RESUMEN
We present a system for the growth of molecular films in vacuum that exhibits high versatility with respect to the choice of molecular species. These can be either evaporated from powders or injected from solutions using an electrospray system, making it possible to handle particularly large and/or fragile molecules in a controlled environment. The apparatus is equipped with a reflectance anisotropy spectroscopy system for the in situ characterization of the optical response of the films and can be directly connected to a photoelectron spectrometer without breaking the vacuum. The system is conceived for the study and characterization of porphyrin films. Here, to showcase the range of possible analyses allowed by the experimental setup and test the operation of the system, novel results are provided on electrospray deposition on highly oriented pyrolytic graphite of Zn tetraphenyl porphyrins and Zn proto porphyrins, the latter featuring fragile side groups that make deposition from solution more attractive. In situ characterization is complemented by ex situ atomic force microscopy. Thanks to this multi-technique approach, changes in the film morphology and spectroscopic response are detected and directly related to the choice of the molecular moiety and growth method.
RESUMEN
The intercalation of graphite by electrochemical methods is an efficient strategy to produce massive graphene flakes. In fact, when graphite is biased inside an acidic solution, anions enter inside the stratified structure of the electrode and reduce the layer-to-layer interaction. Consequently, a gentle sonication is sufficient to disperse the graphene flakes inside the electrolyte. In view of an optimisation of the production protocol, a detailed analysis of the intercalation mechanism at the molecular length scale is mandatory. In the last 30 years, electrochemical (EC) scanning probe microscopies (e.g. EC-STM and in situ AFM) have been widely exploited in this research topic. In fact, these techniques have the possibility of combining the EC characterisation (e.g. cyclic-voltammetry, CV) with mechanical characterisation (e.g. adhesion and friction) and topography acquisition with high (molecular) lateral resolution. In this work, we investigate the tribological properties of the basal surface of graphite before and after the anion intercalation. By comparing the results acquired after the extraction of the graphite electrode from the EC cell with those collected inside the EC cell during the CV by an in situ AFM, we show how some features deriving from anisotropic friction can be exploited to unveil the very early stage of graphite exfoliation.
RESUMEN
In the currently accepted picture, when graphite is immersed and polarized in a diluted sulfuric acid electrolyte, the surface undergoes an invasive process due to the intercalation of solvated sulphate anions inside the crystal. The following evolution of CO, CO2 and O2 promotes the surface swelling and the growth of blisters. Here, we give evidence that the appearance of blisters affects the graphite surface as soon as the oxygen potential is reached, i.e. before the traditionally accepted anion intercalation stage, which instead is demonstrated slowing the blister development. These results suggest a new picture of the solvated anion intercalation in graphite with respect to the current interpretative model.