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 SO(4)˙(-) with oligomers of poly(styrene sulfonic acid) (MW ≈ 1100 Da). At 295 K, this reaction proceeds with k = (4.5 ± 0.6) × 10(8) M(-1) s(-1), both at pH 2.4 and 3.4, and yields benzyl radicals with an estimated yield of ≤60% relative to [SO(4)˙(-)]. 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 × 10(5) 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.
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