RESUMO
In this work, a novel type of fluorine-lean proton exchange membranes is presented, using sulfonamide-sulfonimide functional groups for ion conduction. These groups are constructed on a polystyrene backbone for simple and cost-efficient usage as well as rapid scalability. The polymer is further tailored by adjusting the sulfonamide functionality with various end-groups, namely pentafluorophenyl, 4-fluorophenyl, butyl and octyl groups. These groups affect the pKa, leading to pKa values of 5.7 for the pentafluorophenyl substitution and pKa 10.5 for the alkyl chain. The glass transition temperature of the sulfonamide homopolymers can be reduced from Tg = 151°C (Pentafluorophenyl) to 49°C (Octyl), making the ionomer more flexible at room temperature. The combination of the non-swelling sulfonamide further mitigates the high water uptake of the sulfonimide while maintaining the nominal ion exchange capacity. This combination leads to extremely high proton conductivities with up to σ = 283 mS cm-1 at room temperature, which is clearly outperforming Nafion and approaches values for acid doped systems. This approach can pave the way to a novel type of ion conducting class in proton exchange membrane fuel cells.