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Influence of the Catalyst Layer Structure Formed by Inkjet Coating Printer on PEFC Performance
Yushi Tamaki1, Kimihiko Sugiura1
1Department of Technological Systems, Mechanical Engineering Course, Osaka Prefecture University College of Technology, 26-12 Saiwai-cho, Neyagawa, Osaka 572-8572, Japan.
Polymers
|April 3, 2021
Summary
Catalyst layer thickness and electrode area significantly impact Polymer Electrolyte Fuel Cell (PEFC) performance. Thicker catalyst layers and larger electrode areas increase overpotentials, hindering fuel cell efficiency.
Area of Science:
- Electrochemistry
- Materials Science
- Energy Conversion
Background:
- Polymer Electrolyte Fuel Cells (PEFCs) are crucial for clean energy.
- Optimizing the Catalyst Layer (CL) structure is key to enhancing PEFC performance.
- Inkjet printing offers precise control over CL fabrication.
Purpose of the Study:
- To investigate the impact of Catalyst Layer (CL) thickness on PEFC performance.
- To examine the effect of electrode area on PEFC performance.
- To understand the microstructural changes during CL formation and their consequences.
Main Methods:
- Fabrication of Membrane Electrode Assemblies (MEAs) with varying CL thicknesses (1, 4, 5, and 6 layers).
- Evaluation of PEFC performance using overpotential analysis.
- Microstructural analysis using Energy Dispersive X-ray spectroscopy (EDX).
- Testing MEAs with different electrode areas (1 cm² and 9 cm²).
Main Results:
- Increased CL thickness led to higher activation and diffusion overpotentials.
- EDX analysis revealed platinum aggregation and poor ionomer distribution during drying, hindering the three-phase interface.
- Multilayer CLs exhibited reduced gas diffusivity compared to single-layer CLs.
- Larger electrode areas (9 cm²) resulted in higher diffusion overpotentials, exacerbating flooding/plugging issues due to condensate accumulation.
Conclusions:
- CL thickness is a critical parameter affecting PEFC performance by influencing activation and diffusion overpotentials.
- The drying process significantly impacts CL microstructure, leading to suboptimal platinum-ionomer distribution and reduced performance.
- Electrode area influences diffusion limitations and condensate management, with larger areas being more susceptible to flooding.

