The electro-structural behaviour of yarn-like carbon nanotube fibres immersed in organic liquids.

Yarn-like carbon nanotube (CNT) fibres are a hierarchically-structured material with a variety of promising applications such as high performance composites, sensors and actuators, smart textiles, and energy storage and transmission. However, in order to fully realize these possibilities, a more detailed understanding of their interactions with the environment is required. In this work, we describe a simplified representation of the hierarchical structure of the fibres from which several mathematical models are constructed to explain electro-structural interactions of fibres with organic liquids. A balance between the elastic and surface energies of the CNT bundle network in different media allows the determination of the maximum lengths that open junctions can sustain before collapsing to minimize the surface energy. This characteristic length correlates well with the increase of fibre resistance upon immersion in organic liquids. We also study the effect of charge accumulation in open interbundle junctions and derive expressions to describe experimental data on the non-ohmic electrical behaviour of fibres immersed in polar liquids. Our analyses suggest that the non-ohmic behaviour is caused by progressively shorter junctions collapsing as the voltage is increased. Since our models are not based on any property unique to carbon nanotubes, they should also be useful to describe other hierarchical structures.

Tuning the mechanical properties of composites from elastomeric to rigid thermoplastic by controlled addition of carbon nanotubes.

A commercial thermoplastic polyurethane is identified for which the addition of nanotubes dramatically improves its mechanical properties. Increasing the nanotube content from 0% to 40% results in an increase in modulus, Y, (0.4-2.2 GPa) and stress at 3% strain, σ(ϵ = 3%) , (10-50 MPa), no significant change in ultimate tensile strength, σ(B) , (≈50 MPa) and decreases in strain at break, ϵ(B) , (555-3%) and toughness, T, (177-1 MJ m(-3) ). This variation in properties spans the range from compliant and ductile, like an elastomer, at low mass fractions to stiff and brittle, like a rigid thermoplastic, at high nanotube content. For mid-range nanotube contents (≈15%) the material behaves like a rigid thermoplastic with large ductility: Y = 1.5 GPa, σ(ϵ = 3%) = 36 MPa, σ(B) = 55 MPa, ϵ(B) = 100% and T = 50 MJ m(-3) . Analysis suggests that soft polyurethane segments are immobilized by adsorption onto the nanotubes, resulting in large changes in mechanical properties.

Ordering in a droplet of an aqueous suspension of single-wall carbon nanotubes on a solid substrate.

We report on a series of experiments on the aqueous, nematic liquid crystalline phase of single-wall carbon nanotubes (SWNTs) and their ordered assemblies on the solid substrates. The nanotubes were dispersed at a low concentration of isotropic phase, and the concentration was gradually increased by the controlled evaporation of water. In-situ isotropic-to-liquid crystalline phase transition via a biphasic region was observed during water evaporation. Drying on a substrate demonstrated the effect of surface fields on the order and alignment of SWNTs in the liquid suspension and the influence on the structure of the deposited nanotubes after evaporation.

Investigating the effect of pH on the aggregation of two surfactant-like octapeptides.

The aggregation of two de novo designed surfactant-like peptides, with sequences Ac-IIKKEENN-OH (P1) and Ac-IIEENNDD-OH (P2), has been studied in aqueous solution at various pH values using titration, Circular dichroism (CD), Fourier transform infrared spectroscopy (FTIR), and atomic force microscopy (AFM). It was found that aggregates of P1 and P2 both display 5 pK(a)'s, some of which differ considerably from the tabulated values for those amino acids. In particular, a lysine of P1 titrated to 4.939 +/- 0.066. CD spectra of P1 were insensitive to pH, while CD spectra of P2 demonstrated a random coil-to-beta-sheet transition as pH was decreased. AFM images confirmed that P1 aggregates were spheres at all pH values and ranged in size from 3 to 20 nm. On the other hand, P2 aggregates were twisted ribbons below pH 4 but spheres less than 10 nm above pH 4. In addition, AFM images demonstrated the partial breakup of these twisted ribbons upon elevating the pH from 3.03 to 3.46 and the virtual disappearance of ribbons at pH 3.82. FTIR spectra of P2 indicate a structural transition from random coil to beta-sheet as pH was decreased. The role of backbone hydrogen bonding as well as charge is discussed.

Continuous production of flexible carbon nanotube-based transparent conductive films.

This work shows a simple, single-stage, scalable method for the continuous production of high-quality carbon nanotube-polymer transparent conductive films from carbon feedstock. Besides the ease of scalability, a particular advantage of this process is that the concentration of nanotubes in the films, and thus transparency and conductivity, can be adjusted by changing simple process parameters. Therefore, films can be readily prepared for any application desired, ranging from solar cells to flat panel displays. Our best results show a surface resistivity of the order of 300 Ω square-1 for a film with 80% transparency, which is promising at this early stage of process development.

Orientation dynamics in multiwalled carbon nanotube dispersions under shear flow.

We report studies of the orientation state of multiwalled carbon nanotubes (MWNTs) dispersions in steady and transient shear flows. Uncured epoxy was used as a viscous Newtonian suspending medium and samples were prepared from "aligned" MWNTs using methods previously reported [S. S. Rahatekar et al., J. Rheol. 50, 599 (2006)]. Orientation measurements were performed in both the flow-gradient (1-2) and flow-vorticity (1-3) plane of simple shear flow using in situ x-ray scattering techniques. Steady state measurements in the 1-2 plane indicate that the MWNT orientation is shear rate dependent, with the MWNTs orienting closer to the flow direction at higher shear rates. During steady shear, anisotropy was measured to be higher in the 1-2 plane than in the 1-3 plane, demonstrating that the nanotube orientation state is not unaxially symmetric in shear. It is hypothesized that the steady state MWNT orientation is governed primarily by a rate-dependent state of nanotube aggregation/disaggregation, which was separately characterized by optical microscopy of the same samples under shear. High flux synchrotron radiation allowed for time-resolved structural studies in transient flows. A partial relaxation of flow-induced anisotropy was observed following flow cessation, despite the very small rotational diffusivity estimated for these nanotubes. Long transients are observed in step-down experiments, as the orientation state changes in response to the slow tube aggregation process.

Crystal structure and growth mechanism of unusually long fullerene (C60) nanowires.

Exceptionally long C60 nanowires, with a length to width aspect ratio as large as 3000, are grown from a 1,2,4-trimethylbenzene solution of C60. They have been formed to possess a highly unusual morphology, with each nanowire being composed of two nanobelts joined along the growth direction to give a V-shaped cross section. The crystal structure of these nanowires is found to be orthorhombic, with the unit cell dimensions of a = 10.2 A, b = 20.5 A, and c = 25.6 A. Structural and compositional analyses enable us to explain the observed geometry with an anisotropic molecular packing mechanism that has not been observed previously in C60 crystal studies. The nanowires have been observed to be able to transform into carbon nanofibers following high-temperature treatment, but the original V-shaped morphology can be kept unchanged in the transition. A model for the nanowire morphology based upon the solvent-C60 interactions and preferential growth directions is proposed, and potentially it could be extended for use to grow different types of fullerene nanowires.

Macroscopic fibers of well-aligned carbon nanotubes by wet spinning.

A simple process to spin fibers consisting of multi-walled carbon nanotubes (CNTs) directly from their lyotropic liquid-crystalline phase is reported. Ethylene glycol is used as the lyotropic solvent, enabling a wider range of CNT types to be spun than previously. Fibers spun with CNTs and nitrogen-doped CNTs are compared. X-ray analysis reveals that nitrogen-doped CNTs have a misalignment of only +/-7.8 degrees to the fiber axis. The tensile strength of the CNT and nitrogen-doped CNT fibers is comparable but the modulus and electrical conductivity of the are lower. The electrical conductivity of both types of CNT fibers is found to be highly anisotropic. The results are discussed in context of the microstructure of the CNTs and fibers.

Crystallographic order in multi-walled carbon nanotubes synthesized in the presence of nitrogen.

Multi-walled carbon nanotubes were synthesized by chemical vapor deposition from pure toluene and toluene/diazine mixtures using ferrocene as a catalyst precursor at 760 degrees C. As recently announced, characterization of the resulting nanotube films showed that, unlike pure carbon nanotubes, those grown in the presence of nitrogen have an extremely high degree of internal order, both in terms of the uniform chirality in the nanotube walls and of the crystallographic register between them. Here, the structure, defects, and morphology of the nanotubes were analyzed in depth using advanced electron microscopy techniques, and compared with existing models and observations. Nitrogen, which seems to be responsible for the dramatic structural order, was found to segregate preferentially within the core of the nanotubes.

Self-organization of carbon nanotubes in evaporating droplets.

Here, we report a simple and efficient way for organizing carbon nanotubes, in particular, single-wall carbon nanotubes (SWNTs) into ordered structures from their dilute solutions. It was found that drying a droplet of carbon nanotube solution at room temperature on a wettable surface such as glass or silica wafer led to redistribution, accumulation, and organization of carbon nanotubes along the perimeter of the droplet. Unlike the aggregation behaviors of colloid nanoparticles, anistropic carbon nanotubes tended to show two orientations in a ring deposit: one parallel to the outer perimeter of the ring and the other normal to it in the interior. Drying droplets of SWNT solutions at high temperatures exhibited a long-range ordered structure. In addition, droplet drying may cause size separation of carbon nanotubes and pattern formation through interactions between droplets. This result helps us not only to further understand fluid dynamics during the drying process but also to provide a promising and simple strategy for either assembling carbon nanotubes on a surface or organizing them into well-aligned films and fibers.

Pure rutile nanotubes.

We present a novel method to produce pure rutile nanotubes using a sacrificial carbon nanotube template.

Effect of the elastic constant anisotropy on disclination interaction in the nematic polymers.

In this work, disclination interaction behavior in relation to Frank elastic constant anisotropy in nematics has been studied. A large number of (+(1/2), -(1/2)) disclination pairs are revealed by spontaneous band texture in a semiflexible copolyester. The pairs show no preferential relative orientation, with the intervening fields showing intermediate patterns. A two-dimensional tensor lattice model considering unequal elastic constants is applied to simulate the interaction behavior and patterns of disclination pairs in the presence of elastic anisotropy. Scaling laws for disclination density rho(t) as a function of time step t with different elastic anisotropy are obtained as t(-nu). The value of the exponent nu decreases as elastic anisotropy is increased. Obviously, elastic anisotropy slows the texture coarsening. The simulations also show that angular forces arise in the presence of elastic anisotropy and change the patterns of pairs during the texture coarsening. When disclination density is considerably decreased, some +(1/2) disclinations start to rotate to the energetically favored patterns depending on the sign of the elastic anisotropy. As a result of the disclination rotation, the distribution of patterns of pairs continues to change during the annihilation. However, disclination pairs are influenced not only by elastic anisotropy but also by disclination interaction during the whole annihilation. Therefore, in a real system, the dependence of pairs on elastic anisotropy is not as strong as the theoretical prediction for an isolated pair, and the full pattern range of disclination pairs can be observed.

Production of carbon nanofibers in high yields using a sodium chloride support.

A new route for the highly convenient scalable production of carbon nanofibers on a sodium chloride support has been developed. Since the support is nontoxic and soluble in water, it can be easily removed without damage to the nanofibers and the environment. Nanofiber yields of up to 6500 wt % relative to the nickel catalyst have been achieved in a growth time of 15 min. Electron microscopy (SEM, TEM) and thermal gravimetric analysis (TGA) indicated that the catalytically grown carbon had relatively little thermal over-growth and possessed either a herringbone or a semi-ordered nanostructure, depending on the growth conditions.

Discrete dispersion of single-walled carbon nanotubes.

Single-walled carbon nanotubes (SWNTs) have been effectively wetted and dispersed in saturated sodium hydroxide (NaOH) alcohol-water solutions with little surface damage or shortening of the tubes; the treated material was dissolvable as individual tubes in many common organic solvents.

Multi-walled carbon nanotube induced frustrated phagocytosis, cytotoxicity and pro-inflammatory conditions in macrophages are length dependent and greater than that of asbestos.

The potential toxicity of carbon nanotubes (CNTs) has been compared to pathogenic fibres such as asbestos. It is important to test this hypothesis to ascertain safe methods for CNT production, handling and disposal. In this study aspects reported to contribute to CNT toxicity were assessed: length, aspect ratio, iron content and crystallinity; with responses compared to industrially produced MWCNTs and toxicologically relevant materials such as asbestos. The impacts of these particles on a range of macrophage models in vitro were assessed due to the key role of macrophages in particle clearance and particle/fibre-induced disease. Industrially produced and long MWCNTs were cytotoxic to cells, and were potent in inducing pro-inflammatory and pro-fibrotic immune responses. Short CNTs did not induce any cytotoxicity. Frustrated phagocytosis was most evident in response to long CNTs, as was respiratory burst and reduction in phagocytic ability. Short CNTs, metal content and crystallinity had less or no influence on these endpoints, suggesting that many responses were fibre-length dependent. This study demonstrates that CNTs are potentially pathogenic, as they were routinely found to induce detrimental responses in macrophages greater than those induced by asbestos at the same mass-based dose.

Synthesis of high purity single-walled carbon nanotubes in high yield.

A simple method for the synthesis of high purity single wall carbon nanotubes has been developed by using nickel formate as a precursor for the formation of nearly mono-dispersed nickel seed-nanoparticles as catalysts in the CVD growth process.

Small angle X-ray study of cellulose macromolecules produced by tunicates and bacteria.

The organisation of poly-glucan chains into cellulose macromolecular microfibrils has been studied using small angle X-ray scattering (SAXS). Three kinds of cellulose - bacterial cellulose (BC), nata-de-coco (NdC) (food grade bacterial cellulose) and tunicate cellulose (TC) have been investigated. Given the large ambiguity in literature on the microfibril dimensions owing to different methods and data analysis strategies, a method to extract dimensions of cellulose microfibrils using SAXS has been shown, which was found to be consistent across all the samples. The results have been verified with microscopy data. Two populations of microfibrils with different cross-section dimensions were identified. The dimensions of the rectangular cross-sections of BC were found to be 32nm by 16nm and 21nm by 10nm. The dimensions for NdC were calculated to be 25nm×8nm and 14nm×6nm and that for TC were determined to be 25nm×10nm and 15nm×8nm.

Piezoresistive effect in carbon nanotube fibers.

The complex structure of the macroscopic assemblies of carbon nanotubes and variable intrinsic piezoresistivity of nanotubes themselves lead to highly interesting piezoresistive performance of this new type of conductive material. Here, we present an in-depth study of the piezoresistive effect in carbon nanotube fibers, i.e., yarnlike assemblies made purely of aligned carbon nanotubes, which are expected to find applications as electrical and electronic materials. The resistivity changes of carbon nanotube fibers were measured on initial loading, through the elastic/plastic transition, on cyclic loading and on stress relaxation. The various regimes of stress/strain behavior were modeled using a standard linear solid model, which was modified with an additional element in series to account for the observed creep behavior. On the basis of the experimental and modeling results, the origin of piezoresistivity is discussed. An additional effect on the resistivity was found as the fiber was held under load which led to observations of the effect of humidity and the associated water adsorption level on the resistivity. We show that the equilibrium uptake of moisture leads to the decrease in gauge factor of the fiber decrease, i.e., the reduction in the sensitivity of fiber resistivity to loading.

Electric field-modulated non-ohmic behavior of carbon nanotube fibers in polar liquids.

We report a previously unseen non-ohmic effect in which the resistivity of carbon nanotube fibers immersed in polar liquids is modulated by the applied electric field. This behavior depends on the surface energy, dielectric constant, and viscosity of the immersion media. Supported by synchrotron SAXS and impedance spectroscopy, we propose a model in which the gap distance, and thus the conductance, of capacitive interbundle junctions is controlled by the applied field.

Liquid infiltration into carbon nanotube fibers: effect on structure and electrical properties.

Carbon nanotube (CNT) fibers consist of a network of highly oriented carbon nanotube bundles. This paper explores the ingress of liquids into the contiguous internal pores between the bundles using measurements of contact angles and changes in fiber dimensions. The resultant effects on the internal structure of the fiber have been examined by WAXS and SAXS. A series of time-resolved experiments measured the influence of the structural changes on the electrical resistivity of the fiber. All organic liquids tested rapidly wicked into the fiber to fill its internal void structure. The local regions in which the nanotube bundles are aggregated to give a bundle network were broken up by the liquid ingress. For the range of organic penetrants examined, the strength of the effects on structure and electrical resistivity was correlated, not only with the degree to which the liquid reduced the nanotube surface energy, but also with the Hansen affinity parameters. The fact that liquid environments influence the electrical performance of these fibers is of significance if they are to replace copper as power and signal conductors, with added implications regarding the possible ingress of external insulating materials, and possibly also sensing applications.