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Developing a Cobalt Phosphide Catalyst with Combined Cobalt Defects and Phosphorus Vacancies to Boost Oxygen
Weihua Ou1, Ligui Li1, Wei Zhou1
1New Energy Research Institute, College of Environment and Energy, South China University of Technology, Guangzhou 510006, China.
Defect engineering in cobalt phosphide (CoP) catalysts, specifically creating cobalt and phosphorus vacancies, boosts oxygen evolution reaction (OER) efficiency. This novel Co1-xPv catalyst shows excellent performance in water splitting, outperforming noble metal catalysts.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Defect engineering is crucial for enhancing catalyst performance.
- Optimizing surface charge and active sites of cobalt phosphide (CoP) catalysts improves oxygen evolution reaction (OER) efficiency.
Purpose of the Study:
- To develop a novel Co1-xPv catalyst with coexisting cobalt defects and phosphorus vacancies.
- To evaluate the catalyst's performance in oxygen evolution reaction (OER) and electrocatalytic water splitting (EWS).
Main Methods:
- Synthesis of a Co1-xPv catalyst featuring both cobalt and phosphorus vacancies.
- Electrochemical testing of the catalyst in basic and acidic media for OER.
- Performance evaluation in alkaline electrocatalytic water splitting (EWS) using a Co1-xPv || Pt/C cell.
Main Results:
- The Co1-xPv catalyst demonstrated modest overpotentials of 238 mV (basic) and 249 mV (acidic) at 10 mA cm-2 for OER.
- In alkaline EWS, the Co1-xPv || Pt/C cell operated at a low voltage of 1.51 V, outperforming RuO2 || Pt/C (1.66 V).
- Enhanced catalytic efficiency and longevity were attributed to a tunable electronic structure, facilitated Co2+ to Co3+ transformation, and improved oxygen species interaction.
Conclusions:
- Coexisting cobalt and phosphorus vacancies in CoP catalysts significantly enhance OER efficiency.
- The developed Co1-xPv catalyst offers a promising alternative to noble metal catalysts for water splitting.
- This defect engineering strategy provides a new pathway for designing advanced transition metal phosphide catalysts for energy conversion.
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