Rapid outgassing of hydrophilic TiO2 electrodes achieves long‑term stability of anion exchange membrane water electrolyzers
Shanghai Jiao Tong University Journal Center
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Credit: Shajahan Shaik, Jeonghyeon Kim, Mrinal Kanti Kabiraz, Faraz Aziz, Joon Yong Park, Bhargavi Rani Anne, Mengfan Li, Hongwen Huang, Ki Min Nam, Daeseong Jo, Sang-Il Choi*.
As global demand for green hydrogen surges, anion-exchange membrane water electrolyzers (AEMWEs) are gaining attention as a cost-effective alternative to proton-exchange membrane systems. However, electrode stability remains a critical bottleneck due to gas bubble accumulation that blocks active sites and accelerates catalyst degradation. Now, researchers from Kyungpook National University, led by Prof. Sang-Il Choi, have developed a super-hydrophilic electrode that achieves record operational stability by enabling rapid gas evacuation.
Why Super-Hydrophilic Electrodes Matter
- Gas Management: The NiFe/ATNT (annealed TiO2 nanotube) electrode exhibits zero water contact angle and 155° underwater O2 contact angle, facilitating formation of tiny 23 µm bubbles that detach rapidly compared to 124 µm bubbles on conventional Ti felt.
- Electrochemical Performance: Demonstrates oxygen evolution reaction overpotential of 235 mV at 10 mA cm-2 with a Tafel slope of 60 mV dec-1 in 1.0 M KOH, outperforming commercial IrO2 catalysts.
- Device-Level Impact: When integrated into AEMWE with Pt/C cathode, delivers 1.67 A cm-2 at 1.80 V and consumes only 4.05 kWh Nm-3 H2—surpassing most reported systems and approaching IRENA’s 2050 target.
- Longevity: Operates continuously for 1 500 hours at 0.50 A cm-2 and 80 °C with degradation rate of merely 0.20 mV h-1, while hydrophobic counterparts fail within 500 hours due to bubble-induced dead zones.
Innovative Design & Features
- Hierarchical Nanotube Architecture: Anodization and 500 °C annealing of Ti felt creates 3-D porous anatase TiO2 nanotubes with 120 nm surface roughness, providing abundant nucleation sites for uniform NiFe nanoparticle deposition.
- Electronic Synergy: X-ray spectroscopy reveals electron transfer from TiO2 to NiFe, creating electron-rich catalytic surfaces that enhance OER kinetics while maintaining structural integrity.
- Bubble Dynamics: Real-time imaging shows continuous bubble release without coalescence on ATNT surface, eliminating mass-transfer overpotentials that plague flat hydrophobic substrates.
- Versatility: Performance advantages maintained across different commercial membranes (PiperION, Fumasep) and electrolytes—from concentrated KOH to pure water.
Applications & Future Outlook
The study demonstrates that super-hydrophilic electrode design is crucial for simultaneous enhancement of activity, stability and efficiency in AEMWE systems. The NiFe/ATNT configuration achieves twice the current density of hydrophobic counterparts while eliminating bubble-related degradation pathways. Future research will focus on scaling the anodization process for large-area electrodes and extending the nanotube architecture to cathode materials for symmetric bubble management. This work provides a practical pathway toward durable, low-cost AEMWE stacks competitive with established alkaline and PEM technologies. Stay tuned for scale-up demonstrations from the multi-institutional Korea-China collaboration!
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