RESUMO
Having clear and deep information on the surface/interface of deposited molecules is of crucial importance for the development of efficient optoelectronic devices. This paper reports on a joint experimental/theoretical hybrid approach based on Raman spectroscopy in order to provide information on the orientation of push-pull chromophores deposited onto a gold surface. In addition, several parameters can strongly control or impede the orientation of such molecules on the surface such as: the molecular structure, the surface itself, the method of deposition and the solvents used. From this approach, additional information has been highlighted such as perpendicularly depositing the molecule on the surface, the bithiophene compounds displaying more solvent effects compared to terthiophene molecules and so on. According to the results, the joint SERS/DFT study proves to be an effective tool for probing the arrangement of push-pull chromophores and selecting the right experimental conditions to tune the surface properties.
RESUMO
Aggregates of Au nanoparticles have been extremely easily obtained on glass substrates by physical sputtering under primary vacuum. With such a protocol, we demonstrate that it is possible to control the surface plasmon band absorption. Surface enhanced Raman spectroscopy (SERS) experiments were performed with methylene blue, zinc octacarboxyphthalocyanine, 4-aminothiophenol and cysteamine. The correlation between the absorption band and the wavelength giving the highest SERS intensity is clearly observed for methylene blue, in accordance with the electromagnetic enhancement theory. For the other molecules, effects of the chemical enhancement are also observed. In addition, we noticed a strong influence of the nature of the adsorbed molecule on the enhancement factor for a given wavelength. The origin of this feature is discussed in terms of resonant effects or multipolar surface plasmon modes.