2011
DOI: 10.1021/ma201188e
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Highly Conductive Aromatic Ionomers with Perfluorosulfonic Acid Side Chains for Elevated Temperature Fuel Cells

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Cited by 49 publications
(38 citation statements)
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“…Apart from Ullmann coupling, another synthetic approach using dehalogenation coupling was reported by Wang and coworkers 102 to prepare a fluorinated aromatic poly(arylene ether) 27 with pendent perfluoroalkyl sulfonic acid groups, as shown in Scheme 6. High proton diffusion coefficients were observed due to the hydrophilic nanochannels, as confirmed by TEM images.…”
Section: Proton Exchange Membranesmentioning
confidence: 99%
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“…Apart from Ullmann coupling, another synthetic approach using dehalogenation coupling was reported by Wang and coworkers 102 to prepare a fluorinated aromatic poly(arylene ether) 27 with pendent perfluoroalkyl sulfonic acid groups, as shown in Scheme 6. High proton diffusion coefficients were observed due to the hydrophilic nanochannels, as confirmed by TEM images.…”
Section: Proton Exchange Membranesmentioning
confidence: 99%
“…Wang and co-workers 102 reported the hydrogen/air fuel cell performance of poly(arylene ether) 27 with superacid groups at 120°C. The maximum power density and current density at 0.5 V of 27 were 30% and 43% higher, respectively, than those of Nafion.…”
Section: Applicationsmentioning
confidence: 99%
“…For comparison, the structure of the sulfonated copolymer with two pendent phenyl sulfonic acid groups is presented in Scheme 5 (1-10). The performance of the membranes was evaluated by generating a trade-off plot containing both relative methanol permeability and relative proton conductivity (57,58).…”
Section: Sulfonated Fluorinated Random Copoly(arylene Ether)smentioning
confidence: 99%
“…Therefore, SAPs with ÀSO 3 H attached to a pendent side chain are expected to be more stable to heat, hydrolysis, and oxidation than main-chain-sulfonated analogues. [54,55] Based on this idea, Liu et al designed and synthe- Figure 1. Thermogravimetric analysis of untreated SPPSU, SPPSU treated at 170 8C for 48 h, and SPPSU treated at 170 8C for 64 h. [36] sized di(4-sulfonic acid) phenylated PESs.…”
Section: Optimization Of the Position Of So 3 Hmentioning
confidence: 99%