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
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.
引用
收藏
页数:6
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