Reaction of SO4˙− with an oligomer of poly(sodium styrenesulfonate). Probing the mechanism of damage to fuelcell membranes

Abstract

Clarification of the mechanism of degradation of model compounds for polymers used in polymer electrolyte fuel cells may identify intermediates that propagate damage; such knowledge can be used to improve the lifetime of fuel cell membranes, a central issue to continued progress in fuel cell technology. In proton-exchange membranes based on poly(styrene sulfonic acid), hydroxycyclohexadienyl radicals are formed after reaction with HO˙ and thought to decay to short-lived radical cations at low pH. To clarify subsequent reactions, we generated radical cations by reaction of SO₄˙⁻ with oligomers of poly(styrene sulfonic acid) (MW ≈ 1100 Da). At 295 K, this reaction proceeds with k = (4.5 ± 0.6) × 10⁸ M⁻¹ s⁻¹, both at pH 2.4 and 3.4, and yields benzyl radicals with an estimated yield of ≤60% relative to [SO₄˙⁻]. The radical cation is too short-lived to be observed: based on a benzyl radical yield of 60%, a lower limit of k > 6.8 × 10⁵ s⁻¹ for the intramolecular transformation of the aromatic radical cation of the oligomer to a benzyl radical is deduced. Our results show that formation of the benzyl radical, an important precursor in the breakdown of the polymer, is irreversible.