Green hydrogen produced via electrochemical splitting of water, powered by variable renewable energy, is gaining recognition as a key component of society's transition to low-carbon energy, particularly for the decarbonization of hard-to-abate industrial sectors such as steel, refining, and chemicals. As an energy carrier, green hydrogen can be flexibly converted and stored, enabling the long-term storage of large amounts of renewable energy, which is crucial for facilitating rapid, large-scale renewable energy development. The global total hydrogen indicates a need for 140-170 MtH₂eq by 2030 and 430-600 MtH₂eq by 2050 (Wang
To prepare, membrane thickness directly affects proton
conductivity, gas cross-over and mechanical stability, making it one of the
most important design parameters for PEM fuel cells. In the figure, experiments
demonstrate that thinner membranes enhance the structure design and improve their
properties during the conversion of energy cells. A molecular level of
understanding of PEM functionality further underscores the importance of
membrane thickness. It consists of hydrophobic domains that absorb water,
creating pathways for efficient proton conduction. Hydrogen energy is widely utilised
in this application, ranging from hydrogen cars and drones to naval submarines
and marine unmanned systems, showcasing its versatility and emphasising the
importance of optimising PEMs to meet diverse application needs. If a
thicker membrane structure is good in the diffusion layer and enhances mechanical
robustness, it incurs higher voltage losses and reduced efficiency. In
this study, fabricated Simple PEM-based fuel cells for hydrogen to electricity
with varying thickness, compared their performance, and analysed their
electrochemical behaviour using EIS (Electrochemical impedance spectroscopy) to
evaluate the effect of membrane thickness on device performance. Our results
reveal that performance was the primary focus of our analysis. Durability
testing results were not included, as it is widely recognised that thicker
membranes generally provide better durability.
Figure: Preparation of PEM (Photon Exchange Membrane)-Based Fuel Cell for Energy Conversion
|
Material |
Function |
|
PEEK powder |
Base polymer for the membrane |
|
DMF (Dimethylformamide) |
Solvent for dissolving PEEK |
|
Sulfuric acid (H₂SO₄) or Chlorosulfonic acid
(ClSO₃H) |
Sulfonating agents |
|
Deionized water |
Washing and protonation |
|
Glass plate |
Casting surface for the membrane |
|
Vacuum oven |
For drying membranes |
Procedure for the preparation of PEM for fuel cells
Prepare a solution for the dissolution
of PEEK in DMF. Dissolve PEEK in DMF at a ratio of about 10–20 wt%. Stir the
mixture at 80–120°C for several hours (typically 6–12 hours) under reflux until
a homogeneous solution is obtained. Pour the viscous PEEK/DMF solution onto a
clean glass plate or Petri dish to cast the membrane. Use a doctor blade or
film applicator to ensure even thickness (100–200 µm typical). Dry at room
temperature overnight, then in a vacuum oven at 80°C to remove residual DMF.
Sulfonation of PEEK (to make it proton-conductive). Immerse the dried PEEK film
in chlorosulfonic acid (ClSO₃H) or concentrated sulfuric acid at room
temperature or 50–60°C for 12–24 hours. This introduces –SO₃H groups, making it
a SPEEK (sulfonated PEEK) membrane.
PEEK+SO₃→SPEEK
Washing and Protonation Wash the sulfonated membrane thoroughly with deionised water to remove acid. Optionally, treat with 0.5 M H₂SO₄ and then wash again with DI water. Store in DI water to keep hydrated.
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