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,Jia-Xin 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:2
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 La 3+ /Ca 2+ –Na 0.7 MnO 2.05 (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.
科研通智能强力驱动
Strongly Powered by AbleSci AI