Numerical discrimination of intrachannel cross-phase modulation and intrachannel four-wave mixing and their respective effect on 40 Gbit/s transmissions

We propose a numerical method to accurately discriminate the influence of the different intrachannel nonlinear effects occurring in 40 Gbit/s optical transmissions, following an analogy with methods used to discriminate WDM interchannel effects. In contrast to other studies showing the predominance of intrachannel cross-phase modulation when low-dispersion fibers are used, in our study intrachannel four-wave mixing is the most penalizing effect in all investigated cases.     

Clock shift in a strongly interacting two-dimensional Fermi gas

We derive universal relations for the rf spectroscopy of a two-dimensional Fermi gas consisting of two spin states interacting through an S-wave scattering length. The rf transition rate has a high-frequency tail that is proportional to the contact and displays logarithmic scaling violations, decreasing asymptotically like 1/(ω2ln2ω). Its coefficient is proportional to ln2'(a'(2D)/a(2D)), where a(2D) and a'(2D) are the two-dimensional scattering lengths associated with initial-state and final-state interactions. The clock shift is proportional to the contact and to ln(a'(2D)/a(2D)). If |ln(a'(2D)/a(2D))| > 1, the clock shift arises as a cancellation between much larger contributions proportional to ln2(a'(2D)/a(2D)) from bound-bound and bound-free rf transitions.     

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.     

Spin-dependent electron-hole capture kinetics in luminescent conjugated polymers

The recombination of electron-hole pairs injected in extended conjugated systems is modeled as a multistep interconversion relaxation in monoexcited electronic state space, mediated by electron-phonon coupling. The computed ratio of triplet-to-singlet exciton formation times r=tau(T)/tau(S) increases from 0.9 for a model dimer to 2.5 for a 32-unit chain, in good agreement with recent experiments. We rationalize the conjugation-length dependence of r in terms of spin-specific energetics and mutual vibronic coupling of the excited states.     

The Neutral Part of the Bark of Pinus Luchuensis Mayer

The neutral part of the acetone extract from the bark of Pinus luchuensis Mayer has been investigated and found to consist of alkanes (C₂₂–C₃₄) and triterpenes of serratene type. The triterpenes are 3β–methoxyserrat–14–en–21–one, serrat–14–en–3, 21–dione, 3β–hydroxyserrat–14–en–21–one, 3β–21α–dimethoxyserrat–l4–ene and 3β–methoxyserrat–14–en–21α–ol.     

Polyélectrolytes basiques faibles—I. Détermination du degré de protonation de la poly(vinyl-2 pyridine) par spectrophotométrie dans l'u.v. et par conductimétrie

We have determined the degree of protonation (a) for a weak polybase (poly(2-vinyl-pyridine)) in aqueous solution without added salt by spectrophotometry and conductimetry. For acid solutions of poly(2-vinylpyridine), the use of Kolhrausch's law is adequate; we propose two expressions for the conductance of these solutions (from “ionic association” and “relaxation” models respectively). The values of a, as determined by spectrophotometric and conductimetric measurements, agree well for the highest concentrations and degree of neutralisation (ā).     

Products of the reaction of H2Os3(CO)10 with cyclonona-1,2diene

Treatment of H₂Os₃(CO)₁₀ with cyclonona-l,2-diene produced HOs₃(CO)₉C₉H₁₃ and Os₂(CO)₆(C₉H₄)₂. Single crystal X ray analysis has shown that the latter is not isostructural with Fe₂(CO)₆(C₉H₁₄)₂.