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Abstract:

The temperature dependence of the photoluminescence intensity from frozen single walled carbon nanotube solutions is reported. This is modelled assuming that it is dominated by the small energy splitting between the dark and bright states of the singlet excitons which are found to be in the region of 1-5 meV for nanotubes of 0.8-1.2nm. The luminescence is strongly enhanced by a magnetic field along the tube axis due to the mixing of the different valley states of the excitons.

Abstract:

We report studies of the modification of the band structure of single-walled carbon nanotubes through encapsulation of the inorganic material manganese ditelluride (Mn Te2). Using photoluminescence excitation mapping we show that this leads to a global reduction of their first and second band gap energies by a similar percentage (up to 3.8%). We interpret this as due to the additional screening which causes a change in the internal dielectric constant and a possible lowering of the carbon-carbon transfer integrals. The shifts increase with increasing tube diameter due to the increased quantity of filled materials. © 2006 The American Physical Society.

Abstract:

Using TEM, absorption and photoluminescence-excitation spectroscopy we have shown that nitrogen and nitrogen/boron doping of single-walled carbon nanotubes produce significant changes in both the optical properties and the diameter distribution of nanotubes produced by the arc-discharge method. Smaller diameter tubes are preferentially formed in the presence of boron. In addition the presence of nitrogen is found to significantly affect the emission properties of the nanotube ensemble, causing a shift in the dominant emission to lower energies, possibly due to changes in the bundling structure of the nanotubes in solution, but only very small changes are observed in the emission energies for individual nanotubes. © 2006 Elsevier Ltd. All rights reserved.

Abstract:

Fluorescence intensity from single walled carbon nanotubes in aqueous sodium dodecylsulfate solution is shown to be strongly temperature dependent in the range 5-60 degrees C. Emission peaks corresponding to particular nanotube species which have been quenched due to oxidation by aerated water show sharp transitions at distinct temperatures as the sample is heated. The temperature at which the transition occurs is found to be species dependent and has been interpreted as being proportional to the valence band edge potential of the nanotube. The results are explained quantitatively using the Nernst equation to measure the increase in reduction potential of the solution as the temperature is raised. The removal of dissolved O(2) and CO(2) is thought to be a significant driving force in the reversal of the redox reaction which causes oxidation of the nanotubes.