Modulational instability in dispersion-kicked optical fibers

We study, both theoretically and experimentally, modulational instability in optical fibers that have a longitudinal evolution of their dispersion in the form of a Dirac delta comb. By means of Floquet theory, we obtain an exact expression for the position of the gain bands, and we provide simple analytical estimates of the gain and of the bandwidths of those sidebands. An experimental validation of those results has been realized in several microstructured fibers specifically manufactured for that purpose. The dispersion landscape of those fibers is a comb of Gaussian pulses having widths much shorter than the period, which therefore approximate the ideal Dirac comb. Experimental spontaneous MI spectra recorded under quasi continuous wave excitation are in good agreement with the theory and with numerical simulations based on the generalized nonlinear Schr\"odinger equation

Heteroclinic structure of parametric resonance in the nonlinear Schr\"odinger equation

We show that the nonlinear stage of modulational instability induced by parametric driving in the {\em defocusing} nonlinear Schr\"odinger equation can be accurately described by combining mode truncation and averaging methods, valid in the strong driving regime. The resulting integrable oscillator reveals a complex hidden heteroclinic structure of the instability. A remarkable consequence, validated by the numerical integration of the original model, is the existence of breather solutions separating different Fermi-Pasta-Ulam recurrent regimes. Our theory also shows that optimal parametric amplification unexpectedly occurs outside the bandwidth of the resonance (or Arnold tongues) arising from the linearised Floquet analysis

Fotonima stimulirana desorpcija vodikovih iona iz poluvodičkih površina: dokazi izravnih i posrednih procesa

Photon-stimulated desorption of positive hydrogen ions from hydrogenated diamond and GaAs surfaces have been studied for incident photon energies around core-level binding energies of substrate atoms. In the case of diamond surfaces, the comparison between the H+ yield and the near edge X-ray absorption fine structure (NEXAFS) for electrons of selected kinetic energies reveals two different processes leading to photodesorption: an indirect process involving secondary electrons from the bulk and a direct process involving core-level excitations of surface carbon atoms bonded to hydrogen. The comparison of H+ photodesorption and electron photoemission as the function of photon energy from polar and non-polar GaAs surfaces provides clear evidence for direct desorption processes initiated by ionisation of corresponding core levels of bonding atoms.Proučavali smo fotonima stimuliranu desorpciju pozitivnih iona vodika iz hidrogeniziranih površina dijamanta i GaAs, za fotone energije oko energija vezanja unutarnjih elektrona atoma podloge. U slučaju površine dijamanta, usporedba prinosa H+ i fine strukture blizu-rubne apsorpcije X-zračenja (NEXAFS) za elektrone odabranih kinetičkih energija otkriva dva različita procesa koji uzrokuju fotodesorpciju: posredan proces uz sudjelovanje sekundarnih elektrona iz osnovnog materijala, i izravan proces uzrokovan uzbudom unutarnjih elektrona površinskih atoma ugljika vezanih na vodik. Usporedba fotodesorpcije H+ i emisije elektrona u ovisnosti o energiji fotona iz polarnih i nepolarnih površina GaAs daje jasne dokaze za izravne procese desorpcije uzrokovane ionizacijom odgovarajućih unutarnjih stanja veznih atoma

Fotonima stimulirana desorpcija vodikovih iona iz poluvodičkih površina: dokazi izravnih i posrednih procesa

Photon-stimulated desorption of positive hydrogen ions from hydrogenated diamond and GaAs surfaces have been studied for incident photon energies around core-level binding energies of substrate atoms. In the case of diamond surfaces, the comparison between the H+ yield and the near edge X-ray absorption fine structure (NEXAFS) for electrons of selected kinetic energies reveals two different processes leading to photodesorption: an indirect process involving secondary electrons from the bulk and a direct process involving core-level excitations of surface carbon atoms bonded to hydrogen. The comparison of H+ photodesorption and electron photoemission as the function of photon energy from polar and non-polar GaAs surfaces provides clear evidence for direct desorption processes initiated by ionisation of corresponding core levels of bonding atoms.Proučavali smo fotonima stimuliranu desorpciju pozitivnih iona vodika iz hidrogeniziranih površina dijamanta i GaAs, za fotone energije oko energija vezanja unutarnjih elektrona atoma podloge. U slučaju površine dijamanta, usporedba prinosa H+ i fine strukture blizu-rubne apsorpcije X-zračenja (NEXAFS) za elektrone odabranih kinetičkih energija otkriva dva različita procesa koji uzrokuju fotodesorpciju: posredan proces uz sudjelovanje sekundarnih elektrona iz osnovnog materijala, i izravan proces uzrokovan uzbudom unutarnjih elektrona površinskih atoma ugljika vezanih na vodik. Usporedba fotodesorpcije H+ i emisije elektrona u ovisnosti o energiji fotona iz polarnih i nepolarnih površina GaAs daje jasne dokaze za izravne procese desorpcije uzrokovane ionizacijom odgovarajućih unutarnjih stanja veznih atoma

Fluorescent oxide nanoparticles adapted to active tips for near-field optics

We present a new kind of fluorescent oxide nanoparticles with properties well suited to active-tip based near-field optics. These particles with an average diameter in the range 5-10 nm are produced by Low Energy Cluster Beam Deposition (LECBD) from a YAG:Ce3+ target. They are studied by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), classical photoluminescence, cathodoluminescence and near-field scanning optical microscopy (NSOM). Particles of extreme photo-stability as small as 10 nm in size are observed. These emitters are validated as building blocks of active NSOM tips by coating a standard optical tip with a 10 nm thick layer of YAG:Ce3+ particles directly in the LECBD reactor and by subsequently performing NSOM imaging of test surfaces.Comment: Changes made following Referee's comments; added references; one added figure. See story on this article at: http://nanotechweb.org/cws/article/tech/3606

Conversion of total shoulder arthroplasty to reverse shoulder arthroplasty made possible by custom humeral adapter

AbstractReverse shoulder arthroplasty (RSA) is increasingly being used to revise anatomical total shoulder arthroplasty cases. This procedure's high complication rate has been reduced by the availability of modular shoulder systems, which allows the humeral component to be preserved during the conversion. This case report describes the revision of an anatomical shoulder implant inserted in 1998. Polyethylene wear and the resulting metal-on-metal contact had caused metallosis. Since the existing humeral implant was not compatible with standard conversion products, the manufacturer provided a custom humeral adapter that allowed the humeral stem to be preserved. This approach greatly simplified the surgical procedure and resulted in good anatomical and clinical outcomes after 9 months of follow-up

STM topography and manipulation of single Au atoms on Si(100)

The low-temperature (12 K) adsorption of single Au atoms on Si(100) is studied by scanning tunneling microscopy (STM). Comparison between experimental and calculated STM topographies as well as density-functional-theory calculations of the adsorption energies enable us to identify two adsorption configurations of Au atoms between Si-dimer rows (BDRs) and on top of Si-dimer rows (TDRs). In both adsorption configurations, the Au atoms are covalently bound to two Si atoms through a partial electron transfer from Si to Au. STM manipulation confirms that the TDR adsorption configuration is metastable, whereas the BDR one is the most stable configuration.Peer reviewe

Evaluation de la pollution de l'eau par les Ethers de glycol (Eg)

Les Eg sont des substances largement utilisées dans les produits domestiques et industriels. Certains sont des toxiques, principalement de la reproduction et du sang. Leur présence dans les milieux aqueux a été peu recherchée, car leur polarité fait que les méthodes classiques sont inadéquates pour les détecter. Une méthode d'extraction de type SPME (Solid Phase Micro Extraction), couplée avec une analyse CG/FID ou CG/SM a été mise au point et utilisée pour évaluer la pollution dans un certain nombre de milieux aquatiques. Le traitement dans les stations diminue fortement la pollution de l'eau, mais certains pics de pollution subsistent. Les indications relatives à la pollution des nappes montrent qu'une étude plus systématique est nécessaire, notamment autour de décharges ayant reçu des déchets contenant des Eg