Adsorption of γ-mercaptopropyltrimethoxysilane on zinc: A study of the competition between thiol and silanol functions related to the age of the siloxane solution, its pH and the oxidation state of the surface

We describe the adsorption of γ–mercaptopropyltrimethoxysilane (γ-MPS) on zinc under various experimental conditions, including the age of the siloxane solution (tag), its pH (7 or 4), and the mode of preparation of the surface (RCA treatment or in situ polishing). It is shown by XPS studies that the structure of the adsorbed monolayer varies dramatically with the pH of the solution. At the natural pH of the siloxane solution (pH 7) where no hydrolysis of the SiOCH3 group occurs, adsorption proceeds through the SH moiety and not through SiOCH3 groups. This preferential attachment through SH is found whatever the age of the solution and the treatment of the zinc. It is confirmed by the fact that n-propyltrimethoxysilane (PSi) does not interact with the surface in the case of very old solutions (adsorption is not observed when Zn is polished in situ and only occurs with RCA zinc treatment for tag > 40 min). With siloxane solutions at pH 4, adsorption of γ-MPS is more complex and the structure of the adsorbed layer depends mainly on the age of the solution. With a fresh solution, hydrolysis is not very advanced and, as mentioned previously, adsorption occurs through the SH group. With older solutions and as a consequence of the progressive hydrolysis of the SiOCH3 group to SiOH, the density of the grafted siloxane monolayer increases (6 min < tag < 10 min), followed by a mixed adsorption through SH and SiOH (10 min < tag < 40–50 min) revealed by the decrease in the normalised (Si2p/S2p)* intensity ratio. Finally, adsorption of dimers and oligomers is observed with still older siloxane solutions. In contrast to PSi whose adsorption on zinc is favoured by the RCA treatment, neither treatment of the surface changes the results significantly in the case of γ-MPS. Comparison with alkanethiols confirms the transition from monomer to dimer adsorption and IRRAS studies clearly indicate a condensation reaction between OH and SH groups.