RESUMO
Titanium is the most used material for implant production. To increase its biocompatibility, continuous research on new coatings has been performed by the scientific community. The aim of the present paper is to prepare new coatings on the surfaces of the pure Ti Grade 2 and the Ti6Al4V alloy. Three types of coatings were achieved by applying anodization and chemical vapor deposition (CVD) methods: TiO2 nanotubes (TNTs) were formed by anodization, carbon nanotubes (CNTs) were obtained through a metal-catalyst-free CVD process, and a bilayer coating (TiO2 nanotubes/carbon nanostructures) was prepared via successive anodization and CVD processes. The morphology and structure of the newly developed coatings were characterized using SEM, EDX, AFM, XRD, and Raman spectroscopy. It was found that after anodization, the morphology of the TiO2 layer on pure Ti consisted of a "sponge-like" structure, nanotubes, and nano-rods, while the TNTs layer on the Ti alloy comprised mainly nanotubes. The bilayer coatings on both materials demonstrated different morphologies: the pure Ti metal was covered by a layer of nanotubular and nano-rod TiO2 structures, followed by a dense carbon layer decorated with carbon nanoflakes, and on the Ti alloy, first, a TNTs layer was formed, and then carbon nano-rods were deposited using the CVD method.
RESUMO
A thermoplastic polyurethane (TPU) composite film containing hexadecyl-functionalized low-defect graphene nanoribbons (HD-GNRs) was produced by solution casting. The HD-GNRs were well distributed within the polyurethane matrix, leading to phase separation of the TPU. Nitrogen gas effective diffusivity of TPU was decreased by 3 orders of magnitude with only 0.5 wt % HD-GNRs. The incorporation of HD-GNRs also improved the mechanical properties of the composite films, as predicted by the phase separation and indicated by tensile tests and dynamic mechanical analyses. The improved properties of the composite film could lead to potential applications in food packaging and lightweight mobile gas storage containers.
RESUMO
Although lithium ion batteries have gained commercial success owing to their high energy density, they lack suitable electrodes capable of rapid charging and discharging to enable a high power density critical for broad applications. Here, we demonstrate a simple bottom-up approach toward single crystalline vanadium oxide (VO2) ribbons with graphene layers. The unique structure of VO2-graphene ribbons thus provides the right combination of electrode properties and could enable the design of high-power lithium ion batteries. As a consequence, a high reversible capacity and ultrafast charging and discharging capability is achieved with these ribbons as cathodes for lithium storage. A full charge or discharge is capable in 20 s. More remarkably, the resulting electrodes retain more than 90% of the initial capacity after cycling more than 1000 times at an ultrahigh rate of 190C, providing the best reported rate performance for cathodes in lithium ion batteries to date.
Assuntos
Fontes de Energia Elétrica , Grafite/química , Lítio/química , Eletrodos , Desenho de Equipamento , Nanoestruturas/química , Óxidos/química , Propriedades de SuperfícieRESUMO
Here, we design and develop high-power electric double-layer capacitors (EDLCs) using carbon-based three dimensional (3-D) hybrid nanostructured electrodes. 3-D hybrid nanostructured electrodes consisting of vertically aligned carbon nanotubes (CNTs) on highly porous carbon nanocups (CNCs) were synthesized by a combination of anodization and chemical vapor deposition techniques. A 3-D electrode-based supercapacitor showed enhanced areal capacitance by accommodating more charges in a given footprint area than that of a conventional CNC-based device.
RESUMO
In an effort to combine group III-V semiconductors with carbon nanotubes, a simple solution-based technique for gallium functionalization of nitrogen-doped multi-wall carbon nanotubes has been developed. With an aqueous solution of a gallium salt (GaI(3)), it was possible to form covalent bonds between the Ga(3+) ion and the nitrogen atoms of the doped carbon nanotubes to form a gallium nitride-carbon nanotube hybrid at room temperature. This functionalization was evaluated by x-ray photoelectron spectroscopy, energy dispersive x-ray spectroscopy, Raman spectroscopy, scanning electron microscopy and transmission electron microscopy.
RESUMO
The establishment of covalent junctions between carbon nanotubes (CNTs) and the modification of their straight tubular morphology are two strategies needed to successfully synthesize nanotube-based three-dimensional (3D) frameworks exhibiting superior material properties. Engineering such 3D structures in scalable synthetic processes still remains a challenge. This work pioneers the bulk synthesis of 3D macroscale nanotube elastic solids directly via a boron-doping strategy during chemical vapour deposition, which influences the formation of atomic-scale "elbow" junctions and nanotube covalent interconnections. Detailed elemental analysis revealed that the "elbow" junctions are preferred sites for excess boron atoms, indicating the role of boron and curvature in the junction formation mechanism, in agreement with our first principle theoretical calculations. Exploiting this material's ultra-light weight, super-hydrophobicity, high porosity, thermal stability, and mechanical flexibility, the strongly oleophilic sponge-like solids are demonstrated as unique reusable sorbent scaffolds able to efficiently remove oil from contaminated seawater even after repeated use.
RESUMO
In this paper, a method of strain actuation of single-walled carbon nanotube (SWNT) films using droplets is examined, and the physical origin of an open-circuit voltage (Voc)-observed across the film during this process-is explored. We demonstrate that droplet actuation is driven by the formation of a capillary bridge between the suspended SWNT films and the substrates, which deforms the films by wetting forces during evaporation. The induced strain is further evaluated and analyzed using dynamic Raman and two-dimensional correlation spectra. Supported by theoretical calculations, our experiments reveal the time and strain dependency of the capillary bridge's midpoint directional movement. This relationship is applied to display the correlation between the induced strain and the measured Voc.
RESUMO
We have created stable dispersions of single wall carbon nanotubes (SWNTs) in water by employing a noncovalent functionalization scheme that allows carboxylic acid moieties to be attached to the SWNT surface by a pi-pi stacking interaction. Pyrenecarboxylic acid (PCA) is noncovalently attached to the surface of SWNTs and affords highly uniform and stable aqueous dispersions. This method was developed to provide a noncovalent alternative to the commonly used oxidative acid treatment functionalization of carbon nanotubes. This alternative strategy avoids the damage to the carbon nanotube structure inherent to oxidative acid treatments. Carbon nanotubes are commonly functionalized with oxidative acid treatment schemes to create polymer-nanotube composites and improve the adhesion between the polymer and carbon nanotubes. Composites of SWNTs and polycarbonate were prepared and tested to determine the effect of PCA on the adhesion of the SWNTs to the polymer matrix. These tests confirmed that PCA improved the SWNT-polycarbonate adhesion and improved the dispersion of the SWNTs throughout the matrix. This study demonstrates that stable dispersions of SWNTs can be achieved without substantial cutting, introduction of defects, or covalent modification, by employing a simple and effective noncovalent functionalization with PCA.