Small (3-5 nm in diameter following HRTEM images) Si nanocrystals were produced in a two-stage process including (1) nanosecond laser ablation of a Si target in an organic liquid (chloroform) that results in formation of big composite polycrystalline particles (about 20-100 nm average diameter) and ( 2) ultrasonic post-treatment of Si nanoparticles in the presence of HF. The post-treatment is responsible for disintegration of the composite Si particles, release of small individual nanocrystals, and reduction of their size due to HF-induced etching of Si oxide. The downshift and broadening of the ∼520 cm -1 Raman phonon band of the small Si nanocrystals with respect to the bulk Si Raman band is consistent with the presence of ∼4.5 nm Si nanocrystals. The photoluminescence spectra (450-900 nm) and decay kinetics of small Si nanocrystals were detected, and the possible origin of the luminescence is discussed.

Here we describe a simple, powerful technique based on the laser ablation of a target immersed in a water solution of a metal salt. With this method, nanoparticles of different metals and alloys can be processed very quickly. Both the target and the salt solution can be chosen to produce metal nanoparticles of different sizes, surface-oxidized nanoparticles (silica-silver, for example), or even more complex structures to be defined by the researcher on one or more steps because the technique combines the advantages of both physical and chemical methods. We have applied this technique to the fabrication of inert silica-metal (silver, gold, and silver-gold) nanoparticles with a strong surface plasmon resonance all together in a single step. The advantage of the simultaneous production of silica during laser ablation is the stabilization of the metal nanoparticle colloid but also the possibility to reduce the toxicity of these nanoparticles.

Here we report on the triggering of antibacterial activity by a new type of silver nanoparticle coated with porous silica, Ag@silica, irradiated at their surface plasmon resonant frequency. The nanoparticles are able to bind readily to the surface of bacterial cells, although this does not affect bacterial growth since the silica shell largely attenuates the intrinsic toxicity of silver. However, upon simultaneous exposure to light corresponding to the absorption band of the nanoparticles, bacterial death is enhanced selectively on the irradiated zone. Because of the low power density used for the treatments, we discard thermal effects as the cause of cell killing. Instead, we propose that the increase in toxicity is due to the enhanced electromagnetic field in the proximity of the nanoparticles, which indirectly, most likely through induced photochemical reactions, is able to cause cell death.

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Here we report on the in situ synthesis of Ag and Au nanoparticles inside several polymer matrixes by solid-state chemical reduction of a metallic salt. Poly(ethyleneimine) (PEI), poly(hydroxyethyl methacrylate) (PHEMA), poly(vinylpyrrolidone) (PVP), novolak, poly(4-vinylphenol) (P4VP), poly(4-vinylphenol)-co-(methyl methacrylate) (P4VP-co-MMA) and poly(styrene-co-allyl alcohol) (PS-co-AA) were able to reduce Ag(I) and Au(III) to the corresponding nanoparticles during the baking process. The nanoparticle diameters of Ag and Au were found to range from 2 to 25 nm. TEM also indicated a uniform distribution of nanoparticles embedded in the thin film. This approach is suitable for controlling the size of the nanoparticles and its homogeneous distribution in the polymer matrix.

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This study presents a design of multilayer solar selective absorber for high temperature applications. The optical stack of this absorber is composed of four layers deposited by magnetron sputtering on stainless steel substrates. The first is a back-reflector tungsten layer, which is followed by two absorption layers based on CrAlSiN x / CrAlSiO y N x structure for phase interference. The final layer is an antireflection layer of SiAlO x. The design was theoretically modelled with SCOUT software using transmittance and reflectance curves of individual thin layers, which were deposited on glass substrates. The final design shows simultaneously high solar absorbance α= 95.2 % and low emissivity ε= 9.8% (at 400 ºC) together with high thermal stability at 400 ºC, in air, and 600 ºC in vacuum for 650 h.