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Synthesis of Platinum-nickel Nanowires and Optimization for Oxygen Reduction Performance
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Surface-Engineered Ni2P: An Efficient Oxygen Electrocatalyst for Zinc-Air Battery
Mopidevi Manikanta Kumar1, Rahul Singh1, C Retna Raj1
1Functional Materials and Electrochemistry Lab, Department of Chemistry, IIT Kharagpur, 721302, Kharagpur, West Bengal, India.
Chemistry, an Asian Journal
|September 9, 2024
Summary
Surface engineering of nickel phosphide (Ni2P) enhances its activity for oxygen electrocatalysis. This improved catalyst powers rechargeable zinc-air batteries (ZABs) with high energy density and stability.
Area of Science:
- Materials Science
- Electrochemistry
- Energy Storage
Background:
- Surface engineering of electrocatalysts is crucial for enhancing intrinsic activity.
- Defect generation (anion/cation vacancies) and increased surface area are key outcomes.
- Nickel phosphide (Ni2P) is a potential electrocatalyst material.
Purpose of the Study:
- To engineer the surface of Ni2P to improve bifunctional oxygen electrocatalytic activity.
- To develop a high-performance rechargeable zinc-air battery (ZAB) using the engineered catalyst.
Main Methods:
- Synthesis of N and P-dual doped carbon encapsulated Ni2P (Ni2P@NPC) using a single-source precursor.
- Surface engineering via controlled room-temperature acid treatment.
- Characterization of catalyst properties and performance in a ZAB.
Main Results:
- Acid treatment exfoliated carbon, increased P-vacancy, and boosted electrochemically active surface area.
- Engineered Ni2P@NPC showed enhanced oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) activity.
- The ZAB achieved a specific capacity of 770.25 mAh gZn−1 and energy density of 692 Wh kgZn−1.
Conclusions:
- Surface engineering effectively tunes Ni2P for superior bifunctional oxygen electrocatalysis.
- The engineered catalyst enables high-performance rechargeable zinc-air batteries with excellent cycling stability.
- P-vacancy creation is beneficial for forming active oxyhydroxide species for OER.
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