4.7 Article

Sulfonated poly(arylene ether sulfone)s membranes with distinct microphase-separated morphology for PEMFCs

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 68, Pages 33978-33990

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2021.07.199

Keywords

Proton exchange membranes; Poly(arylene ether sulfone)s; Atom transfer radical; polymerization; Side-chain length; Phase-separated-morphology

Funding

  1. National Key Research and Development Plan [2017YFB0103004]
  2. National Natural Science Foundation of China [51975049, 52006009, 52006010]

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Copoly (arylene ether sulfone)s were used for proton exchange membrane preparation, achieving enhanced phase-separated morphology and favorable proton conductivity. The membranes exhibited higher water uptake and reasonably high proton conductivity, making them suitable for use in PEMFCs.
Copoly (arylene ether sulfone)s was employed for proton exchange membrane preparation via atom transfer radical polymerization followed by mild sulfonation, enhanced phase-separated morphology and favorable proton conductivity were achieved. The comprehensive ex-situ properties of a range of membranes with different ion exchange capacities were characterized alongside the fuel cell performances investigation. The membranes exhibit higher water uptake, which is beneficial to the proton conduction, compared to Nafion (R) 211 while maintaining similar swelling ratio. The prepared membranes exhibit reasonably high proton conductivity (0.16 S/cm at 85 degrees C) benefitting from the well-defined microstructure and high connectivity of the hydrophilic domains. Considering the comprehensive property, membrane with moderate ion exchange capacity (1.39 mmol/g) was employed to fabricate the membrane electrode assembly and peak power density of 0.65 W/cm(2) at 80 degrees C, 60% relative humidity was achieved for a H-2/O-2 fuel cell, these hydrocarbon membranes can therefore be implemented in PEMFCs. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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