local coordinates that are spatially harmonic in each CMC slice. The results and techniques in this paper should be useful in the context of general relativity for investigating the long-time behavior of solutions to the Einstein equations.     

Enhanced quantum well infrared photodetector focal plane arrays for space applications

A 30 months European Space Agency project started in March 2008, whose overall purpose is to expand and assess the performance of broadband (11–15 μm) quantum detectors for spectro-imaging applications: Dispersive Spectrometers and Fourier Transform Spectrometers. We present here the technical requirements, the development approach chosen as well as preliminary experimental results. Our approach is fully compatible with the final array format (1024 × 256, pitch 50–60 μm). We expect the requested uniformity, operability and SNR levels to be achieved at temperatures close to the goal values. The performance level will be demonstrated on 256 × 256, 50 μm pitch arrays. Also, operability and uniformity issues will be addressed on large mechanical 1024 × 256 hybrid arrays.     

Aligned synthesis of multi-walled carbon nanotubes with high purity by aerosol assisted chemical vapor deposition: Effect of water vapor

Aligned multi-walled carbon nanotubes (MWCNTs) with high purity and bulk yield were achieved on a silicon substrate by an aerosol-assisted chemical vapor deposition. The introduction of specific amounts of water vapor played a key role in in situ controlling the purity and surface defects of the nanotubes. The morphology, surface quality and structure of MWCNTs were characterized by secondary and backscattered electron imaging in a field emission scanning electron microscope (FESEM) and transmission electron microscope (TEM). Crystallinity and defects of the MWCNTs’ were investigated by high-resolution transmission electron microscopy (HRTEM) and Raman spectroscopy. In this work, water vapor was found to provide a weak oxidative environment, which enhanced and purified the MWCNTs’ growth. However, excessive water vapor would inhibit the MWCNTs growth with a poor surface quality. In addition, it has been found that the surface morphology of the CNTs can be modified intentionally through producing some surface defects by tuning the amount of the water vapor, which may offer more nucleation sites on the chemically inert CNT surface for various applications such as catalyst support.     

Laser–Induced Fluorescence Detection of Carbamates Traces in Water

The absorption and fluorescence spectra of carbaryl (CB), carbofuran (CF) and carbendazim (MBC) have been studied. Fluorescence lifetime and fluorescence quantum yields are also reported as well as the influence of pH, solvent and presence of humic acids on fluorescence. The limit of detection (LD) of the three compounds has been measured by direct analysis by laser-induced fluorescence (LIF) using a pulsed YAG laser with an Optical Parametric Oscillator (OPO) as excitation source and an Intensified Charged Coupled Device (ICCD) camera for the fluorescence detection. Instrumental LD found for CB, for MBC and for CF are respectively 4, 50 and 1000 ng L⁻¹. In tap water, the LD obtained is 800 ng L⁻¹ for MBC and 20,000 ng L⁻¹ for CF. For CB, the use of a time shift between excitation and emission allows to reach a LD of 20 ng L⁻¹ in tap water.     

Intermolecular interactions in the chiral and racemic forms of 3‐­hydroxy‐2‐(1‐oxoisoindolin‐2‐yl)­butanoic acid derived from threonine

The title compounds, C₁₂H₁₃NO₄, are derived from l ‐threonine and dl ‐threonine, respectively. Hydro­gen bonding in the chiral derivative, (2S/3R)‐3‐hydroxy‐2‐(1‐oxoisoindolin‐2‐yl)­butanoic acid, consists of O—H_acid?O_alkyl—H?O=C_indole chains [O?O 2.659 (3) and 2.718 (3) Å], Csp³—H?O and three C—H?π_arene interactions. In the (2R,3S/2S,3R) racemate, conventional carboxylic acid hydrogen bonding as cyclical (O—H?O=C)₂ [graph set R₂²(8)] is present, with O_alkyl—H?O=C_indole, Csp³—H?O and C—H?π_arene interactions. The COOH group geometry differs between the two forms, with C—O, C=O, C—C—O and C—C=O bond lengths and angles of 1.322 (3) and 1.193 (3) Å, and 109.7 (2) and 125.4 (3)°, respectively, in the chiral structure, and 1.2961 (17) and 1.2210 (18) Å, and 113.29 (12) and 122.63 (13)°, respectively, in the racemate structure. The O—C=O angles of 124.9 (3) and 124.05 (14)° are similar. The differences arise from the contrasting COOH hydrogen‐bonding environments in the two structures.     

The [CH2CHOH.+, CH3CHO] solvated enol radical cation

The bimolecular reaction of the CH₂CHOH^.+ enol ion (m/z 44) with acetaldehyde gives a strongly dominant product,m/z 45, formed mainly by proton transfer from the ion to the molecule. The abundance of the product coming from a H^. abstraction reaction from the neutral, albeit more exothermic, is negligible. In order to explain this result, the long lived [CH₂CHOH^.+, CH₃CHO] solvated ion was generated by reaction of the CH₂CHOH^.+ enol ion with (CH₃CHO) _n in the cell of a Fourier transform ion cyclotron resonance mass spectrometer. The structure of this solvated ion was clearly established. Labeling indicates that [CH₂CHOH^.+, CH₃CHO], upon low energy collisions, reacts by H^. abstraction more rapidly than by H⁺ transfer to the neutral moiety. This shows that the entropic factors are determinant when the enol ion reacts directly with acetaldehyde.