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We report an innovative method for the fast preparation of wafer-scale uniform single-wall carbon nanotubes (SWCNT) films with controllable density by NaHCO3 tuning the interaction between amine-functionalized substrates and surfactant-dispersing SWCNTs in aqueous solution. With this technique, a 4-inch SWCNT film with a linear density of ∼30 tubes/μm can be achieved in 1 s, and over 60 tubes/μm within 30 s using a high-concentration SWCNT solution. The SWCNT density changes by less than 8% over a 4-inch area. The electrical uniformity of the as-prepared wafer-scale single-chirality SWCNT film was demonstrated to be within 10.8% for subthreshold swing and 12% for carrier mobility and 13.5% for their on-current, which is the most uniform SWCNT films reported so far fabricated from the surfactant-dispersed SWCNT solution. Further, the photodetectors made by the uniform semiconducting SWCNT films exhibit excellent cascading ability, which linearly amplify the output photovoltages and could produce a photovoltage responsivity of 2.5 × 106 V/W. When three-stage cascading photodetectors are used as optical gate to establish an integrated photoelectric system, a 20-mW/cm2 light illumination produces the current responsivity of 147.3 A/W under a source/drain voltage of −0.1 V. Our present technique lays an important foundation for their applications in integrated circuits.

Transition metal phosphides (TMPs) are emerging as high-performance and promising electrode materials for use in asymmetric supercapacitors (ASCs). Herein, we demonstrate that cobalt phosphide (CoP...

We quantitatively analyze the effect of reabsorption on the Raman spectroscopy of (10, 3) and (8, 3) single-chirality single-wall carbon nanotube (SWCNT) solutions by varying the detection depth in confocal micro-Raman measurements and SWCNT concentration the in sample solution. The increase of the detection depth and concentration of SWCNTs enhances the reabsorption effect and decreases the intensities of the Raman features. More importantly, reabsorption exhibits different effects on different Raman features such as the radial breathing mode (RBM) and G+ band, strongly depending on the resonance degree of the scattered light energy and the interband transition of SWCNTs. When (10, 3) SWCNTs are excited with a 633 nm laser, the scattered light from RBM has stronger resonance with the interband transition of the SWCNTs than that from the G+ band, leading to a faster reduction in the RBM intensity and a lower intensity ratio of RBM to the G+ band. In contrast, when (8, 3) SWCNTs are excited with a 633 nm laser, reabsorption has the same effect on the RBM and G+ band intensities and thus maintains a constant intensity ratio of RBM to the G+ band. Furthermore, we precisely establish a quantitative relationship of the intensities of the Raman features such as RBM, the G+ band and their intensity ratio as a function of the focal depth and SWCNT concentration by theoretical calculations and numerical simulation, which reproduces the experimental results well. These results are very useful in the precise analysis of the Raman spectroscopy of SWCNTs and thus their applications in molecular detection and imaging.

Mass production of high-purity semiconducting single-wall carbon nanotubes (s-SWCNTs) is critical for their application in the electronic and optoelectronic devices. Here we reported a method for h...

Submilligram-scale separation of near-zigzag single-chirality carbon nanotubes has been achieved by gel chromatography., Mass production of zigzag and near-zigzag single-wall carbon nanotubes (SWCNTs), whether by growth or separation, remains a challenge, which hinders the disclosure of their previously unknown property and practical applications. Here, we report a method to separate SWCNTs by chiral angle through temperature control of a binary surfactant system of sodium cholate (SC) and SDS in gel chromatography. Eleven types of single-chirality SWCNT species with chiral angle less than 20° were efficiently separated including multiple zigzag and near-zigzag species. Among them, (7, 3), (8, 3), (8, 4), (9, 1), (9, 2), (10, 2), and (11, 1), were produced on the submilligram scale. The spectral detection results indicate that lowering the temperature induced selective adsorption and reorganization of the SC/SDS cosurfactants on SWCNTs with different chiral angles, amplifying their interaction difference with gel. We believe that this work is an important step toward industrial separation of single-chirality zigzag and near-zigzag SWCNTs.

Continuous uniform, The direct growth of single-walled carbon nanotubes (SWCNTs) with narrow chiral distribution remains elusive despite substantial benefits in properties and applications. Nanoparticle catalysts are vital for SWCNT and more generally nanomaterial synthesis, but understanding their effect is limited. Solid catalysts show promise in achieving chirality-controlled growth, but poor size control and synthesis efficiency hampers advancement. Here, we demonstrate the first synthesis of refractory metal nanoparticles (W, Mo, and Re) with near-monodisperse sizes. High concentrations (N = 105 to 107 cm−3) of nanoparticles (diameter 1 to 5 nm) are produced and reduced in a single process, enabling SWCNT synthesis with controlled chiral angles of 19° ± 5°, demonstrating abundance >93%. These results confirm the interface thermodynamics and kinetic growth theory mechanism, which has been extended here to include temporal dependence of fast-growing chiralities. The solid catalysts are further shown effective via floating catalyst growth, offering efficient production possibilities.

Single-walled carbon nanotube (SWCNT) films are promising materials as flexible transparent conductive films (TCFs). Here, inspired by the extrusion blown plastic film technique and the SWCNT synthesis approach by floating catalyst chemical vapor deposition (FCCVD), a novel blown aerosol chemical vapor deposition (BACVD) method is reported to directly and continuously produce freestanding SWCNT TCFs at several hundred meters per hour. The synthesis mechanism, involving blowing a stable aerosol bubble and transforming the bubble into an aerogel, is investigated, and a general phase diagram is established for this method. For the SWCNT TCFs via BACVD, both carbon conversion efficiency and SWCNT TCF yield can reach three orders of magnitude higher than those with the conventional FCCVD. The film displays a sheet resistance of 40 ohm sq-1 at 90% transmittance after being doped, representing the record performance based on large-scale SWCNT films. Transparent, flexible, and stretchable electrodes based on BACVD films are demonstrated. Moreover, this high-throughput method of producing SWCNT TCFs can be compatible with the roll-to-roll process for mass production of flexible displays, touch screens, solar cells, and solid-state lighting, and is expected to have a broad and long-term impact on many fields from consumer electronics to energy conversion and generation.

As possible alternatives to traditional thermoelectric (TE) materials, carbon nanomaterials and their hybrid materials have great potential in the future application of flexible and lightweight temperature detection. In this work, an integrated, highly flexible, and tailorable TE temperature detector with high performance has been fabricated based on a continuous single-walled carbon nanotube (SWCNT) fiber. The detector consists of more than one pairs of thermocouples composed of p-type SWCNT fiber and n-type SWCNT hybrid fiber in situ doped by polyethylenimine. Due to the node contact mechanism of the detection, the sensitivity of the detector can be improved with the increase of the number of p-n thermocouples, independent of the length of the thermocouple. The temperature detection process of the detector has been studied in detail. In particular, the integrated and flexible detector can be divided into several sub-detectors easily by cutting, illustrating the prospect of large-scale preparation of this kind of novel temperature detectors. Its high flexibility ensures the detector to maintain excellent detection performance after 15 000 bending circles. Furthermore, the as-designed TE type temperature detector demonstrates a great application promise for real-time temperature detection and temperature change sensing even in complex surface and harsh environment.

In this work, we put forward an effective approach by combining both highly transparent and conductive carbon nanotube (CNT) network and poly (3, 4-ethylene dioxythiophene):poly (styrenesulfonate) (PEDOT:PSS) film to co-form-coordinate heterojunctions with silicon, and have developed a hybrid PEDOT:PSS-CNT/n-Si solar cell. The power conversion efficiency (PCE) of the as-designed solar cell can be improved up to 10.2%, which is much higher than the PCE values of both PEDOT:PSS/n-Si (5.5%) and CNT/n-Si (6.1%) solar cells fabricated using the same materials and process. PEDOT:PSS can fill the hundreds nanometer scale pores of the CNT network, both CNT network and PEDOT:PSS patches contact with the silicon concomitantly and form p Synergy -n heterojunctions through seamless contact with n-Si. The PEDOT:PSS-CNT composite film exhibits a much lower sheet resistance and remains high optical transmittance. Once the photo-generated holes are extracted to the PEDOT:PSS-CNT composite film, CNT network can serve as a carrier transport bridge, which is different from the design that inserts an ultrathin polymer between the CNT and Si. Incorporation of the continuous CNT network with PEDOT:PSS jointly in the as-designed simple and explicit structure has generated synergistic effects, which can make full use of the respective merits and then considerably enhance the PCE of hybrid PEDOT:PSS-CNT/n-Si solar cells.

Recent development in epidermal and bionic electronics systems has promoted the increasing demand for supercapcacitors with micrometer-thickness and good compatibility. Here, a highly flexible free-standing epidermal supercapacitor (SC-E) with merely 1 μm thickness and high performance is developed. Single-walled carbon nanotube/poly(3,4-ethylenedioxythiophene) hybrid films with unique inner-connected reticulation are adopted as electrodes for ultrathin structure and high electric conductivity. Then, based on two substrates with different surface energies, a stepwise lift-off method is presented to peel off the ultrathin integrated supercapacitor from the substrates nondestructively. As a result of the high conductive hybrid electrodes and the thin electrolyte layer, the as-designed supercapacitors (based on the total mass of two electrodes) achieve a good capacitance of 56 F g−1 and a superhigh power density of 332 kW kg−1, which manifest superior performance in contrast to the other devices fabricated by traditional electrodes. Meanwhile, the ultrashort response time of 11.5 ms enables the epidermal supercapacitor (SC-E) work for high-power units. More importantly, the free-standing structure and outstanding flexibility (105 times bending) endow the SC-E with excellent compatibility to be integrated and work in the next generation of smart and epidermal systems.

Based on polyaniline-single-walled carbon nanotubes -sponge electrodes, highly compressible all-solid-state supercapacitors are prepared with an integrated configuration using a poly(vinyl alcohol) (PVA)/H2 SO4 gel as the electrolyte. The unique configuration enables the resultant supercapacitors to be compressed as an integrated unit arbitrarily during 60% compressible strain. Furthermore, the performance of the resultant supercapacitors is nearly unchanged even under 60% compressible strain.

In order to meet the growing need for smart bionic devices and epidermal electronic systems, biaxial stretchability is essential for energy storage units. Based on porous single-walled carbon nanotube/poly(3,4-ethylenedioxythiophene) (SWCNT/PEDOT) hybrid fiber, we designed and fabricated a biaxially stretchable supercapacitor, which possesses a unique configuration of the parallel buckled hybrid fiber array. Owing to the reticulate SWCNT film and the improved fabrication technique, the hybrid fiber retained its porous architecture both outwardly and inwardly, manifesting a superior capacity of 215 F g(-1). H3PO4-polyvinyl alcohol gel with an optimized component ratio was introduced as both binder and stretchable electrolyte, which contributed to the regularity and stability of the buckled fiber array. The buckled structure and the quasi one-dimensional character of the fibers endow the supercapacitor with 100% stretchability along all directions. In addition, the supercapacitor exhibited good transparency, as well as excellent electrochemical properties and stability after being stretched 5000 times.

It is a great challenge to substantially improve the practical performance of flexible thermoelectric modules due to the absence of air-stable n-type thermoelectric materials with high-power factor. Here an excellent flexible n-type thermoelectric film is developed, which can be conveniently and rapidly prepared based on the as-grown carbon nanotube continuous networks with high conductivity. The optimum n-type film exhibits ultrahigh power factor of ∼1,500 μW m−1 K−2 and outstanding stability in air without encapsulation. Inspired by the findings, we design and successfully fabricate the compact-configuration flexible TE modules, which own great advantages compared with the conventional π-type configuration modules and well integrate the superior thermoelectric properties of p-type and n-type carbon nanotube films resulting in a markedly high performance. Moreover, the research results are highly scalable and also open opportunities for the large-scale production of flexible thermoelectric modules., Thermoelectric modules can generate electricity directly from heat and have applications to waste heat-energy conversion. Here Zhou et al. have fabricated a thermoelectric module based on an air-stable n-type single-walled carbon nanotube sheet which can reach a high power factor of 1500 μWm−1K−2.

Carbon nanotube thin film transistors (CNT-TFTs) have been regarded as strong competitors to currently commercialized TFT technologies. Though much progress has been achieved recently, CNT-TFT research is still in the stage of laboratory research. One critical challenge for commercializing CNT-TFT technology is that the commonly used device fabrication method is a lift-off based process, which is not suitable for mass production. In this paper, we report an etching based fabrication process for CNT-TFTs, which is fully manufacturing compatible. In our process, the CNT thin film channel was patterned by dry etching, while wet etching was used for patterning the layers of metal and insulator. The CNT-TFTs were successfully fabricated on a 4 inch wafer in both top-gate and buried-gate geometries with low Schottky barrier contact and pretty uniform performance. High output current (>1.2 μA μm−1), high on/off current ratio (>105) and high mobility (>30 cm2 V−1 s−1) were obtained. Though the fabrication process still needs to be optimized, we believe our research on the etching fabrication process pushes CNT-TFT technology a step forward towards real applications in the near future.

In order to develop an excellent pseudocapacitor with both high specific capacitance and outstanding stretchability to match with other devices applicable in future wearable and bio-implantable systems, we focus our studies on three vital aspects: Stretchability of hybrid film electrodes, the interface between different components, and the integrated performance in stretchability and electrochemistry of supercapacitors based on single-walled carbon nanotube/polyaniline (SWCNT/PANI) composite films on pre-elongated elastomers. Owing to the moderate porosity, the buckled hybrid film avoids the cracking which occurs in conventional stretchable hybrid electrodes, and both a high specific capacitance of 435 F·g−1 and a high strain tolerance of 140% have been achieved. The good SWCNT/PANI interfacial coupling and the reinforced solid electrolyte penetration structure enable the integrated pseudocapacitors to have stretch-resistant interfaces between different units and maintain a high performance under a stretching of 120% elongation, even after 1,000 cyclic elongations.

Single-walled carbon nanotubes (SWNTs) grown by chemical vapor deposition (CVD) are widely used for fabrication of high-performance nanotube devices. However, the high-temperature growth is incompatible with the current complementary metal-oxide semiconductor (CMOS) technology. We demonstrate a low-temperature and direct deposition of the CVD-grown SWNTs. The nanotubes are synthesized by floating catalytic CVD technique and further carried by the flowing gas directly to the low- temperature area. Individual SWNTs have been successfully deposited on Si/ SiO2 substrates covered with a polymethylmethacrylate layer, which results in a suspended geometry of the nanotube in the fabricated devices. We subsequently investigate the electrical-transport properties of a representative small band gap nanotube, which exhibits an ambipolar feature with p-channel mobility up to 1410 cm 2 V −1 S −1 at room temperature. Furthermore, low- temperature measurements down to 4 K reveal different transport characteristics with the gate voltage biased near zero or at a large negative value, respectively.

Single Walled Carbon Nanotube (SWCNT) films were directly synthesized via Floating Catalyst Chemical Vapor Deposition (FCCVD) method. Temperature dependent resistance measurements were carried out on the as-grown and chemical treated SWCNTs films. A "U" shaped curve was obtained for each sample, with a significant variation in the crossover temperatures between the as-grown and treated samples. A heterogeneous model was adopted to interpret the experimental data, revealing the coexistence of anisotropic 1D metallic conduction, conventional metallic conduction and fluctuation assisted tunneling. Our results implied very low barriers, verifying the good intertube and interbundle contacts in the directly synthesized SWCNTs films. We speculated that oxidization and acid treatments would affect the overall configuration of the films, leading to the changes in the temperature dependence of resistance. In addition, Raman and absorption spectra indicated that oxidization and acid process would cause moderate changes in the hole carrier concentration of the films.

In-situ Raman spectra under continuous strain have been carried out to follow the load transfer efficiency in a single-walled carbon nanotube/epoxy nanocomposite film, which was fabricated by a facile and filter-free infiltration method using directly synthesized SWNT film as skeleton. It was found that in the low elastic range of 1%, with the increase of applied strain, the G(-) and G(+) Raman bands downshift nearly lineally with corresponding ultrahigh rates up to -12 and -17 cm(-1)/% strain, respectively. As the applied strain decrease, these Raman bands upshift to their original frequencies with almost the same rates. These precise relationships between the Raman band shift and the applied strain enable this nanocomposite film promising stress or stain sensors. Furthermore, some Raman radial breathing modes (RBMs) disappear (appear) under larger strain (1.6%) and recover (vanish) when the strain is released, also verify the effective deformation of micro SWNTs induced by extra macro strain applied on the nanocomposite film. More interestingly, these frequency shifts and intensity vibrations are recoverable and repeatable, indicating the high elasticity of deformation in this strain region of 2%.

Carbon nanotube (CNT) fibers are a novel type of fibrous materials that show potential in polymeric composite fields. In this study, we investigated the interfacial behavior of a single single-walled carbon nanotube (SWCNT) fiber embedded in isotactic polypropylene (iPP) matrix. The SWCNT fibers were found to be able to act as a heterogeneous nucleating agent which inducing the formation of transcrystals around the fiber surface. According to the theory of heterogeneous nucleation, the interfacial free energy difference Delta sigma of iPP on the SWCNT fibers was determined and compared with that on the conventional fibers. By carefully controlling the crystallizing conditions, three types of alpha-iPP supramolecular microstructures with different optical birefringences were obtained. Raman spectra were utilized to investigate the influences of the supra-molecular microstructures of the transcrystalline (tc) layer on the strain transfer efficiency from the matrix to the fibers at a microscopic level. Conventional single-fiber pull-out tests were further employed to compare with the results derived from the Raman tests. (C) 2012 Elsevier Ltd. All rights reserved.

Hybrid hydro-responsive actuators are developed by infiltrating carbon nanotube yarns using poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate). These actuators demonstrate impressive rotation and contraction in response to water due to volumetric expansion of the helical arrangement of carbon nanotubes. The total torsional stroke is 3720 revolutions per m and the simultaneously generated contractive strain reaches 24% at a paddle-to-yarn mass ratio of 350. The contraction output can furthermore be significantly enhanced by constraining the rotational motion and it reaches 68% with an applied stress of 1 MPa. Additionally, hybrid yarns exhibit an approximately linear response to humidity changes and show extra capability of electrical actuation, which, combined with the excellent hydro-actuation performance, endow them with great potential for a variety of applications including artificial muscles, hydro-driven generators, moisture switches and microfluidic mixers.

An ingenious strategy is put forward to evaluate accurately the thermoelectric performance of carbon nanotube (CNT) thin films, including thermal conductivity, electrical conductivity, and Seebeck coefficient in the same direction. The results reveal that the as-prepared CNT interconnected films and CNT fibers possess enormous potential of thermoelectric applications because of their ultrahigh power factors.

Ultrathin SWCNT transparent and conductive films on flexible and transparent substrates are prepared via repeatedly halving the directly grown SWCNT films and flexible and transparent supercapacitors with excellent performance were fabricated.

A critical challenge in nanocomposite fabrication by adding SWCNTs as reinforcement is to realize an effective transfer of the excellent mechanical properties of the SWCNTs to the macroscale mechanical properties of the matrix. Using directly grown SWCNT films with continuous reticulate structure as the template, Cu/SWCNTs/Cu laminated nanocomposites are fabricated by an electrodepositing process. The resulting Cu/SWCNTs/Cu laminated nanocomposites exhibit extremely high strength and Young's modulus. The estimated Young's modulus of the SWCNT bundles in the composite are between 860 and 960 GPa. Such a high strength and an effective load-transfer capacity are ascribed to the unique continuous reticulate architecture of SWCNT films and the strong interfacial strength between the SWCNTs and Cu matrix. Raman spectroscopy is used to characterize the loading status of the SWCNTs in the strained composite. It provides a route to investigate the load transfer of SWCNTs in the metal matrix composites.

Free-standing, hierarchical reticulate single-walled carbon nanotube (SWCNT) films are embedded in poly(dimethylsiloxane) (PDMS) to fabricate stretchable conductors (SWCNT/PDMS stretchable conductors). The stretchable conductors are highly transparent in visible light region and retain excellent conductance under large tensile strains. Strain tests reveal a unique strain-history dependence behavior of the resistance, and resistance stabilization is achieved upon repetitive stretching and releasing, implying that the SWCNT/PDMS stretchable conductors can be programmed to be reversibly stretched to a defined strain without resistance changes. A quantitative description of the increase in resistance is determined by adopting the Weibull distribution. Moreover, a light-emitting diode is illuminated using a repetitively stretched SWCNT/PDMS strip as the connecting wire, demonstrating the utility of the stretchable conductors as interconnects for stretchable electronics. Because of the high transparency, high conductivity, and excellent stretchability, in addition to the facile fabrication, the SWCNT/PDMS stretchable conductors might be widely used as interconnects and electrodes for stretchable intelligent and functional devices.

A physical route is proposed to obtain highly crystalline graphene sheets with minimal oxygen content similar to the precursor graphite. The functional graphene sheets obtained from graphite oxide by low temperature thermal exfoliation are annealed at high temperature (1900 degrees C) in a vacuum (10(-6) torr). The D band intensity in Raman spectroscopy is reduced significantly, while the G band intensity is recovered, similar to the level of precursor graphite. No appreciable oxygen content is observed from X-ray photoelectron spectroscopy and an electrical conductivity of similar to 56 500 S m(-1) is obtained, comparable to 100 900 S m(-1) of the precursor graphite.

High mechanical performances of macroscopic-scale fibers hierarchically constructed with carbon nanotubes (CNTs) are attracting great interest in the materials community owing to their merits of light weight and multiple functionalities. However, from the viewpoint of structural design, many fundamental issues, for example, modulus, strength, and deformation mechanisms of such CNT fibers are not yet well understood. In this Full Paper, the axial compression of hierarchical CNT fibers embedded in epoxy is investigated with the assistance of in situ Raman spectroscopy. Experimental results reveal that the conspicuous stiffening and strengthening effects of embedded CNT fibers are dominated by the constituent CNTs within the fiber, and have not yet been observed for conventional carbon fibers. Moreover, hierarchically structured CNT fibers exhibit notable flexibility without permanent deformation and failure under large-strain compression.

The progress on novel interconnects for carbon nanotube (CNT)-based electronic circuit is by far behind the remarkable development of CNT-field effect transistors. The Cu interconnect material used in current integrated circuits seems not applicable for the novel interconnects, as it requires electrochemical deposition followed by chemical-mechanical polishing. We report our experimental results on the failure current density, resistivity, electromigration effect and failure mechanism of patterned stripes of Pd, Sc and Y thin-films, regarding them as the potential novel interconnects. The Pd stripes have a failure current density of (8∼10)×106 A/cm2 (MA/cm2), and they are stable when the working current density is as much as 90% of the failure current density. However, they show a resistivity around 210 μΩ·cm, which is 20 times of the bulk value and leaving room for improvement. Compared to Pd, the Sc stripes have a similar resistivity but smaller failure current density of 4∼5 MA/cm2. Y stripes seem not suitable for interconnects by showing even lower failure current density than that of Sc and evidence of oxidation. For comparison, Au stripes of the same dimensions show a failure current density of 30 MA/cm2 and a resistivity around 4 μΩ·cm, making them also a good material as novel interconnects.

The selective interaction is systematically explored between the surfactants (sodium deoxycholate (DOC), sodium dodecyl sulfate (SDS), and sodium cholate (SC)) and the single-wall carbon nanotubes (SWCNTs) by the gel chromatography technique. The results show that DOC preferentially interacts with small-diameter semiconducting SWCNTs (S-SWCNTs), exhibiting the strongest interaction strength for the SWCNTs, and the highest structural selectivity. The surfactant SC shows high selectivity toward the chiral angles of the SWCNTs. Its interaction strength and structural recognition ability are slightly higher than that of SDS but lower than that of DOC. Combining with the proved selectivity of SDS in the adsorption onto the S-SWCNTs with small CC bond curvature, it is discovered that the synergistic effect of the triple surfactants amplified the interaction difference among the different SWCNTs and the gel, and thus dramatically improved the separation efficiency and structural purity of the SWCNTs, achieving the separation of distinct (n, m) single-chirality species and their enantiomers in one step. This work not only provides deeper insights into the separation mechanism of SWCNTs with the surfactant sorting techniques, but also has a profound significance in studying the interaction between the SWCNTs and other small molecules.

Using the carbon nanotube (CNT) arrays embedded in anodic aluminum oxide (AAO) template as an electrode, large amounts of Ni nanoparticles have been encapsulated into the CNTs by an alternating current (AC) electrodepostion technique. As deposited Ni nanoparticles with a typical size of 50-60 nm randomly nucleated on the CNT walls, thus inhomogeneously distributed in the CNTs. After annealing at 600 degrees C, the nanoparticles transformed into quasi-spherical structures with the diameter increasing to 60-80 nm. The quasi-spherical nanoparticles were aligned in orderly rows along the axis of the CNT channels. Magnetic hysteresis measured at 5 K showed that the coercivity was 450 Oe for the as-deposited sample and 385 Oe for annealed sample, with the applied magnetic field parallel with the CNT's axis. The structures and magnetic properties were discussed for both as-deposited and annealed samples. (C) 2009 Published by Elsevier Ltd

Carbon nanotubes have unprecedented mechanical properties as defect-free nanoscale building blocks, but their potential has not been fully realized in composite materials due to weakness at the interfaces. Here we demonstrate that through load-transfer-favored three-dimensional architecture and molecular level couplings with polymer chains, true potential of CNTs can be realized in composites as initially envisioned. Composite fibers with reticulate nanotube architectures show order of magnitude improvement in strength compared to randomly dispersed short CNT reinforced composites reported before. The molecular level couplings between nanotubes and polymer chains results in drastic differences in the properties of thermoset and thermoplastic composite fibers, which indicate that conventional macroscopic composite theory fails to explain the overall hybrid behavior at nanoscale.

The resistance of single-walled carbon nanotube (SWNT) bundles has been investigated by two-terminal measurements. We find that the time dependence of resistance (dR/dt) exhibits different behaviors at different currents. At low currents, a positive dR/dt is observed. However, dR/dt shows a negative sign when the applied current exceeds a critical current (I-c). I-c coincides with the current when the sample begins to emit light. The variation of dR/dt can be interpreted as the thermal effects owing to Joule heating in the SWNTs. Our lighting SWNTs sample has a small change in resistance and exhibits high stability.

The photocurrent generated in single-walled carbon nanotube bundles upon camera flash illumination has been studied under different ambient pressures and light intensities. The results show that the intensity of photocurrent depends closely on the ambient pressure and light intensity. With the ambient pressure reduced, the photocurrent exhibits a logarithmic growth behaviour. Meanwhile, the photocurrent increases with the increase in light intensity. In this work, a dynamic model is employed to unveil the origins of the observed photocurrent. A much smaller lifetime of photocarriers (~10?ms) is observed than that needed for gas molecular desorption or photodesorption (seconds or longer). Our results are consistent with the model of Schottky barriers being responsible for photocurrent generation.

In this letter, the sandwich-like single-walled carbon nanotube (SWNT) paper/polyetheretherketone (PEEK) composites were successfully prepared by using a hot-compress method. Based on SEM observation, it was found that the PEEK macromolecules could diffuse into the voids of SWNT paper and were able to form very good bonding to the nanotube bundles, which ensure effective stress transfer between two phases. Some typical problems in preparing conventional carbon nanotube/polymer composites, e.g. the difficulty to obtain well-dispersed high-loading nanotubes into polymer matrices, were successfully overcome. Moreover, the compact networks of SWNTs were not destroyed at the appropriate processing condition. Correspondingly, the resulting composite (with one layer of SWNT paper) exhibited about 40% increased in Young’s modulus and 4% enhanced in failure strength when comparing with that of neat PEEK, respectively. According to rule-of-mixtures of the special sandwich-like structure, the estimated Young’s modulus can reach up to about 8 GPa, which was nearly three times of that of neat matrix. Moreover, the surface electric conductivity and thermal conductivity of the PEEK films were also increased after the addition of SWNT paper. The preliminary results suggest that the SWNT paper has great potential for being used to reinforce polymers.

Surfactants or polymers are usually used for the liquid processing of carbon nanotubes for their structure separation. However, they are difficult to remove after separation, affecting the intrinsic properties and applications of the separated species. Here, we report an ethanol-assisted gel chromatography for the chirality separation of single-walled carbon nanotubes (SWCNTs), in which ethanol is employed to finely tune the density/coverage of sodium dodecyl sulfate (SDS) on nanotubes, and thus the interactions between SWCNTs and an allyl dextran-based gel. Incrementally increasing the ethanol content in a low-concentration SDS eluent leads to successive desorption of the different structure SWCNTs adsorbed on the gel, and to achieve multiple distinct (n, m) single-chirality species. The use of ethanol enables the working concentration of SDS to be reduced dramatically and also avoids the introduction of other surfactants or chemical reagents. More importantly, ethanol can be easily removed after separation. The ability of ethanol to tune the interactions between SWCNTs and the gel also gives a deeper insight into the separation mechanism of SWCNTs using gel chromatography.

Structural defects play an important role in the physics of carbon nanototube. However, very few investigations of the structural changes induced by purifying process and other treatments have been performed by means of X-ray absorption near-edge structure (XANES) spectroscopy. We used XANES spectroscopy to detect the presence of defects induced in single-walled carbon nanotubes (SWNTs) by nitric acid treated processes and by an Ar+ ion bombardment. The relationship between the features in XANES spectrum and the structural defects has been discussed systematically. Data also addresses evidence of oxygen effect induced by aging on nanotubes. (c) 2006 Elsevier Ltd. All rights reserved.

Many applications based on single-walled carbon nanotubes (SWNTs) require chemical modification of carbon nanotube to optimize the functionalities of the device. In this contribution we discuss the properties of SWNTs immersed in a hydrobromic acid (HBr) solution. Changes of atomic and electronic structures of bromine modified SWNTs were investigated using photoelectron spectroscopy (PES). Spectra of SWNTs before and after immersion in the HBr solution exhibit different features. To understand the mechanism of interaction between SWNTs and bromine, we performed density-functional theory calculations to reveal the structural changes, adsorption energy and chemical bonding information of SWNTs interacting with bromine. In addition, based on the Gelius model, from the molecular orbitals (MOs), we calculated ultraviolet photoelectron spectra (UPS) of SWNTs with and without functionalizing and compared them with the experiment. The present study is a first step in the understanding of the functionalization mechanism of carbon nanotubes.

A Fe nanowires-filled amorphous carbon nanotubes (FeNW-filled a-CNTs) array was synthesized by sequential growth of electrodeposited Fe nanowires and subsequent chemical vapour deposition of amorphous CNTs in the nanochannels of alumina template. Structural characterizations of as-prepared FeNW-filled a-CNTs were carried out via field emission scanning electron microscope (FE-SEM), x-ray diffraction (XRD), elemental mapping, high-resolution transmission electron microscope (HRTEM) and Raman scattering. The formation mechanism of such Fe/C nanoheterostructure was proposed according to the detailed HRTEM analyses. Furthermore, the room temperature magnetic property of the as-prepared FeNW-filled a-CNTs array was also investigated, and obvious anisotropic behaviour in magnetization was observed.

Water molecules adsorbed on a double-walled carbon nanotube (DWCNT) serve as charge trapping centers when present in low density and as electron donors when present in high density. There is a discontinuous change between the low- and high-density regions. H2O molecules are apt to be adsorbed on the outer surface of DWCNTs, and in this case the electrical transport properties are extremely sensitive to environment, which suggests that DWCNTs are hole doped and act as an electric dipole with the inner tube.

Rings of bundled single-walled carbon nanotubes with perfectly toroidal geometries (see figure), are fabricated in high yields by a floating chemical vapor deposition process involving the thermal decomposition of acetylene. The nano-tube rings can be grown with varying densities on a wide variety of substrates at relatively low temperatures, which is a significant advantage for nanoelectronics applications.

Rings of single-walled carbon nanotubes (SWNTs) with a high yield of 30-50% have been fabricated through a floating catalytic chemical vapor deposition (FCCVD) method. The SWNT rings, which were characterized as the self-looping nanotube coils, feature a relative small diameter of 100-300 nm and a thin thickness of 1-8 nm. The high yield of the SWNT rings has been ascribed to the unique experimental configuration which could favor the as-synthesized straight SWNTs to bend freely and easily to form the coil-shaped structures. The technique presented here may advance the new understanding to bulk-prepare the nanotube rings. (c) 2006 Elsevier B.V. All rights reserved.

Single-walled carbon nanotube (SWNT) rings with a diameter of about 100 nm have been prepared by thermally decomposing hydrocarbon in a floating catalyst system. These rings appeared to consist mostly of SWNT toroids. High resolution transmission electron microscopy showed that these rings were composed of tens of SWNTs with a tightly packed arrangement. The production of SWNT rings was improved through optimizing various growth parameters, such as growth temperature, sublimation temperature of the catalyst, different gas flows and different catalyst components. The growth mechanism of the SWNT rings is discussed. In the field emission measurements we found that field emission from a halved ring is better than that from a whole SWNT ring, which contributed to the better emission from two opened ends of the nanotubes of the halved SWNT ring.

The adsorption behavior of human fibrinogen (Hfg) on single-walled carbon nanotube (SWNT) films was investigated using scanning electron microscopy (SEM) and near edge X-ray absorption fine structure (NEXAFS) spectroscopy. It was shown in the SEM images that fibrinogen was adsorbed strongly on the surface of SWNT when the samples were incubated in the Hfg solutions for 10 min. The dependence of adsorption on the concentration of fibrinogen was also investigated and it was found that adsorption increased with increasing concentration. In order to further explore the adsorption of fibrinogen on SWNT surface, NEXAFS spectra were obtained at the N K-edge and the C K-edge. The results confirmed the conclusion regarding the dependence of adsorption on fibrinogen concentration. It is demonstrated that, due to its high sensitivity to the surface elements, NEXAFS spectroscopy is a powerful tool to investigate the adsorption of fibrinogen on SWNT films.

X-ray absorption near-edge structure (XANES) spectroscopy and photoelectron spectroscopy (PES) have been used to investigate single-walled carbon nanotubes (SWNTs) modified by immersion in a HBr solution at room temperature. After treatment XANES spectra of SWNTs show a new pronounced feature, which has been assigned to new bonds between the sidewall of the SWNTs and Br atoms. This investigation demonstrates the unique capabilities of the XANES spectroscopy as a tool to achieve structural and bonding information of carbon nanotubes induced by chemical processes.

By investigating the morphologies and microstructures of the cathode deposits prepared by self-sustained arc discharge between graphite rods, we consider that there are two electron emission mechanisms occurring on the cathode: field emission and thermionic emission. The former occurs mainly on the edge of the growing surface, by which we can explain the formation of the outer hard shell of the cathode deposit; while the latter occurs mainly on the growing surface except for the edge area and it is the main cause for the growth of carbon nanotubes.

Ultrafast time-resolved optical transmissions in purified and as-grown single-walled carbon nanotube films are measured at a temperature of 200K. The signal of the purified sample shows a crossover from photobleaching to photoabsorption. The former and the latter are interpreted as the state filling and the red shift of the pi-plasmon, respectively. The signal of the as-grown sample can be perfectly fitted by a single-exponential with a time constant of 232fs. The disappearance of the negative component in the as-grown sample is attributed to the charge transfer between the semiconducting nanotubes and the impurities.

A new experimental technique has been presented to investigate the surface-enhanced Raman scattering (SERS) on “individual and untouched” single-walled carbon nanotubes (SWNTs) deposited onto gold or silver film-covered substrate through a direct CVD method. It was found that the radial breathing mode for SERS shows a narrower linewidth than the normal Raman spectroscopy (NRS). Relative to NRS, the SERS spectra also revealed a preferable contribution to some metallic component of the G line. However no obvious difference for D and G′ between SERS and NRS has been revealed, which is different from the previous results on bulk SWNT samples.

Light-induced difference THz spectroscopy was used to investigate the dielectric response of free-stand single-walled carbon nanotubes (SWCNTs) films in THz region. We observed an enhanced transmission of the peak-signal of THz wave through SWCNTs films under 800 nm pump. In frequency domain, the transparency came from 0.5 to 2.1 THz and the absorption was in 2.1–3.0 THz region. The pump power dependency of the transmission showed this was a nonlinear effect. The dielectric constant response of the SWCNTs films was analyzed theoretically. The analysis suggests that the nonlinear optical properties stem from two factors, which are Drude and Lorentz term for metallic and semiconducting SWCNTs, respectively.