Andre S. Ferlauto

On the growth and electrical characterization of CuO nanowires by thermal oxidation

We present a detailed study on the growth process of cupric oxide (CuO) nanowires by thermal oxidation. The morphology of nanowires, obtained at different oxidation temperatures and times, was determined. The diameter of nanowires was found to depend linear on temperature whereas the time dependence of their length is modeled by a parabolic law. The results suggest that CuO nanowires are formed as a result of the competition between grain boundary and lattice diffusion of Cu atoms across a Cu2O layer. Electrical characterization of the nanowires was also performed. A field effect transistor was produced with an isolated nanowire showing p-type characteristics. The resistivity, mobility, and density of carriers were calculated. Nanowire growth by thermal oxidation is very simple and has great potential to be used for large scale production; this opens possibilities for various kinds of application.

Nafion–Titanate Nanotube Composite Membranes for PEMFC Operating at High Temperature

Nafion-titanate nanotube composites were investigated as electrolytes for proton exchange membrane fuel cells (PEMFCs) operating at high temperature T. With the addition of 5-15 wt % of nanotubes to the ionomer, PEMFC performance can be significantly sustained for T up to 130°C. The polarization curves of PEMFCs using the composite electrolytes reflect a competing effect between an increase in water uptake due to the extremely large surface area of the nanotubes and a decrease in proton conductivity of the composites.

Direct production of carbon nanotubes/metal nanoparticles hybrids from a redox reaction between metal ions and reduced carbon nanotubes.

A method to decorate single-walled and multiwalled carbon nanotubes (CNTs) with metal nanoparticles (NPs) based on the formation of a CNT polyelectrolyte is reported. Such a method does not rely on CNT surface functionalization or the use of surfactants. It has been tested for gold (Au) and palladium (Pd). The resulting hybrids present metal NPs highly dispersed along the tube walls and with small size dispersion. The average diameters of the Au and Pd NPs were approximately 5 and approximately 3 nm, respectively. This method paves the way for large-scale decoration of CNTs with metal NPs.

Gene expression and biochemical responses in brain of zebrafish Danio rerio exposed to organic nanomaterials: carbon nanotubes (SWCNT) and fullerenol (C60(OH)18-22(OK4)).

Nanomaterials (NM) industry had grown in the last decade, although there are few studies concerning its potential toxicity effects on aquatic organisms. In this study the freshwater zebrafish (Danio rerio) was exposed to two kinds of carbon NM, single-wall carbon nanotubes (SWCNT) and fullerenol [C60(OH)18-22(OK4)] to analyze oxidative stress responses on fish brain. Adult zebrafish (mean mass: 0.52±0.01g) were submitted to intraperitoneal injections of SWCNT suspension and fullerenol solution (30mg/kg of fish), receiving one or two doses with a time interval of 24h. Results showed that total antioxidant capacity was lowered in brains of fish exposed 24h to fullerenol when compared to those from SWCNT treatment (p<0.05). After 48h, fullerenol induced higher expression of both catalytic and regulatory subunits of enzyme glutamate cysteine ligase when compared to control group (p<0.05), indicating an antioxidant behavior. In vitro assays showed a dual effect of SWCNT, since a pro-oxidant behavior was observed at low concentrations (0.1 and 1.0mg/L) and an antioxidant one at the highest concentration (10.0mg/L). Few biological responses were altered by this NM: decrease in total antioxidant capacity and induction of the expression of the transcription factor Nrf2 when compared to control group.

Asymmetric effect of oxygen adsorption on electron and hole mobilities in bilayer graphene: long- and short-range scattering mechanisms.

We probe electron and hole mobilities in bilayer graphene under exposure to molecular oxygen. We find that the adsorbed oxygen reduces electron mobilities and increases hole mobilities in a reversible and activated process. Our experimental results indicate that hole mobilities increase due to the screening of long-range scatterers by oxygen molecules trapped between the graphene and the substrate. First principle calculations show that oxygen molecules induce resonant states close to the charge neutrality point. Electron coupling with such resonant states reduces the electron mobilities, causing a strong asymmetry between electron and hole transport. Our work demonstrates the importance of short-range scattering due to adsorbed species in the electronic transport in bilayer graphene on SiO2 substrates.

Determination of the epitaxial growth of zinc oxide nanowires on sapphire by grazing incidence synchrotron x-ray diffraction

This letter shows that aligned zinc oxide (ZnO) nanowires growth on sapphire substrates is epitaxial and demonstrates the crystallographic relation between the two using grazing incidence synchrotron x-ray diffraction (XRD). The in-plane lattice match between the sapphire and the nanowires was directly probed by using XRD at grazing angles of incidence, where the lattice match between the (0001) plane of the sapphire and the (11−20) plane of the ZnO were observed simultaneously. It will also be shown that gold acts as a catalyst to initiate ZnO nanowire growth, but it does not interfere with the epitaxial mechanism between the nanowires and the sapphire substrate.

Mixed ionic-electronic conductivity in yttria-stabilized zirconia/carbon nanotube composites

The fabrication of yttria stabilized-zirconia/single-wall carbon nanotube (YSZ/SWCNT) composites is reported. Electrical conductivity measurements from 25to800°C revealed that the composites exhibit mixed ionic-electronic conduction. At room temperature, the conductivity increases by 11 orders of magnitude with the addition of SWCNT to the YSZ. At high temperatures (>300°C), the ionic conduction of the YSZ becomes relevant and a mixed ionic-electronic transport is observed. It is found that the transport can be described by a sum of two parallel contributions: thermally activated ionic conduction from the YSZ and fluctuation-assisted tunneling within the SWCNT network.

One-pot in situ photochemical synthesis of graphene oxide/gold nanorod nanocomposites for surface-enhanced Raman spectroscopy

Nanoscale engineered plasmonic materials that can efficiently sustain surface enhanced Raman scattering (SERS) have been strongly pursued for high sensitivity molecular detection. In this work, we report the production of gold nanorod/graphene oxide (GNR/GO) nanocomposites by a simple, one-pot process whereby GNR are formed directly onto the GO flakes in solution by UV light irradiation. The proposed method is easily scalable and results in GNRs with low dispersion in size and aspect ratio of ∼3. The GNR/GO hybrids were deposited in glass by filtration yielding homogenous films that were systematically tested as SERS active substrates. Raman spectroscopy mapping revealed that the tested substrates present spatially homogenous and reproducible SERS responses. Analysis of Raman spectroscopy by using a model molecule (cresyl violet perchlorate) indicates that the produced substrates can provide very large SERS enhancement factors (∼106) and very low molecular detection limits (10−11 M).

Fabrication of gas nanosensors and microsensors via local anodic oxidation.

A nanosensor and microsensor fabrication method employing scanning probe microscopy (SPM) is demonstrated. Within such process, nano- or microscale metal oxide (MoO(x) or TiO(x)) structures, constituting the active region of a sensor, are directly fabricated onto a microscopic metal track via SPM-assisted local anodic oxidation (LAO). Two distinct LAO routes, a slow (conventional) or a fast (unusual) one, are employed to produce nano- and microsensors, which are tested at different temperatures using CO2 and H2 as test gases. Sensitivities down to ppm levels are demonstrated, and the possibility of easy integration into microfabrication processes is also discussed.

Graphene chemical vapor deposition at very low pressure: The impact of substrate surface self-diffusion in domain shape

The initial stages of graphene chemical vapor deposition at very low pressures ( 900 °C), graphene grain shape and symmetry were found to depend on the underlying symmetry of the Cu crystal, whereas for lower temperatures (<900 °C), mostly rounded grains are observed. The temperature dependence of graphene nucleation density was determined, displaying two thermally activated regimes, with activation energy values of 6 ± 1 eV for temperatures ranging from 900 °C to 960 °C and 9 ± 1 eV for temperatures above 960 °C. The comparison of such dependence with the temperature dependence of Cu surface self-diffusion suggests that graphene growth at high temperatures and low pressures is strongly influenced by copper surface rearrangement. We propose a model that incorporates Cu surface self-diffusion as an essential process to explain the orientation correlation between graphene and Cu crystals, and which can clarify the difference generally observed between graphene domain shapes in atmospheric-pressure and low-pressure chemical vapor deposition.