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Improving the Oxygen Evolution Reaction: Exsolved Cobalt Nanoparticles on Titanate Perovskite Catalyst
Shangshang Zuo1, Yuan Liao1, Chenchen Wang1
1School of Chemistry, University of St Andrews, St Andrews, Fife, KY16 9ST, UK.
Small (Weinheim an Der Bergstrasse, Germany)
|October 29, 2023
Summary
Exsolving cobalt nanoparticles from perovskite catalysts significantly enhances oxygen evolution reaction (OER) performance. This strategy improves atom utilization efficiency and catalytic activity, outperforming traditional catalysts.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Perovskites are tunable catalysts for oxygen evolution reaction (OER) but often suffer from low atom utilization efficiency due to large particle sizes.
- Improving mass activity and atom utilization is crucial for efficient OER catalysis.
Purpose of the Study:
- To enhance the atom utilization efficiency and OER performance of perovskite catalysts by exsolving cobalt nanoparticles.
- To investigate the catalytic activity and stability of the exsolved cobalt nanoparticle perovskite catalyst.
Main Methods:
- Synthesis of La0.2+2x Ca0.7-2x Ti1-x Cox O3 perovskite.
- Exsolution of cobalt nanoparticles via reduction in H2/N2 atmosphere.
- Electrochemical characterization including OER performance testing and electrochemical impedance spectroscopy (EIS).
- Accelerated durability testing (10 h electrolysis, 1000 CV cycles).
Main Results:
- The exsolved cobalt nanoparticle catalyst (R-LCTCo0.11) achieved a mass activity of ≈1700 mA mg-1 at 450 mV overpotential, significantly higher than parent perovskite and benchmark RuO2.
- R-LCTCo0.11 exhibited the lowest charge transfer resistance (58 Ω), indicating superior catalytic and kinetic activity.
- The catalyst demonstrated high stability over 10 hours of electrolysis and 1000 cyclic voltammetry cycles.
Conclusions:
- Nanoparticle exsolution from doped perovskites is an effective strategy to boost atom utilization efficiency for OER.
- The R-LCTCo0.11 catalyst presents a promising alternative for efficient and stable oxygen evolution catalysis.
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