Porous poly(perfluorosulfonic acid) membranes for alkaline water electrolysis

被引:58
作者
Aili, David [1 ]
Hansen, Martin Kalmar [2 ]
Andreasen, Jens Wenzel [3 ]
Zhang, Jingdong [4 ]
Jensen, Jens Oluf [1 ]
Bjerrum, Niels J. [1 ]
Li, Qingfeng [1 ]
机构
[1] Tech Univ Denmark, Sect Proton Conductors, Dept Energy Convers & Storage, DK-2800 Lyngby, Denmark
[2] Siemens Corp Technol, DK-2750 Ballerup, Denmark
[3] Tech Univ Denmark, Sect Imaging & Struct Anal, Dept Energy Convers & Storage, DK-4000 Roskilde, Denmark
[4] Tech Univ Denmark, Dept Chem, DK-2800 Lyngby, Denmark
关键词
Poly(perfluorosulfonic acid); Membranes; Porous; Water electrolysis; Alkaline; ANION-EXCHANGE MEMBRANES; FUEL-CELL APPLICATIONS; ANGLE X-RAY; POTASSIUM HYDROXIDE; DOPED POLYBENZIMIDAZOLE; CONDUCTING MEMBRANES; STEAM ELECTROLYSIS; IONOMER MEMBRANES; HIGH-TEMPERATURE; DEGREES-C;
D O I
10.1016/j.memsci.2015.06.057
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Poly(perfluorosulfonic acid) (PFSA) is one of a few polymer types that combine excellent alkali resistance with extreme hydrophilicity, It is therefore of interest as a base material in separators for alkaline water electrolyzers. In the pristine form it, however, shows high cation selectivity. To increase its ion conductivity in aqueous KOH, a method for the preparation of porous PFSA membranes was developed. It was based on an approach where PFSA was co-cast with poly(vinylpyrrolidone) (PVP) at different ratios to give transparent and colorless blend membranes. The PVP was subsequently dissolved and washed out and the obtained porous materials allowed for swelling to reach water contents up to lambda=85 [H2O] [-SO3K](-1). After equilibration in 22 wt% aqueous KOH, ion conductivity of 0.2 S cm(-1) was recorded for this membrane type at room temperature, which is significantly higher than 0.01 S cm(-1) for the unmodified membrane. The technological feasibility was demonstrated by testing the membranes in an alkaline water electrolysis cell with encouraging performance. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:589 / 598
页数:10
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