Abstract
With the aim to develop vanadium redox flow battery (VRFB) membranes beyond state of the art, we have in the present work functionalized poly(p-terphenylene)s with highly acidic perfluorosulfonic groups and investigated their performance as proton exchange membranes (PEMs). Consequently, two poly(p-terphenylene alkylene)s tethered with perfluoroalkylsulfonic acid and perfluorophenylsulfonic acid, respectively, were synthesized through superacid-mediated polyhydroxyalkylations and cast into PEMs. Compared with Nafion 212, the PEM carrying perfluorophenylsulfonic acid groups (PTPF-Phenyl-SA) was found to exhibited higher ionic conductivity and eight times lower vanadium (IV) permeation rate. The latter explains the longer self-discharge duration of the VRFB based on the PTPF-Phenyl-SA. In addition, the VRFB assembled with the PTPF-Phenyl-SA PEM exhibited a high average coulombic efficiency of 99.6% for over 100 cycles with a capacity fade of 0.24% per cycle, which was 50% lower than when Nafion 212 was used. More importantly, an excellent capacity retention was achieved through electrochemical rate performance experiments at different current densities.
Original language | English |
---|---|
Article number | 121390 |
Number of pages | 11 |
Journal | Journal of Membrane Science |
Volume | 671 |
DOIs | |
Publication status | Published - 2023 |
Subject classification (UKÄ)
- Energy Systems
- Polymer Technologies
- Polymer Chemistry
- Materials Chemistry
- Analytical Chemistry