Thomas W. Chamberlain

Self-assembly of a sulphur-terminated graphene nanoribbon within a single-walled carbon nanotube

The ability to tune the properties of graphene nanoribbons (GNRs) through modification of the nanoribbons width and edge structure widens the potential applications of graphene in electronic devices. Although assembly of GNRs has been recently possible, current methods suffer from limited control of their atomic structure, or require the careful organization of precursors on atomically flat surfaces under ultra-high vacuum conditions. Here we demonstrate that a GNR can self-assemble from a random mixture of molecular precursors within a single-walled carbon nanotube, which ensures propagation of the nanoribbon in one dimension and determines its width. The sulphur-terminated dangling bonds of the GNR make these otherwise unstable nanoribbons thermodynamically viable over other forms of carbon. Electron microscopy reveals elliptical distortion of the nanotube, as well as helical twist and screw-like motion of the nanoribbon. These effects suggest novel ways of controlling the properties of these nanomaterials, such as the electronic band gap and the concentration of charge carriers.

Size, Structure, and Helical Twist of Graphene Nanoribbons Controlled by Confinement in Carbon Nanotubes

Carbon nanotubes (CNTs) act as efficient nanoreactors, templating the assembly of sulfur-terminated graphene nanoribbons (S-GNRs) with different sizes, structures, and conformations. Spontaneous formation of nanoribbons from small sulfur-containing molecules is efficiently triggered by heat treatment or by an 80 keV electron beam. S-GNRs form readily in CNTs with internal diameters between 1 and 2 nm. Outside of this optimum range, nanotubes narrower than 1 nm do not have sufficient space to accommodate the 2D structure of S-GNRs, while nanotubes wider than 2 nm do not provide efficient confinement for unidirectional S-GNR growth, thus neither can support nanoribbon formation. Theoretical calculations show that the thermodynamic stability of nanoribbons is dependent on the S-GNR edge structure and, to a lesser extent, the width of the nanoribbon. For nanoribbons of similar widths, the polythiaperipolycene-type edges of zigzag S-GNRs are more stable than the polythiophene-type edges of armchair S-GNRs. Both the edge structure and the width define the electronic properties of S-GNRs which can vary widely from metallic to semiconductor to insulator. The encapsulated S-GNRs exhibit diverse dynamic behavior, including rotation, translation, and helical twisting inside the nanotube, which offers a mechanism for control of the electronic properties of the graphene nanoribbon via confinement at the nanoscale.

Assembly, Growth, and Catalytic Activity of Gold Nanoparticles in Hollow Carbon Nanofibers

Graphitized carbon nanofibers (GNFs) act as efficient templates for the growth of gold nanoparticles (AuNPs) adsorbed on the interior (and exterior) of the tubular nanostructures. Encapsulated AuNPs are stabilized by interactions with the step-edges of the individual graphitic nanocones, of which GNFs are composed, and their size is limited to approximately 6 nm, while AuNPs adsorbed on the atomically flat graphitic surfaces of the GNF exterior continue their growth to 13 nm and beyond under the same heat treatment conditions. The corrugated structure of the GNF interior imposes a significant barrier for the migration of AuNPs, so that their growth mechanism is restricted to Ostwald ripening. Conversely, nanoparticles adsorbed on smooth GNF exterior surfaces are more likely to migrate and coalesce into larger nanoparticles, as revealed by in situ transmission electron microscopy imaging. The presence of alkyl thiol surfactant within the GNF channels changes the dynamics of the AuNP transformations, as surfactant molecules adsorbed on the surface of the AuNPs diminished the stabilization effect of the step-edges, thus allowing nanoparticles to grow until their diameters reach the internal diameter of the host nanofiber. Nanoparticles thermally evolved within the GNF channel exhibit alignment, perpendicular to the GNF axis due to interactions with the step-edges and parallel to the axis because of graphitic facets of the nanocones. Despite their small size, AuNPs in GNF possess high stability and remain unchanged at temperatures up to 300 °C in ambient atmosphere. Nanoparticles immobilized at the step-edges within GNF are shown to act as effective catalysts promoting the transformation of dimethylphenylsilane to bis(dimethylphenyl)disiloxane with a greater than 10-fold enhancement of selectivity as compared to free-standing or surface-adsorbed nanoparticles.

Interactions and Reactions of Transition Metal Clusters with the Interior of Single-Walled Carbon Nanotubes Imaged at the Atomic Scale

Clusters of transition metals, W, Re, and Os, upon encapsulation within a single-walled carbon nanotube (SWNT) exhibit marked differences in their affinity and reactivity with the SWNT, as revealed by low-voltage aberration-corrected high-resolution transmission electron microscopy (AC-HRTEM). Activated by an 80 keV electron beam, W reacts only weakly with the SWNT, Re creates localized defects on the sidewall, and Os reacts readily causing extensive defect formation and constriction of the SWNT sidewall followed by total rupture of the tubular structure. AC-HRTEM imaging at the atomic level of structural transformations caused by metal-carbon bonding of π- and σ-character demonstrates what a crucial role these types of bonds have in governing the interactions between the transition metal clusters and the SWNT. The observed order of reactivity W < Re < Os is independent of the metal cluster size, shape, or orientation, and is related to the metal to nanotube bonding energy and the amount of electronic density transferred between metal and SWNT, both of which increase along the triad W, Re, Os, as predicted by first-principles density functional theory calculations. By selecting the appropriate energy of the electron beam, the metal-nanotube interactions can be controlled (activated or precluded). At an electron energy as low as 20 keV, no visible transformations in the nanotube in the vicinity of Os-clusters are observed.

Harnessing the Synergistic and Complementary Properties of Fullerene and Transition-Metal Compounds for Nanomaterial Applications

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Functionalized Fullerenes in Self-Assembled Monolayers

Anisotropy of intermolecular and molecule-substrate interactions holds the key to controlling the arrangement of fullerenes into 2D self-assembled monolayers (SAMs). The chemical reactivity of fullerenes allows functionalization of the carbon cages with sulfur-containing groups, thiols and thioethers, which facilitates the reliable adsorption of these molecules on gold substrates. A series of structurally related molecules, eight of which are new fullerene compounds, allows systematic investigation of the structural and functional parameters defining the geometry of fullerene SAMs. Scanning tunnelling microscopy (STM) measurements reveal that the chemical nature of the anchoring group appears to be crucial for the long-range order in fullerenes: the assembly of thiol-functionalized fullerenes is governed by strong molecule-surface interactions, which prohibit formation of ordered molecular arrays, while thioether-functionalized fullerenes, which have a weaker interaction with the surface than the thiols, form a variety of ordered 2D molecular arrays owing to noncovalent intermolecular interactions. A linear row of fullerene molecules is a recurring structural feature of the ordered SAMs, but the relative alignment and the spacing between the fullerene rows is strongly dependent on the size and shape of the spacer group linking the fullerene cage and the anchoring group. Careful control of the chemical functionality on the carbon cages enables positioning of fullerenes into at least four different packing arrangements, none of which have been observed before. Our new strategy for the controlled arrangement of fullerenes on surfaces at the molecular level will advance the development of practical applications for these nanomaterials.

Multi‐Electron‐Acceptor Dyad and Triad Systems Based on Perylene Bisimides and Fullerenes

Fullerene (C(60)) and 3,4,9,10-perylene tetracarboxylic diimide (PTDCI) were used as building blocks for an electron acceptor dyad (C(60)-PTCDI) and triad (C(60)-PTCDI-C(60)). As the first reduction potentials for C(60) and PTCDI are very close, simultaneous introduction of two or three electrons is possible into the dyad and triad, respectively. Further stepwise electrochemical reduction leads to formation of a series of well-defined anionic species in which electrons associated with the fullerene or the PTDCI components of the molecule can be clearly distinguished. In total, up to four electrons can be reversibly injected into the dyad C(60)-PTCDI and up to six into the triad C(60)-PTCDI-C(60) system. The optical absorption properties in the UV/Vis range are also crucially defined by the distribution of electrons between the acceptor parts, as the injection/removal of electrons causes drastic colour changes in the dyad and the triad systems.

Azafullerenes encapsulated within single-walled carbon nanotubes.

Methods of insertion of azafullerenes in single-walled carbon nanotubes (SWNTs) at different temperatures were investigated, while the effects of the conditions applied on the structure of azafullerene-based peapods, namely, C59N@SWNTs, were explored. Morphological characteristics of C59N@SWNTs were assessed and evaluated by means of high-resolution transmission electron microscopy (HR-TEM). Pathways and chemical reactions that occur upon encapsulation of C59N within SWNTs were evaluated. Monomeric azafullerenyl radical C59N. as inserted into SWNTs at high temperature, from purified (C59N)2 in the gas phase, can undergo a variety of different transformations forming dimers, oligomers or existing in its monomeric form inside SWNTs due to the stabilization effect by nanotube side walls. However, under milder conditions, that is, at lower temperature, bisazafullerene (C59N)2 can be inserted into SWNTs in its pristine dimeric form.

The Role of Molecular Clusters in the Filling of Carbon Nanotubes

We have demonstrated that the ability of fullerenes to form clusters is essential for the filling of single-walled carbon nanotubes in solution. In solutions where C60 exists in the form of discrete solvated molecules (e.g., in CS2) no fullerene encapsulation in nanotubes takes place, as the large molar excess of solvent compared to solute prohibits C60 from entering the nanotubes. However, in solutions containing large clusters of C60 (e.g., in n-hexane) nanotubes become densely filled with fullerene molecules despite the large excess of solvent. The interactions between carbon nanotubes and fullerene clusters provide an efficient transport of C60 into nanotubes that avoids the detrimental effects of the solvent molecules. This new mechanism provides the first rational explanation of experiments involving nanotube filling with guest-molecules in solution.

Interactions and chemical transformations of coronene inside and outside carbon nanotubes

By exposing flat and curved carbon surfaces to coronene, a variety of van der Waals hybrid heterostructures are prepared, including coronene encapsulated in carbon nanotubes, and coronene and dicoronylene adsorbed on nanotubes or graphite via π-π interactions. The structure of the final product is determined by the temperature of the experiment and the curvature of the carbon surface. While at temperatures below and close to the sublimation point of coronene, nanotubes with suitable diameters are filled with single coronene molecules, at higher temperatures additional dimerization and oligomerization of coronene occurs on the surface of carbon nanotubes. The fact that dicoronylene and possible higher oligomers are formed at lower temperatures than expected for vapor-phase polymerization indicates the active role of the carbon surface used primarily as template. Removal of adsorbed species from the nanotube surface is of utmost importance for reliable characterization of encapsulated molecules: it is demonstrated that the green fluorescence attributed previously to encapsulated coronene is instead caused by dicoronylene adsorbed on the surface which can be solubilized and removed using surfactants. After removing most of the adsorbed layer, a combination of Raman spectroscopy and transmission electron microscopy was employed to follow the transformation dynamics of coronene molecules inside nanotubes.