Résumé
The one-dimensional structure of single-walled carbon nanotubes (NT) display optical absorption and near-infrared emission (thanks to van Hove singularities). Chromophore encapsulation into host single-walled carbon nanotubes allows to create hybrid nano-systems with tunable opto-electronic properties. Up to now, we have been confining different kinds of chromophores,1-4 absorbing from the blue/ green (400/500 nm) range (tetracyanoquinodimethane (TNCQ), quaterthiophene derivatives (4T) and tetramethyl-paraphenylenediamine (TMPD)) to the red (700 nm) range (phthalocyanine (MPc)). In addition then can be either electron donor (4T, TMPD) or acceptor (TNCQ). In this study, we investigate, at both the macroscopic and the individual scales, the electronic and the optical properties of our hybrid systems by means of Raman and photoluminescence spectroscopies. Photoluminescence experiments clearly demonstrate changes on the emission properties after encapsulation. The intensities can be increased or reduced depending on the nature of the confined chromophores (electron donor or acceptor) and on the NT diameter. From Raman measurements, a significant charge transfer from the confined dye to the nanotube is evidenced. The main relevant parameters that govern the charge transfer are the nanotube diameter and the nature of the chromophores (electron donor or acceptor). Therefore, Raman and photoluminescence experiments strongly suggest charge transfer between the confined molecules and the nanotubes, leading to a Fermi level shift which governs the radiative de-excitation efficiency.