Synthesis of graphene nanoribbons encapsulated in single-walled carbon nanotubes

A novel material, graphene nanoribbons encapsulated in single-walled carbon nanotubes (GNR@SWNT), was synthesized using confined polymerization and fusion of polycyclic aromatic hydrocarbon (PAH) molecules. Formation of the GNR is possible due to confinement effects provided by the one-dimensional space inside nanotubes, which helps to align coronene or perylene molecules edge to edge to achieve dimerization and oligomerization of the molecules into long nanoribbons. Almost 100% filling of SWNT with GNR is achieved while nanoribbon length is limited only by the length of the encapsulating nanotube. The PAH fusion reaction provides a very simple and easily scalable method to synthesize GNR@SWNT in macroscopic amounts. First-principle simulations indicate that encapsulation of the GNRs is energetically favorable and that the electronic structure of the encapsulated GNRs is the same as for the free-standing ones, pointing to possible applications of the GNR@SWNT structures in photonics and nanoelectronics.     

Ferromagnetism in graphene nanoribbons: split versus oxidative unzipped ribbons

Two types of graphene nanoribbons: (a) potassium-split graphene nanoribbons (GNRs), and (b) oxidative unzipped and chemically converted graphene nanoribbons (CCGNRs) were investigated for their magnetic properties using the combination of static magnetization and electron spin resonance measurements. The two types of ribbons possess remarkably different magnetic properties. While a low-temperature ferromagnet-like feature is observed in both types of ribbons, such room-temperature feature persists only in potassium-split ribbons. The GNRs show negative exchange bias, but the CCGNRs exhibit a "positive exchange bias". Electron spin resonance measurements suggest that the carbon-related defects may be responsible for the observed magnetic behavior in both types of ribbons. Furthermore, information on the proton hyperfine coupling strength has been obtained from hyperfine sublevel correlation experiments performed on the GNRs. Electron spin resonance finds no evidence for the presence of potassium (cluster) related signals, pointing to the intrinsic magnetic nature of the ribbons. Our combined experimental results may indicate the coexistence of ferromagnetic clusters with antiferromagnetic regions leading to disordered magnetic phase. We discuss the possible origin of the observed contrast in the magnetic behaviors of the two types of ribbons studied.     

Defect- and dopant-controlled carbon nanotubes fabricated by self-assembly of graphene nanoribbons

Molecular dynamics simulations showed that a basal carbon nanotube can activate and guide the fabrication of single-walled carbon nanotubes (CNTs) on its internal surface by self-assembly of edge-unpassivated graphene nanoribbons with defects. Furthermore, the distribution of defects on self-assembled CNTs is controllable. The system temperature and defect fraction are two main factors that influence the success of self-assembly. Due to possible joint flaws formed at the boundaries under a relatively high constant temperature, a technique based on increasing the temperature is adopted. Self-assembly is always successful for graphene nanoribbons with relatively small defect fractions, while it will fail in cases with relatively large ones. Similar to the self-assembly of graphene nanoribbons with defects, graphene nanoribbons with different types of dopants can also be self-assembled into carbon nanotubes. The finding provides a possible fabrication technique not only for carbon nanotubes with metallic or semi-conductive properties but also for carbon nanotubes with electromagnetic induction characteristics.

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Aligned conical carbon nanotubes

Aligned conical carbon nanotubes (CCNTs) have been synthesized on catalyst-coated Si (100) substrates by a D.C. plasma-assisted hot filament chemical vapor deposition process. The same technique under slightly different deposition conditions has been used to grow aligned conventional carbon nanotubes. The conical shape is due to secondary graphitic growth on the main nanotube. This growth results in the formation of a series of inverted lampshade-type structures stacked over each other, which gives the CNT the appearance of a cone. The CCNT structures are typically 2 m at the base with an inner diameter of 100 nm and 2000 nm long. Patterned growth, e.g., arrays of 6 m × 6 m square, has been achieved. Field emission from CCNTs for use in flat panel displays is also reported.     

Synthesis of carbon nanotubes by rolling up patterned graphene nanoribbons using selective atomic adsorption

We demonstrate a new method (U.S. Patent Appl., serial no. 60/908039) for synthesizing carbon nanotubes (CNTs), using first-principles and classical molecular dynamics simulations. The single-walled nanotubes (SWNTs) are formed by folding graphene nanoribbons patterned on graphite films through adsorption of atoms of varying coverage, which introduces an external stress to drive the folding process. The diameter and chirality of SWNTs can be a priori controlled by patterning graphene nanoribbons with predefined width and direction so that the postsynthesis sorting process is eliminated. Our method allows potentially mass production of identical tubes and easy integration into device structures on a substrate.     

Divacancies in graphene and carbon nanotubes

Divacancies are among the most important defects that alter the charge transport properties of single-walled carbon nanotubes (SWNT), and we here study, using ab initio calculations, their properties. Two structures were investigated, one that has two pentagons side by side with an octagon (585) and another composed of three pentagons and three heptagons (555777). We investigate their stability as a function of tube diameter, and calculate their charge transport properties. The 585 defect is less stable in graphene due to two broken bonds in the pentagons. We estimate that the 555777 becomes more stable than the 585 for a diameter of about 40 A (53 A) for an armchair (zigzag) SWNTs, indicating that they will prevail in large diameter multiwalled carbon nanotubes and graphene ribbons.     

Hybrids of carbon nanotubes and graphene/graphene oxide

This paper reviews recent progress in hybrids based on carbon nanotubes (CNTs) and graphene (G) or graphene oxide (GO). The combination of CNTs, including single-walled (SW), double-walled (DW) and multi-walled (MW), and G or GO resulted in various hybrids. CNTs–G/GO hybrid thin films are usually prepared by using solution/suspension casting and layer-by-layer (LbL) deposition, free-standing sheets are fabricated by using vacuum filtration and 3D hierarchical structures are produced by using chemical vapor deposition (CVD). CNTs–G/GO hybrids have also been used as fillers to fabricate polymer composites with synergistic effects. The composites have significantly improved electrical, mechanical and thermal properties, which make them very useful for various potential applications, such as transparent electrodes replacing ITO, electrodes for supercapacitors, lithium-ion batteries and dye-sensitized solar cells.     

Luminescent graphene quantum dots from oxidized multi-walled carbon nanotubes

Fluorescent nano-graphene quantum dots (GQD) were isolated from oxidized carbon nanotube suspension with the aid of cysteamine. The oxidized GQD were thiol functionalized with cysteamine in presence of dicyclohexylcarbodiimide as coupling agent. The GQD chemistry and morphology were characterized by means of X-ray photoelectron spectroscopy and atomic force microscopy. The thiolated graphene quantum dots exhibit an intense luminescence (quantum yield around 10%) in the visible range with an excitation wavelength-dependent fluorescence.     

Catalyst nanocomposites templates of carbon nanoribbons, nanospheres and nanotubes

Several attractive types of amorphous or crystalline carbon nanostructure were obtained by a single catalytic process, during natural gas decomposition using different nanostructured catalysts as template. The nanostructured catalyst templates were based on transition metal nanoparticles embedded in carbon matrixes and nanoceramic supports which consist of magnesium oxide doped with ceria rare earths, prepared by the high-energy mechanical milling. The yield and the nature of the nanostructured carbon are strongly influenced by the preparation method of the template and the chemical composition of the catalysts.     

Synthesis and characterization of carbon nanoribbons and single crystal iron filled carbon nanotubes

Carbon nanoribbons and single crystal iron filled multiwall carbon nanotubes (MWCNTs) have been synthesized by simple pyrolysis technique. SEM investigation shows that the material consist mainly carbon nanoribbons and carbon nanotubes (CNTs). X-ray diffraction (XRD), electron energy loss spectroscopy (EELS), electron energy dispersive X-ray (EDX), transmission electron miscroscopy (TEM) and highresolution transmission electron miscroscopy (HRTEM) studies reveal carbon nanotubes are filled with α-Fe. Closer inspection of HRTEM images indicated that the bcc structure α-Fe nanowires are monocrystalline and Fe (1 1 0) plane is indeed perpendicular to the G (0 0 2) plane, whereas orientation of (0 0 2) lattice planes of carbon nanoribbon is perpendicular to the axis of growth. Magnetic properties studied by superconducting quantum interference device (SQUID) at 300 K and 10 K exhibited coercivity of 1037 Oe and 2023 Oe. The large coercitivity is strongly attributed to the small size monocrystalline single phase α-Fe, single domain nature of the encapsulated Fe crystal, magnetocrystalline shape anisotropy and ferromagnetic behaviour of localized states at the edges of the carbon nanoribbons.     

Nonlinear damping in mechanical resonators made from carbon nanotubes and graphene

The theory of damping is discussed in Newton's Principia and has been tested in objects as diverse as the Foucault pendulum, the mirrors in gravitational-wave detectors and submicrometre mechanical resonators. In general, the damping observed in these systems can be described by a linear damping force. Advances in nanofabrication mean that it is now possible to explore damping in systems with one or more atomic-scale dimensions. Here we study the damping of mechanical resonators based on carbon nanotubes and graphene sheets. The damping is found to strongly depend on the amplitude of motion, and can be described by a nonlinear rather than a linear damping force. We exploit the nonlinear nature of damping in these systems to improve the figures of merit for both nanotube and graphene resonators. For instance, we achieve a quality factor of 100,000 for a graphene resonator.     

Efficient synthesis of graphene nanoribbons sonochemically cut from graphene sheets

We report a facile approach to synthesize narrow and long graphene nanoribbons (GNRs) by sonochemically cutting chemically derived graphene sheets (GSs). The yield of GNRs can reach ∼5 wt% of the starting GSs. The resulting GNRs are several micrometers in length, with ∼75% being single-layer, and ∼40% being narrower than 20 nm in width. A chemical tailoring mechanism involving oxygen-unzipping of GSs under sonochemical conditions is proposed on the basis of experimental observations and previously reported theoretical calculations; it is suggested that the formation and distribution of line faults on graphite oxide and GSs play crucial roles in the formation of GNRs. These results open up the possibilities of the large-scale synthesis and various technological applications of GNRs.      

Low-loss, high-permittivity composites made from graphene nanoribbons

A new composite material was prepared by incorporation of graphene nanoribbons into a dielectric host matrix. The composite possesses remarkably low loss at reasonably high permittivity values. By varying the content of the conductive filler, one can tune the loss and permittivity to desirable values over a wide range. The obtained data exemplifies how nanoscopic changes in the structure of conductive filler can affect macroscopic properties of composite material.     

Solar cells with graphene and carbon nanotubes on silicon

Graphene and carbon nanotubes (CNTs) represent attractive materials for photovoltaic (PV) devices due to their unique electronic and optical properties. Graphene and single-wall carbon nanotubes (SWNTs) layers can be directly configured as energy conversion materials to fabricate thin-film solar cells, serving as both photogeneration sites and charge carrier collecting/transport layers. SWNTs can be modified into either p-type conductor through chemical doping (like acidic purification) or n-type conductor through polymer functionalisation. The solar cells can be simply made of a semitransparent thin film of graphene (or SWNTs) deposited on a proper type of silicon substrate to create high-density Schottky (or p–n) junctions at the interface. The high aspect ratios and large surface area of these carbon nano-structured materials can benefit exciton dissociation and charge carrier transport thus improving the power conversion efficiency.     

Infrared photodetectors based on reduced graphene oxide and graphene nanoribbons

The use of reduced graphene oxide (RGO) and graphene nanoribbons (GNRs) as infrared photodetectors is explored, based on recent results dealing with solar cells, light-emitting devices, photodetectors, and ultrafast lasers. IR detection is demonstrated by both RGO and GNRs in terms of the time-resolved photocurrent and photoresponse. The responsivity of the detectors and their functioning are presented.     

Raman spectroscopy as a probe of graphene and carbon nanotubes

Progress in the use of Raman spectroscopy to characterize graphene samples for the number of graphene layers and doping level they contain is briefly reviewed. Comparisons to prior studies on graphites and carbon nanotubes are used for inspiration to define future promising directions for Raman spectroscopy research on few layer graphenes.