相间
阴极
插层(化学)
阳极
材料科学
水溶液
电化学
化学工程
电池(电)
电极
电解质
纳米技术
电流密度
金属
串联
动力学
降级(电信)
工作(物理)
作者
Dingtao Ma,Jing Lin,Xiaodan Yang,Zhu Jianhui,Xuanlong He,Jiaxin Xie,Liang He,Ming Yang,Yanyi Wang,Hongwei Mi,Peixin Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-12-17
卷期号:20 (1): 1181-1195
被引量:1
标识
DOI:10.1021/acsnano.5c17102
摘要
The practical operation of aqueous zinc-ion batteries is greatly influenced by the microenvironment of the electrode-electrolyte interface, while the structural instability and sluggish interfacial reaction kinetics at both cathode and anode sides are still critical challenges. This work develops a heterocation intercalation approach to unlock a robust La3+/Ca2+-Na0.7MnO2.05 (LCNMO) cathode material, which enables simultaneously constructing an efficient cathode-electrolyte interphase (CEI) and a compressed double electric layer (EDL) interphase during the first few charging cycles. These in situ-formed interphases can simultaneously alleviate the interrelated adverse issues including cathode dissolution, uneven deposition, severe side reactions, and sluggish reaction kinetics. Benefiting from that, the constructed aqueous Zn||LCNMO system was demonstrated to exhibit self-enhanced electrochemical performance. Impressively, it can display a 6000-cycle lifespan with a 73.7% capacity retention even at a high current density of 10 A g-1. Besides, the corresponding pouch cell with a 10 mg cm-2 loading enables providing a high reversible capacity of 14.8 mAh at 1 A g-1 after 100 cycles. Such a heterogeneous intercalation paradigm creates a tandem effect to expand the regulatory area of guest cations, deepen the understanding of host intercalation chemistry, and boost the development of high-performance aqueous zinc-ion batteries.
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