In this work we develop surface-micromachinedRF MEMS switches in III-V technology making use ofmaterials which can be alternative to the ones commonly used.In this way, some technological constraints concerning RFMEMS reliability can be overcome. Specifically, we evaluatethe potential of tantalum nitride (TaN) and tantalumpentoxide (Ta2O5) to be used for the switches actuation padsand dielectric layers, respectively. To this scope, acompositional, structural and electrical characterization ofTaN and Ta2O5 films as a function of the depositionparameters (temperature, sputtering mixture composition, andfilm thickness) is performed. Both shunt and series switchesare prepared and show good switching capabilities by apreliminary analysis. The complete device characterization isin progress and will be presented.

TiO2 microspheres (TMS) with perfect spherical morphology were synthesized by spray drying of a hydrothermally cured aqueous suspension of TiO2 nanoparticles. TiO2 powders (TP) obtained by drying the nanoparticle suspension were studied simultaneously to determine which was the most efficient photocatalyst. SEM images and laser granulometry on TMS show spherical morphology with the diameter ranging from 2 to 10 mu m. TMS had high specific surface area after annealing as seen from BET analyses. XRD analyses show that TMS consist of anatase and rutile crystalline phases where the rutile fraction increases with annealing temperature and above 500 degrees C rutile dominates anatase. Raman spectroscopy shows several Raman bands from anatase and rutile phases and supports the XRD results of phase transformation with increasing annealing temperature. Photodegradation of organic pollutants in aqueous solution under UV light irradiation establishes the higher photocatalytic activity of TMS with respect to TP. The highest efficiency was found on the 400 degrees C annealed TMS.

In this paper, shunt capacitive RF microelectromechanical systems (MEMS) switches are developed in III-V technology using tantalum nitride (TaN) and tantalum pentoxide (Ta2O5) for the actuation lines and the dielectric layers, respectively. A compositional, structural, and electrical characterization of the TaN and Ta2O5 films is preliminarily performed, demonstrating that they are valid alternatives to the conventional materials used in III-V technology for RF MEMS switches. Specifically, it is found that the TaN film resistivity can be tuned from 0.01 to 30 ohmcm . cm by changing the deposition parameters. On the other hand, dielectric Ta2O5 films show a low leakage-current density of few nanoamperes per square centimeter for E similar to 1 MV/cm, a high breakdown field of 4 MV/cm, and a high dielectric constant of 32. The realized switches show good actuation voltages, in the range of 15-20 V, an insertion loss better than -0.8 dB up to 30 GHz, and an isolation of similar to -40 dB at the resonant frequency, which is, according to bridge length, between 15 and 30 GHz. A comparison between the measured S-parameter values and the results of a circuit simulation is also presented and discussed, providing useful information on the operation of the fabricated switches.

The detection of the DNA hybridization mechanism using monodispersed gold nanoparticles as labels is an interesting alternative to increase the sensitivity of the SPR imaging technique. DNA-modified Au nanoparticles (DNA-Au NPs) containing single-stranded (ss) portions of DNA were prepared by monitoring their monolayer formation by UV-vis spectroscopy. The hybridization process between specific thio-oligonucleotides immobilized on the DNA-Au NPs and the corresponding complementary strands is reported and compared with the traditional hybridization process on properly self-assembled thin gold films deposited on glass substrates. A remarkable signal amplification is observed, following the incorporation of colloidal Au into a SPR biosensing experiment, resulting in an increased SPR response to DNA-DNA interactions. In particular Fusarium thiolated DNA (5'HS poly(T)(15)ATC CCT CAA AAA CTG CCG CT-3) and trichothecenes complementary DNA (5'-AGC GGC AGT TTT TGA GGG AT-3') sequences have been explored due to their possible application to agro-industry for the control of food quality.

In this paper we report on the effects of the insertion of Cr atoms on the electrical and optical properties of indium tin oxide (ITO) films to be used as electrodes in spinpolarized light-emitting devices. ITO films and ITO(80 nm)/Cr-doped ITO(20 nm) bilayers and Cr-doped ITO films with a thickness of 20 nm were grown by pulsed ArF excimer laser deposition. The optical, structural, morphological wand electrical properties of ITO films and ITO/Cr-doped structures were characterized by UV-Visible transmission and reflection spectroscopy, transmission electron microscopy (TEM), atomic force microscopy (AFM) and Hall-effect analysis. For the different investigations, the samples were deposited on different substrates like silica and carbon coated Cu grids. ITO films with a thickness of 100 nm, a resistivity as low as similar to 4 x 10(-4) Omega cm, an energy gap of similar to 4.3 eV and an atomic scale roughness were deposited at room temperature without any post-deposition process. The insertion of Cr into the ITO matrix in the upper 20 nm of the ITO matrix induced variations in the physical properties of the structure like an increase of average roughness (similar to 0.4-0.5 nm) and resistivity (up to similar to 8x10(-4) Omega cm). These variations were correlated to the microstructure of the Cr-doped ITO films with particular attention to the upper 20 nm.

Brookite titanium dioxide (TiO2) nanorods. synthesized by a surfactant-assisted aminolysis route, were used as precursors for the fabrication of thin films by using the matrix-assisted pulsed-laser deposition (MAPLE) technique. Thin films with controllable thickness were grown on a variety of substrates for different characterizations. High-resolution scanning and transmission electron microscopy investigations evidenced the formation of rough TiO2 films incorporating individually distinguishable nanocrystals with different shapes. Suitable alumina substrates equipped with interdigitated electrical contacts (IDC) and heating elements were used to fabricate gas-sensing devices based on resistive transduction mechanism. Electrical characterization measurements in controlled environment were carried out. Typical gas sensor parameters (such as gas response, sensitivity, stability and detection limit) towards selected oxidizing and reducing gases, namely NO2 and CO, respectively, were extracted in dark condition. Very interesting optically activated enhancement of the response towards NO2 oxidizing gas was achieved in controlled atmosphere upon irradiating the sensing layer with UV light with low energy close to the TiO2 sensing layer band-gap width. (C) 2011 Elsevier B.V. All rights reserved.

Fe3O4/gamma-Fe2O3 nanoparticles (NPs) based thin films were used as active layers in solid state resistive chemical sensors. NPs were synthesized by high temperature solution phase reaction. Sensing NP monolayers (ML) were deposited by Langmuir-Blodgett (LB) techniques onto chemoresistive transduction platforms. The sensing ML were UV treated to remove NP insulating capping. Sensors surface was characterized by scanning electron microscopy (SEM). Systematic gas sensing tests in controlled atmosphere were carried out toward NO2, CO, and acetone at different concentrations and working temperatures of the sensing layers. The best sensing performance results were obtained for sensors with higher NPs coverage (10 ML), mainly for NO2 gas showing interesting selectivity toward nitrogen oxides. Electrical properties and conduction mechanisms are discussed.

Pd nanoparticles generated onto gel type ion-exchange resins under catalytic conditions show high activity, selectivity and durability in partial hydrogenation reactions under mild condition, thus providing a green, low-cost option to fine-chemicals production. The application to the continuous-flow synthesis of the leaf alcohol fragrance cis-3-hexen-1-ol is demonstrated.

Shunt capacitive radio-frequency microelectromechanical system (RF MEMS) switches were fabricated on silicon substrate and characterized in the RF domain. Various switch typologies were obtained by three different approaches, which are: (1) the change of the bridge geometric parameters, (2) the covering of the actuator with a floating metal, and (3) the deposition of the bridge directly on the actuator. The S parameters of the fabricated switches were measured in the up and down states, observing the impact on the RF performance of the variation of the geometric parameters and the fabrication process. The electromagnetic modelling of the fabricated switches was used to interpret the measured RF behaviour, allowing to elucidate the drawbacks of the non-perfect conforming of the bridge on the actuator. Finally, the reliability of the fabricated RF MEMS switches under a bipolar voltage excitation was evaluated by cycling tests. Hence, the study presented here provides guidelines to solve some issues of the tight correlation between design, fabrication, performance, and reliability of RF MEMS switches, in view of a large-scale development of these devices.

The matrix-assisted pulsed laser evaporation (MAPLE) has been recently exploited for depositing films of nanomaterials by combining the advantages of colloidal inorganic nanoparticles and laser-based techniques. MAPLE-deposition of nanomaterials meeting applicative purposes demands their peculiar properties to be taken into account while planning depositions to guarantee a congruent transfer (in terms of crystal structure and geometric features) and explain the deposition outcome. In particular, since nanofluids can enhance thermal conductivity with respect to conventional fluids, laser-induced heating can induce different ablation thermal regimes as compared to the MAPLE-treatment of soft materials. Moreover, nanoparticles exhibit lower melting temperatures and can experience pre-melting phenomena as compared to their bulk counterparts, which could easily induce shape and or crystal phase modification of the material to be deposited even at very low fluences. In this complex scenario, this review paper focuses on examples of MAPLE-depositions of size and shape controlled nanoparticles for different applications highlights advantages and challenges of the MAPLE-technique. The influence of the deposition parameters on the physical mechanisms which govern the deposition process is discussed. © 2013 Elsevier B.V.

Concentrated solar power (CSP) plants are one of several renewable energy technologies with significant potential to meet a part of our future energy demand. By now, CSP systems are used to supply photovoltaic or thermal power plant, but results on nanorectennas suggest the possibility to use this technology for direct energy conversion of solar radiation into electricity. A rectenna is a rectifying antenna that can be used to directly convert wave energy into DC electricity. Experiences in microwave applications have shown energy conversion efficiency in the order of 85%, and recently empirical tests have demonstrated that this technology can be used up to the infrared wavelength. The present paper, together with first preliminary results on the fabrication of the rectifier (the key element of a rectenna) and its electrical behavior, proposes the numerical simulation of a new CSP system where a receiver, heated by concentrated solar radiation, reemits infrared energy on the nanorectenna, which converts the incoming energy into electricity. In this way the receiver plays the role of a sunlight radiation converter to infrared energy. The numerical simulation of the system consists of two steps. The first is a ray-tracing model to calculate the concentrator optical efficiency and the energy distribution on the focusing area of the parabolic mirror. The second step consists in the receiver temperature calculation as function of the incident solar radiation. The numerical procedure allows the calculation of the concentrator/receiver assembly performance which returns the energy incident on the nanorectenna as a function of external environmental conditions. Copyright © 2012 by ASME.

The aim of this study is to analyze the evolution of microstructural and room temperature mechanical properties of air plasma sprayed (APS) CoNiCrAlY coatings before and after early stage high-temperature oxidation. To this purpose, selected samples were isothermally heat treated at 1110 A degrees C for different durations. Phase analysis and oxide scale characterization were performed using x-ray diffraction. Morphological and microstructural features of as-sprayed and oxidized CoNiCrAlY coatings were analyzed by scanning electron microscopy and energy dispersive x-ray spectroscopy. After heat treatment, a duplex oxide scale, composed of an inner alpha-Al2O3 layer and an outer spinel-type oxide layer, was observed on coating top-surface. The nanoindentation technique was employed to study the evolution of the mechanical properties. An increase in Young's modulus and hardness with increasing the aging time was observed, this effect was mainly addressed to the partial densification of coating microstructure.

In this paper we report on optical absorption measurements performed on several metal oxide nanoparticles (ZnO, CeO2, Fe2O3) as a function of temperature in the range 25500 °C, in order to study the optical properties, and to investigate how several heating cycles could affect nanoparticle structural stability and absorption characteristics. These are quite important issues to be investigated in order to assess the possibility to use such metal-oxide nanoparticles as gas-based high temperature nanofluid in concentrated solar power (CSP).

The photoconduction properties of individual GaAs/AlGaAs core-shell nanowires under uniform and local optical excitation are investigated, allowing the external quantum efficiency, the polarization anisotropy, and the role of the nanocontacts to be valuated. © OSA 2013.

Conductivity and photoconductivity properties of individual GaAs/AlGaAs core-shellnanowires (NWs) are reported. The NWs were grown by Au-assisted metalorganic vaporphase epitaxy, and then dispersed on a substrate where electrical contacts were defined on theindividual NWs by electron beam induced deposition. Under dark conditions, the carriertransport along the NW is found to be limited by Schottky contacts, and influenced by thepresence of an oxide layer. Nonetheless, under illumination, the GaAs/AlGaAs core-shell NWshows a significant photocurrent, much higher than the bare GaAs NW. The spatialdependence of the photocurrent within the single core-shell NW, evaluated by a mappingtechnique, confirms the blocking behavior of the contacts. Moreover, local spectralmeasurements were performed which allow one to discriminate the contribution of carriersphotogenerated in the core and in the shell.

The optical response by NO2 gas adsorption at different concentrations has been investigated, at room temperature, in ZnO nanostructured films grown by controlled vapor phase deposition. The variation (quenching) in the photoluminescence signal from excitonic and defects bands, due to the interactions between the oxidizing gas molecules and the sample surface, has been detected and dynamic responses and calibration curves as a function of gas concentration have been obtained and analyzed for each band. We showed that the sensing response results larger in excitonic band than in defect one and that the emission signal rises from two different quenchable and unquenchable states. A simple model was proposed in order to explain the quenching processes on the emission intensity and to correlate them to the morphological features of the samples. Finally, the reversibility of the quenching effects has also been tested at high gas concentration. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.3700251]

We investigate the photodetection properties of individual core/shell GaAs/AlGaAs nanowires (NWs) and, in particular, their behavior under linearly polarized light. The NWs are grown by Au-assisted metalorganic vapor phase epitaxy and electrical contacts are defined on NWs by electron beam induced deposition. The spectral photocurrent of the single NW is measured and the dependence of the polarization anisotropy rho (varying from similar to 0.1 to similar to 0.55) on the absorption wavelength is found to be clearly affected by the core/shell structure. High quantum efficiency values (10% at 600 nm) are obtained which are attractive for a wide range of optoelectronic devices.

A reliable strategy is presented to combine the preparation of functional building blocks based on polymer beads decorated with luminescent nanocrystals (NCs) and their precise positioning onto suitable patterns by capillary assembly technique. In particular, a layer-by-layer (LbL) polyelectrolyte (PE) deposition procedure has been implemented to provide uniform NC coverage on PS beads, thus conveying the optical properties of luminescent nanocrystals to highly processable PS beads. The latter have then been integrated into patterned stamps by means of template-driven capillary assembly. Their selective positioning has been directed by means of pattern geometry. The use of luminescent (CdSe)ZnS NCs offers a direct optical probe to evaluate the efficiency of the positioning procedure on the substrate, enabling the extension of the method to a wide range of materials, i.e., NCs with different compositions and specific geometry-dependent properties. Moreover, the precise control over the pattern geometry and the micrometer accuracy in positioning achieved by capillary assembly make such functional patterned structures excellent candidates for integration into devices exploiting specific size-dependent NC properties.

A highly dense and uniform layer of Au nanoparticles (NPs) on poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) film has been produced by the pulsed laser deposition (PLD) technique toward the production of an improved efficiency photovoltaic device. The advantage of PLD over other techniques is the easy and precise control of the Au NPs size and spatial distribution, without needing of further NP surface functionalization. The efficiency enhancement factor related to Au NPs doping has been evaluated in a solar cell based on poly-(3-hexylthiophene):[6,6]-phenyl-C-61-butyric acid methyl ester (P3HT:PCBM) diffused bilayer. The short-circuit current density, J (SC), increases by 18 % and the power conversion efficiency by 22 %, respectively, in comparison with an equivalent device without Au NPs. The optical and morphological properties of the Au NPs layer have been selected in order to evaluate the contribution of the surface plasmon resonance as enhancement factor of the solar cell efficiency, in a range size where light scattering is negligible.

This paper reports an investigation into the aging of pyrolyzed cobalt/polypyrrole (Co/PPy) oxygen reduction reaction (ORR) electrocatalysts, based on quasi-in-situ photoelectron microspectroscopy. The catalyst precursor was prepared by potentiostatic reverse-pulse coelectrodeposition from an acetonitrile solution on graphite. Accelerated aging was obtained by quasi-in-situ voltammetric cycling in an acidic electrolyte. Using photoelectron imaging and microspectroscopy of single Co/PPy grains at a resolution of 100 nm, we tracked the ORR-induced changes in the morphology and chemical state of the pristine material, consisting of uniformly distributed similar to 20 nm nanoparticles, initially consisting of a mixture of Co(II) and Co(III) oxidation states in almost equal amounts. The evolution of the Co 2p, O 1s, and N 1s spectra revealed that the main effects of aging are a gradual loss of the Co present at the surface and the reduction of Co(III) to Co(II), accompanied by the emergence and growth of a N 1s signal, corresponding to electrocatalytically active C-N sites.

In this paper we report on the growth and structural characterization of very thin (20 nm) Cr-doped ITO films, deposited at room temperature by double-target pulsed laser ablation on amorphous silica substrates. The role of Cr atoms in the ITO matrix is carefully investigated with increasing doping content by transmission electron microscopy (TEM). Selected-area electron diffraction, conventional bright field and dark field as well as high-resolution TEM analyses, and energy dispersive x-ray spectroscopy demonstrate that (i) crystallization features occur despite the low growth temperature and small thickness, (ii) no chromium or chromium oxide secondary phases are detectable, regardless of the film doping levels, (iii) the films crystallize as crystalline flakes forming large-angle grain boundaries; (iv) the observed flakes consist of crystalline planes with local bending of the crystal lattice. Thickness and compositional information about the films are obtained by Rutherford back-scattering spectrometry. Results are discussed by considering the combined effects of growth temperature, smaller ionic radius of the Cr cation compared with the trivalent In ion, doping level, film thickness, the double-target doping technique and peculiarities of the pulsed laser deposition method.

The objective of this paper is to study the morphology, structure, and composition, as well as the thermal-induced morphological, structural, and chemical changes of copper(Cu)/titanium nitride(TiN) bilayers versus Cu single layers, deposited on silicon substrates for microelectronic applications. These characterizations aimed to assess the reliability of Cu metallization for local interconnect and to investigate the barrier capability of TiN against Cu diffusion into the silicon (Si) substrate. Moreover, this paper provides a fundamental study of the temperature-induced interactions between Cu and Si, intermediated by the presence of a thin TiN layer. Cu thin films were sputtered onto Si substrates, with and without the interposition of thin TiN layers, and were successively annealed at temperature as high as 600. C. Different nitrogen flux percentages in the sputtering mixture (Ar + N-2) were used for the deposition of the barriers. X-ray diffraction (XRD) analyses were carried out in order to study the structural evolution of the layers, before and after the annealing. Scanning electron microscopy (SEM) observations gave information about the surface and cross section morphology, and spatially resolved energy dispersive X-ray Spectroscopy (EDS) profiles provided chemical information about the cross-sectional distribution of the atomic species and their possible interdiffusion. The barrier efficacy has been demonstrated by comparing the morphological and chemical modifications of the annealed Cu layers, with and without the presence of the TiN layer, and their effects on the electrical properties of the Cu films.

In this work, the evolution of the Au assisted-growth of ZnO nanorods deposited by vapour phase deposition both on sapphire and on indium-tin-oxide on glass (ITO-glass) substrates has been studied. Our investigation demonstrates that the growth proceeds first as a 3D growth, giving rise to a buffer layer, few microns thick, formed by ZnO grains with different orientation. Then a 1D transition occurs with the nucleation of a dense array of vertically aligned nanorods. A different degree of crystalline order and nanorods alignment was found between the samples grown on ITO-glass and sapphire substrates, which was ascribed to the different morphology that the Au seed layer acquires on the two different substrates. A semi-quantitative analysis of the ZnO crystalline orientation was carried out by X-ray diffraction (XRD) measurements performed at fixed incidence configuration and supported by high resolution scanning electron microscopy (HR-SEM) investigations on focused ion beam (FIB) prepared cross-sections.

In this work, we synthesized porous nanohydroxyapatite/collagen composite scaffold (nHA-COL), which resemble extracellular matrices in bone and cartilage tissues. Nano hydroxyapatite (nHA) was successfully nucleated in to the collagen matrix using hen eggshell as calcium biogenic source. Porosity was evaluated by apparent and theoretical density measurement. Porosity of all scaffolds was in the range of 95-98%. XRD and TEM analyses show the purity and size of nucleated HA around 10 nm and selected area electron diffraction (SAED) analysis reveals the polycrystalline nature of nucleated HA. SEM analysis reveals (i) all the scaffolds have interconnected pores with an average pore diameter of 130 micron and (ii) aggregates of hydroxyapatite were strongly embedded in the collagen matrix for both composite scaffolds compared with pure collagen scaffold. EDS analysis shows the Ca/P stoichiometric ratio around 1.67 and FTIR reveals the chemical interaction between the collagen molecule and HA particles. The testing of mechanical properties evidenced that incorporation of HA resulted in up to a two-fold increase in compressive modulus with high reinforcement level (similar to 7 kPa for 50HA-50COL) compared to pure collagen scaffold.

Shunt capacitive RF MEMS switches have been developed using III-V technology and employing (tantalum pentoxide) Ta2O5 thin films as dielectric layers. In order to evaluate the potential of the Ta2O5 thin films for the considered application, the compositional, structural, and electrical characterization of the deposited films has been performed, demonstrating that they are good candidates to be used as dielectric layers for the fabrication of RF MEMS switches. Specifically, Ta2O5 films are found to show a leakage current density of few nA/cm2 for MV/cm and a high dielectric constant of 32. Moreover, the charging process has been investigated, finding that it follows a stretched exponential law. The fabricated switches show actuation voltages in the range 15-20 V, an insertion loss better than -0.8 dB up to 30 GHz, and an isolation of ~-40 dB at the resonant frequency which is around 25 GHz.

Shunt capacitive radio-frequency microelectromechanical (RF MEMS) switches were modelled, fabricated and characterized in the K-band domain. Design allowed to predict the RF behaviour of the switches as a function of the bridge geometric parameters. The modelled switches were fabricated on silicon substrate, using a surface micromachining approach. In addition to the geometric parameters, the material structure in the bridge-actuator area was modified for switches fabricated on the same wafer, thanks to the removal/addition of two technological steps of crucial importance for RF MEMS switches performance, which are the use of the sacrificial layer and the deposition of a floating metal layer on the actuator. Surface profilometry analysis was used to check the material layer structure in the different regions of the bridge area as well as to investigate the mechanical behaviour of the moveable bridge under the application of a loaded force. The RF behaviour of all the fabricated switches was measured, observing the impact on the isolation of the manipulation of the bridge size and of the variations in the fabrication process.

Investigations on surface properties of poly(dimethylsiloxane) (PDMS) are justified by its large application ranges especially as coating polymer in fluidic devices. At a micrometer scale, the liquid dynamics is strongly modified by interactions with a solid surface. A crucial parameter for this process is microchannel wettability that can be tuned by acting on surface chemistry and topography. In literature, a number of multi-step, time and cost consuming chemical and physical procedures are reported. Here we selectively modify both wetting and mechanical properties by a single step treatment. Changes of PDMS surface were investigated by X-ray photoelectron spectroscopy and atomic force microscopy and the effects of interface properties on the liquid displacement inside a microfluidic system were evaluated. The negative capillary pressure obtained tailoring the PDMS wettability is believed to be promising to accurately control sample leakage inside integrated lab-on-chip by acting on the liquid confinement and thus to reduce the sample volume, liquid drying as well as cross-contamination during the operation. © 2012 Elsevier B.V. All rights reserved.

In this work, we report on similar to 4% power conversion efficiency (PCE) depleted bulk heterojunction (DBH) solar cells based on a high-quality electrode with a three-dimensional nanoscale architecture purposely designed so as to maximize light absorption and charge collection. The newly conceived architecture comprises a mesoporous electron-collecting film made of networked anisotropic metal-oxide nanostructures, which accommodates visible-to-infrared light harvesting quantum dots within the recessed regions of its volume. The three-dimensional electrodes were self-assembled by spin-coating a solution of colloidal branched anatase TiO2 NCs (BNC), followed by photocatalytic removal of the native organic capping from their surface by a mild UV-light treatment and filling with small PbS NCs via infiltration. The PCE similar to 4% of our TiO2 BNC/PbS QD DBH solar cell features an enhancement of 84% over the performance obtained for a planar device fabricated under the same conditions. Overall, the DBH device fabrication procedure is entirely carried out under mild processing conditions at room temperature, thus holding promise for low-cost and large-scale manufacturing.