Vertically aligned carbon-nanotube arrays showing Schottky behavior at room temperature

Vertically aligned carbon-nanotube (CNT) arrays were fabricated in the thin-film anodic aluminum oxide (AAO) templates on silicon wafers utilizing a niobium (Nb) thin film as the source electrode. The average diameter of the CNTs was 25 nm, and the number density was 3 x 10(10) cm(-2). The CNT arrays synthesized at 700 degrees C and above exhibited Schottky behavior even at 300 K, with energy gaps between 0.2 eV and 0.3 eV. However, individual CNTs obtained by removal of the template behaved as resistors at 300 K. The CNT/Nb oxide/Nb junction is thought to be responsible for the Schottky behavior. This structure can be a useful cornerstone in the fabrication of nanotransistors operating at room temperature.     

Frictionless sliding of single-stranded DNA in a carbon nanotube pore observed by single molecule force spectroscopy

Smooth inner pores of carbon nanotubes (CNT) provide a fascinating model for studying biological transport. We used an atomic force microscope to pull a single-stranded DNA oligomer from a carbon nanotube pore. DNA extraction from CNT pores occurs at a nearly constant force, which is drastically different from the elastic profile commonly observed during polymer stretching with atomic force microscopy. We show that a combination of the frictionless nanotube pore walls and an unfavorable DNA solvation energy produces this constant force profiles.     

Investigation of metal/carbon-related materials for fuel cell applications by electronic structure calculations

The potential of carbon-related materials, such as carbon nanotubes (CNTs) and graphite nanofibers (GNFs), supported metal catalysts as an electrode for fuel cell application was investigated using the first-principle electronic structure calculations. The stable binding geometries and energies of metal catalysts are determined on the CNT surface and the GNF edge. The catalyst metal is more tightly bound to the GNF edge than to the CNT surface because of the existence of active dangling bonds of edge carbon atoms.The diffusion barrier of metal atoms on the surface and edge is also obtained. From our calculation results, we have found that high dispersity is achievable for GNF due to high barrier against the diffusion of metal atoms, while CNT appears less suitable. The GNF with a large edge-to-wall ratio is more suitable for the high-performance electrode than perfect crystalline graphite or CNT.     

Nickel Oxide/Carbon Nanotubes Nanocomposite for Electrochemical Capacitance

A nanocomposite of nickel oxide/carbon nanotubes was prepared through a simple chemical precipitation followed by thermal annealing. The electrochemical capacitance of this electrode material was studied. When the mass fraction of CNTs (carbon nanotubes) in NiO/CNT composites increases, the electrical resistivity of nanocomposites decreases and becomes similar to that of pure CNTs when it reaches 30%. The specific surface area of composites increases with increasing CNT mass fraction and the specific capacitance reaches 160 F/g under 10 mA/g discharge current density at CNT mass fraction of 10%.     

Deposition of platinum nanoparticles on organic functionalized carbon nanotubes grown in situ on carbon paper for fuel cells

Deposition of small Pt nanoparticles of the order of 2-2.5?nm on carbon nanotubes (CNTs) grown directly on carbon paper is demonstrated in this work. Sulfonic acid functionalization of CNTs is used as a means to facilitate the uniform deposition of Pt on the CNT surface. The organic molecules attached covalently to the CNT surface via electrochemical reduction of corresponding diazonium salts are treated with concentrated sulfuric acid and the sulfonic acid sites thus attached are used as molecular sites for Pt ion adsorption, which are subsequently reduced to yield the small Pt nanoparticles. Cyclic voltammograms reveal that, after removal of the organic groups during high temperature reduction, these Pt nanoparticles are in electrical contact with the carbon paper backing. A typical Pt loading of 0.09?mg?cm(-2) is achieved, that shows higher specific surface area of Pt than an E-TEK electrode with Pt loading of 0.075?mg?cm(-2). A membrane and electrode assembly (MEA) is prepared with a Pt/CNT electrode as cathode and an E-TEK electrode as anode, and it offers better performance than a conventional E-TEK MEA.     

Fabrication of highly crystalline NbOx nanotube/cup-stacked CNT nanocomposites

Carbon nanotubes (CNTs) are promising catalyst supports for fuel cell applications. Metal oxide/CNT nanocomposites are also being studied for dye-sensitized solar-cell, photocatalyst, and sensor applications. The fabrication of nanocomposites consisting of highly crystalline NbOx nanotubes and cup-stacked carbon nanotubes (CSCNTs) is reported herein. The CSCNTs were selected for the carbon materials because of their distinctive structure. The CSCNTs were photochemically treated with vacuum ultraviolet light, which increased the amount of oxygen-containing functional groups therein. NbOx nanotubes with no defects were successfully prepared with the chemical treatment of highly crystalline, layered, flux-grown K4Nb6O17 crystals. First, K4Nb6O17 crystals were grown from a KCl flux at a holding temperature of 800 degrees C. Next, NbOx nanosheets were prepared from the layered K4Nb6O17 crystals via a two-step exfoliation process, which consists of proton exchange in an acid solution and intercalation of the tetrabutylammonium ions. The NbOx nanosheets were rolled up into nanotubes with diameters of about 20 nm and lengths of 100-500 nm on the surfaces of the CSCNTs; thus, unique and complex NbOx/CSCNT nanocomposites were successfully fabricated.     

A nanostructured electrode of IrOx foil on the carbon nanotubes for supercapacitors

IrO(x) nanofoils (IrO(x)NF) of high surface area are sputtered on multi-wall carbon nanotubes (CNT) in the preparation of a structured electrode on a stainless steel (SUS) substrate for supercapacitor applications. This IrO(x)/CNT/SUS electrode is featured with intriguing IrO(x) curved foils of 2-3 nm in thickness and 400-500 nm in height, grown on top of the vertically aligned CNT film with a tube diameter of ～ 40 nm. These nanofoils are moderately oxidized during reactive sputtering and appeared translucent under the electron microscope. Detailed structural analysis shows that they are comprised of contiguous grains of iridium metal, iridium dioxide, and glassy iridium oxide. Considerable Raman line broadening is also evidenced for the attributed nanosized iridium oxides. Two capacitive properties of the electrode are significantly enhanced with addition of the curved IrO(x) foils. First, IrO(x)NF reduces the electrode Ohmic resistance, which was measured at 3.5 Ω cm(2) for the CNT/SUS and 2.5 Ω cm(2) for IrO(x)NF/CNT/SUS using impedance spectroscopy. Second, IrO(x)NF raises the electrode capacitance from 17.7 F g(-1) (CNT/SUS) to 317 F g(-1) (IrO(x)/CNT/SUS), measured with cyclic voltammetry. This notable increase is further confirmed by the galvanostatic charge/discharge experiment, measuring 370 F g(-1) after 2000 uninterrupted cycles between - 1.0 and 0.0 V (versus Ag/AgCl).     

A combination of capillary and dielectrophoresis-driven assembly methods for wafer scale integration of carbon-nanotube-based nanocarpets

The wafer scale integration of carbon nanotubes (CNT) remains a challenge for electronic and electromechanical applications. We propose a novel CNT integration process relying on the combination of controlled capillary assembly and buried electrode dielectrophoresis (DEP). This process enables us to monitor the precise spatial localization of a high density of CNTs and their alignment in a pre-defined direction. Large arrays of independent and low resistivity (4.4 × 10(-5) Ω m) interconnections were achieved using this hybrid assembly with double-walled carbon nanotubes (DWNT). Finally, arrays of suspended individual CNT carpets are realized and we demonstrate their potential use as functional devices by monitoring their resonance frequencies (ranging between 1.7 and 10.5 MHz) using a Fabry-Perot interferometer.     

Experimental-computational study of shear interactions within double-walled carbon nanotube bundles

The mechanical behavior of carbon nanotube (CNT)-based fibers and nanocomposites depends intimately on the shear interactions between adjacent tubes. We have applied an experimental-computational approach to investigate the shear interactions between adjacent CNTs within individual double-walled nanotube (DWNT) bundles. The force required to pull out an inner bundle of DWNTs from an outer shell of DWNTs was measured using in situ scanning electron microscopy methods. The normalized force per CNT-CNT interaction (1.7 ± 1.0 nN) was found to be considerably higher than molecular mechanics (MM)-based predictions for bare CNTs (0.3 nN). This MM result is similar to the force that results from exposure of newly formed CNT surfaces, indicating that the observed pullout force arises from factors beyond what arise from potential energy effects associated with bare CNTs. Through further theoretical considerations we show that the experimentally measured pullout force may include small contributions from carbonyl functional groups terminating the free ends of the CNTs, corrugation of the CNT-CNT interactions, and polygonization of the nanotubes due to their mutual interactions. In addition, surface functional groups, such as hydroxyl groups, that may exist between the nanotubes are found to play an unimportant role. All of these potential energy effects account for less than half of the ~1.7 nN force. However, partially pulled-out inner bundles are found not to pull back into the outer shell after the outer shell is broken, suggesting that dissipation is responsible for more than half of the pullout force. The sum of force contributions from potential energy and dissipation effects are found to agree with the experimental pullout force within the experimental error.     

Nanoelectromechanical contact switches

Nanoelectromechanical (NEM) switches are similar to conventional semiconductor switches in that they can be used as relays, transistors, logic devices and sensors. However, the operating principles of NEM switches and semiconductor switches are fundamentally different. These differences give NEM switches an advantage over semiconductor switches in some applications--for example, NEM switches perform much better in extreme environments--but semiconductor switches benefit from a much superior manufacturing infrastructure. Here we review the potential of NEM-switch technologies to complement or selectively replace conventional complementary metal-oxide semiconductor technology, and identify the challenges involved in the large-scale manufacture of a representative set of NEM-based devices.     

Cover Picture: Direct Growth of Flexible Carbon Nanotube Electrodes (Adv. Mater. 3/2008)

Entangled networks of multiwalled carbon nanotubes (CNTs) integrated into a highly conducting carbon layer can be grown on a range of substrates including glassy carbon and metal foils. On p. 566, Gordon Wallace and co‐workers report the fabrication of a continuous flexible CNT electrode with high surface area and conductivity. The electrode demonstrates a stable battery capacity of 572 mAh g^–1. This discovery provides a direct route for the generation of large‐scale flexible CNT electrode materials.     

Carbon nanotube electron ionization source for portable mass spectrometry

Cold cathode carbon nanotubes (CNTs) are used in a low-voltage quadrupole ion trap mass spectrometer and shown to be a viable low-power alternative to filament sources for portable mass spectrometry instrumentation. No heating is necessary, and the power consumption depends only on the switching characteristics of the electronics. The CNT electron sources are mounted directly in the ring electrode, and their performance is compared directly with a filament source also mounted in the ring electron. Up to a 5 × 10(-4) Torr CO(2) environment, reflecting conditions expected during operation in a Mars atmosphere, the CNT emitters may provide up to 1 μA of current over more than 200 h.     

碳纳米管增强PA6纤维的性能

将碳纳米管(CNT)在分散剂或分散剂和聚合物(PA6)载体中处理后制备出两种母粒,将其作为增强材料分别和PA6切片熔融共混纺丝,制备出碳纳米管的增强PA6纤维,研究其结构和力学性能.CNT含量低于0.5%(质量分数)时,使用两种母粒制备出的纤维强度和模量都提高,NT含量为0.03%时增强的效果最好.由碳纳米管和分散剂组成的母粒增强效果更好,NT的含量为0.03%时就能使PA6纤维的强度和模量分别提高23%和76%.这种增强纤维是一种微纤增强纤维,纳米CNT在纤维中均匀分散且沿着纤维轴的方向取向.这种结构能有效地转移载荷,具有增强作用,且取向性越好,增强效果越好.     

SnO2 nanoparticles distributed on multi-walled carbon nanotubes and ball-milled graphite as anode materials of lithium ion batteries

SnO2 nanoparticles were supported on ball-milled graphite (BMG) or carbon nanotubes (CNTs) using a chemical reduction method with ethylene glycol, and the electrochemical properties of the nanocomposites were evaluated as anode active materials of lithium-ion batteries. The BMG and CNTs contributed to an increase in both the capacity enhancement and cyclic stability compared to that of commercial graphite. In particular, the mixture electrode of SnO2/BMG:SnO2/CNT = 3:1 (in weight ratio) showed higher performance in the reversible capacity and cyclic stability than did the SnO2/BMG and SnO2/CNT electrodes. This might be resulted from the network formation for excellent electronic path by CNT distributed on SnO2/BMG composites.     

Synthesis of flake-like MnO2/CNT composite nanotubes and their applications in electrochemical capacitors

MnO2/CNT composite nanotubes with nanometer-sized flake-like MnO2 on carbon nanotubes' surfaces have been synthesized through an easy and efficient solution-based method. Similarly, Mn3O4/CNT composite nanotubes have also been synthesized by using the same method but different heat treatment process. The structures and compositions of the two types of composite nanotubes are characterized by using scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and nitrogen adsorption-desorption isotherms. Electrochemical measurements indicate that the MnO2/CNT composites nanotubes exhibit significantly enhanced supercapacitance performance compared with the Mn3O4/CNT composite nanotubes, the as-synthesized MnO2 nanoparticles and commercial MnO2. The possibilities of the enhanced properties are illustrated on the basis of analysis of XRD and X-ray photoelectron spectroscopy measurements. Our results presented here can give clear evidence of the superiority of nanocrystalline MnO2 to nanocrystalline Mn3O4 toward the applications as electrode materials in electrochemical capacitors.     

Hydrothermal synthesis of titanate nanoparticle/carbon nanotube hybridized material for dye sensitized solar cell application

With the hydrothermal treatment, titanate nanostructure with distinctively different morphology and surface characteristics was successfully synthesized from commercial rutile titania powder dispersed in accommodating media which were deionized water or NaOH solution. Hybridized materials of titanate nanoparticles and carbon nanotubes (CNT) were also synthesized by the hydrothermal treatment process. Intrinsic interaction of titanate nanoparticles and CNTs could be confirmed by spectroscopic analysis. The synthesized titanate nanoparticle/CNT hybridized material was then employed for fabricating a working electrode of dye-sensitized solar cells (DSSC). Based on experimental results, DSSC fabricated from the hybridized titanate nanoparticles and carbon nanotubes could provide the highest photoconversion efficiency of approximately 3.92%.     

Modeling and in-situ observation of mechanical resonances in single, vertically-oriented carbon nanofibers

In this paper, we have analyzed mechanical resonances in carbon nanotubes (CNTs) based on single, vertically-oriented tubes for their potential application in high-frequency, high-Q, miniaturized resonators. The nano-electro-mechanical (NEM) resonators were modeled using a commercially available finite-element-simulator, where the electro-mechanical coupling of the CNT to an incoming AC signal on a probe in close proximity was examined. The modeling results confirmed that the mechanical resonance was maximized when the frequency of the input signal was equal to the first order harmonic of the CNT. An investigation of the resonance frequency was also performed for various geometrical parameters of our unique three-dimensional (3D) NEMS architecture. Finally, in-situ observations of mechanical resonance in single, vertically oriented tubes is also reported, where such measurements were conducted inside a scanning-electron-microscope. This work suggests that our vertically oriented tubes are potentially well-suited for resonator applications, such as filter banks in communication systems or for mass sensing applications.     

High conductivity transparent carbon nanotube films deposited from superacid

Carbon nanotubes (CNTs) were deposited from a chlorosulfonic superacid solution onto PET substrates by a filtration/transfer method. The sheet resistance and transmission (at 550 nm) of the films were 60 Ω/sq and 90.9% respectively, which corresponds to a DC conductivity of 12,825 S cm(-1) and a DC/optical conductivity ratio of 64.1. This is the highest DC conductivity reported for CNT thin films to date, and attributed to both the high quality of the CNT material and the exfoliation/doping by the superacid. This work demonstrates that CNT transparent films have not reached the conductivity limit; continued improvements will enable these films to be used as the transparent electrode for applications in solid state lighting, LCD displays, touch panels, and photovoltaics.     

Mechanical properties of carbon nanotubes and their polymer nanocomposites

More than 10 years have passed since carbon nanotubes (CNT) have been found during observations by transmission electron microscopy (TEM). Since then, one of the major applications of the CNT is the reinforcements of plastics in processing composite materials, because it was found by experiments that CNT possessed splendid mechanical properties. Various experimental methods are conducted in order to understand the mechanical properties of varieties of CNT and CNT-based composite materials. The systematized data of the past research results of CNT and their nanocomposites are extremely useful to improve processing and design criteria for new nanocomposites in further studies. Before the CNT observations, vapor grown carbon fibers (VGCF) were already utilized for composite applications, although there have been only few experimental data about the mechanical properties of VGCF. The structure of VGCF is similar to that of multi-wall carbon nanotubes (MWCNT), and the major benefit of VGCF is less commercial price. Therefore, this review article overviews the experimental results regarding the various mechanical properties of CNT, VGCF, and their polymer nanocomposites. The experimental methods and results to measure the elastic modulus and strength of CNT and VGCF are first discussed in this article. Secondly, the different surface chemical modifications for CNT and VGCF are reviewed, because the surface chemical modifications play an important role for polymer nanocomposite processing and properties. Thirdly, fracture and fatigue properties of CNT/polymer nanocomposites are reviewed, since these properties are important, especially when these new nanocomposite materials are applied for structural applications.     

Fabrication of carbon nanotube-emitters on Ag-Cu alloy film by thermal welding

A field emission electron source was fabricated on a Si substrate using Ag-Cu alloy (ACa) and carbon nanotubes (CNTs). The ACa was adopted as a binder material due to its excellent electrical conductivity, oxidation stability, and suitable melting point (783 degrees C). The surface morphology of the ACa-film was improved by introducing an Nb layer as an adhesion layer between the ACa-film and the Si substrate. The ACa-film thickness was varied from 100 to 500 nm. The spray method was employed to deposit a CNT film on the ACa/Nb/Si substrate for large area fabrication. After annealing the substrate at 700 degrees C for 10 min, the CNT film was tightly welded on the ACa-films, and the CNT-emitters fabricated on the 400-nm-thick ACa-film exhibited high current density and stability with a low turn-on voltage. It is worth noting that ACa could be applied to the glass substrate because the CNT-emitters fabricated at 500 degrees C exhibited good field emission characteristics.