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Surface engineered CoP/Co3O4 heterojunction for high-performance bi-functional water splitting electro-catalysis
Xintong Li1, Yizhe Liu1, Qidi Sun1
1Department of Chemistry, City University of Hong Kong, Kowloon, 999077, Hong Kong. zonglzhu@cityu.edu.hk.
This study developed a novel CoP/Co3O4 heterostructure catalyst for efficient electrochemical water splitting. The engineered catalyst demonstrates excellent bifunctional activity in alkaline solutions, paving the way for cost-effective hydrogen production.
Area of Science:
- Electrochemistry
- Materials Science
- Catalysis
Background:
- Electrochemical water splitting integrates hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) for energy efficiency.
- Existing catalysts face challenges with stability in acidic media (OER) or poor kinetics in alkaline media (HER).
Purpose of the Study:
- To develop a bifunctional catalyst for efficient electrochemical water splitting in alkaline environments.
- To address the limitations of current catalysts in terms of stability and kinetics.
Main Methods:
- Fabrication of a CoP/Co3O4 heterostructure.
- Surface engineering to introduce oxygen (O) and phosphorus (P) defects, creating s-CoP/Co3O4.
- Evaluation of the catalyst's performance in alkaline HER and OER.
Main Results:
- The s-CoP/Co3O4 catalyst achieved a current density of -10 mA cm-2 at an overpotential of 106 mV vs. RHE for alkaline HER.
- For OER, the catalyst required an overpotential of 211 mV vs. RHE at 10 mA cm-2 with a low Tafel slope of 58.4 mV dec-1.
- Demonstrated bifunctional catalytic activity in 1 M KOH.
Conclusions:
- The developed s-CoP/Co3O4 heterostructure serves as an effective bifunctional catalyst for alkaline water splitting.
- Surface engineering creating unsaturated metal sites offers a low-cost approach to enhance electro-catalytic activity.
- This work presents a promising strategy for scalable and cost-effective hydrogen production.
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