A Graphene Surface Force Balance

We report a method for transferring graphene, grown by chemical vapor deposition, which produces ultraflat graphene surfaces (root-mean-square roughness of 0.19 nm) free from polymer residues over macroscopic areas (>1 cm2). The critical step in preparing such surfaces involves the use of an intermediate mica template, which itself is atomically smooth. We demonstrate the compatibility of these model surfaces with the surface force balance, opening up the possibility of measuring normal and lateral forces, including friction and adhesion, between two graphene sheets either in contact or across a liquid medium. The conductivity of the graphene surfaces allows forces to be measured while controlling the surface potential. This new apparatus, the graphene surface force balance, is expected to be of importance to the future understanding of graphene in applications from lubrication to electrochemical energy storage systems

Effects of temperature and ammonia flow rate on the chemical vapour deposition growth of nitrogen-doped graphene

We doped graphene in situ during synthesis from methane and ammonia on copper in a low-pressure chemical vapour deposition system, and investigated the effect of the synthesis temperature and ammonia concentration on the growth. Raman and X-ray photoelectron spectroscopy was used to investigate the quality and nitrogen content of the graphene and demonstrated that decreasing the synthesis temperature and increasing the ammonia flow rate results in an increase in the concentration of nitrogen dopants up to ca. 2.1% overall. However, concurrent scanning electron microscopy studies demonstrate that decreasing both the growth temperature from 1000 to 900 1C and increasing the N/C precursor ratio from 1/50 to 1/10 significantly decreased the growth rate by a factor of six overall. Using scanning tunnelling microscopy we show that the nitrogen was incorporated mainly in substitutional configuration, while current imaging tunnelling spectroscopy showed that the effect of the nitrogen on the density of states was visible only over a few atom distances

Controlling pyridinic, pyrrolic, graphitic, and molecular nitrogen in multi-wall carbon nanotubes using precursors with different N/C ratios in aerosol assisted chemical vapor deposition

Nitrogen-containing multi-wall carbon nanotubes (N-MWCNTs) were synthesized using aerosol assisted chemical vapor deposition (CVD) techniques in conjunction with benzylamine:ferrocene or acetonitrile: ferrocene mixtures. Different amounts of toluene were added to these mixtures in order to change the N/C ratio of the feedstock. X-ray photoelectron and near-edge X-ray absorption fine structure spectroscopy detected pyridinic, pyrrolic, graphitic, and molecular nitrogen forms in the N-MWCNT samples. Analysis of the spectral data indicated that whilst the nature of the nitrogen-containing precursor has little effect on the concentrations of the different forms of nitrogen in N-MWCNTs, the N/C ratio in the feedstock appeared to be the determining factor. When the N/C ratio was lower than ca. 0.01, all four forms existed in equal concentrations, for N/C ratios above 0.01, graphitic and molecular nitrogen were dominant. Furthermore, higher concentrations of pyridinic nitrogen in the outer shells and N2 molecules in the core of the as-produced N-MWCNTs suggest that the precursors were decomposed into individual atoms, which interacted with the catalyst surface to form CN and NH species or in fact diffused through the bulk of the catalyst particles. These findings are important for a better understanding of possible growth mechanisms for heteroatom-containing carbon nanotubes (CNTs) and therefore paving the way for controlling the spatial distribution of foreign elements in the CNTs using CVD processes

Synthesis and characterization of new polyaniline/nanotube composites

New polyaniline/nanotube (PANI/NT) composites have been synthesized by “in situ” polymerization processes using both multi-wall carbon nanotubes (MWNTs) and single-wall carbon nanotubes (SWNTs) in concentrations ranging from 2 to 50 wt.%. Although no structural changes are observed using MWNTs above a concentration of 20 wt.%, the in situ synthesis results in electronic interactions between nanotubes and the quinoid ring of PANI leading to enhanced electronic properties and thus to the formation of a genuine PANI/MWNT composite material. On the other hand, using SWNTs favors the formation of inhomogeneous mixtures rather than of a homogeneous composite materials, independent of the SWNT concentration. X-ray diffraction, Raman and transport measurements show the different behavior of both classes of nanotubes in PANI/NT materials. The difficulties in the formation of a true PANI/SWNT composite are related to the far more complex structure of the SWNT material itself, i.e. to the presence of entangled bundles of SWNTs, amorphous carbon and even catalytic metal particles.This work was supported by the EC RTN contract NANOCOMP (HPRN-CT-2000-00037).Peer reviewe

Effect of the experimental parameters on the structure of nitrogen-doped carbon nanotubes produced by aerosol chemical vapour deposition

We describe the systematic study of multi-walled carbon nanotubes with different nitrogen doping produced by aerosol chemical vapour deposition. Benzylamine:toluene mixtures of 0:100, 5:95, 10:90, 25:75, 50:50, 75:25 and 100:0 were thermally decomposed at 800-900 °C under argon at atmospheric pressure, whereby the nitrogen content of the bulk material was varied between 0 and 2.2 at%. We also show how the presence of nitrogen in the precursor changed the nanotube morphology, i.e. nitrogen decreaed the number of kinks incorporated into the carbon nanotubes, decreased their length and diameter and increased the proportion of 'bamboo' shaped nanotubes. Furthermore, due to the nitrogen doping, the oxidation resistance of the nanotube material was decreased. With concentrations above 10% benzylamine the increase of the reaction temperature had no significant effect on the quality of the nanotubes, however, at higher temperatures the nitrogen content was decreased. We demonstrate the control over the nanotube geometry, the nitrogen content and oxidation resistance of the nanotubes, and show that these properties are interlinked

Graphene covered gold nanoparticles produced by focused laser irradiation

The Figure shows a scanning electron microscopy (SEM) image of gold nanoparticles produced by laser irradiation of a thin (5 nm) gold film. The nanoparticles are covered by a graphene overlayer. Graphene “bridges” are observed between neighbouring nanoparticles.<div>The laser irradiation not only produces the gold nanoparticles, but also induces dynamic strain in the nanoparticle supported graphene, an effect which is completely reversible upon switching off the laser.</div