Raman spectroscopy can be used to probe the aggregation state of single-walled carbon nanotubes in solution or as solids with a range of varying morphologies. Carbon nanotubes experience an orthogonal electronic dispersion when in electrical contact that broadens (from 40 meV to roughly 80 meV) and shifts the interband transition to lower energy (by 60 meV). We show that the magnitude of this shift is dependent on the extent of bundle organization and the inter-nanotube contact area. In the Raman spectrum, aggregation shifts the effective excitation profile and causes peaks to increase or decrease, depending on where the transition lies, relative to the excitation wavelength. The results are modeled using a simplified δ-function representation of nanotube electronic structure. The findings are particularly relevant for evaluating nanotube separation processes, where relative peak changes in the Raman spectrum can be confused for selective enrichment.

Gel electrophoresis and column chromatography conducted on individually dispersed, ultrasonicated single-walled carbon nanotubes yield simultaneous separation by tube length and diameter. Electroelution after electrophoresis is shown to produce highly resolved fractions of nanotubes with average lengths between 92 and 435 nm. Separation by diameter is concomitant with length fractionation, and nanotubes that have been cut shortest also possess the greatest relative enrichments of large-diameter species. Longer sonication time causes increased electrophoretic mobility in the gels; thus, ultrasonic processing determines the degree of both length and diameter separation of the nanotubes. The relative quantum yield decreases nonlinearly as the nanotube length becomes shorter. These techniques constitute a preparative, scalable method for separating nanotubes by two important attributes required for electronic and sensor applications.

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Breast cancer incidence is increasing worldwide. Early detection is critical for long-term patient survival, as is monitoring responses to chemotherapy for management of the disease. Magnetic resonance imaging and spectroscopy (MRI/MRS) has gained in importance in the last decade for the diagnosis and monitoring of breast cancer therapy. The sensitivity of MRI/MRS for anatomical delineation is very high and the consensus is that MRI is more sensitive in detection than x-ray mammography. Advantages of MRS include delivery of biochemical information about tumor metabolism, which can potentially assist in the staging of cancers and monitoring responses to treatment. The roles of MRS and MRI in screening and monitoring responses to treatment of breast cancer are reviewed here. We rationalize how it is that different histological types of breast cancer are differentially detected and characterized by MR methods.