Abstract

Polymer electrolyte fuel cells (PEFCs) provide efficient and carbon-free power by converting the hydrogen chemical energy. The PEFCs can reach their greatest performance in humidified condition, as proton exchange membranes (PEMs) should be humidified for their proton transportation function. Thus, external humidifiers are commonly employed to increase the water content of reactants. However, being burdened with external humidifiers can make the control of PEFCs complicated and costly, in particular for transportation application. To overcome this issue, self-humidifying PEMs have been introduced, with which PEFC can be fed by dry reactants. In fact, internal humidification is accomplished by produced water from the recombination of permeated hydrogen and oxygen gases on the incorporated platinum catalysts within the PEM. While the water production agent remains constant, there is a broad range of additives that are utilized to retain the generated water and facilitate the proton conduction path in the PEM. This review paper has classified the aforementioned additives in three categories: inorganic materials, proton-conductive materials, and carbon-based additives. Moreover, synthesis methods, preparation procedures, and characterization tests are overviewed. Eventually, self-humidifying PEMs endowed with platinum and different additives are compared from performance and stability perspectives, such as water uptake, proton conductivity, fuel cell performance, gas cross-over, and the overall durability. In addition, their challenges and possible solutions are reviewed. Considering the concerns regarding the long-term durability of such PEMs, it seems that further investigations can be beneficial to confirm their reliability for prolonged PEFC operation.

Highlights

  • Even though the transition to renewable energies has not yet been achieved [1], it is fortunate that measures are increasingly being taken to tackle environmental problems caused by the conventional combustion of fossil fuels [2,3]

  • This paper aims to review the advances of self-humidifying proton exchange membranes (PEMs) as well as their prevailing challenges

  • Pt nanoparticles for internal water production and other additives that are classified into three categories of inorganic, proton-conductive, and carbon-based materials

Read more

Summary

Introduction

Even though the transition to renewable energies has not yet been achieved [1], it is fortunate that measures are increasingly being taken to tackle environmental problems caused by the conventional combustion of fossil fuels [2,3]. Similar to the way cactus retains water in arid conditions, the nano-sized cracks on the deposited hydrophobic layer can swell in humidified conditions or become narrower in anhydrous conditions in order to minimize the water loss These nanocracks can act as nanovalves at low humidity levels and maintain an appropriate degree of hydration for the membrane. External humidifiers have remained as a burden for fuel cell vehicles To address this problem, the term “self-humidifying proton exchange membranes” was introduced, where the PEMs are endowed with Pt nanoparticles as internal water production catalytic sites together with other additives to retain hydration and improve proton conductivity. The term “self-humidifying proton exchange membranes” was introduced, where the PEMs are endowed with Pt nanoparticles as internal water production catalytic sites together with other additives to retain hydration and improve proton conductivity In these cases, external humidifiers were no longer needed [41]. This paper aims to review the advances of self-humidifying PEMs as well as their prevailing challenges

Self-Humidifying PEMs Incorporated with Inorganic Additives
Self-Humidifying PEMs Incorporated with Highly Proton-Conductive Additives
Hsuperior
Self-Humidifying
Self-Humidifying PEMs Incorporated with Carbon-Based Additives
Prevailing Challenges and Possible Remedies
Future Prospects of Self-Humidifying PEMs
Findings
Conclusions
Full Text
Published version (Free)

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