Abstract

Acid-doped reinforced polymer electrolyte membranes for high-temperature polymer electrolyte membrane fuel cell applications (HT PEMFCs) are presented and spectroscopically studied. Fully aromatic polyethers are employed bearing main chain pyridine units as the proton accepting sites, which have two different substitution patterns of the pyridine units, namely, 2,5- or 2,6-pyridine. This fact enables control of the solubility and of the acid doping ability of the polymeric membranes. Reinforcement is accomplished via incorporation of a PTFE woven fabric during the casting procedure for fabrication of the membranes. High acid uptake of the reinforced membranes was maintained for the 2,6-pyridine-based copolymers with high pyridine unit content. Studies of the swelling behavior of these reinforced membranes revealed that they expand mainly along the z-axis, which helps to avoid extensive damage in case of humidity or temperature changes during the fuel cell operation. Additionally, spectroscopic techniques are employed, namely, X-ray photoelectron spectroscopy, X-ray photoelectron spectroscopy with depth profile, near-edge X-ray absorption fine structure, and reflection electron energy loss spectroscopy, for the in-depth study of the two copolymer membranes doped with phosphoric acid. Through these spectroscopic evaluations, modifications in the membranes’ chemical structure, orientation, composition, and electronic structure after the reinforcement and doping processes were elaborated and unveiled.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.