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Understanding the microstructure of a core-shell anode catalyst layer for polymer electrolyte water electrolysis
Salvatore De Angelis1,2, Tobias Schuler1, Mayank Sabharwal1
1Electrochemistry Laboratory, Paul Scherrer Institute, 5232, Villigen PSI, Switzerland.
Scientific Reports
|March 16, 2023
Summary
This study reveals the nanostructure of a titanium dioxide-supported iridium dioxide catalyst layer for water electrolysis. The ionomer distribution is non-uniform, impacting conductivity and cost reduction efforts.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Reducing precious metal loading in catalyst layers (CLs) is crucial for lowering costs in polymer electrolyte water electrolysis.
- Developing efficient and durable catalysts is key to widespread adoption of this clean energy technology.
Purpose of the Study:
- To present the first 3D reconstruction of a TiO2-supported IrO2 core-shell CL using X-ray ptychographic tomography.
- To analyze the nanostructure, phase distribution, and connectivity within the catalyst layer.
Main Methods:
- High-resolution X-ray ptychographic tomography at cryogenic temperature (90 K).
- 3D reconstruction of pore space, IrO2, TiO2 support, and ionomer network.
- Analysis of ionic and electronic conductivity.
Main Results:
- IrO2 forms thin, nanoporous shells around TiO2 particles.
- The ionomer exhibits non-uniform thickness and incomplete catalyst coverage.
- TiO2 particles do not form a percolating network, but other phases show high connectivity.
- Ionic conductivity is significantly lower than electronic conductivity in a dry CL.
Conclusions:
- The nanostructure of the catalyst layer, particularly ionomer distribution, influences its performance.
- Support conductivity has a limited impact on the overall CL electrical conductivity.
- Understanding catalyst layer morphology is vital for optimizing water electrolysis efficiency and cost.

