Studying single-wall carbon nanotubes through encapsulation: from optical methods till magnetic resonance

Encapsulating fullerenes, magnetic fullerenes, 13C isotope enriched fullerenes, and organic solvents inside SWCNTs enables to yield unprecedented insight into their electronic, optical, and interfacial properties and to study SWCNT growth. In addition to customary methods of their studies such as e.g., optical absorption or Raman spectroscopy, these efforts enables to employ electron spin resonance (ESR) and nuclear magnetic resonance (NMR) spectroscopy. Encapsulated C60 fullerenes are transformed to inner tubes by a high temperature annealing. The diameter distribution of the inner tubes follow that of the outer ones and their unique, low defect concentration makes them an ideal model system for high resolution and energy dependent Raman studies. The observation of Raman modes of individual inner-outer tube pairs allows to measure the inner-outer tube interaction strength that is also well described theoretically. Reversible closing and opening of SWCNT can be studied in a diameter selective manner by encapsulating C60 and transforming it to an inner tube. The growth of inner tubes can be achieved from 13C enriched encapsulated organic solvents, which shows that the geometry of the fullerene does not play a particular role in the inner tube growth as it was originally thought. In addition, it opens new perspectives to explore the in-the-tube chemistry. Growth of inner tubes from 13C enriched fullerenes provides a unique isotope engineered heteronuclear system, where the outer tubes contain natural carbon and the inner walls are controllably 13C isotope enriched. The material enables to identify the vibrational modes of inner tubes which otherwise strongly overlap with the outer tube modes. The 13C NMR signal of the material has an unprecedented specificity for the small diameter SWCNTs. Temperature and field dependent 13C T1 studies show a uniform metallic-like electronic state for all inner tubes rather than distributed metallic and isolating behavior. A low energy, 3 meV gap is observed that is tentatively assigned to a long sought Peierls transition in the small diameter SWCNTs. Encapsulating magnetic fullerenes, such as N@C60 and C59N opens the way for local probe ESR studies of the electronic properties of the SWCNTs.     

Synthesis of fullerenes from carbon powder by using high power induction thermal plasma

Radio frequency (rf) inductively coupled thermal plasma (ICTP) was used to fabricate fullerenes (C₆₀,C₇₀, etc.) by direct evaporation of carbon powder injected into the plasma. Spectroscopic observation of the plasma was made for molecular band spectra of C₂ and atomic lines of C. The formation of fullerenes C₆₀ and C₇₀ as well as higher fullerenes were checked and recognized by high performance liquid chromatography (HPLC) and time-of-flight mass spectrometer (TFMS). The suitable conditions for the synthesis of fullerenes within the experimental conditions adopted were 10-kPa plasma pressure, with a considerably higher flow rate of approximately 150 l/min for mixed-gas condition of Ar, He and CO₂, with carbon powder of average diameter 20 μm. The results showed that the productivity of fullerenes has a relation to the intensity of C₂ molecular and C atomic spectra from the induction plasma. Mixing of Si with C particles has a kind of role in enhancing the synthesis rate of fullerenes C₆₀, as well as the higher order fullerenes.     

Li+ and Li interactions with carbon nanocage structures

Molecular dynamics simulations have been carried out to explore the structural properties of Li and Li+ confined inside single-walled carbon nanotubes (SWCNTs) and fullerene molecules. C-Li, C-Li+, Li-Li and Li+-Li+ interactions have been represented by pair functions and parameterized for the corresponding interactions. C-C interactions have been modeled by Tersoff potential. Open-ended SWCNTs with various sizes and chirality, as well as fullerenes with various sizes have been considered in the simulations. C-Li interaction is stronger than that of C-Li+. Endohedral Li+ doping caused structural deformations in C60. It has been found that for both Li and Li+ cases endohedral doping is favorable with respect to exohedral doping. This result is valid for both fullerenes and nanotubes.     

Raman study on single-walled carbon nanotubes with different laser excitation energies

The industrial use of carbon nanotubes is increasing day by day; therefore, it is very important to identify the nature of carbon nanotubes in a bundle. In this study, we have used the Raman spectroscopic analysis on vertically aligned single-walled carbon nanotubes (SWCNTs) grown by the chemical vapour deposition (CVD) technique. The grown sample is excited with two laser excitation wavelengths, 633 nm from He-Ne laser and 514·5 nm from Ar⁺ laser. Raman spectrum in the backscattering geometry provides the characteristic spectra of SWCNTs with its radial breathing mode (RBM), defect-induced disorder mode (D band), and high-energy modes (G and M bands). The Raman signal positions of the spectra in RBM, G and M bands confirm the grown sample to be of semiconducting type in nature.     

ON THE MECHANISM OF CARBON CLUSTERS FORMATION UNDER LASER IRRADIATION. THE CASE OF DIAMOND GRAINS AND SOLID C60 FULLERENE

It is shown by FT-ICR (Fourier transform ion cyclotron resonance) mass spectrometry that carbon clusters considered to be the superior homologues of C₆₀ fullerene are formed by laser irradiation of both synthetic diamond grains or from pure C₆₀ fullerene crystals. The surfaces of the laser irradiated diamond or C₆₀ have been examined by Raman spectroscopy. In the case of diamond the Raman spectrum suggests the superficial formation of mixed carbon nanostructures consisting of disordered graphite, fullerenic nanostructures, onion-like carbon nanostructures and diamond-like carbon. Based on the Raman spectra of the surface and on data taken from the phase diagram of carbon, it is shown that the graphitization is needed in order to produce fullerenes from diamond under laser ablation conditions. In the case of C₆₀ fullerene, it is shown by Raman spectroscopy that the laser irradiation of the crystals causes initially their photopolymerization and after further irradiation their transformation into disordered graphite. Based on these results and on a literature survey on the formation of fullerenes from more than 15 completely different substrates, it is concluded that fullerenes are formed always when laser ablation leads to a graphitization of the laser-irradiated substrate. Some astrochemical implications of the conclusions have been discussed.     

ON THE MECHANISM OF CARBON CLUSTERS FORMATION UNDER LASER IRRADIATION. THE CASE OF DIAMOND GRAINS AND SOLID C60 FULLERENE

ABSTRACT

It is shown by FT-ICR (Fourier transform ion cyclotron resonance) mass spectrometry that carbon clusters considered to be the superior homologues of C₆₀ fullerene are formed by laser irradiation of both synthetic diamond grains or from pure C₆₀ fullerene crystals. The surfaces of the laser irradiated diamond or C₆₀ have been examined by Raman spectroscopy. In the case of diamond the Raman spectrum suggests the superficial formation of mixed carbon nanostructures consisting of disordered graphite, fullerenic nanostructures, onion-like carbon nanostructures and diamond-like carbon. Based on the Raman spectra of the surface and on data taken from the phase diagram of carbon, it is shown that the graphitization is needed in order to produce fullerenes from diamond under laser ablation conditions. In the case of C₆₀ fullerene, it is shown by Raman spectroscopy that the laser irradiation of the crystals causes initially their photopolymerization and after further irradiation their transformation into disordered graphite. Based on these results and on a literature survey on the formation of fullerenes from more than 15 completely different substrates, it is concluded that fullerenes are formed always when laser ablation leads to a graphitization of the laser-irradiated substrate. Some astrochemical implications of the conclusions have been discussed.     

Employing Raman spectroscopy to qualitatively evaluate the purity of carbon single-wall nanotube materials

Carbon single-wall nanotubes (SWNTs) have highly unique electronic, mechanical and adsorption properties, making them interesting for a variety of applications. Raman spectroscopy has been demonstrated to be one of the most important methods for characterizing SWNTs. For example, Raman spectroscopy may be employed to differentiate between metallic and semi-conducting nanotubes, and may also be employed to determine SWNT diameters and even the nanotube chirality. Single-wall carbon nanotubes are generated in a variety of ways, including arc-discharge, laser vaporization and various chemical vapor deposition (CVD) techniques. In all of these methods, a metal catalyst must be employed to observe SWNT formation. Also, all of the current synthesis techniques generate various non-nanotube carbon impurities, including amorphous carbon, fullerenes, multi-wall nanotubes (MWNTs) and nano-crystalline graphite, as well as larger micro-sized particles of graphite. For any of the potential nanotube applications to be realized, it is, therefore, necessary that purification techniques resulting in the recovery of predominantly SWNTs at high-yields be developed. It is, of course, equally important that a method for determining nanotube wt.% purity levels be developed and standardized. Moreover, a rapid method for qualitatively measuring nanotube purity could facilitate many laboratory research efforts. This review article discusses the application of Raman spectroscopy to rapidly determine if large quantities of carbon impurities are present in nanotube materials. Raman spectra of crude SWNT materials reveal tangential bands between 1500-1600 cm(-1), as well as a broad band at approximately 1350 cm(-1), attributed to a convolution of the disorder-induced band (D-band) of carbon impurities and the D-band of the SWNTs themselves. Since the full-width-at-half-maximum (FWHM) intensity of the various carbon impurity D-bands is generally much broader than that of the nanotube D-band, an indication of the SWNT purity level may be obtained by simply examining the line-width of the D-band. We also briefly discuss the effect of nanotube bundling on SWNT Raman spectra. Finally, sections on employing Raman spectroscopy, and Raman spectroscopy coupled with additional techniques, to identify the separation and possible isolation of a specific nanotube within purified SWNT materials is provided. Every SWNT can be considered to be a unique molecule, with different physical properties, depending on its (n, m) indices. The production of phase-pure (n, m) SWNTs may be essential for some nanotube applications.     

Molecular dynamics simulation of mechanical, vibrational and electronic properties of carbon nanotubes

A theoretical investigation of the mechanical, vibrational and electronic properties of single walled carbon nanotubes (SWCNTs) with the armchair (5,5) and zigzag (10,0) geometry is carried out in detail. The Poisson ratio, Young modulus and Raman active frequencies for these types of SWCNTs are calculated within a simple vibrational model. The electronic spectra of the SWCNTs are obtained using a tight-binding calculation. The theoretical results are compared with the available experimental ones.     

Shape and complexity at the atomic scale: the case of layered nanomaterials

In nature there are numerous layered compounds, some of which could be curved so as to form fascinating nanoshapes with novel properties. Graphite is at present the main example of a very flexible layered structure, which is able to form cylinders (nanotubes) and cages (fullerenes), but there are others. While fullerenes possess positive curvature due to pentagonal rings of carbon, there are other structures which could include heptagonal or higher membered rings. In fact, fullerenes and nanotubes could display negative curvature, thus forming nanomaterials possessing unexpected electronic and mechanical properties. The effect of curvature in other nano-architectures, such as in boron nitride and metal dichalcogenides, is also discussed in this account. Electron irradiation is a tool able to increase the structural complexity of layered materials. In this context, we describe the coalescence of carbon nanotubes and C(60) molecules. The latter results now open up an alternative approach to producing and manipulating novel nanomaterials in the twenty-first century.     

Characteristics of multi-walled carbon nanotubes and background aerosols by carbon analysis; particle size and oxidation temperature

Novel carbonaceous nanomaterials such as carbon nanotubes and fullerenes have many beneficial characteristics as industrial materials, but exposure to these nanomaterials also poses health risks. As part of an exposure assessment, we characterized the following carbonaceous nanomaterials, using an aerosol carbon monitor: nine samples of multi-walled carbon nanotubes (MWCNTs), a sample of single-walled carbon nanotubes (SWCNTs), a standard sample of diesel exhaust particles (DEPs), and an ambient particulate matter (APM). The amounts of elemental carbon (EC) determined by the monitor coincided with the mass of MWCNTs calibrated by a microbalance. The carbonaceous nanomaterials were oxidized in three steps of oven temperatures (550, 700 and 920 °C) in this method. The portion of oxidized carbon at each temperature depended on the sample characteristic. We used the monitor to analyze the aerosol samples collected in five stages by a Sioutas cascade impactor (SCI), which collects size-segregated airborne particles having aerodynamic diameters from 6.6 μm to less than 0.25 μm. As MWCNTs aggregate/agglomerate easily, the size was of a good parameter to distinguish the MWCNTs from other materials. Two-dimensional mapping by size and oxidized temperature suggested the origin of the carbonaceous aerosol samples. Based on the results, we reanalyzed our previous data obtained at a factory manufacturing MWCNTs. The characteristics of workplace samples by particle size and carbon analysis were similar to those of MWCNT aerosol particles.     

Interaction between fullerenes and single-wall carbon nanotubes: the influence of fullerene size and electronic structure

A series of fullerenes and endohedral metallofullerenes peapods have been synthesized by supercritical method in high filling rate. The interaction between SWNTs and various kinds of fullerenes (C60, C70, C78, C84) and metallofullerenes (Gd@C82, Er@C82, Ho@C82, Y@C82) has been further investigated. The slight blue shift of G-band in Raman spectra with respect to pristine SWNTs was attributed to the charge transfer from SWNTs to fullerenes cage. The obvious RBM shift strongly depended on the distance between the inner wall of the SWNTs and the fullerene cage and also partly associated with the electronic structure of the fullerene. These results indicated that the interaction between fullerenes and SWNTs, which was considered to be the van de walls interaction, can be influenced by the cage size and the kind of fullerenes.     

Purification of single-walled carbon nanotubes

The discovery of carbon nanotubes (CNTs) created much excitement and stimulated extensive research into the properties of nanometer-scale cylindrical networks. From then on, various methods for the synthesis and characterization of aligned CNTs-both single-walled (SWCNTs) and multi-walled (MWCNTs) by different methods have been hotly pursued. Unfortunately, most methods currently in use produce raw multi component solid products, only a small fraction of which contains carbon nanotubes. The balance of the material is composed of residual catalyst particles (some of which are encased in concentric graphitic shells), fullerenes, other graphitic materials and amorphous carbon. These impurities cause a serious impediment for their detailed characterization and applications. If the carbon nanotube is ever to fulfill its promise as an engineering material, large, high quality aliquots will be required. A number of purification methods involving elimination processes such as physical separation, gas phase and liquid phase oxidation in combination with chemical treatments have been developed for nanotube materials. Though the quantitative determination of purity remains controversial, reported yields are best regarded with an appropriate level of skepticism on the method of assay. In this article, a review is given on the past and recent advances in purification of SWCNTs.     

Raman Spectra of Chlorinated C60 and C70 Fullerenes

Raman spectra of chlorinated C₆₀ and C₇₀ fullerenes prepared by photochlorination have been reported and discussed. The Raman lines suggest structural analogies with already fully characterized brominated fullerenes. Intense laser light irradiation cause a decomposition of fullerene chloro-derivatives leading to the formation of C₆₀ polymer.     

可降解碳纳米管/聚乳酸复合材料的制备及性能

利用丙交酯的开环聚合反应成功地制备了单壁碳纳米管/聚乳酸复合材料, 研究了其降解性和热稳定性。通过红外光谱(FTIR)、 Raman光谱、 热失重分析(TGA)和扫描电子显微镜(SEM)研究, 证明乙二醇功能化的单壁碳纳米管能够参与丙交酯的开环聚合反应, 并在碳纳米管侧壁成功接枝聚乳酸链, 得到的复合材料在碱性溶液中容易降解。差示热分析(DSC)表明, 功能化单壁碳纳米管/聚乳酸复合材料的玻璃化转变温度与纯聚乳酸相比有所提高。      

Industrially synthesized single-walled carbon nanotubes: compositional data for users, environmental risk assessments, and source apportionment

Commercially available single-walled carbon nanotubes (SWCNTs) contain large percentages of metal and carbonaceous impurities. These fractions influence the SWCNT physical properties and performance, yet their chemical compositions are not well defined. This lack of information also precludes accurate environmental risk assessments for specific SWCNT stocks, which emerging local legislation requires of nanomaterial manufacturers. To address these needs, we measured the elemental, molecular, and stable carbon isotope compositions of commercially available SWCNTs. As expected, catalytic metals occurred at per cent levels (1.3-29%), but purified materials also contained unexpected metals (e.g., Cu, Pb at 0.1-0.3?ppt). Nitrogen contents (up to 0.48%) were typically greater in arc-produced SWCNTs than in those derived from chemical vapor deposition. Toluene-extractable materials contributed less than 5% of the total mass of the SWCNTs. Internal standard losses during dichloromethane extractions suggested that metals are available for reductive dehalogenation reactions, ultimately resulting in the degradation of aromatic internal standards. The carbon isotope content of the extracted material suggested that SWCNTs acquired much of their carbonaceous contamination from their storage environment. Some of the SWCNTs, themselves, were highly depleted in (13)C relative to petroleum-derived chemicals. The distinct carbon isotopic signatures and unique metal 'fingerprints' may be useful as environmental tracers allowing assessment of SWCNT sources to the environment.     

Resonant laser-induced formation of double-walled carbon nanotubes from peapods under ambient conditions

The selective excitation of fullerenes encapsulated in single-walled carbon nanotubes (SWCNTs) is carried out by irradiating them using a UV laser, the wavelength of which corresponds exactly to their maximum of absorption. Under such conditions, fullerenes strongly absorb the laser energy, open, and break, while the containing SWCNT merely acts as both a nanoreactor and a mold which is only weakly heated by the laser. The containing tube confines the fullerene fragments, promotes their reconstruction into an inner tube, and protects them from air oxidation. This leads to the overall formation of double-walled carbon nanotubes (DWCNTs). The transformation is found to strongly depend on the laser irradiance and dose. This proves that the related mechanism is a multiphoton photolysis, different from the previous heat-induced transformation attempts found in the literature, whether the heat is produced by means of a thermostat, infrared laser, or nonresonant UV laser. The actual peapod-to-DWCNT transformation is monitored by Raman spectroscopy and high-resolution transmission electron microscopy.     

High-quality single-walled carbon nanotubes synthesis by hot filament CVD on Ru nanoparticle catalyst

We investigated the single-walled carbon nanotubes (SWCNTs) growth on Ru nanoparticle catalyst via hot filament assisted chemical vapor deposition (HFCVD) with two independent W filaments for the carbon precursor (methane) and the hydrogen dissociation respectively. The Ru nanoparticles were obtained following a two-step strategy. At first the growth substrate is functionalized by silanisation, then a self assembly of a ruthenium porphyrin complex monolayer on pyridine-functionalized metal oxide substrates. We have studied the impact of the filaments power and we optimized the SWCNTs growth temperature. The as grown SWCNTs were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM) and Raman spectroscopy. It was found that the quality, density and the diameter of SWCNTs depends on the filament and growth temperature. Results of this study can be used to improve the understanding of the growth of SWCNTs by HFCVD.     

Organometallic radical-adducts of fullerenes C60, C70, and single-walled carbon nanotubes derived from (cyclopentadienyl)molybdenumtricarbonyl dimer

Interaction of the metal-centered free radicals [CpMo(CO)3]* generated photochemically from the corresponding dimer [CpMo(CO)3]2 with fullerenes C60, C70, or single-walled carbon nanotubes in toluene results in the radical-adducts investigated by using TGA, ESR, Raman and X-ray Photo-electron spectroscopy. Comparison was made with the chromium analogues previously studied.     

拉曼光谱表征石墨烯结构的研究进展

石墨烯是一种只有一个原子层的二维原子晶体,它是构成零维富勒烯、一维碳纳米管和三维石墨等其他碳同素异形体的基本结构单元,具有很多独特的电子及力学性能,因而吸引了化学、材料及其他领域众多科学家的高度关注。拉曼光谱作为一种灵敏便捷的表征方法,在石墨烯的研究中起到重要的作用。该综述总结了近年来拉曼光谱在石墨烯表征中的应用,在对单层石墨烯的典型特征峰作详细介绍的基础上,通过对拉曼谱图中D峰、G峰和2D峰的强度、位置和半峰宽变化情况的分析,可以快速而准确地表征出石墨烯的层数,并可以对石墨烯的堆垛方式、边缘手性和掺杂程度进行判定。同时,也系统地分析了在石墨烯制备与测试过程中基底、掺杂、温度和激光功率等因素对拉曼谱图中D峰、G峰和2D峰的强度、位置和半峰宽的影响。     

Ag nanoparticles coated SWCNT with surface enhanced Raman scattering (SERS) signals

We report here a simple method to fabricate the silver nanoparticles (AgNPs) coated DNA-SWCNTs that give SERS signals. Dynamic light scattering (DLS), atomic force microscopy (AFM), and high resolution transmission electron microscopy (HRTEM) suggested the products are dispersive and soluble in aqueous solution. The Raman scattering spectra show AgNPs coated SWCNTs have enhanced the Raman signal when compared with pure SWCNT. From the radial breathing mode (RBM) of the Raman spectra, we can disclose that this DNA-SWCNT has unique chirality, which implies that it could be a good nanoprobe for cell marking.