4.6 Article

Dual-Side-Chain-Grafted Poly(phenylene oxide) Anion Exchange Membranes for Fuel-Cell and Electrodialysis Applications

Journal

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 9, Issue 25, Pages 8611-8622

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.1c02189

Keywords

anion exchange membrane; additional side chain; extender; fuel cell; electrodialysis

Funding

  1. National Natural Science Foundation of China [22075037, 21776042]
  2. fund for Creative Research Groups of the National Natural Science Foundation of China [22021005]
  3. Fundamental Research Fund for the Central Universities of China [DUT19ZD214, DUT19TD33]
  4. Science and Technology Innovation Fund of Dalian [2018J12GX052]

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The synthesized AEMs with specific side-chain structures achieved a good balance between ion conduction and stability, exhibiting excellent electrochemical performance and providing a new effective pathway for the research of AEMs.
Anion exchange membranes (AEMs) usually suffer from the trade-off between ion conduction and stability. In this work, a series of dual-side-chain-grafted poly(phenylene oxide) AEMs were synthesized to explore how the side-chain architectures influence membrane performance. Our investigations suggest that the AEM containing both a long hydrophobic extender (attached to the cation's central atom) and a hydrophilic additional side chain (beside the cation) show high hydroxide conductivity (21.3 mS/cm at 30 degrees C) and good chemical and dimensional stability (90.5% conductivity retention after 1 M NaOH treatment at 60 degrees C for 528 h). In addition, when a tri-cation side chain and a hydrophobic side chain are incorporated simultaneously, the resulting AEM shows further improved conductivity and stability (50.0 mS/cm at 30 degrees C; 90.6% conductivity retention after 1 M NaOH treatment at 60 degrees C for 528 h); it also shows excellent electrochemical performance when applied in a fuel cell and an electrodialyzer, accomplishing a peak power density of 506 mW/cm(2) and a current efficiency of 96.11%, respectively. Our side-chain manipulation strategy provides a new and effective pathway to balance the ionic conductivity and stability of AEMs.

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