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Highly Active IrOx Formation on Strontium Manganite for Acidic Oxygen Evolution
Jia Wei Zhao1, Kaihang Yue2, Zhihao Pei1
1Department of Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong, 999077, China.
Researchers developed a novel catalyst using low iridium loading for the oxygen evolution reaction (OER). This advancement enhances OER activity and durability, overcoming a key challenge in electrochemical applications.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Iridium-based oxides are effective oxygen evolution reaction (OER) catalysts but require high iridium (Ir) content, hindering commercial use.
- Reducing Ir loading while maintaining high activity and durability is a critical challenge in OER catalysis.
Purpose of the Study:
- To synthesize a low-Ir-loading catalyst with enhanced OER activity and stability.
- To investigate the mechanism behind the catalyst's performance using advanced characterization and theoretical calculations.
Main Methods:
- Electrospinning of porous strontium manganate nanofibers.
- Hydrothermal synthesis to load short-range ordered Iridium oxide (IrOx).
- In situ characterizations (X-ray absorption spectroscopy, Raman spectroscopy, differential electrochemical mass spectrometry, synchrotron-radiation infrared spectroscopy) and theoretical calculations.
Main Results:
- Successfully synthesized low-Ir-loading porous strontium manganate nanofibers decorated with short-range ordered IrOx.
- Confirmed structural stability of IrOx during OER using in situ techniques.
- Demonstrated that Manganese (Mn) suppresses the lattice oxygen mechanism, favoring the adsorbate evolution mechanism for OER stabilization.
Conclusions:
- The synthesized catalyst exhibits high OER activity (221 mV overpotential at 10 mA cm-2) and excellent stability (≈1000 h) with significantly reduced Ir loading.
- The findings offer a promising strategy for developing cost-effective and high-performance OER catalysts.
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