Aligned coaxial nanocables were grown on Si substrates by a vapor-deposition technique. The lengths of the nanocables increased as the distance between the substrate and the source decreased. The nanocables were characterized as homogeneously crystallized shells of about 25 nm thick, diameters of about 100 nm, and round top ends. It was found that the shell emits an intense middle-ultraviolet about 300 nm at room temperature. This emission was attributed to the thin double-layer structure in the Zn-Zn2SiO4 core-shell nanocable where the Zn2SiO4 shell has the potential to serve as more ideal luminophors. The results demonstrated that the nanocable density could be changed by altering nucleation density at the steps on the substrate surface. The unique growth manner described herein provides a new technique for the homogeneous crystallization of Zn-Zn2SiO4 core-shell nanocables. 相似文献
A simple one-step thermal evaporation of CdSe powder using Si substrate at controlled conditions results in ultrauniform Si-core/CdSe-sheath nanocables. These nanocables are approximately 80 nm in diameter and several tens of micrometers in length. Detailed microstructure and chemical composition analysis of the nanocables indicates that they are composed of a single crystalline Si (cubic) core and CdSe (hexagonal) sheath. The experimental evidence suggested that the Si nanowires can be directly grown from the Si substrate via an oxide-assisted growth mechanism and further served as templates for CdSe, resulting in nanocable heterostructures. 相似文献
One-dimensional gold/polyaniline (Au/PANI-CSA) coaxial nanocables with an average diameter of 50-60 nm and lengths of more than 1 mum were successfully synthesized by reacting aniline monomer with chlorauric acid (HAuCl(4)) through a self-assembly process in the presence of D-camphor-10-sulfonic acid (CSA), which acts as both a dopant and surfactant. It was found that the formation probability and the size of the Au/PANI-CSA nanocables depends on the molar ratio of aniline to HAuCl(4) and the concentration of CSA, respectively. A synergistic growth mechanism was proposed to interpret the formation of the Au/PANI-CSA nanocables. The directly measured conductivity of a single gold/polyaniline nanocable was found to be high (approximately 77.2 S cm(-1)). Hollow PANI-CSA nanotubes, with an average diameter of 50-60 nm, were also obtained successfully by dissolving the Au nanowire core of the Au/PANI-CSA nanocables. 相似文献
A novel Ag/C nanocable and epoxy resin composite was obtained by compounding Ag/C nanocables and epoxy resin. The nanocable is composed of a nanowire (core) wrapped with one or more outer layers (shell). Scanning electron microscopy images proved that the nanocables consisted of a silver nanowire core and a carbon outer shell. The Ag/C nanocables were modified by hyperbranched poly (amine ester) to improve their mechanical properties for further application. We separately compounded raw and modified Ag/C nanocables with epoxy resin, and then tested the thermal performance, tensile properties, and fracture morphology of each composite. We found that the tensile strengths of the two composite systems were enhanced by the epoxy resin, with the modified (Ag/C)/epoxy resin composite system improving more significantly. Differential scanning calorimeter (DSC) results showed that the glass transition temperature of the unmodified (Ag/C)/epoxy resin composite is increased when the Ag/C nanocable is filled, while that of the modified system slightly decreased. Fracture morphology results showed that both (Ag/C)/epoxy composite systems featured increased toughness. The modified Ag/C nanocables had better compatibility with the epoxy resin. The relationship between the properties and microstructure of the composites were discussed in detail to explain the mechanism behind the observed changes in material properties. 相似文献
Summary: In this paper, PEDOT/PSS‐ZnO coaxial nanocables with diverse inner core sizes are prepared by a new and facile method that involves two‐steps: the synthesis of ZnO nanoparticles through a sol‐gel process, followed by dewetting‐controlled self‐assembly of the nanoparticles and charged polymers to generate a cable‐like nanostructure with the aid of a vacuum. The nanocables have an outer diameter of ca. 100 nm with a polycrystalline ZnO inner core of 7–25 nm in diameter. The length and morphology of the nanocables are determined by external vacuum conditions as well as the ZnO concentration in the composite. A photoluminescence study shows an enhanced green light emission arising from ZnO with a size‐dependence feature.
TEM image of a PEDOT/PSS‐ZnO nanocable at high magnification. 相似文献
We describe a new synthetic approach to fabricate Ni/Cu nanocable arrays by co-depositing nickel and copper atoms into the pores of anodic alumina membranes and to fabricate Ni nanotube arrays by selectively etching the Cu cores from the Ni/Cu nanocable arrays. The formation of the Ni-shelled Ni/Cu nanocables is attributed to the Ni ions adsorbed on the pore walls by a chemical complexation through hydroxyl groups. By varying electrodepositon parameters in this technique, we can control the lengths of nanocables and nanotubes, the shell thickness of the nanocables, and the wall thickness and surface morphology of the nanotubes. 相似文献
Summary: Copper/poly(vinyl alcohol) (PVA) nanocables have been successfully obtained by electrospinning a PVA‐protected copper nanoparticle solution. The molar ratio of copper ions to PVA (in terms of VA repeating units) plays an important role in the formation of copper/PVA nanocables. The average diameter of the copper cores and PVA shells is about 100 and 400 nm, respectively. The structures of the copper/PVA nanocables are characterized by transmission electron microscopy (TEM) and their formation is confirmed by scanning electron microscopy (SEM).
