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Surface Defect Engineering on Perovskite Oxides as Efficient Bifunctional Electrocatalysts for Water Splitting
RuoQi Zong1, YeGui Fang1, Changrong Zhu1
1College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060, China.
ACS Applied Materials & Interfaces
|September 1, 2021
Summary
Surface defect engineering enhances perovskite oxide electrocatalysts for sustainable hydrogen production via water splitting. Selective acid etching optimizes activity by modifying metal coordination and electronic structure while maintaining catalyst stability.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Efficient and cost-effective electrocatalysts are crucial for sustainable hydrogen production through water splitting.
- Perovskite oxides show promise but require optimization for enhanced electrocatalytic activity.
Purpose of the Study:
- To develop a surface defect engineering method for optimizing perovskite oxide electrocatalysts.
- To enhance the performance of perovskite oxide electrocatalysts for water electrolysis.
Main Methods:
- Utilized selective acid etching to engineer surface defects in a ferrite-based perovskite oxide, La$_{0.6}$Sr$_{0.4}$Co$_{0.2}$Fe$_{0.8}$O$_{3-δ}$ (LSCF).
- Identified optimal parameters for surface treatment to create a bifunctional electrocatalyst (LSCF-30).
- Maintained the perovskite bulk crystal lattice integrity during surface modification.
Main Results:
- Selective corrosion of the A-site Sr element in the surface region was achieved.
- Increased exposure and decreased coordination of B-site metals were observed.
- Modulation of the electronic structure of B-site metals and enhanced structural stability were confirmed.
Conclusions:
- Surface defect engineering is an effective strategy for enhancing perovskite oxide electrocatalyst performance.
- The developed method provides a pathway for designing high-performance electrocatalysts for water splitting.
- The study highlights the importance of surface modification while preserving bulk structure for catalyst stability and activity.

