Solvent-Dependent Adsorption of Perfluorosulfonated Ionomers on a Pt(111) Surface Using Atomic Force Microscopy

The adsorption behavior of perfluorosulfonated ionomers (PFSIs) on a Pt(111) surface in various solvents is investigated by in situ atomic force microscopy (AFM) and discussed on the basis of aggregation of PFSIs in the liquid phase. The AFM images show that, in an aqueous solution of PFSI (0.1 wt % Nafion + 99.9 wt % water), PFSI aggregates with a lateral size of 20-200 nm adsorb on the Pt(111) surface. In a PFSI solution containing a small amount of 1-propanol (0.1 wt % Nafion + 99.5 wt % water + 0.4 wt % 1-propanol), however, slightly smaller aggregates adsorb on the Pt(111) surface. Such solvent-dependent sizes of adsorbed aggregates are in reasonable agreement with apparent hydrodynamic radii of PFSIs in the corresponding solutions determined by dynamic light scattering (DLS) while assuming the formation of spherical aggregation. Interestingly, a step-terrace structure characteristic to a clean Pt(111) surface is observed in a propanol-rich PFSI solution (0.1 wt % Nafion + 44.45 wt % water + 55.45 wt % 1-propanol) but X-ray photoelectron spectroscopy clearly indicates the existence of fluorocarbon species at the Pt(111) surface, suggesting the formation of a smooth adsorbed layer of PFSIs in a lying down configuration. Absence of any features assignable to aggregates in DLS data suggests well-dispersion of PFSIs in such propanol-rich solution without aggregations. Thus, the adsorbed structure of PFSIs at Pt surfaces can be controlled by tuning the composition of mixed solvent, which affects the aggregation of PFSI in the liquid phase.