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Updated: Jul 17, 2025

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
Published on: August 17, 2016
Efficient Alkaline Hydrogen Evolution Reaction Using Superaerophobic Ni Nanoarrays with Accelerated H2 Bubble
Jaerim Kim1, Sang-Mun Jung1, Noho Lee1
1Department of Materials Science and Engineering, Pohang University of Science and Technology, 77 Cheongam-Ro, Nam-Gu, Pohang, 37673, Republic of Korea.
Highly porous nickel nanorods enhance water electrolysis by promoting superaerophobic surfaces for efficient hydrogen bubble release. This boosts catalytic activity, especially at high current densities, optimizing hydrogen evolution reaction performance.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Hydrogen bubbles adhering to catalysts impede water electrolysis performance.
- Understanding hydrogen bubble release mechanisms in the alkaline hydrogen evolution reaction (HER) is crucial.
Purpose of the Study:
- Investigate the impact of nanoscale surface morphologies on bubble release and HER performance.
- Utilize earth-abundant nickel (Ni) catalysts with controlled surface porosities.
Main Methods:
- Systematic investigation of Ni nanorods (NRs) with varying surface porosities.
- Analysis of surface aerophobicity, hydrophilicity, and HER performance.
- Evaluation of bubble release dynamics and catalytic activity.
Main Results:
- Ni catalyst with ≈52% porosity exhibited superaerophobic nature and superior HER performance.
- Superaerophobicity and open pore channels accelerated H2 bubble release.
- Significant improvements in geometric, specific, and mass activities were observed, especially at high current densities.
Conclusions:
- Highly porous Ni NRs with superaerophobic surfaces effectively release H2 bubbles, enhancing HER performance.
- Optimized surface morphology is key to improving catalyst efficiency.
- Combining superaerophobic Ni NRs with Pt and Cr can further enhance electrocatalytic performance.
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