Dispersion of single-walled carbon nanotubes modified with poly-l-tyrosine in water

In this study, complexes composed of poly-l-tyrosine (pLT) and single-walled carbon nanotubes (SWCNTs) were produced and the dispersibility of the pLT/SWCNT complexes in water by measuring the ζ potential of the complexes and the turbidity of the solution were investigated. It is found that the absolute value of the ζ potential of the pLT/SWCNT complexes is as high as that of SWCNTs modified with double-stranded DNA (dsDNA) and that the complexes remain stably dispersed in the water at least for two weeks. Thermogravimetry analysis (TGA) and visualization of the surface structures of pLT/SWCNT complexes using an atomic force microscope (AFM) were also carried out.     

Preparation of single-walled carbon nanotube/TiO2 hybrid atmospheric gas sensor operated at ambient temperature

Single-walled carbon nanotubes (SWCNTs)/TiO₂ hybrid gas sensors operated at a room temperature were fabricated. SWCNTs were stabilized on a Si substrate with interdigitated Pt-electrodes to prepare a gas sensor. Sensing properties of the gas sensor were measured in various concentrations of NO gas. Resistance of the prepared SWCNT based gas sensor decreased with increase of NO gas concentration due to electron transfer from p-type SWCNTs to NO molecules. The SWCNT gas sensor showed high sensitivity and rapid response to the test gas. The hybrid gas sensor using SWCNTs doped with anatase TiO₂ nano-particles was developed, which could work at room temperature under UV-LED (λ = 377 nm) irradiation. It showed rapid recovery to the initial state and higher sensitivity than the SWCNT gas sensor due to TiO₂ photocatalytic effect.     

Using oxidation to increase the electrical conductivity of carbon nanotube electrodes

Recent studies have demonstrated that significantly low sheet resistance (Rs) (<100 Ω/sq; comparable to ITO) were achieved in single-walled carbon nanotube (SWCNT) films treated with HNO₃ followed by thionyl chloride. Here we show that H₂SO₄ can effectively reduce the Rs of SWCNT electrodes. H₂SO₄ treatment generates defects (COOH and SO₃H functionalities) on SWCNTs and the produced chemical functionalities are beneficial for enhancing the electrical conductivity in SWCNT electrodes. It is plausible that the H₂SO₄p-dopes the SWCNTs and the attachment of chemical functionalities helps to stabilize p-doping owing to their electron-deficient property.     

Adsorption of single-ringed N- and S-heterocyclic aromatics on carbon nanotubes

Adsorption of single-ringed N- and S-heterocyclic aromatics on single-walled carbon nanotubes (SWCNTs) was examined to explore the potential of using carbon nanotubes (CNTs) as drug carriers and environmental adsorbents. Adsorbates included pyrimidine, 2-aminopyrimidine, 4,6-diaminopyrimidine, thiophene, benzene and aniline. Adsorbents included pristine SWCNTs, oxidized SWCNTs, and nonporous graphite. Adsorption of N- and S-heterocyclic aromatics was significantly enhanced by non-hydrophobic interactions. Particularly, the -NH₂-substituted compounds exhibited much stronger (up to 2 orders of magnitude) adsorption affinities to oxidized SWCNTs than benzene, even though they are much less hydrophobic. The π-π coupling or electron donor-acceptor (EDA) interactions are likely adsorption-enhancement mechanisms for all six compounds. The lone-pair electrons of the N heteroatoms and the -NH₂ group can enable n-π EDA interactions with SWCNT surfaces. Lewis acid-base interactions are another significant adsorption-enhancement mechanism for the -NH₂-substituted compounds (and possibly for pyrimidine) on SWCNTs. For the N-heterocyclic aromatics, adsorption affinity is highly dependent on the O-functionality of the SWCNT surface and on solution pH, due to the speciation reactions of both adsorbates and SWCNT surface O-functional groups, indicating that selective adsorption of N-heterocyclic aromatics is possible by combining the surface functionality of CNTs and solution chemistry.     

Chirality fingerprinting and geometrical determination of single-walled carbon nanotubes: Analysis of fine structure of X-ray diffraction pattern

Single-walled carbon nanotubes (SWCNTs) are seamless cylindrical tubes consisting of carbon atoms with diameters ranging from less than one nanometer to a few nanometers. The arrangement of carbon atoms in a SWCNT is uniquely specified by using a pair of integers (n, m) referred to as the chiral indices. While the detailed structures, such as a carbon–carbon bond length, should be important, they have not been fully clarified yet. In this work, we examine the possibility of powder X-ray diffraction (XRD) method to characterize structures of SWCNTs. It is found that the XRD is a useful tool to “fingerprint” the chiral indices of bulk SWCNT samples. Besides, we find that information on the detailed structure within a SWCNT can be obtained from the XRD pattern. The application to a highly concentrated SWCNTs clarifies that the (6,5) SWCNT is expanded along the radial direction compared to that of ideal rolling up structure of graphene, with a negligible change along the tube axis.     

Fabrication of single-walled carbon nanotube Schottky diode with gold contacts modified by asymmetric thiolate molecules

We have fabricated single-walled carbon nanotube (SWCNT) Schottky diodes by asymmetrically modifying the two Au/SWCNT contacts using different thiolate molecules, methanethiol (CH₃SH) and trifluoroethanethiol (CF₃CH₂SH). Characterization has revealed that highly asymmetrical contacts with Schottky barrier heights of ∼190 and ∼40 meV (increased by over 70% and decreased by over 60%, respectively with respect to that of pristine Au/SWCNT contact of ∼110 meV) were achieved for the Au/SWCNT contacts modified by CH₃SH and CF₃CH₂SH, respectively. The performance of our SWCNT Schottky diodes is as follows: the forward and reverse current ratio (I_forward/I_reverse) higher than 10⁴, a forward current as high as ∼5 μA, a reverse leakage current as low as ∼100 pA, and a current ideality factor as low as ∼1.42. This is at least comparable to, if not better than SWCNT Schottky diodes fabricated with asymmetrical metals, where one contact is a metal with a work function lower than that of SWCNTs to yield a Schottky contact, while the other has a work function higher than that of SWCNTs to achieve an ohmic (more near ohmic) contact.     

Evidence for large hydrogen capacity in single-walled carbon nanotubes encapsulated by thin Pd layers onto a Pd substrate

We report a study of hydrogen storage and its mechanism in a novel material, representing single-walled carbon nanotubes (SWCNTs) encapsulated by thin Pd layers onto a Pd substrate. A synergetic effect resulting in combination of the Pd and the SWCNT properties with regard to hydrogen has been achieved. We showed that adding SWCNTs increases the H₂-capacity of the Pd–SWCNT composite under electrochemical loading only by up to 25% relative to the Pd metal alone. At the same time, with regard to the added SWCNTs, such synergetic approach (providing high H₂ pressure from highly H-loaded massive Pd substrate into a small fraction of deposited SWCNT) allowed us to achieve a net capacity of 8–12 wt.%. H₂, thus, bringing a unique chance to study hydrogen storage mechanism in highly H-loaded SWCNT. Using ESR technique it was established that the Pd–C_x π-complexes forming at the openings of SWCNTs could be considered as hydrogen adsorption sites, providing both high gravimetric capacity (H/C > 1) and low hydrogen binding energy in the Pd encapsulated SWCNT.     

The synthesis of covalent bonded single‐walled carbon nanotube/polyvinylimidazole composites by in situ polymerization and their physical characterization

Single‐walled carbon nanotube (SWCNT) polyvinylimidazole (PVI) composites have been prepared by in situ emulsion polymerization. Dispersion of raw SWCNTs in the PVI matrix was improved by surface modification of the SWCNTs using nitric acid treatment and air oxidation. The carbonyl‐terminated SWCNTs were covalently bonded to PVI by in situ polymerization and the SWCNT/PVI composite was thus obtained. The morphological and structural characterizations of the surface‐functionalized SWCNTs and SWCNT/PVI composites were carried out by Fourier transform infrared spectroscopy, X‐ray diffraction, conductivity measurements, scanning, and transmission electron microscopy. Thermograms of the materials were determined by the differential scanning calorimetry technique. The characterization results indicate that PVI was covalently bonded to SWCNTs and a new material was then obtained. The functionalized SWCNTs showed homogenous dispersion in the composites, whereas purified SWCNT resulted in poor dispersion and nanotube agglomeration. SWCNT/PVI composites exhibited chemical stability enhancement in many common solvents. I–V curves of the samples exhibit an ohmic character. Conductivity values for pure SWCNTs, pure PVI and SWCNT/PVI composite were measured to be 3.47, 2.11 × 10⁻⁹, and 2.3 × 10⁻³ S/m, respectively. Because of resonance, a large dielectric constant is obtained for SWCNT/PVI composite, which is not observed for ordinary materials. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Surfactant-free assembling of functionalized single-walled carbon nanotube buckypapers

The electrical and textural properties of single-walled carbon nanotube buckypapers were tunned through chemical functionalization processes. Single-walled carbon nanotubes (SWCNTs) were covalently functionalized with three different chemical groups: Carboxylic acids (-COOH), benzylamine (-Ph-CH₂-NH₂), and perfluorooctylaniline (-Ph-(CF₂)₇-CF₃). Functionalized SWCNTs were dispersed in water or dimethylformamide (DMF) by sonication treatments without the addition of surfactants or polymers. Carbon nanotube sheets (buckypapers) were prepared by vacuum filtration of the functionalized SWCNT dispersions. The electrical conductivity, textural properties, and processability of the functionalized buckypapers were studied in terms of SWCNT purity, functionalization, and assembling conditions. Carboxylated buckypapers demonstrated very low specific surface areas (< 1 m²/g) and roughness factor (R_a = 14 nm), while aminated and fluorinated buckypapers exhibited roughness factors of around 70 nm and specific surface areas of 160-180 m²/g. Electrical conductivity for carboxylated buckypapers was higher than for as-grown SWCNTs, but for aminated and fluorinated SWCNTs it was lower than for as-grown SWCNTs. This could be interpreted as a chemical inhibition of metallic SWCNTs due to the specificity of the diazonium salts reaction used to prepare the aminated and fluorinated SWCNTs. The utilization of high purity as-grown SWCNTs positively influenced the mechanical characteristics and the electrical conductivity of functionalized buckypapers.     

Electrochemical doping of pure single-walled carbon nanotubes used as supercapacitor electrodes

Pure single-walled carbon nanotubes (SWCNTs) with little bundling show an excellent capacitor performance attributable to the intrinsic nature of the SWCNTs, and possess unusual electrochemical properties characterized by a butterfly shaped cyclic voltammogram which differs from those for conventional activated carbon electrodes. Electrochemical doping in semi-conductor nanotubes occurred at the interface between the electrolyte and the SWCNT surface. In situ measurements showed a remarkable increase of electric conductivity with the polarization from the flat band potential. Because of the potential dependence, the capacitance of the SWCNT electrodes was higher at the higher charging potentials.     

Controllable bulk growth of few-layer graphene/single-walled carbon nanotube hybrids containing Fe@C nanoparticles in a fluidized bed reactor

A family of layered double hydroxides (LDHs) with varied Fe contents were employed as catalyst precursors for the controllable bulk growth of few-layer graphene/single-walled carbon nanotube (G/SWCNT) hybrids in a fluidized-bed reactor through chemical vapor deposition of methane at 950 °C. All the G/SWCNT hybrids exhibited the morphology of SWCNTs interlinked with graphene layers. The purity, thermal stability, graphitization degree, specific surface area, and total pore volume of the G/SWCNT hybrids decreased with the increasing Fe contents in the LDH precursors. A high yield of 0.97 g_G/SWCNTs/g_cat can be achieved by tuning the Fe content in the FeMgAl LDHs after a 15-min growth. After the removal of the as-calcined FeMgAl layered double oxide flakes, a high carbon purity of ca. 98.3% for G/SWCNT hybrids was achieved when the mole ratio of Fe–Al is 0.05:1. The size and density of Fe nanoparticles decorated in the as-obtained G/SWCNT hybrids depend largely on Fe content in the FeMgAl LDH precursors. Furthermore, the mass ratio of graphene materials to SWCNTs in the as-prepared G/SWCNT hybrids can be well controlled in a range of 0.4–15.1.     

Fluidized-bed synthesis of sub-millimeter-long single walled carbon nanotube arrays

The rapid growth method for vertically aligned, single walled carbon nanotube (SWCNT) arrays on flat substrates was applied to a fluidized-bed, using ceramic beads as catalyst supports as a means to mass produce sub-millimeter-long SWCNT arrays. Fe/Al₂O_x catalysts were deposited on the surface of Al₂O₃ beads by sputtering and SWCNTs were grown on the beads by chemical vapor deposition (CVD) using C₂H₂ as a feedstock. Scanning electron microscopy and transmission electron microscopy showed that SWCNTs of 2–4 nm in diameter grew and formed vertically aligned arrays of 0.5 mm in height. Thermogravimetric analysis showed that the SWCNTs had a catalyst impurity level below 1 wt.%. Furthermore, they were synthesized at a carbon yield as high as 65 at.% with a gas residence time as short as <0.2 s. Our fluidized-bed CVD, which efficiently utilizes the three-dimensional space of the reactor volume while retaining the characteristics of SWCNTs on substrates, is a promising option for mass-production of high-purity, sub-millimeter-long SWCNT arrays.     

Doping single-walled carbon nanotubes with surfactant peptides containing electron-donor substituents and nitrogen heterocycles

We examined the potential of a series of aromatic moieties with different electron-donating ability to alter SWCNT electronic properties. The selected aromatic moieties included p-amino-phenylalanine, 3-[4-(dimethylamino)phenyl]propanoic acid, tyrosine, tryptophan, and 4-pyridylalanine. These moieties contained exocyclic electron-donor substituents, such as amine, dimethylamine, and hydroxyl groups, as well as nitrogen-containing heterocycles, including indole and pyridine. We attached these aromatic molecules to the N-terminus of an amphiphilic surfactant peptide and obtained stable aqueous peptide/SWCNT dispersions. Atomic force microscopy images and ultraviolet–visible–near-infrared spectra revealed that, under the conditions used, all peptides, except for the one with 4-pyridylalanine, disperse SWCNTs well in solution. The local electron density of states of the peptide-coated SWCNTs was examined using scanning tunneling spectroscopy dI/dV plots. All spectra showed an additional peak in the conduction band side very close to the Fermi level, indicating n-type doping of the SWCNTs. The doping behavior was further verified by Raman spectroscopy G-band peak downshifts. Additionally, we found that the location of the heteroatom contributes significantly to the interaction between the aromatic moieties and the SWCNTs.     

Polyaniline/single-wall carbon nanotube (PANI/SWCNT) composites for high performance supercapacitors

PANI/SWCNT composites were prepared by electrochemical polymerisation of polyaniline onto SWCNTs and their capacitive performance was evaluated by means of cyclic voltammetry and charge-discharge cycling in 1 M H₂SO₄ electrolyte. The PANI/SWCNT composites single electrode showed much higher specific capacitance, specific energy and specific power than pure PANI and SWCNTs. The highest specific capacitance, specific power and specific energy values of 485 F/g, 228 W h/kg and 2250 W/kg were observed for 73 wt.% PANI deposited onto SWCNTs. PANI/SWCNT composites also showed long cyclic stability. Based upon the variations in the surface morphologies and specific capacitance of the composite, a mechanism is proposed to explain enhancement in the capacitive characteristics. The PANI/SWCNT composites have demonstrated the potential as excellent electrode materials for application in high performance supercapacitors.     

Solubilization of single-walled carbon nanotubes by entanglements between them and hyperbranched phenolic polymer

Hyperbranched phenolic polymer (HBP) was prepared by Lewis acid-catalyzed polycondensation of bifunctional phenolic monomer with trifunctional phenolic monomer. By choosing an appropriate Lewis acid, HBP was successfully obtained. By using physical adsorption of HBP on a single-walled carbon nanotube (SWCNT) surface, solubilization of SWCNTs was examined. SWCNTs were soluble with extended branches of HBP in N,N-dimethylformamide (DMF) solution, while they were insoluble in a linear phenolic polymer. In the presence of shrinking branches of HBP in tetrahydrofuran, SWCNTs were hardly soluble. Entanglements between extended branches of HBP and SWCNT in DMF solution resulted in high solubility of SWCNTs.     

Electrochemical characterization of single-walled carbon nanotubes for electrochemical double layer capacitors using non-aqueous electrolyte

Single-walled carbon nanotubes (SWCNTs) were investigated by cyclic voltammetry and electrochemical impedance spectroscopy in a non-aqueous electrolyte, 1 M Et₄NBF₄ in acetonitrile, suitable for supercapacitors. Further, in situ dilatometry and in situ conductance measurements were performed on single electrodes and the results compared to an activated carbon, YP17. Both materials show capacitive behavior characteristic of high surface area electrodes for supercapacitors, with the maximum full cell gravimetric capacitance being 34 F/g for YP17 and 20 F/g for SWCNTs at 2.5 V with respect to the total active electrode mass. The electronic resistance of SWCNTs and activated carbon decreases significantly during charging, showing similarities of the two materials during electrochemical doping. The SWCNT electrode expands irreversibly during the first electrochemical potential sweep as verified by in situ dilatometry, indicative of at least partial debundling of the SWCNTs. A reversible periodic swelling and shrinking during cycling is observed for both materials, with the magnitude of expansion depending on the type of ions forming the double layer.     

Electrochemical doping of single-walled carbon nanotubes in double layer capacitors studied by in situ Raman spectroscopy

The electrochemical doping of single-walled carbon nanotubes (SWCNTs) in 1 M Et₄NBF₄ in acetonitrile was investigated by in situ Raman spectroscopy. The capacitance was determined to be 82 F/g for the positive and 71 F/g for the negative SWCNT electrode, respectively, which approaches the typical values for microporous activated carbons used in supercapacitors. The changes in the Raman intensities and shifts of the D and G⁺ bands as well as of the radial breathing modes (RBMs) during electron and hole injection were studied as a function of the electrode potential. For the D and G⁺ bands, hole doping leads to strong upshifts which can be attributed to a stiffening of C-C bonds and the corresponding phonon modes. Electron doping results in much less pronounced changes in the band positions. The intensity attenuation of the RBM bands was found to be markedly different for semi-conducting and metallic SWCNTs, whereby sufficiently high doping leads to a loss of Raman intensity due to bleaching of electronic transitions. The main RBM bands upshift upon both electron and hole doping, which is attributed to changes in the chemical environment of individual SWCNTs upon charging and discharging of the electrochemical double layer within SWCNT bundles.     

Spectroscopic studies and electrical properties of transparent conductive films fabricated by using surfactant-stabilized single-walled carbon nanotube suspensions

This study evaluates the effect of anionic and cationic surfactants on the dispersion of purified SWCNTs in water in terms of dispersibility and on electrical conductivity of TCFs and electronic band structures of SWCNTs. The dispersibility of surfactants in an aqueous SWCNT suspension is assessed with the amount of SWCNTs dispersed, the content of surfactants required to suspend SWCNTs, and the long-term stability of dispersion. Sodium dodecylbenzene sulfonate (SDBS) shows better dispersibility and electrical conductivity of SWCNTs than sodium dodecyl sulfate, sodium cholate, and cetyltrimethyl ammonium bromide. Electronic band structures of SWCNTs vary with surfactants and nitric acid treatment, investigated by using UV–Vis–NIR and Raman spectroscopy. Metallic and semiconducting SWCNTs and surfactants make electrostatic charge interactions between them, which occur in different manners according to the electronic types of tubes and the natures of surfactants. TCFs are fabricated by using the SWCNT suspension dispersed with SDBS, which reveal a low percolation threshold with the two dimensional percolation behavior. The highest ratio of dc to optical conductivity (σ_dc/σ_op) is observed to be ∼23.1, corresponding to sheet resistance of 69 Ω/sq at the 550-nm optical transmission of 80%, upon nitric acid treatment of the SWCNT films.     

Advanced carbon nanotube/polymer composite infrared sensors

We demonstrate that both single-walled carbon nanotube (SWCNT) types and nanotube-matrix polymer-nanotube (CNT-P-CNT) junctions have profound impact on electro-optical properties of SWCNT/polymer composites. Composite IR sensors based on CoMoCAT^®-produced SWCNTs (SWCNTs_CoMoCAT) significantly outperform those based on HiPco^®-produced SWCNTs (SWCNTs_HiPco). Higher semiconducting nanotube concentration in a SWCNT material is critical to enhance the photo effect of IR light on SWCNT/polymer nanocomposites, whereas CNT-P-CNT junctions play a dominant role in the thermal effect of IR light on supported SWCNT/polymer composite films.     

An easy method for direct metal coordination reaction on unoxidized single-walled carbon nanotubes

The transition metal copper (II) ion (Cu²⁺) was effectively coordinated with a single-walled carbon nanotube (SWCNT) to produce a SWCNT–Cu²⁺ complex by a metal coordination reaction. Since the complex was very reactive towards the carboxylic acid group, the chemical functionalization of SWCNTs was easy to accomplish. This approach was used to functionalize the surface of the SWCNTs with stearic acid or ethylenediaminetetraacetic acid for tuning of the relative hydrophobicity and hydrophilicity of the surface, respectively. The mild reaction conditions used for metal coordination of the SWCNTs minimized the defects that result from chemical modification of SWCNT. Thus, the electrical properties of unmodified SWCNTs were preserved. Various analytical techniques, including Fourier transform infrared spectroscopy, thermal gravimetric analysis, ultraviolet–visible spectroscopy, and water sorption isotherm measurements, were used to characterize the surface properties of the functionalized SWCNTs. Functionalization of SWCNTs by metal coordination reaction effectively modified the SWCNT surface, while conserving the excellent physical properties of the SWCNTs. The surface properties of the SWCNTs were easily tuned by introduction of the functional groups required for specific applications.