Optimisation of 40 Gb/s wavelength converters based on four-wave mixing in a semiconductor optical amplifier

The optimum operating powers and wavelengths for a 40 Gb/s wavelength converter based on four-wave mixing in a semiconductor optical amplifier are inferred from experimental results. From these measurements, some general rules of thumb are derived for this kind of devices. Generally, the optimum signal power should be 10 dB lower than the pump power (−16 dB conversion efficiency) whereas the wavelength separation between the signal and the pump carrier should not be lower than about four times the signal bitrate (1.3 nm for 40 Gb/s RZ signals).     

Internal energy distribution in electrospray ionization

Internal energies and energy distributions were studied using the 'survival yield' method developed previously. In addition to conventional benzylpyridinium salts, protonated esters (fragmenting by rearrangement) and protonated leucine enkephalin were also used, extending the validity of the technique. Fragmentation processes were studied in the cone voltage region and modeled by the RRKM-based MassKinetics program. The results show that the shapes of the energy distributions are similar to thermal distributions. The mean internal energies are very similar for all compound classes studied, and show a linear increase with collision energy in the 10-50 eV region.     

Proton shock acceleration in laser-plasma interactions

The formation of strong, high Mach number (2-3), electrostatic shocks by laser pulses incident on overdense plasma slabs is observed in one- and two-dimensional particle-in-cell simulations, for a wide range of intensities, pulse durations, target thicknesses, and densities. The shocks propagate undisturbed across the plasma, accelerating the ions (protons). For a dimensionless field strength parameter a(0)=16 (Ilambda(2) approximately 3 x 10(20) W cm(-2) microm(2), where I is the intensity and lambda the wavelength), and target thicknesses of a few microns, the shock is responsible for the highest energy protons. A plateau in the ion spectrum provides a direct signature for shock acceleration.     

Analysis of adiabatic coupling between photonic crystal single-line-defect and coupled-resonator optical waveguides

A detailed analysis of adiabatic coupling between conventional photonic crystal single-line-defect and coupled-resonator optical waveguides is reported. Adiabatic coupling by progressive variation of the radii of the spacing defects between cavities is investigated. Flat transmission spectra with coupling efficiencies greater than 90% are achieved in a broad frequency range with short coupling lengths. Moreover, we find that flat transmission at low frequencies requires longer coupling lengths partly because the requirements imposed for adiabatic transmission in photonic crystals are violated.     

Nonlinear distortion generated by semiconductor optical amplifier boosters in analog optical systems

Closed-form theoretical expressions for the second- and third-order harmonic distortions generated by a semi-conductor optical amplifier (SOA) operating under slight saturation conditions are derived for what is believed to be the first time. The distortion results provided by these expressions agree very well with those obtained by means of simulation and experiments, showing that one should carefully adjust the optical power launched into the SOA to obtain both the good linearity and high dynamic range required by analog optical systems.     

Synthesis and evaluation of aminocyclopentitol inhibitors of beta-glucosidases

[reaction: see text] (1R,2S,3S,4R,5R)-4-Amino-5-(hydroxymethyl)cyclopentane-1,2,3-triol 1, prepared from D-glucose, inhibits beta-glucosidases from Caldocellum saccharolyticum (Ki = 1.8 x 10(-7) M) and from almonds (Ki = 3.4 x 10(-6) M). Inhibition is not influenced by N-ethylation (--> 15) but is strongly reduced upon N-acetylation (--> 12). Inversion of stereochemistry at C(5) (--> 14) has little effect on inhibition of beta-glucosidases. These experiments suggest that 1 acts as an analogue of a protonated beta-glucoside.     

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