Abstract

Series of partially fluorinated sulfonated poly(arylene ether)s were synthesized through nucleophilic substitution polycondensation from three types of diols and superhydrophobic tetra-trifluoromethyl-substituted difluoro monomers with postsulfonation to obtain densely sulfonated ionomers. The membranes had similar ion exchange capacities of 2.92 ± 0.20 mmol g−1 and favorable mechanical properties (Young’s moduli of 1.60–1.83 GPa). The membranes exhibited considerable dimensional stability (43.1–122.3% change in area and 42.1–61.5% change in thickness at 80 °C) and oxidative stability (~55.5%). The proton conductivity of the membranes, higher (174.3–301.8 mS cm−1) than that of Nafion 211 (123.8 mS cm−1), was the percent conducting volume corresponding to the water uptake. The membranes were observed to comprise isolated to tailed ionic clusters of size 15–45 nm and 3–8 nm, respectively, in transmission electron microscopy images. A fuel cell containing one such material exhibited high single-cell performance—a maximum power density of 1.32 W cm2 and current density of >1600 mA cm−2 at 0.6 V. The results indicate that the material is a candidate for proton exchange membranes in fuel cell applications.

Highlights

  • The fuel cell is a type of energy conversion device, and the prototype fuel cell, which converted chemical energy into electrical energy through an electrochemical mechanism, was produced at the beginning of the 19th century [1,2,3]

  • Hydrogen is produced following the opposite principle of fuel cells, according to which it is produced from water splitting and used as a carrier for energy storage

  • Bipolar domains form in the molecule which become partially fluorinated sulfonated poly(arylene ether)s with highly efficien proton transport.the free volume effect and hydrogen bond cohesion of b we report a series of novel poly(arylene ether)s synthesized using a multisphenol monomers with different degrees of sulfonation provide phenylated difluoro monomer with a trifluoromethylphenyl side chaincorresponding and three types wate of multiphenylated bisphenol monomer

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Summary

Introduction

The fuel cell is a type of energy conversion device, and the prototype fuel cell, which converted chemical energy into electrical energy through an electrochemical mechanism, was produced at the beginning of the 19th century [1,2,3]. Sulfonated HC-based polymers have a wide diversity of morphology types because hydrophobic and hydrophilic moieties are multiscale distributed by structural effects These are microphase separations to form proton transport channels. Bipolar domains form in the molecule which become partially fluorinated sulfonated poly(arylene ether)s with highly efficien proton transport.the free volume effect and hydrogen bond cohesion of b we report a series of novel poly(arylene ether)s synthesized using a multisphenol monomers with different degrees of sulfonation provide phenylated difluoro monomer with a trifluoromethylphenyl side chaincorresponding and three types wate of multiphenylated bisphenol monomer. The synthesis of sulfonate through treatment with chlorosulfuric acid, with the trifluoromethyl (-CF3 ) substituent poly(arylene expected ether)s towas confirmed using proton nuclear magnetic resonance (1H NMR inhibit the SN Ar reaction in specific moieties, effectively dividing the local, and Fourier transform infrared (FTIR).

General Methods
General
General Procedure for Sulfonation
2.10. Measurements
2.11. Stability
2.12. Water Uptake and Dimensional Stability
2.13. Ion Exchange Capacity
2.14. Hydrated Molar Volume per Charge
2.15. Percent Conducting Volume
2.16. Proton Conductivity
2.17. Microstructure Analysis
2.18. Single-Cell Performance
Synthesis and Characterization of the Monomers and Polymers
Mechanical Properties
Hydration Behavior
Water uptake as a function of temperature for s-P12FmB-Ave and Nafion 2
Microstructure Analysis
Fuel Cell Performance
Conclusions
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