Dispersion and alignment of carbon nanotubes in polycarbonate

Dispersion and alignment of carbon nanotubes in thermoplastic polymers such as polycarbonate have been studied. Dispersion was accomplished by mixing in a conical twin-screw extruder and alignment was carried out using a fiber-spinning apparatus. The effects of mixing time and fiber draw rates on dispersion and alignment were investigated. Uniform dispersions were produced with relatively short residence times in the extruder. Excellent alignment of carbon nanotubes in nanocomposite filaments was obtained when the fiber draw rate was greater than 70 m/min. The ability to closely control the dispersion and alignment of carbon nanotubes in polymers is expected to lead to the development of nanocomposites with desirable electronic and structural properties. Received: 7 January 2002 / Accepted: 11 April 2002 / Published online: 10 September 2002 RID="*" ID="*"Corresponding author. Fax: +1-508/233-5521, E-mail: Michael.Sennett@natick.army.mil     

Carbon nanotubes formed in graphite after mechanical grinding and thermal annealing

Multi-walled carbon nanotubes with cylindrical and bamboo-type structures are produced in a graphite sample after mechanical milling at ambient temperature and subsequent thermal annealing up to 1400 °C. The ball milling produces a precursor structure and the thermal annealing activates the nanotube growth. Different nanotubular structures indicate different formation mechanisms: multi-wall cylindrical carbon nanotubes are probably formed upon micropores and the bamboo tubes are produced because of the metal catalysts. A two-dimensional growth governed by surface diffusion is believed to be one important factor for the nanotube growth. A potential industrial production method is demonstrated with advantages of large production quantity and low cost. Received: 17 May 2002 / Accepted: 12 September 2002 / Published online: 4 December 2002 RID="*" ID="*"Corresponding author. Fax: +61-2/6125-8338, E-mail: ying.chen@anu.edu.au     

High yield incorporation and washing properties of halides incorporated into single walled carbon nanotubes

We describe here the high yield filling (i.e. >50%) of single walled nanotubes (SWNTs) with a variety of halides, achieved according to various modified filling procedures. Both bundles and discrete SWNTs can be filled continuously up to lengths of several hundred nm, often with filling yields approaching 60–70% or better. In addition some high yield filled SWNTs were subjected to long-term washing in either boiling or room temperature. aqueous media, which does not remove the filling from the tubules, but enables effective removal of water-soluble extraneous materials . Received: 10 May 2002 / Accepted: 25 October 2002 / Published online: 10 March 2003 RID="*" ID="*"Corresponding author. Fax: +44-1865/272-690, E-mail: jeremy.sloan@chem.ox.ac.uk     

Field emission from single-walled carbon nanotubes aligned on a gold plate using a self-assembly monolayer

Field emission from single-walled carbon nanotubes (SWNTs) aligned on a patterned gold surface is reported. The SWNT emitters were prepared at room temperature by a self-assembly monolayer technique. SWNTs were cut into sub-micron lengths by sonication in an acidic solution. Cut SWNTs were attached to the gold surface by the reaction between the thiol groups and the gold surface. The field-emission measurements showed that the turn-on field was 4.8 V/μm at an emission current density of 10 μA/cm². The current density was 0.5 mA/cm² at 6.6 V/μm. This approach provides a novel route for fabricating CNT-based field-emission displays. Received: 3 May 2002 / Accepted: 6 May 2002 / Published online: 4 December 2002 RID="*" ID="*"Corresponding author. Fax: +82-54/279-8298, E-mail: ce20047@postech.ac.kr     

Nanotube growth during annealing of mechanically milled Boron

Boron powder, finely ground in a tungsten carbide ball mill in an ammonia atmosphere, has been annealed at 1200 °C in flowing nitrogen to produce small quantities of cylindrical BN nanotubes, both as isolated individuals and grouped into ropes. Thick-walled conical BN tubes are abundant in specimens annealed for longer times, and their growth was catalysed once WC debris was converted into W metal particles. Some catalytic effect of small W nanoparticles could be necessary for nanotube formation, though no tip particles have been imaged here. Given the low temperature of mechanical milling and annealing, BN growth must involve surface diffusion and solid-state reconfiguration. It could be possible to engineer desirable physical and chemical properties by exploiting the variation in cylindrical versus conical BN structures as a function of annealing time. Received: 19 December 2001 / Accepted: 3 April 2002 / Published online: 19 July 2002 RID="*" ID="*"Corresponding author. Fax: +61-2/6125-8253, E-mail: john.fitzgerald@anu.edu.au     

Microstructural properties of bulk nanocrystalline Ag–Ni alloy prepared by hot pressing of mechanically pre-alloyed powders

A bulk nanocrystallined Ag50Ni alloy has been prepared by hot-pressing the mechanically pre-alloyed powders at 620 °C under a normal pressure of 58 MPa in vacuum. The microstructural characteristics of the alloy were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results of the precise determination of the lattice parameters of the phases in the powders and in the alloy by XRD show that, after mechanical alloying for 200 h, the solid solubility of Ag in Ni reaches 4.85±0.21 at %, while that of Ni in Ag reaches 0.84±0.30 at %. After hot pressing, the Ag- and Ni-rich phases in the alloy still show a certain degree of supersaturation, with a solid solubility of 0.45±0.11 at % of Ag in Ni. After further annealing of the alloy at 700 °C for 24 h, the solubility decreases to a value of 0.21±0.11 at % for Ag in Ni and to less than 0.1 at % for Ni in Ag. The grain size of the mechanically alloyed powders was of ca 6 nm. After hot pressing, the grain size of the alloy increased to 40–60 nm and then grew further to 100–110 nm after annealing. The influence of the variation of the grain size and the internal stress on the line breadth of the X-ray diffraction peaks has been evaluated in detail. Finally, the role of the nanocrystalline structure in the fast densification process of the powders is also discussed. Received: 12 September 2001 / Accepted: 18 Febraury 2002 / Published online: 10 September 2002 RID="*" ID="*"Corresponding author. Fax: +86-24/2389-3624, E-mail: wwt@icpm.syb.ac.cn     

High-yield synthesis of multi-walled carbon nanotubes by arc discharge in liquid nitrogen

Synthesis of multi-walled carbon nanotubes (MWNTs) by arc discharge in liquid nitrogen is reported. As liquid nitrogen substituted both vacuum and cooling systems, high-quality MWNTs were produced at a low cost. The content of the MWNTs can be as high as 70% of the reaction product. Auger-spectroscopy analysis revealed that no nitrogen is incorporated in the MWNTs. This method can be an economical route for the mass production of highly crystalline MWNTs. Received: 5 July 2002 / Accepted: 8 July 2002 / Published online: 10 September 2002 RID="*" ID="*"Corresponding author. Fax: +82-54/279-8298, E-mail: ce20047@postech.ac.kr     

WS<Subscript>2</Subscript> layer formation on multi-walled carbon nanotubes

Time-dependent powder X-ray-diffraction analyses reveal that the conversion of WO₃ into WS₂ on carbon nanotube surfaces in the presence of H₂S is a one-step process. The WS₂ layers grow simultaneously along the tube in the radial and axial directions. Received: 17 June 2002 / Accepted: 19 June 2002 / Published online: 15 January 2003 RID="*" ID="*"Corresponding author. Fax: +44-1273/677-196, E-mail: d.walton@sussex.ac.uk     

A simple wet-chemical synthesis and characterization of CuO nanorods

Using a simple wet-chemical route, we synthesized CuO nanorods with diameters of ca. 5–15 nm and lengths of up to 400 nm. The purity, crystallinity, morphology, structure features, and chemical composition of the as-prepared CuO nanorods were investigated by powder X-ray diffraction, transmission electron microscopy, high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, and Raman spectroscopy. Received: 22 March 2002 / Accepted: 12 June 2002 / Published online: 28 October 2002 RID="*" ID="*"Corresponding author. Fax: +86-25/359-5535, E-mail: wangqun@nju.edu.cn     

High-resolution electron microscopy of individual metallofullerene molecules on the dipole orientations in peapods

Electron microscopy with atomic sensitivity enables us to obtain a direct image of the intra-molecular structure of metallofullerenes encapsulated inside single-walled carbon nanotubes. By a comparison of high-resolution images with a simulation to extract the relative atom positions for encaged metal atoms in each molecule, the distribution of the molecular orientations and interactions between adjacent molecules in metallofullerene peapods have been statistically analyzed. The results are suggestive of strong interactions between fullerene–fullerene and fullerene–tube in peapods at room temperature. Received: 10 October 2002 / Accepted: 25 October 2002 / Published online: 10 March 2003 RID="*" ID="*"Corresponding author. Fax: +81-298/61-6310, E-mail: suenaga-kazu@aist.go.jp     

Giant field amplification in tungsten nanowires

The original RF-sputtering-assisted technique to produce metal wires with tip-curvature radii at the nanometer scale was developed and applied to tungsten. The wire tips were characterized by scanning electron microscopy. Field-emission tests of those wires exhibit excellent performance and reliable processability. Very high field-amplification factors of 18000 were demonstrated. Received: 1 November 2002 / Accepted: 30 November 2002 / Published online: 11 April 2003 RID="*" ID="*"Corresponding author. Fax: +1-972/479-4482, E-mail: alexander.umnov@fla.fujitsu.com     

Catalytic growth and characterization of Ga<Subscript>2</Subscript>O<Subscript>3</Subscript> nanowires

β-Ga₂O₃ nanowires have been synthesized using Ga metal and H₂O vapor at 800 °C in the presence of Ni catalyst on the substrate. Remarkable reduction of the diameter and increase of the length of the Ga₂O₃ nanowires are achieved by separation of Ga metal and H₂O vapor before they reach the substrate. Transmission electron microscopy analyses indicate that the β-Ga₂O₃ nanowires possess a single-crystalline structure. Photoluminescence measurements show two broad emission bands centered at 290 nm and 390 nm at room temperature. Received: 27 June 2002 / Accepted: 7 October 2002 / Published online: 17 December 2002 RID="*" ID="*"Corresponding author. Fax: +886-6/234-4496, E-mail: wujj@mail.ncku.edu.tw     

Electro-responsive asymmetric nanopores in polyimide with stable ion-current signal

For the preparation of a single asymmetrically shaped nanopore in a polyimide membrane, Kapton foils were irradiated with single heavy ions and subsequently etched from one side in sodium hypochlorite (NaOCl). The other side of the membrane was protected from etching by a stopping medium containing a reducing agent for hypochlorite ions (OCl^-). The resulting conical nanopore rectified ion current and exhibited a stable ion-current flow. Received: 23 May 2002 / Accepted: 2 September 2002 / Published online: 15 January 2003 RID="*" ID="*"Corresponding author. Fax: +49-6159/712-179, E-mail: Z.Siwy@gsi.de     

Effect of nickel,iron and cobalt on growth of aligned carbon nanotubes

The effect of pure nickel, iron and cobalt on growth of aligned carbon nanotubes was systematically studied by plasma-enhanced hot-filament chemical vapor deposition. It is found that the catalyst has a strong effect on the nanotube diameter, growth rate, wall thickness, morphology and microstructure. Ni yields the highest growth rate, largest diameter and thickest wall, whereas Co results in the lowest growth rate, smallest diameter and thinnest wall. The carbon nanotubes catalyzed by Ni have the best alignment and the smoothest and cleanest wall surface, whereas those from Co are covered with amorphous carbon and nanoparticles on the outer surface. The carbon nanotubes produced from Ni catalyst also exhibit a reasonably good graphitization. Therefore, Ni is considered as the most suitable catalyst for growth of aligned carbon nanotubes. Received: 30 November 2001 / Accepted: 3 December 2001 / Published online: 4 March 2002     

Electrochemical synthesis of ordered CdTe nanowire arrays

Semiconductor CdTe nanowire arrays embedded in the nanochannels of the porous anodic alumina (PAA) template have been prepared by using a potentiostatic electrochemical deposition method. The morphology and structure of the CdTe nanowire arrays have been characterized by X-ray powder diffraction, transmission electron microscopy, and high-resolution transmission electron microscopy. It is found that the CdTe nanowires with diameters and lengths of about 60 nm are single-crystalline with cubic phase structure, uniformly and continuously embedded in the nanochannels of the PAA template. X-ray energy-dispersion analysis and X-ray photoelectron spectroscopy analysis indicate that stoichiometric CdTe was formed. The growth mechanism of the CdTe nanowires is also discussed. Received: 11 June 2002 / Accepted: 2 July 2002 / Published online: 8 January 2003 RID="*" ID="*"Corresponding author. Fax: +86-551/559-1434, E-mail: aiwuzhao@yahoo.com.cn     

Synthesis and morphology of boron nitride nanotubes and nanohorns

Boron nitride (BN) nanotubes have been synthesized by evaporating a mixture of boron and gallium oxide in the presence of ammonia gas. The synthesized BN nanotubes exhibit a well-crystallized concentric structure with diameters less than 30 nm, and no carbon contamination or defects could be observed, while the BN nanotubes with large diameters usually show a number of defects. Some BN nanohorn structures could also be observed in the product. The carbon-free growth of BN nanotubes was explained based on the vapor–liquid–solid growth mechanism, and the catalytic activity of liquid gallium for BN one-dimensional growth was also demonstrated. Received: 16 April 2002 / Accepted: 25 May 2002 / Published online: 19 July 2002     

Self-assembly of length-tunable gold nanoparticle chains in organic solvents

The one-dimensional coagulation of gold colloidal particles dispersed in organic solvent was investigated with transmission electron microscopy. The results indicate that the length of the nanoparticle chains can be modulated by changing the concentration of the solutions. It was also demonstrated that the wetting of the substrate surface hardly influenced the morphology of the nanoparticle chains, which revealed that the particle chains had been formed in the solution before deposition on the substrates. A general theoretical interpretation is provided to explain the linear coagulation of gold colloidal particles, on the basis of the asymmetrical distribution of the charges absorbed on the surface of the gold colloidal particles, as well as the action of the solvent molecules. Received: 8 April 2002 / Accepted: 1 July 2002 / Published online: 4 December 2002 RID="*" ID="*"Corresponding author. Fax: +86-025/361-9983, E-mail: jhliao@seu.edu.cn     

Growth of vertically aligned carbon-nanotube array on large area of quartz plates by chemical vapor deposition

A simple method has been developed for growth of well-aligned carbon nanotubes (CNTs) on nickel-film quartz plates by chemical vapor deposition (CVD) with organic ethylenediamine as a precursor. High-density carbon nanotubes were vertically aligned on a large area of the quartz plates. The height of the nanotube array could be controlled by varying the CVD time. High-resolution transmission electron microscopy analysis revealed that the multiwalled CNTs were composed of crystalline graphitic sheets with a bamboo structure. Received: 28 May 2001 / Accepted: 3 December 2001 / Published online: 4 March 2002     

Preparation of Mn<Subscript>3</Subscript>O<Subscript>4</Subscript> nanowires by calcining the precursor powders synthesized in a novel inverse microemulsion

Manganese oxide (hausmannite) nanowires were prepared by annealing precursor powders at a temperature of 800 °C for 3 h, which were produced in a novel inverse microemulsion (IμE) system. The microstructures of the as-prepared Mn₃O₄ nanowires were investigated by means of X-ray diffraction, transmission electron microscopy, and Raman spectra. It has been found that the Mn₃O₄ nanowires were relatively straight and their surfaces were smooth with a typical diameter of 75–150 nm. The formation mechanism of the Mn₃O₄ nanowires is discussed. Received: 30 May 2002 / Accepted: 7 October 2002 / Published online: 17 December 2002 RID="*" ID="*"Corresponding author. Fax: +86-25/359-5535, E-mail: wangqun@nju.edu.cn