Functionalization and Dissolution of Nitric Acid Treated Single-Walled Carbon Nanotubes

We report an investigation of the nature and chemical functionalization of nitric acid treated single-walled carbon nanotubes (SWNTs). SWNTs washed with diluted sodium hydroxide solutions were characterized by near-IR, mid-IR, and Raman spectroscopy as well as TEM, and the remaining carboxylic acid content was determined to assess the effect of base washing on the removal of carboxylated carbon fractions, which are generated by the nitric acid treatment. It was found that even after exhaustive washing with aqueous base the purified SWNTs contain carboxylic acid groups in sufficient quantity to prepare high quality soluble SWNT materials by covalent functionalization with octadecylamine

Bone Cell Proliferation on Carbon Nanotubes

We explored the use of carbon nanotubes (CNTs) as suitable scaffold materials for osteoblast proliferation and bone formation. With the aim of controlling cell growth, osteosarcoma ROS 17/2.8 cells were cultured on chemically modified single-walled (SW) and multiwalled (MW) CNTs. CNTs carrying neutral electric charge sustained the highest cell growth and production of plate-shaped crystals. There was a dramatic change in cell morphology in osteoblasts cultured on MWNTs, which correlated with changes in plasma membrane functions

A ¹³C INADEQUATE and HF-GIAO Study of C₆₀H₂ and C₆₀H₆ Identification of Ring Currents in a 1,2-Dihydrofullerene

The hydrofullerenes C60H2 (1) and C60H6 (2) have been prepared in 13C-enriched form and 2D INADEQUATE NMR spectra were measured. These spectra have provided unambiguous 13C assignments for 2, and nearly unambiguous assignments for 1. In both cases, the most downfield resonances are immediately adjacent to the sp3 carbons, despite the fact that these carbons are the least pyramidalized carbons in the molecule. Typically, 13C chemical shifts move downfield with increasing pyramidalization (ϑp), but in these systems there is no strong correlation between ϑp and δ. HF-GIAO calculations are able to predict the chemical shifts, but provide little chemical insight into the origin of these chemical shifts. London theory reveals a significant paramagnetic ring current in 1, a feature that helps explain the 1H shifts in these compounds and may contribute to the 13C chemical shifts as well

Thermal Conductivity Measurements of Semitransparent Single-Walled Carbon Nanotube Films by a Bolometric Technique

We introduce a new technique for measurement of the thermal conductivity of ultrathin films of single-walled carbon nanotubes (SWNTs) utilizing IR radiation as heat source and the SWNT film as thermometer. The technique is applied to study the temperature dependence of the thermal conductivity of an as-prepared SWNT film obtained in the electric arc discharge process and a film of purified SWNTs prepared by vacuum filtration. The interplay between thermal and electrical transport in SWNT networks is analyzed in relation to the type of intertube junctions and the possibility of optimizing the thermal and electrical properties of SWNT networks for specific applications is discussed

Hexathiophenalenylium Cations: Syntheses, Structures, and Redox Chemistry

Preparations of two hexathiophenalenylium compounds as stable salts from the reaction of 3,4,6,7-tetrathio-9-hydroxyphenalenone with Lawesson’s reagent have been reported. The presence of three disulfide linkages on the periphery of the core phenalenyl unit is confirmed by X-ray crystallographic characterizations. Electrochemical cell potentials are lower than those of related dithio- and tetrathio-bridged phenalenyl radicals, and the hexathiophenalenyl radical shows a strong electron paramagnetic resonance (EPR) signal in the solid state

Hexathiophenalenylium Cations: Syntheses, Structures, and Redox Chemistry

Preparations of two hexathiophenalenylium compounds as stable salts from the reaction of 3,4,6,7-tetrathio-9-hydroxyphenalenone with Lawesson’s reagent have been reported. The presence of three disulfide linkages on the periphery of the core phenalenyl unit is confirmed by X-ray crystallographic characterizations. Electrochemical cell potentials are lower than those of related dithio- and tetrathio-bridged phenalenyl radicals, and the hexathiophenalenyl radical shows a strong electron paramagnetic resonance (EPR) signal in the solid state

Chemically Engineered Graphene-Based 2D Organic Molecular Magnet

Carbon-based magnetic materials and structures of mesoscopic dimensions may offer unique opportunities for future nanomagnetoelectronic/spintronic devices. To achieve their potential, carbon nanosystems must have controllable magnetic properties. We demonstrate that nitrophenyl functionalized graphene can act as a room-temperature 2D magnet. We report a comprehensive study of low-temperature magnetotransport, vibrating sample magnetometry (VSM), and superconducting quantum interference (SQUID) measurements before and after radical functionalization. Following nitrophenyl (NP) functionalization, epitaxially grown graphene systems can become organic molecular magnets with ferromagnetic and antiferromagnetic ordering that persists at temperatures above 400 K. The field-dependent, surface magnetoelectric properties were studied using scanning probe microscopy (SPM) techniques. The results indicate that the NP-functionalization orientation and degree of coverage directly affect the magnetic properties of the graphene surface. In addition, graphene-based organic magnetic nanostructures were found to demonstrate a pronounced magneto-optical Kerr effect (MOKE). The results were consistent across different characterization techniques and indicate room-temperature magnetic ordering along preferred graphene orientations in the NP-functionalized samples. Chemically isolated graphene nanoribbons (CINs) were observed along the preferred functionality directions. These results pave the way for future magnetoelectronic/spintronic applications based on promising concepts such as current-induced magnetization switching, magnetoelectricity, half-metallicity, and quantum tunneling of magnetization

Networks of Semiconducting SWNTs: Contribution of Midgap Electronic States to the Electrical Transport

ConspectusSingle-walled carbon nanotube (SWNT) thin films provide a unique platform for the development of electronic and photonic devices because they combine the advantages of the outstanding physical properties of individual SWNTs with the capabilities of large area thin film manufacturing and patterning technologies. Flexible SWNT thin film based field-effect transistors, sensors, detectors, photovoltaic cells, and light emitting diodes have been already demonstrated, and SWNT thin film transparent, conductive coatings for large area displays and smart windows are under development. While chirally pure SWNTs are not yet commercially available, the marketing of semiconducting (SC) and metallic (MT) SWNTs has facilitated progress toward applications by making available materials of consistent electronic structure. Nevertheless the electrical transport properties of networks of separated SWNTs are inferior to those of individual SWNTs. In particular, for semiconducting SWNTs, which are the subject of this Account, the electrical transport drastically differs from the behavior of traditional semiconductors: for example, the bandgap of germanium (<i>E</i> = 0.66 eV) roughly matches that of individual SC-SWNTs of diameter 1.5 nm, but in the range 300–100 K, the intrinsic carrier concentration in Ge decreases by more than 10 orders of magnitude while the conductivity of a typical SC-SWNT network decreases by less than a factor of 4. Clearly this weak modulation of the conductivity hinders the application of SC-SWNT films as field effect transistors and photodetectors, and it is the purpose of this Account to analyze the mechanism of the electrical transport leading to the unusually weak temperature dependence of the electrical conductivity of such networks. Extrinsic factors such as the contribution of residual amounts of MT-SWNTs arising from incomplete separation and doping of SWNTs are evaluated. However, the observed temperature dependence of the conductivity indicates the presence of midgap electronic states in the semiconducting SWNTs, which provide a source of low-energy excitations, which can contribute to hopping conductance along the nanotubes following fluctuation induced tunneling across the internanotube junctions, which together dominate the low temperature transport and limit the resistivity of the films. At high temperatures, the intrinsic carriers thermally activated across the bandgap as in a traditional semiconductor became available for band transport. The midgap states pin the Fermi level to the middle of the bandgap, and their origin is ascribed to defects in the SWNT walls. The presence of such midgap states has been reported in connection with scanning tunneling spectroscopy experiments, Coulomb blockade observations in low temperature electrical measurements, selective electrochemical deposition imaging, tip-enhanced Raman spectroscopy, high resolution photocurrent spectroscopy, and the modeling of the electronic density of states associated with various defects.Midgap states are present in conventional semiconductors, but what is unusual in the present context is the extent of their contribution to the electrical transport in networks of semiconducting SWNTs. In this Account, we sharpen the focus on the midgap states in SC-SWNTs, their effect on the electronic properties of SC-SWNT networks, and the importance of these effects on efforts to develop electronic and photonic applications of SC-SWNTs

Chemically Functionalized Water-Soluble Single-Walled Carbon Nanotubes Modulate Morpho-Functional Characteristics of Astrocytes

We report the use of chemically functionalized water-soluble single-walled carbon nanotubes (ws-SWCNTs) for the modulation of morpho-functional characteristics of astrocytes. When added to the culturing medium, ws-SWCNTs were able to make astrocytes larger and stellate/mature, changes associated with the increase in glial fibrillary acidic protein immunoreactivity. Thus, ws-SWCNTs could have more beneficial effects at the injury site than previously thought; by affecting astrocytes, they could provide for a more comprehensive re-establishment of the brain computational power

Single-Walled Carbon Nanotube–Poly(porphyrin) Hybrid for Volatile Organic Compounds Detection

Porphyrins due to their unique and interesting physicochemical properties have been widely investigated as functional materials for chemical sensor fabrication. However, their poor conductivity is a major limitation toward the realization of porphyrin-based field-effect transistor/chemiresistor sensor. The issue of conductivity can be overcome by exploiting the excellent electrical property of single-walled carbon nanotubes (SWNTs) to make a SWNTs-based hybrid device in which SWNTs would act as a transducer and porphyrin as a sensory layer. The present attempt was to fabricate a SWNTs–poly­(tetraphenylporphyrin) hybrid through electrochemical route and to evaluate its potential as a low-power chemiresistor sensor for sensing acetone vapor as a model for volatile organic compounds. Functionalization of SWNTs with porphyrin polymer by the electrochemical method resulted in a fuller coverage of SWNTs surface compared to a partial coverage by adsorption and thereby higher sensitivity. SWNTs were coated with poly­(tetraphenylporphyrin) of different thickness by applying different charge density to optimize sensing performance. Differences in sensing performance were noticed for hybrids fabricated at varying charge densities, and the optimum sensing response was found at 19.65 mC/cm². The hybrid exhibited a wide dynamic range for acetone vapor sensing from 50 to ∼230 000 ppm with a limit of detection of 9 ppm. The field-effect transistor studies showed a negative threshold voltage shift and almost constant transconductance when exposed to air/analyte, indicating electrostatic gating dominated sensing mechanism. Further, the results confirmed a good stability of the device over a period of 180 days. The long-term device stability along with the sensing capability at low analyte concentration with a wide dynamic range and easily scalable fabrication technique signify the potential of SWNT–poly­(porphyrin) hybrid for volatile organic compound sensing applications