Carlo Scian

Sub-nanometric metallic Au clusters as efficient Er3+ sensitizers in silica

Silica films co-implanted with Er and Au ions show an enhancement of rare earth photoluminescence after gold introduction in the matrix. Er excitation originates in a broad spectral region, from the red to the near ultraviolet. We have investigated the influence of gold aggregation on the optical properties of co-doped samples by varying the temperature of post-Au implantation annealing in the 400–900°C range. Optical measurements and extended x-ray absorption analysis support the hypothesis of an energy transfer process mediated by sub-nanometric Au aggregates with metallic character that are optically activated mostly through electron interband transitions between d and sp-conduction levels.

Structure and optical properties of Au-polyimide nanocomposite films prepared by ion implantation

Au-polyimide nanocomposites have been synthesized by implanting different doses of Au+ ions in 100nm thick films of pyromellitic dianhydride-4,4′ oxydianiline polyimide, prepared by glow discharge vapor deposition polymerization. Unambiguous evidence of Au nanoclusters growth is found only at the highest implantation doses (5×1016Au+∕cm2). Structural, compositional, and optical characterizations show that the implantation induces the compactation of the initial film due to H and C loss. The resulting structure is a composite containing 2–3nm gold nanoparticles arranged in a layer of about 40nm and, just beneath the sample surface, a 15nm thick carbon-rich layer. Optical simulations suggest the presence of a gold-carbon core-shell structure in the nanoparticles.

Optimal geometric parameters of ordered arrays of nanoprisms for enhanced sensitivity in localized plasmon based sensors

Plasmonic sensors based on ordered arrays of nanoprisms are optimized in terms of their geometric parameters like size, height, aspect ratio for Au, Ag or Au0.5-Ag0.5 alloy to be used in the visible or near IR spectral range. The two figures of merit used for the optimization are the bulk and the surface sensitivity: the first is important for optimizing the sensing to large volume analytes whereas the latter is more important when dealing with small bio-molecules immobilized in close proximity to the nanoparticle surface. A comparison is made between experimentally obtained nanoprisms arrays and simulated ones by using Finite Elements Methods (FEM) techniques.

Oxidation effects on the SERS response of silver nanoprism arrays

Silver nanostructures are widely employed for Surface Enhanced Raman Scattering (SERS) characterizations owing to their excellent properties of field confinement in plasmonic resonances. However, the strong tendency to oxidation at room temperature of these substrates may represent a major limitation to their performances. In the present work, we investigated in detail the effects of oxidation on the SERS response of a peculiar kind of Ag nanostructured substrates, i.e., bi-dimensional ordered arrangements of Ag nanoprisms synthesized by nanosphere lithography. Particularly, wavelength-scanned SERS measurements were performed on Ag nanoprism arrays with a different level of oxidation to determine the SERS enhancement curves as a function of the excitation wavelength around the dipolar plasmonic resonance of the arrays. The experimental results were compared with those obtained by finite elements method simulations. With this approach, we were able to decouple the effects of spectral shift and decrease of the maximum value of the SERS enhancement observed for the different oxidation conditions. The results could be interpreted taking into account the inhomogeneities of the electromagnetic field distribution around the Ag nanostructures, as demonstrated by the simulations.

Silver nanoprism arrays coupled to functional hybrid films for localized surface plasmon resonance-based detection of aromatic hydrocarbons.

We report the achievement of sensitive gas detection using periodic silver nanoprisms fabricated by a simple and low-cost lithographic technique. The presence of sharp tips combined with the periodic arrangement of the nanoprisms allowed the excitement of isolated and interacting localized surface plasmon resonances. Specific sensing capabilities with respect to aromatic hydrocarbons were achieved when the metal nanoprism arrays were coupled in the near field with functional hybrid films, providing a real-time, label-free, and reversible methodology. Ultra-high-vacuum temperature-programmed desorption measurements demonstrated an interaction energy between the sensitive film and analytes in the range of 55-71 kJ/mol. The far-field optical properties and the detection sensitivity of the sensors, modeled using a finite element method, were correlated to experimental data from gas sensing tests. An absorbance variation of 1.2% could be observed and associated with a theoretical increase in the functional film refractive index of ∼0.001, as a consequence to the interaction with 30 ppm xylene. The possibility of detecting such a small variation in the refractive index suggests the highly promising sensing capabilities of the presented technique.

Strengths of the resonances at 436, 479, 639, 661, and 1279 keV in theNe22(p,γ)Na23reaction

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Energy-transfer from ultra-small Au nanoclusters to Er3+ ions: a short-range mechanism

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Ion implantation for manufacturing bent and periodically bent crystals

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Amplified sensitization of Er3+ luminescence in silica by AuN quantum clusters upon annealing in a reducing atmosphere

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Au clustering formation by implantation in silica: optical, magnetic and sensing properties

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