A quantitative in situ investigation of the structure of the catalytic layer of polymer electrolyte membrane fuel cells using material-sensitive and conductive atomic force microscopy is reported. The distribution and size of the ionomer phase at the surface of the catalytic layer is retrieved from adhesion force mappings, measured at high humidity and up to 75 °C. The average ionomer layer thickness varies between 7 and 13 nm for three differently prepared samples, as concluded from the histograms. Evidence of a lamellar structure of the thinner ionomer layers is presented. A significant thinning of the ionomer layers after long-term fuel cell operation is observed.

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Proton Exchange Membrane Fuel Cells (PEM-FC) are considered an alternative to the internal combustion engine for transportation. Despite the existence of relevant demonstrations and few commercial fleets, there are still a series of issues such as the durability of the materials and the cost of platinum which limit a wider application in this field. To this regard, better utilization and consequently loading reduction of Pt in electrodes is of outstanding importance. Herein we report the synthesis, characterization and application of an ionomer in the cathode catalyst layer; thanks to its higher oxygen permeability the quantity of Pt may be minimized. This ionomer is a modification of commercial Aquivion ® PFSA obtained by incorporation of a third monomer (2,2,4-trifluoro-5trifluoromethoxy-1,3-dioxole, MDO). Results on cast membrane demonstrate a 20% higher oxygen permeability of the new ionomer compared to Aquivion PFSA E87-05S and Nafion NR212 at 100% RH. Furthermore, an improvement of the performance of a PEM-FC in automotive conditions (RH=40-70%) is obtained with the assembly where this ionomer is used as cathode binder. In particular polarization curve at 70% RH shows improvement of 20% of power density peak and electrochemical impedance confirms higher oxygen permeability due to lower mass transport resistance than Aquivion.

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A holistic detection system, in principle sensitive to any molecular species in the vapor phase is proposed. The sensor consists of a polymeric multilayered distributed Bragg reflector made of a perfluorinated polar polymer, Aquivion, and a nonpolar polymer, poly(N‐vinylcarbazole). Alternated layers of the two polymers provide a characteristic optical response that depends on the chemical species intercalating within the structure. Such differences arise from Flory–Huggins polymer–solvent interactions. Then, the presence of polar, nonpolar, and perfluorinated moieties in the structures, potentially, allows sensitivity to any molecular species, providing a detection system with no need for any additional chemical receptors. As a proof of concept, the study demonstrates the sensitivity of the sensor to very diverse classes of molecules in the vapor phase including perfluorinated, nonpolar hydrophobic, and hydrophilic species and the capability to distinguish them, even in binary mixtures. Additionally, a connection between the dynamic temporal response of the sensors and the chemical–physical properties of the analytes, their concentration, and effective diffusion coefficient within the polymer structure is revealed.