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Register a new userIncrease of SRG modulation depth in azopolymers-nanoparticles hybrid materials
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Thin films of azopolymer-nanoparticles hybrid materials were fabricated with poly[1-[4-(3-carboxy-4-hydroxyphenylazo) benzenesulfonamido]-1,2-ethanediyl] (PAZO) and different concentrations of Ag and AgAu nanoparticles (NPs). By illuminating the films with polarized interference patterns, surface relief gratings (SRGs) were recorded. It was found that for some concentrations of NPs their modulations and diffraction efficiency were higher than the obtained for PAZO films without NPs. The effect was mainly explained by the increase of the free volume available for the photoisomerization for certain concentrations of NPs. The dependence of the diffraction efficiency on concentration was directly related to changes in modulation depth. When doping with NPs, the maximum efficiency increases more than two times the efficiency without NPs.
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When polyelectrolyte-neutral block copolymers are mixed in solutions to oppositely charged species (e.g. surfactant micelles, macromolecules, proteins etc), there is the formation of stable supermicellar aggregates combining both components. The resulting colloidal complexes exhibit a core-shell structure and the mechanism yielding to their formation is electrostatic self-assembly. In this contribution, we report on the structural properties of supermicellar aggregates made from yttrium-based inorganic nanoparticles (radius 2 nm) and polyelectrolyte-neutral block copolymers in aqueous solutions. The yttrium hydroxyacetate particles were chosen as a model system for inorganic colloids, and also for their use in industrial applications as precursors for ceramic and opto-electronic materials. The copolymers placed under scrutiny are the water soluble and asymmetric poly(sodium acrylate)poly(acrylamide) diblocks. Using static and dynamical light scattering experiments, we demonstrate the analogy between surfactant micelles and nanoparticles in the complexation phenomenon with oppositely charged polymers. We also determine the sizes and the aggregation numbers of the hybrid organic-inorganic complexes. Several additional properties are discussed, such as the remarkable stability of the hybrid aggregates and the dependence of their sizes on the mixing conditions.
Nanoparticles of superconducting YBa2Cu3O7-delta (YBCO) (Tc = 91 K) exhibit ferromagnetism at room temperature while the bulk YBCO, obtained by heating the nanoparticles at high temperature (940 degree C), shows a linear magnetization curve. Across the superconducting transition temperature, the magnetization curve changes from that of a soft ferromagnet to a superconductor. Furthermore, our experiments reveal that not only nanoparticles of metal oxides but also metal nitrides such as NbN (Tc = 6 - 12 K) and delta-MoN (Tc ~ 6 K) exhibit room-temperature ferromagnetism.
The vibrational density of states (VDOS) of nanoclusters and nanocrystalline materials are derived from molecular-dynamics simulations using empirical tight-binding potentials. The results show that the VDOS inside nanoclusters can be understood as that of the corresponding bulk system compressed by the capillary pressure. At the surface of the nanoparticles the VDOS exhibits a strong enhancement at low energies and shows structures similar to that found near flat crystalline surfaces. For the nanocrystalline materials an increased VDOS is found at high and low phonon energies, in agreement with experimental findings. The individual VDOS contributions from the grain centers, grain boundaries, and internal surfaces show that, in the nanocrystalline materials, the VDOS enhancements are mainly caused by the grain-boundary contributions and that surface atoms play only a minor role. Although capillary pressures are also present inside the grains of nanocrystalline materials, their effect on the VDOS is different than in the cluster case which is probably due to the inter-grain coupling of the modes via the grain-boundaries.
Current optical coherent transponders technology is driving data rates towards 1 Tb/s/{lambda}and beyond. This trend requires both high-performance coded modulation schemes and efficient implementation of the forward-error-correction (FEC) decoder. A possible solution to this problem is combining advanced multidimensional modulation formats with low-complexity hybrid HD/SD FEC decoders. Following this rationale, in this paper we combine two recently introduced coded modulation techniques:the geometrically-shaped 4D-64 polarization ring-switched and the soft-aided bit-marking-scaled reliability decoder. This joint scheme enabled us to experimentally demonstrate the transmission of 11x218 Gbit/s channels over transatlantic distances at 5.2bit/4D-sym. Furthermore, a 30% reach increase is demonstrated over PM-8QAM and conventional HD-FEC decoding for product codes.
The energy barrier distribution Eb of five samples with different concentrations x of Ni nanoparticles using scaling plots from ac magnetic susceptibility data has been determined. The scaling of the imaginary part of the susceptibility Chi(nu, T) vs. Tln(t/tau_0) remains valid for all samples, which display Ni nanoparticles with similar shape and size. The mean value <E_b> increases appreciably with increasing x, or more appropriately with increasing dipolar interactions between Ni nanoparticles. We argue that such an increase in <Eb> constitutes a powerful tool for quality control in magnetic recording media technology where the dipolar interaction plays an important role.
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