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Optimizing reaction pathways through inner surface ion confinement for high energy efficiency neutral zinc-air batteries
被引:0
|作者:
Luo, Sha
[1
]
Chen, Haotian
[1
]
Wang, Jiaqi
[1
]
Feng, Yu
[1
]
Zhang, Bao
[1
]
Sun, Wei
[1
]
机构:
[1] Univ Elect Sci & Technol China, Sch Mat & Energy, Chengdu 611731, Sichuan, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
Non-alkaline electrolyte;
Zinc-air batteries;
Zinc hydroxyacetate dihydrate;
Interface pH;
Ion confinement;
ACETATE;
D O I:
10.1016/j.nanoen.2025.110806
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Near-neutral rechargeable zinc-air batteries (ZABs) offer high energy density, safety, and economic benefits but suffer from higher polarization due to low-conductivity discharge products. Herein, we demonstrate an inner surface ion confinement effect within hydrophilic porous carbon to accelerate cathodic reaction kinetics of neutral ZABs. Operando electrochemical pH and in-situ XRD measurements reveal that microporous structure can temporarily store intermediate OH-, shifting the reaction pathway to a more efficient electrolyte mechanism, similar to high-performance aprotic Li-O2 batteries. This reduces basic zinc salt precipitation and ORR/OER overpotential, boosting energy efficiency from 46.0 % to 74.5 % at 0.1 mA cm- 2 and 2 mAh cm- 2. The resulting 10 Ah pouch cell and flexible belt-shaped cell offer scalable solutions for neutral zinc-air batteries across various applications, opening new avenues for high-performance metal-air batteries.
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页数:6
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