4.3 Article

Durable and highly proton conducting poly(arylene perfluorophenylphosphonic acid) membranes

期刊

JOURNAL OF MEMBRANE SCIENCE
卷 623, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.memsci.2021.119074

关键词

Proton exchange membranes; Fuel cells; Phosphonic acid; Proton conductivity; Stability against radicals; Polyhydroxyalkylation

资金

  1. Swedish Energy Agency [45057-1, 37806-3]
  2. Swedish Research Council [45397-1, 2015-04820]
  3. Swedish Foundation for Strategic Research [EM16-0060]
  4. Royal Physiographic Society of Lund
  5. Swedish Research Council [2015-04820] Funding Source: Swedish Research Council

向作者/读者索取更多资源

Phosphonated aromatic polymers functionalized with highly acidic perfluorophenylphosphonic acid show high conductivity, efficient ionic clustering, excellent proton conductivity, and outstanding thermal stability, making them attractive for applications in catalyst layers and proton exchange membranes.
Phosphonated aromatic polymers show several important advantages as proton exchange membranes (PEMs), including high thermal and chemical stability. However, the conductivity generally needs to be significantly enhanced for most electrochemical applications. Here, we have prepared a series poly(p-terphenyl perfluoroalkylene)s functionalized with highly acidic perfluorophenylphosphonic acid by first carrying out triflic acid mediated polyhydroxylations involving p-terphenyl, 2,2,2-trifluoroacetophenone and perfluomacetophenone. Subsequently, the resulting polymers were quantitatively and selectively phosphonated in the para positions of the pendant perfluorophenyl units by employing an efficient Michaelis-Arbuzov reaction. X-ray scattering of proton exchange membranes (PEMs) based on the phosphonated polymers showed efficient ionic clustering with the interdomain distance depending on the acid content of the polymer. Although the water uptake and swelling was moderate (even at high temperature) the PEMs showed high proton conductivity, up to 111 mS cm(-1) at 80 degrees C fully hydrated, and reaching 4 mS cm(-1) at 50% RH at the same temperature. This may be ascribed to the distinct phase separation and high acidity of the polymers. The stability of the PEMs was excellent with thermal decomposition only above similar to 400 degrees C. Moreover, no change in weight, appearance or molecular structure was detected after 5 h immersion in Fenton's reagent at 80 degrees C, demonstrating an excellent chemical resistance of the PEMs towards free-radical attack. The radical resistance of the present phosphonated PEMs was found to increase with the acid content, which is in contrast to corresponding sulfonated PEMs. The combination of high thermochemical stability and high conductivity implies that the present materials are attractive for use as ionomers in catalyst layers and as PEMs in fuel cells and water electrolyzer applications.

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