4.7 Article

Fuel cell electrolyte membranes based on copolymers of protic ionic liquid [HSO3-BVIm] [TfO] with MMA and hPFSVE

期刊

POLYMER
卷 179, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.polymer.2019.121583

关键词

Copolymerization; Ionic liquid; Fuel cell; conductivity; membranes; photopolymerization

资金

  1. Xunta de Galicia (REGALIs Network) [ED431D2017/06]
  2. Spanish Ministry of Science, Innovation and Universities (grant 'Juan de la Cierva-Formacion') [FJCI-2017-32404]
  3. [SOE1/P1/E0293]
  4. [CTQ2015-66078-R]

向作者/读者索取更多资源

Polymeric ionic liquids (PILs) have recently been attracting great attention as new types of electrolytes for polymer exchange membrane fuel cells (PEMFCs), clean energy devices, due to their outstanding properties. In this work, the copolymerization of the ionic liquid (IL) 1-(4-sulphobutyl)-3-vinylimidazolium trifluoromethanesulphonate, [HSO3-BVIm][TfO], with methyl methacrylate (MMA) and perfluoro-3,6-dioxa-4-methyl-7-octene sulfonyl fluoride in its hydrolyzed form (hPFSVE), respectively, was performed for the preparation of structurally new IL copolymer membranes with enhanced conductive properties in comparison with the pristine PIL form. Membranes were synthesized through a facile photopolymerization method under UV radiation. The effect of temperature under wet and dry conditions on the ionic conductivities of the resulting membranes was analyzed. The performances of the new membranes were also assessed in a proton exchange fuel cell for power generation. Both poly ([HSO3-BVIm][TfO]-co-MMA) and poly ([HSO3-BVIm][TfO]-co-hPFSVE) electrolyte membranes offered high conductivity even in dry conditions (in the order 10(-3) - 10(-2)S cm(-1)). At low MMA and hPFSVE amounts (10 mol%), the ionic conductivity and power performances of the resulting membranes were enhanced in comparison with the membrane only constituted of the polymerizable IL showing the promising prospects of these ionic liquid-based copolymers as proton exchange membranes, with power outputs up to 45 mW cm(-2).

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据