Sulfonate side chains grafted poly(terphenyl piperidine) membranes with improved chemical stability for vanadium redox flow battery applications

Ether-free ion exchange membranes with high ion selectivity and excellent oxidative stability are highly desirable for vanadium redox flow batteries (VRFBs), yet achieving a balanced combination of fast proton transport and suppressed vanadium ion crossover remains a major challenge. Herein, an ether-free, N -unsubstituted poly(terphenyl piperidine) (PTP) was synthesized via superacid-catalyzed polymerization and employed as the polymer backbone for membrane fabrication. Subsequently, sodium 2-bromoethanesulphonate (ES), 1,3-propane sultone (PS), and 1,4-butane sultone (BS) are grafted onto the active N H site in piperidine ring to introduce sulfonic acid side chains with different alkyl lengths and grafting degrees under mild conditions without additional catalysts. Unlike conventional N -methyl substituted poly(terphenyl N -methyl-4-piperidine)-based membranes, the grafted PTPs don't contain quaternary ammonium structures in polymer main chains, which improves oxidative stability in strongly acidic VO 2 + environments. The effects of side-chain alkyl length and sulfonation degree on membrane properties were systematically investigated. Among all samples, the PTP-55%PS membrane exhibited the best overall performance, achieving a low area resistance of 0.52 Ω cm 2 , low vanadium ion permeability of 2.0 × 10 −7 cm 2 min −1 and high ion selectivity of 4.0 × 10 4 S min cm −3 , which was approximately 13 times higher in ion selectivity than Nafion 115. When applied in VRFBs, the PTP-55%PS membrane delivered a maximum energy efficiency of 82.7% at 100 mA cm −2 and maintained coulombic efficiencies above 97% with stable electrochemical performance over 200 charge-discharge cycles. This work demonstrates that the regulation of sulfonic acid side-chain length and grafting degree of PTP provides an effective strategy for constructing high-performance membranes for VRFB applications.

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Journal
Journal of Energy Storage
Published
2026-09-15
DOI
https://doi.org/10.1016/j.est.2026.124683
Primary Topic
Advanced battery technologies research
Type
article
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article

Sulfonate side chains grafted poly(terphenyl piperidine) membranes with improved chemical stability for vanadium redox flow battery applications

Jingshuai Yang, Di Ke, Bin Chen, Xinquan Cheng et al.
Journal of Energy Storage
Advanced battery technologies research
article

Sulfonate side chains grafted poly(terphenyl piperidine) membranes with improved chemical stability for vanadium redox flow battery applications

Jingshuai Yang, Di Ke, Bin Chen, Xinquan Cheng, Yang Wu, Peiru Lv
article en

Abstract

Ether-free ion exchange membranes with high ion selectivity and excellent oxidative stability are highly desirable for vanadium redox flow batteries (VRFBs), yet achieving a balanced combination of fast proton transport and suppressed vanadium ion crossover remains a major challenge. Herein, an ether-free, N -unsubstituted poly(terphenyl piperidine) (PTP) was synthesized via superacid-catalyzed polymerization and employed as the polymer backbone for membrane fabrication. Subsequently, sodium 2-bromoethanesulphonate (ES), 1,3-propane sultone (PS), and 1,4-butane sultone (BS) are grafted onto the active N H site in piperidine ring to introduce sulfonic acid side chains with different alkyl lengths and grafting degrees under mild conditions without additional catalysts. Unlike conventional N -methyl substituted poly(terphenyl N -methyl-4-piperidine)-based membranes, the grafted PTPs don't contain quaternary ammonium structures in polymer main chains, which improves oxidative stability in strongly acidic VO 2 + environments. The effects of side-chain alkyl length and sulfonation degree on membrane properties were systematically investigated. Among all samples, the PTP-55%PS membrane exhibited the best overall performance, achieving a low area resistance of 0.52 Ω cm 2 , low vanadium ion permeability of 2.0 × 10 −7 cm 2 min −1 and high ion selectivity of 4.0 × 10 4 S min cm −3 , which was approximately 13 times higher in ion selectivity than Nafion 115. When applied in VRFBs, the PTP-55%PS membrane delivered a maximum energy efficiency of 82.7% at 100 mA cm −2 and maintained coulombic efficiencies above 97% with stable electrochemical performance over 200 charge-discharge cycles. This work demonstrates that the regulation of sulfonic acid side-chain length and grafting degree of PTP provides an effective strategy for constructing high-performance membranes for VRFB applications.

Journal of Energy StorageVol. 181
Liaoning University (CN), Shaoxing University (CN), Zhejiang Medicine (China) (CN), Northeastern University (CN)
Affordable and clean energy
Openalex Percentile: Top 21%
Advanced battery technologies research
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