Optical Absorption
Optical absorption in carbon nanotubes differs from absorption in conventional 3D materials by presence of sharp peaks (1D nanotubes) instead of an absorption threshold followed by an absorption increase (most 3D solids). Absorption in nanotubes originates from electronic transitions from the v2 to c2 (energy E22) or v1 to c1 (E11) levels, etc. The transitions are relatively sharp and can be used to identify nanotube types. Note that the sharpness deteriorates with increasing energy, and that many nanotubes have very similar E22 or E11 energies, and thus significant overlap occurs in absorption spectra. This overlap is avoided in photoluminescence mapping measurements (see below), which instead of a combination of overlapped transitions identifies individual (E22, E11) pairs.
Interactions between nanotubes, such as bundling, broaden optical lines. While bundling strongly affects photoluminescence, it has much weaker effect on optical absorption and Raman scattering. Consequently, sample preparation for the latter two techniques is relatively simple.
Optical absorption is routinely used to quantify quality of the carbon nanotube powders.
The spectrum is analyzed in terms of intensities of nanotube-related peaks, background and pi-carbon peak; the latter two mostly originate from non-nanotube carbon in contaminated samples. However, it has been recently shown that by aggregating nearly single chirality semiconducting nanotubes into closely packed Van der Waals bundles the absorption background can be attributed to free carrier transition originating from intertube charge transfer.
Read more about this topic: Optical Properties Of Carbon Nanotubes
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