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Fe-Doping-Accelerated Deep Reconstruction of KCoF3 for Enhanced Alkaline Oxygen Evolution Reaction
Luyao Yang1, Xue Yang1, Xueying Cao1
1State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources; College of Chemistry, Xinjiang University, Urumqi, Xinjiang, People's Republic of China.
Designing efficient oxygen evolution reaction (OER) catalysts is crucial. This study introduces a self-reconstructing KCoFeF3 catalyst that forms active oxyhydroxides, significantly boosting OER performance and stability.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Developing efficient catalysts for the oxygen evolution reaction (OER) is critical for energy conversion technologies.
- Catalyst deep reconstruction into active oxyhydroxides presents a significant challenge.
Purpose of the Study:
- To design and synthesize a catalyst capable of self-reconstruction for enhanced alkaline OER.
- To investigate the role of Fe doping in catalyst reconstruction and OER mechanism.
Main Methods:
- Rational synthesis of KCo1-xFexF3 perovskite materials.
- Electrochemical characterization of OER performance in alkaline media.
- In situ Raman spectroscopy to study catalyst reconstruction.
Main Results:
- KCo1-xFexF3 undergoes self-reconstruction via ion leaching to form amorphous (Co, Fe)OOH active layers.
- Fe incorporation enhances bond dissociation, promotes deep reconstruction, and switches the OER mechanism to lattice oxygen-mediated mechanism (LOM).
- Reconstructed KCo0.7Fe0.3F3 exhibits a low overpotential (257 mV at 10 mA cm-2) and excellent stability (>100 h at 100 mA cm-2).
Conclusions:
- A rational strategy for deep catalyst reconstruction is demonstrated.
- Fe-doped KCoF3 perovskites serve as efficient precursors for highly active and stable OER electrocatalysts.
- The findings provide fundamental insights into enhancing OER catalytic activity through controlled reconstruction.
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