Elena Messina
University of Catania
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Publication
Featured researches published by Elena Messina.
ACS Nano | 2013
Cristiano D’Andrea; Jörg Bochterle; Andrea Toma; Christian Huck; Frank Neubrech; Elena Messina; Barbara Fazio; Onofrio M. Maragò; Enzo Di Fabrizio; Marc Lamy de la Chapelle; Pietro G. Gucciardi; Annemarie Pucci
In this article we show that linear nanoantennas can be used as shared substrates for surface-enhanced Raman and infrared spectroscopy (SERS and SEIRS, respectively). This is done by engineering the plasmonic properties of the nanoantennas, so to make them resonant in both the visible (transversal resonance) and the infrared (longitudinal resonance), and by rotating the excitation field polarization to selectively take advantage of each resonance and achieve SERS and SEIRS on the same nanoantennas. As a proof of concept, we have fabricated gold nanoantennas by electron beam lithography on calcium difluoride (1-2 μm long, 60 nm wide, 60 nm high) that exhibit a transverse plasmonic resonance in the visible (640 nm) and a particularly strong longitudinal dipolar resonance in the infrared (tunable in the 1280-3100 cm(-1) energy range as a function of the length). SERS and SEIRS detection of methylene blue molecules adsorbed on the nanoantennas surface is accomplished, with signal enhancement factors of 5×10(2) for SERS (electromagnetic enhancement) and up to 10(5) for SEIRS. Notably, we find that the field enhancement provided by the transverse resonance is sufficient to achieve SERS from single nanoantennas. Furthermore, we show that by properly tuning the nanoantenna length the signals of a multitude of vibrational modes can be enhanced with SEIRS. This simple concept of plasmonic nanosensor is highly suitable for integration on lab-on-a-chip schemes for label-free chemical and biomolecular identification with optimized performances.
ACS Nano | 2011
Elena Messina; Emanuele Cavallaro; Adriano Cacciola; Maria Antonia Iatì; Pietro G. Gucciardi; Ferdinando Borghese; Paolo Denti; Rosalba Saija; Giuseppe Compagnini; Moreno Meneghetti; Vincenzo Amendola; Onofrio M. Maragò
We show how light forces can be used to trap gold nanoaggregates of selected structure and optical properties obtained by laser ablation in liquid. We measure the optical trapping forces on nanoaggregates with an average size range 20-750 nm, revealing how the plasmon-enhanced fields play a crucial role in the trapping of metal clusters featuring different extinction properties. Force constants of the order of 10 pN/nmW are detected, the highest measured on a metal nanostructure. Finally, by extending the transition matrix formalism of light scattering theory to the optical trapping of metal nanoaggregates, we show how the plasmon resonances and the fractal structure arising from aggregation are responsible for the increased forces and wider trapping size range with respect to individual metal nanoparticles.
Scientific Reports | 2016
Barbara Fazio; Cristiano D’Andrea; Antonino Foti; Elena Messina; Alessia Irrera; M. G. Donato; Valentina Villari; Norberto Micali; Onofrio M. Maragò; Pietro G. Gucciardi
Strategies for in-liquid molecular detection via Surface Enhanced Raman Scattering (SERS) are currently based on chemically-driven aggregation or optical trapping of metal nanoparticles in presence of the target molecules. Such strategies allow the formation of SERS-active clusters that efficiently embed the molecule at the “hot spots” of the nanoparticles and enhance its Raman scattering by orders of magnitude. Here we report on a novel scheme that exploits the radiation pressure to locally push gold nanorods and induce their aggregation in buffered solutions of biomolecules, achieving biomolecular SERS detection at almost neutral pH. The sensor is applied to detect non-resonant amino acids and proteins, namely Phenylalanine (Phe), Bovine Serum Albumin (BSA) and Lysozyme (Lys), reaching detection limits in the μg/mL range. Being a chemical free and contactless technique, our methodology is easy to implement, fast to operate, needs small sample volumes and has potential for integration in microfluidic circuits for biomarkers detection.
Plasmonics | 2013
Antonino Foti; Cristiano D’Andrea; Francesco Bonaccorso; Maurizio Lanza; Giuseppe Calogero; Elena Messina; Onofrio M. Maragò; Barbara Fazio; Pietro G. Gucciardi
Surface-enhanced Raman scattering (SERS) takes advantage of the giant electromagnetic field enhancement provided by localized surface plasmons in metal nanoparticles to amplify the weak Raman scattering of the molecules. Optical fibers coated with noble metal nanoparticles can therefore be used as SERS-based sensors for remote detection of molecular species. In this article, we report on the development of an optical fiber SERS sensor capable to operate on a range of excitation wavelengths from the visible to the near-infrared. We introduce a quasistatic chemical etching protocol to engineer the tip shape and investigate the effects of the tip shape on the sensor performances.
ACS Applied Materials & Interfaces | 2016
Elena Messina; Nancy Leone; Antonino Foti; Gaetano Di Marco; C. Riccucci; Gabriella Di Carlo; Francesco Di Maggio; Antonio Cassata; Leonardo Gargano; Cristiano D’Andrea; Barbara Fazio; Onofrio M. Maragò; Benedetto Robba; C. Vasi; Gabriel Maria Ingo; Pietro G. Gucciardi
Improving the electrical and thermal properties of conductive adhesives is essential for the fabrication of compact microelectronic and optoelectronic power devices. Here we report on the addition of a commercially available conductive resin with double-wall carbon nanotubes and graphene nanoplatelets that yields simultaneously improved thermal and electrical conductivity. Using isopropanol as a common solvent for the debundling of nanotubes, exfoliation of graphene, and dispersion of the carbon nanostructures in the epoxy resin, we obtain a nanostructured conducting adhesive with thermal conductivity of ∼12 W/mK and resistivity down to 30 μΩ cm at very small loadings (1% w/w for nanotubes and 0.01% w/w for graphene). The low filler content allows one to keep almost unchanged the glass-transition temperature, the viscosity, and the curing parameters. Die shear measurements show that the nanostructured resins fulfill the MIL-STD-883 requirements when bonding gold-metalized SMD components, even after repeated thermal cycling. The same procedure has been validated on a high-conductivity resin characterized by a higher viscosity, on which we have doubled the thermal conductivity and quadrupled the electrical conductivity. Graphene yields better performances with respect to nanotubes in terms of conductivity and filler quantity needed to improve the resin. We have finally applied the nanostructured resins to bond GaN-based high-electron-mobility transistors in power-amplifier circuits. We observe a decrease of the GaN peak and average temperatures of, respectively, ∼30 °C and ∼10 °C, with respect to the pristine resin. The obtained results are important for the fabrication of advanced packaging materials in power electronic and microwave applications and fit the technological roadmap for CNTs, graphene, and hybrid systems.
Scientific Reports | 2015
Maria Josè Lo Faro; Cristiano D’Andrea; Elena Messina; Barbara Fazio; P. Musumeci; R. Reitano; G. Franzò; Pietro G. Gucciardi; C. Vasi; Francesco Priolo; Fabio Iacona; Alessia Irrera
The realization of an innovative hybrid light source operating at room temperature, obtained by embedding a carbon nanotube (CNT) dispersion inside a Si nanowire (NW) array is reported. The NW/CNT system exhibits a peculiar photoluminescence spectrum, consisting of a wide peak, mainly observed in the visible range, due to quantum confined Si NWs, and of several narrower IR peaks, due to the different CNT chiralities present in the dispersion. The detailed study of the optical properties of the hybrid system evidences that the ratio between the intensity of the visible and the IR emissions can be varied within a wide range by changing the excitation wavelength or the CNT concentration; the conditions leading to the prevalence of one signal with respect to the other are identified. The multiplicity of emission spectra obtainable from this composite material opens new perspectives for Si nanostructures as active medium in light sources for Si photonics applications.
Radiation Effects and Defects in Solids | 2010
Elena Messina; Giuseppe Compagnini; Luisa D'Urso; Orazio Puglisi; S. Bagiante; S. Scalese
We have produced silver colloids by ablating metal targets in water and using two different laser wavelengths. The obtained sols have been characterized by optical spectroscopy and electron microscopy, revealing a definite double size distribution centered at a few tens and a few hundreds of nanometers with a mild difference between the two wavelengths employed. On the contrary, a marked difference in shape has been found for the biggest aggregates, revealing sharp cubic or octahedral structures when visible or infrared radiations are used, respectively. This fact is explained by the re-irradiation processes induced on the already formed colloid and taking place during the ablation.
Radiation Effects and Defects in Solids | 2008
Giuseppe Compagnini; Elena Messina; Orazio Puglisi
We have successfully synthesized noble metal colloids by laser ablation of metal targets in liquids and Au/Ag colloidal nano-alloys with a wide range of compositions by a re-irradiation of mixed colloidal suspensions. Optical extinction spectra as well as electron microscopy data can give a clear picture of the structure and properties of the obtained particles, while an X-ray photoelectron spectroscopy is used for an estimation of the clusters’ composition.
The Open Surface Science Journal | 2010
Giuseppe Compagnini; Gabriele C. Messina; Luisa D'Urso; Elena Messina; Marco G. Sinatra; Orazio Puglisi; Massimo Zimbone
Silver colloids prepared by laser ablation in water have been linked using sp-hybridized carbon chains thus obtaining a plasmonic transfer between the metallic nanoparticles. It has been found that the state of the metallic surface is of fundamental importance for the plasmonic transfer. The role of the carbon �- electron system has been considered in order to justify the electromagnetic field amplification and the observed surface enhanced Raman signals. These findings open the possibility to control the electronic transfer between different metallic nanostructures for the application in future plasmonic devices.
Nanospectroscopy | 2015
Antonino Foti; Cristiano D’Andrea; Elena Messina; Alessia Irrera; Onofrio M. Maragò; Barbara Fazio; Pietro G. Gucciardi
Abstract The Raman depolarization ratio is a quantity that can be easily measured experimentally and offers unique information on the Raman polarizability tensor of molecular vibrations. In Surface Enhanced Raman Scattering (SERS), molecules are near-field coupled with optical nanoantennas and their scattering properties are strongly affected by the radiation patterns of the nanoantenna. The polarization of the SERS photons is consequently modified, affecting, in a non trivial way, the measured value of the SERS depolarization ratio. In this article we elaborate a model that describes how the SERS depolarization ratio is influenced by the nanoantenna re-radiation properties, suggesting how to retrieve information on the Raman polarizability from SERS experiments.