NMR detection of single-walled carbon nanotubes in solution

The detection of nanotube carbons in solution by (13)C NMR is reported. The highly soluble sample was from the functionalization of (13)C-enriched single-walled carbon nanotubes (SWNTs) with diamine-terminated oligomeric poly(ethylene glycol) (PEG(1500N)). The ferromagnetic impurities due to the residual metal catalysts were removed from the sample via repeated magnetic separation. The nanotube carbon signals are broad but partially resolved into two overlapping peaks, which are tentatively assigned to nanotube carbons on semiconducting (upfield) and metallic (downfield) SWNTs. The solid-state NMR signals of the same sample are similarly resolved. Mechanistic and practical implications of the results are discussed.     

Dispersions of individual single-walled carbon nanotubes of high length

In summary, we have presented a suitable approach to obtain surfactant-stabilized suspensions of long, individually dispersed SWCNTs essentially free of bundles. The combination of mild tip and bath ultrasonication has proven effective in unbundling the SWCNT ropes and, at the same time, in minimizing tube shortening. This method is expected to be useful for applications that critically depend on the availability of bulk dispersions of long, individual tubes with minimized defect densities, such as for nanotube-based electronics and composite materials. Furthermore, the observed purification-induced changes in the electronic structure of HiPco SWCNTs indicate that care has to be taken when comparing their properties with those of the as-produced material.     

Preparation and characterization of individual peptide-wrapped single-walled carbon nanotubes

Two challenges for effectively exploiting the remarkable properties of single-walled carbon nanotubes (SWNTs) are the isolation of intact individual nanotubes from the raw material and the assembly of these isolated SWNTs into useful structures. In this study, we present atomic force microscopy (AFM) evidence that we can isolate individual peptide-wrapped SWNTs, possibly connected end-to-end into long fibrillar structures, using an amphiphilic alpha-helical peptide, termed nano-1. Transmission electron microscopy (TEM) and well-resolved absorption spectral features further corroborate nano-1's ability to debundle SWNTs in aqueous solution. Peptide-assisted assembly of SWNT structures, specifically in the form of Y-, X-, and intraloop junctions, was observed in the AFM and TEM images.     

Raman spectroscopy of individual single-walled carbon nanotubes from various sources

Resonance Raman spectroscopy/microscopy was used to study individualized single-walled carbon nanotubes (SWNTs) both in aqueous suspensions as well as after spin-coating onto Si/SiO2 surfaces. Four different SWNT materials containing nanotubes with diameters ranging from 0.7 to 1.6 nm were used. Comparison with Raman data obtained for suspensions shows that the surface does not dramatically affect the electronic properties of the deposited tubes. Raman features observed for deposited SWNTs are similar to what was measured for nanotubes directly fabricated on surfaces using chemical vapor deposition (CVD) methods. In particular, individual semiconducting tubes could be distinguished from metallic tubes by their different G-mode line shapes. It could also be shown that the high-power, short-time sonication used to generate individualized SWNT suspensions does not induce defects in great quantities. However, (additional) defects can be generated by laser irradiation of deposited SWNTs in air, thus giving rise to an increase of the D-mode intensity for even quite low power densities (approximately 10(4) W/cm2).     

Bioelectrochemical single-walled carbon nanotubes

Metalloproteins and enzymes can be immobilized on SWNTs of different surface chemistry. The combination of high surface area, robust immobilization and inherent nanotube electrochemical properties is of promising application in bioelectrochemistry.     

Direct electrochemistry of uric acid at chemically assembled carboxylated single-walled carbon nanotubes netlike electrode

Carboxylated single-walled carbon nanotubes (SWCNT) chemically assembled on gold substrate was employed as netlike electrode to investigate the charge-transfer process and electrode process kinetics using uric acid as an example. The electrochemical behavior of uric acid in carboxylated SWCNT system was investigated using cyclic voltammetry, chronoamperometry, and single potential time-based techniques. The properties of raw SWCNT electrode were also studied for comparison purpose. Uric acid has better electrochemical behavior whereas ascorbic acid has no effective reaction on the carboxylated SWCNT electrode. Cyclic voltammograms indicate that the assembled carboxylated SWCNT increases more active sites on electrode surface and slows down the electron transfer between the gold electrode and uric acid in solution. The charge-transfer coefficient (alpha) for uric acid and the rate constant (k) for the catalytic reaction were calculated as 0.52 and 0.43 s(-1), respectively. The diffusion coefficient of 0.5 mM uric acid was 7.5 x 10(-6) cm2 x s(-1). The results indicate that electrode process in the carboxylated SWCNT electrode system is governed by the surface adsorption-controlled electrochemical process.     

Direct electrochemistry and reagentless biosensing of glucose oxidase immobilized on chitosan wrapped single-walled carbon nanotubes

Single-walled carbon nanotubes (SWCNTs) selectively wrapped by a water-soluble, environmentally friendly, biocompatible polymer chitosan (CHI) were employed for the construction of a bioelectrochemical platform for the direct electron transfer (DET) of glucose oxidase (GOD) and biosensing purposes. Scanning electron microscopy and Raman spectroscopy were used to investigate the properties of the SWCNT-CHI film. The results show that the preferentially wrapped small-diameter SWCNTs are dispersed within the CHI film and exist on the surface of the electrode as small bundles. The DET between GOD and the electrode surface was observed with a formal potential of about ca. -460 mV vs. SCE in phosphate buffer solution. The heterogeneous electron transfer rate constant and the surface coverage of GOD are estimated to be 3.0 s(-1) and 1.3 x 10(-10)mol/cm(2), respectively. The experimental results demonstrate that the immobilized GOD retains its catalytic activity towards the oxidation of glucose. Such a GOD/SWCNT-CHI film-based biosensor not only exhibits a rapid response time, a wide linear rang and a low detection limits at a detection potential of -400 mV but also shows the effective anti-interference capability. Significantly improved analytical capabilities of the GOD/SWCNT-CHI/GC electrode could be ascribed to the unique properties of the individual SWCNTs and to the biocompatibility of CHI.     

The effects of the lengths and orientations of single-walled carbon nanotubes on the electrochemistry of nanotube-modified electrodes

The influence of both nanotube orientation and length on the electrochemical properties of electrodes modified with single-walled carbon nanotubes was investigated. Gold electrodes were modified with either randomly dispersed or vertically aligned nanotubes to which ferrocenemethylamine was attached. Electron transfer kinetics were found to depend strongly on the orientation of the nanotube, with electron transfer between the gold electrode and the ferrocene moiety being 40 times slower through randomly dispersed nanotubes than through vertically aligned nanotubes. The difference is hypothesized to be due to electron transfer being more direct through a single tube than that with electrodes modified with randomly dispersed nanotubes. With the vertically aligned nanotubes the rate constant for electron transfer varied inversely with the mean length of the nanotubes. The results indicate there is an advantage in using aligned carbon nanotube arrays over randomly dispersed nanotubes for achieving efficient electron transfer to bound redox active species such as in the case of bioelectronic or photovoltaic devices.     

Assembly of layer-by-layer films of heme proteins and single-walled carbon nanotubes: electrochemistry and electrocatalysis

After being treated by mixed acids, single-walled carbon nanotubes (SWNTs) were shortened and had negatively charged groups on the surface. Positively charged hemoglobin or myoglobin at pH 5.0 was successfully assembled with SWNTs into layer-by-layer films on solid surfaces, designated as {SWNT/protein} _n . While only those proteins in the first few bilayers closest to the electrode surface exhibited electroactivity, the {SWNT/protein} _n films demonstrated a much higher fraction of electroactive proteins and better controllability in film construction compared with cast films of the proteins and carbon nanotubes. The proteins in the {SWNT/protein} _n films retained their near-native structure at medium pH. The stable protein film electrode showed good electrocatalytic properties toward reduction of oxygen and hydrogen peroxide, demonstrating the potential application of the {SWNT/protein} _n films as a new type of biosensor based on the direct electrochemistry of proteins without using mediators. Figure Cyclic voltammograms at 0.2 V s⁻¹ in pH 7.0 buffers with different number of bilayers (n) for layer-by-layer {single-walled carbon nanotube/hemoglobin} _n films.     

Ultrathin anisotropic films assembled from individual single-walled carbon nanotubes and amine polymers

Oxidized individual single-walled carbon nanotubes and amine polymers have been assembled into 11-32-nm-thick well-ordered conductive films. The films show highly anisotropic electrical conductivity, which is dominated by the nanotubes in the horizontal plane and by polymer-mediated tunneling in the vertical direction. The ratio of the "along" to "across" conductivity is approximately 10(3). The subnanometer thick polymer layers interleaved with monolayers of nanotubes show conductivity several orders of magnitude higher than films of pristine polymers.     

Lithium storage in single-walled carbon nanotubes

Here, we investigated the lithium insertion/extraction mechanism in single-walled carbon nanotubes (SWNTs) based both on the empty SWNTs and filled SWNTs, including ferrocene-filled SWNTs (Fc@SWNTs) and C₆₀-filled SWNTs (C₆₀@SWNTs). SWNTs, C₆₀@SWNTs and Fc@SWNTs were systematically investigated as anode materials for Li-ion batteries. The electrochemical performance of the C₆₀@SWNT electrode was slightly better than that of the SWNTs, and the reversible capacity of Fc@SWNTs per unit weight was ～1.7 times greater than that of the empty SWNTs due to its special tube internal structure. It was proved that the dominant reversible sites for lithium storage in empty SWNTs are the trigonal interstitial channels. Meanwhile, lithium can reversibly insert or extract the inner channels of the tubes after doping with ferrocene; the reversible capacity presented in the inner channels of Fc@SWNTs is about Li_1.13C₆.     

Soluble ultra-short single-walled carbon nanotubes

Soluble, ultra-short (length < 60 nm), carboxylated, single-walled carbon nanotubes (SWNTs) have been prepared by a scalable process. This process, predicated on oleum's (100% H2SO4 with excess SO3) ability to intercalate between individual SWNTs inside SWNT ropes, is a procedure that simultaneously cuts and functionalizes SWNTs using a mixture of sulfuric and nitric acids. The solubility of these ultra-short SWNTs (US-SWNTs) in organic solvents, superacid and water is about 2 wt %. The availability of soluble US-SWNTs could open opportunities for forming high performance composites, blends, and copolymers without inhibiting their processibility.     

Dispersion of single-walled carbon nanotubes in aqueous solution with a thermo-responsive pentablock terpolymer

Single-walled carbon nanotubes (SWNTs) were dispersed in pure water with a thermo-responsive amphiphilic PNIPAM₁₅₀-F108-PNIPAM₁₅₀ pentablock terpolymer in comparison with its precursor PEO₁₃₆-PPO₄₅-PEO₁₃₆ (F108) triblock copolymer. The stability, dispersibility, and thermo-responsive behaviors of the polymer/SWNT hybrids were characterized by UV–vis–NIR spectroscopy, thermal gravimetric analysis, viscosity measurement, Raman spectroscopy, and high-resolution transmission electron microscopy. The pentablock/SWNT hybrids showed superior ability in stabilization over F108/SWNT hybrids, and no sign of sedimentation was found at room temperature for 6 weeks or even 2 months of storage. The pentablock terpolymer can efficiently disperse SWNTs into individual tubes or small bundles with average diameter of about 5 nm, and their chains were helically wrapped onto the nanotube surface, whereas the larger bundles of the nanotubes with sizes of 15–25 nm were observed in F108/SWNT hybrids. Moreover, the pentablock/SWNT hybrids switched reversibly between the well-exfoliated and the aggregated states when cyclically increasing and decreasing temperature.     

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.     

Protein-assisted solubilization of single-walled carbon nanotubes

We report a simple method that uses proteins to solubilize single-walled carbon nanotubes (SWNTs) in water. Characterization by a variety of complementary techniques including UV-Vis spectroscopy, Raman spectroscopy, and atomic force microscopy confirmed the dispersion at the individual nanotube level. A variety of proteins differing in size and structure were used to generate individual nanotube solutions by this noncovalent functionalization procedure. Protein-mediated solubilization of nanotubes in water may be important for biomedical applications. This method of solubilization may also find use in approaches for controlling the assembly of nanostructures, and the wide variety of functional groups present on the adsorbed proteins may be used as orthogonal reactive handles for the functionalization of carbon nanotubes.     

Encapsulation of carbon chain molecules in single-walled carbon nanotubes

The vacuum space inside carbon nanotubes offers interesting possibilities for the inclusion, transportation, and functionalization of foreign molecules. Using first-principles density functional calculations, we show that linear carbon-based chain molecules, namely, polyynes (C(m)H(2), m = 4, 6, 10) and the dehydrogenated forms C(10)H and C(10), as well as hexane (C(6)H(14)), can be spontaneously encapsulated in open-ended single-walled carbon nanotubes (SWNTs) with edges that have dangling bonds or that are terminated with hydrogen atoms, as if they were drawn into a vacuum cleaner. The energy gains when C(10)H(2), C(10)H, C(10), C(6)H(2), C(4)H(2), and C(6)H(14) are encapsulated inside a (10,0) zigzag-shaped SWNT are 1.48, 2.04, 2.18, 1.05, 0.55, and 1.48 eV, respectively. When these molecules come inside a much wider (10,10) armchair SWNT along the tube axis, they experience neither an energy gain nor an energy barrier. They experience an energy gain when they approach the tube walls inside. Three hexane molecules can be encapsulated parallel to each other (i.e., nested) inside a (10,10) SWNT, and their energy gain is 1.98 eV. Three hexane molecules can exhibit a rotary motion. One reason for the stability of carbon chain molecules inside SWNTs is the large area of weak wave function overlap. Another reason concerns molecular dependence, that is, the quadrupole-quadrupole interaction in the case of the polyynes and electron charge transfer from the SWNT in the case of the dehydrogenated forms. The very flat potential surface inside an SWNT suggests that friction is quite low, and the space inside SWNTs serves as an ideal environment for the molecular transport of carbon chain molecules. The present theoretical results are certainly consistent with recent experimental results. Moreover, the encapsulation of C(10) makes an SWNT a (purely carbon-made) p-type acceptor. Another interesting possibility associated with the present system is the direction-controlled transport of C(10)H inside an SWNT under an external field. Because C(10)H has an electric dipole moment, it is expected to move under a gradient electric field. Finally, we derive the entropies of linear chain molecules inside and outside an open-ended SWNT to discuss the stability of including linear chain molecules inside an SWNT at finite temperatures.     

Fluorimetric characterization of single-walled carbon nanotubes

Single-walled carbon nanotubes (SWCNTs) are a family of structurally related artificial nanomaterials with unusual properties and many potential applications. Most SWCNTs can emit spectrally narrow near-IR fluorescence at wavelengths that are characteristic of their precise diameter and chiral angle. Near-IR fluorimetry therefore offers a powerful approach for identifying the structural species present in SWCNT samples. Such characterization is increasingly important for nanotube production, study, separation, and applications. General-purpose and specialized instruments suitable for SWCNT fluorimetric analysis are described, and methods for interpreting fluorimetric data to deduce the presence and relative abundances of different SWCNT species are presented. Fluorescence methods are highly effective for detecting SWCNTs in challenging samples such as complex environmental or biological specimens because of the methods’ high sensitivity and selectivity and the near absence of interfering background emission at near-IR wavelengths. Current limitations and future prospects for fluorimetric characterization of SWCNTs are discussed.     

Long super-bundles of single-walled carbon nanotubes

200 nm-thick super bundles showing a novel polygonization and densely aligned arrangement are found in long single-walled carbon nanotube (SWNT) strands prepared by the vertical floating catalytic method.     

Stability of supershort single-walled carbon nanotubes

How short can single-walled carbon nanotubes (SWNTs) be? How stable are such supershort SWNTs (ss-SWNTs)? This work is the first to address these questions. On the basis of binding energy (E(B)), standard heats of formation , and strain energy (E(S)), we found that SWNTs with only one benzene ring in the axial direction, which we refer to as supershort SWNTs (ss-SWNTs), can be thermodynamically stable. On the basis of the data of E(B), , and E(S), the relative stabilities of ss-SWNTs, fullerenes, polycyclic aromatic hydrocarbons, and butadiyne are discussed. This study has laid a theoretical foundation for the possible synthesis of ss-SWNTs.     

Infrared spectroscopy of single-walled carbon nanotubes

By using the spectral moments method, we calculate the infrared spectra of chiral and achiral single-walled carbon nanotubes (SWCNTs) of different diameters and lengths. We show that the number of the infrared modes, their frequencies, and intensities depend on the length and chirality of the nanotubes. Furthermore, the dependence of the infrared spectrum as a function of the size of the SWCNT bundle is analyzed. These predictions are useful to interpret the experimental infrared spectra of SWCNTs.