Restitution pluridisciplinaire du milieu et des activités humaines sur le site de Villa Romana

Restitution pluridisciplinaire du milieu et des activités humaines sur le site de Villa Roman

Un habitat de la fin de l’âge du Bronze entre lagune et fleuve : le site immergé de la Motte (Agde, Hérault)

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ZnO-Based Quantum Structures for Terahertz Sources

In this paper we report on the numerical study of the terahertz devices based on metal oxide semiconductors and its application in biology and medicine. We also report on the recent progress of the theoretical and experimental studies of ZnO-based THz quantum cascade lasers (QCLs) and resonant tunneling diodes (RTDs). We show that ZnO-based semiconductor compounds are promising materials for fabrication terahertz sources operating up to room temperature due to their unique properties such as large bandgap and conduction band offset (CBO) energy, high LO-phonon energy, and high resistant to the high breakdown electric field. Moreover, it was established that the ZnO-based terahertz sources can cover the spectral region of 5--12 THz, which is very important for THz imaging and detection of explosive materials, and which could be not covered by conventional GaAs-based terahertz devices. In terms of the reported significant progress in growth of non-polar m-plane ZnO-based heterostructures and devices with low density defects, it is open a wide perspective towards design and fabrication of non-polar m-plane ZnO-based high power terahertz sources with capabilities of operation at room temperature

Une occupation lagunaire palafittique au IXe-VIIIe s. a.C.: La Motte (Agde) au fond du fleuve Hérault

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Une occupation lagunaire palafittique au IXe-VIIIe s. a.C.: La Motte (Agde) au fond du fleuve Hérault

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α-Amination of keto-nitrones via Multihetero-Cope rearrangement employing an imidoyl chloride reagent

α-Aminations of ketone-derived nitrones have been developed via [3,3]-rearrangement of the intermediates generated upon condensation with imidoyl chlorides. Careful reagent selection provides synthetically attractive amino protecting groups. The enediamide or α′-carbamoyl enamide products can be hydrolyzed to the desired carbonyl, or exposed to electrophiles for further α-functionalization