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Self-adaptive ZrN coating enables stable acidic oxygen evolution on Co3O4 through dynamic surface reconstruction
Zheng Han1, Ali Sufyan2,3, Jiaxian Zheng1,4
1State Key Laboratory of Physical Chemistry of Solid Surfaces, Tan Kah Kee Innovation Laboratory (IKKEM), College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China. hfliang@xmu.edu.cn.
Developing stable, non-precious catalysts for the oxygen evolution reaction (OER) in water electrolyzers is key. This study introduces a self-adaptive ZrN coating on Co3O4 that reconstructs dynamically, enhancing catalyst stability and performance in acidic conditions.
Area of Science:
- Electrochemistry
- Materials Science
- Catalysis
Background:
- Proton exchange membrane water electrolyzers (PEMWEs) require acid-stable, non-precious oxygen evolution reaction (OER) catalysts.
- Cobalt oxide (Co3O4) exhibits good OER activity but suffers from dissolution in acidic media.
Purpose of the Study:
- To develop a self-adaptive protection strategy for Co3O4 catalysts to improve stability in acidic environments.
- To investigate the dynamic reconstruction of protective coatings under OER conditions.
Main Methods:
- Magnetron sputtering of ZrN onto Co3O4 precursors.
- Controlled calcination to form a mixed-phase Zr2ON2 and ZrO2 surface layer.
- Electrochemical testing in 0.1 M HClO4 and integration into PEMWEs.
Main Results:
- The ZrN coating transformed into a dual-phase Zr2ON2/ZrO2 layer, providing both conductivity and corrosion resistance.
- The catalyst achieved a low overpotential (362 mV at 10 mA cm-2) and excellent stability (>140 h at 100 mA cm-2).
- Dynamic reconstruction of the coating under OER conditions optimized charge transfer and suppressed cobalt dissolution.
Conclusions:
- Dynamic coating reconstruction is an effective strategy for designing stable acidic OER catalysts.
- The developed catalyst demonstrates practical viability for PEMWE applications, showing sustained performance at high current densities.
- This approach offers a pathway to overcome the stability limitations of non-precious metal catalysts in acidic electrochemical systems.
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