Abstract

In this work, two different functionalized graphene oxide (GO), sulfonic acid functionalized GO (SGO) and amino functionalized GO (NGO), were synthesized and incorporated into the sulfonated poly(arylene ether nitrile) (SPEN) by single doping and codoping. It was found that the codoping of SGO and NGO contributed to the enhancement of proton exchange membrane performance. These two functionalized GO as fillers were uniformly dispersed in SPEN matrix and their synergistic effect created the long-range proton transfer channels along fillers/SPEN matrix interfaces. Meanwhile, acid-base pairs which was induced by strong interfacial interactions between fillers and SPEN matrix provided new and low-energy-barrier pathways for proton hopping, facilitating the proton conduction via Grotthuss mechanism. Among all the membranes, the codoped S/N-3 composite membrane exhibited the highest proton conductivity (0.064 S·cm−1 at 20 °C and 0.21 S·cm−1 at 80 °C). Besides, it was endowed with unprecedented dimensional stability, especially in high temperature (just 12.75% at 80 °C). Also, low methanol permeability was conferred owing to methanol trapping effect of two functionalized GO. Furthermore, S/N-3 composite membrane showed a superior selectivity of 4.48 × 105S⋅cm−3⋅s, which was nearly 10 times of that of commercialized Nafion 117. Our investigation provides a new strategy on the design of high performance composite membranes for applications of PEMs and other related fields.

Full Text
Paper version not known

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.