Solubilizing and purifying carbon nanotubes remains one of the foremost technological hurdles in their investigation and application. We report a dramatic improvement in the preparation of single-walled carbon nanotube solutions based on the ability of specific aromatic polymers to efficiently disperse certain nanotube species with a high degree of selectivity. Evidence of this is provided by optical absorbance and photoluminescence excitation spectra, which show suspensions corresponding to up to approximately 60% relative concentration of a single species of isolated nanotubes with fluorescence quantum yields of up to 1.5%. Different polymers show the ability to discriminate between nanotube species in terms of either diameter or chiral angle. Modelling suggests that rigid-backbone polymers form ordered molecular structures surrounding the nanotubes with n-fold symmetry determined by the tube diameter.

Combinations of different aromatic polymers and organic solvents have been studied as dispersing agents for preparing single-walled carbon nanotubes solutions, using optical absorbance, photoluminescence-excitation mapping, computer modeling, and electron microscopic imaging to characterize the solutions. Both the polymer structure and solvent used strongly influence the dispersion of the nanotubes, leading in some cases to very high selectivity in terms of diameter and chiral angle. The highest selectivities are observed using toluene with the rigid polymers PFO-BT and PFO to suspend isolated nanotubes. The specific nanotube species selected are also dependent on the solvent used and can be adjusted by the use of THF or xylene. Where the structure has more flexible conformations, the polymers are shown to be less selective but show an enhanced overall solubilization of nanotube material. When chloroform is used as the solvent, there is a large increase in the overall solubilization, but the nanotubes are suspended as bundles rather than as isolated tubes which leads to a quenching of their photoluminescence.

Single-walled carbon nanotubes have been efficiently dispersed in an organic solvent using the semiconducting polymers MEHPPV and PFO. It has been found that energy is transferred to the carbon nanotubes when the polymer is photo-excited across its minimum energy gap. This is shown using photoluminescence excitation mapping in the range of both the polymer's and the nanotube's optical absorbance. Possible mechanisms for the energy transfer are discussed.

We report a correlation between carrier mobility and defect density in large-scaled graphene films prepared by chemical vapor deposition (CVD). Raman spectroscopy is used for investigating the layer number and the crystal quality of graphene films, and the defect density is estimated by the intensity ratios of the D and G peaks. By carefully controlling the growth parameters, especially the H(2)/CH(4) ratios during growth, and employing H(2) during cooling, monolayer-dominant graphene films can be obtained with different D peak intensities in Raman spectra, which show good correspondence with their carrier mobility obtained by Hall measurements. Also, a progressive shift of neutrality points to a more negative gate voltage is observed with the increase in defect density. Both the connections of carrier mobility and the shift of neutrality points to a negative direction in relation to the defect density in graphene are observed for the first time in CVD-grown graphene films. With the best growth conditions, a cm-scaled graphene film with carrier mobility of ∼ 1350 cm(2) V(-1) s(-1) (p-type in air) can be obtained.