Structural properties of some conducting polymers and carbon nanotubes investigated by SERS spectroscopy

Abstract

In this paper, we present Surface Enhanced Raman Scattering (SERS) experiments performed successfully on some conducting polymers and carbon nanotubes deposited in thin films on rough metallic surfaces. The enhancement mechanism in SERS has a twofold origin: electromagnetic and chemical. The electromagnetic enhancement is, however, the dominant mechanism and consists in the excitation of localized and delocalized surface plasmons (SP). The second enhancing mechanism for SERS, not yet convincingly supported by experimental data, is of chemical origin. This mechanism is due to the increase of the polarizability of the molecules on the metal surface under the action of the incident radiation, leading to the formation of new chemical bonds between the molecules and the metal surface. Unfortunately, the experimental data available to argue the presence of a chemical process are scarce and scattered. In this paper, we try to present some details regarding this aspect. In order to do so, we studied poly 3-hexylthiophene (3-PHT) and polyaniline (PAN) as a function of the type of the rough metallic support (Ag, Au or Cu), the oxidization state and thickness of the polymer layer. We studied also carbon single walled nanotubes. Our experiments reveal the existence of a chemical surface effect. The results obtained for 3-PHT show that SERS spectra depend on the oxidizing properties of the metal surface and on the nature of the solvent. This dependence is explained by the existence of some interfacial reactions that lead to the formation of interface compounds. The SERS measurements reported here reveal an increase of the intensities of the Raman lines, accompanied by a modification of the corresponding intensity ratios, when the degree of doping is increased. We observe for the first time by SERS spectroscopy that doping of 3-PHT with FeCl 3 leads to the appearance of a state of disorder in the structure of the macromolecular chain, as a result of steric hindrance effects. The type of the rough metallic support can modify SERS spectra and such an effect is clearly shown for the polyaniline case. No such dependence on metallic support type is observed on the SERS spectra of carbon nanotubes.