电解质
阴极
金属锂
容量损失
锂(药物)
储能
电化学
图层(电子)
金属
材料科学
剥离(纤维)
相间
化学
化学工程
纳米技术
复合材料
物理
生物
冶金
电极
阳极
物理化学
工程类
量子力学
内分泌学
医学
功率(物理)
遗传学
作者
Mengyu Tian,Ronghan Qiao,Guanjun Cen,Tian Li,Liubin Ben,Hailong Yu,Michaël De Volder,Chenglong Zhao,Qidi Wang,Xuejie Huang
标识
DOI:10.1038/s41467-025-62163-5
摘要
Pairing high-energy nickel-rich cathodes with current collectors as anodes presents a compelling strategy to significantly boost the specific energy of rechargeable lithium-ion batteries, driving progress toward a transportation revolution. However, the limited active lithium inventory sourced by the cathodes tend to be rapidly consumed by irreversible Li plating/stripping and interfacial side reactions. To address these limitations, we propose a dual-gradient metal layer as an innovative solution to mitigate active Li loss by promoting uniform Li deposition and in situ formation of a stable solid electrolyte interphase. The operation of these batteries is investigated using a combination of electrochemical and chemical techniques to differentiate dead Li and interphase-bound Li inventory loss as well as material characterization methods to analyse the plated Li and interfacial composition and morphology. The developed dual gradient metal layer-based 600 mAh LiNi0.9Co0.05Mn0.05O2 | |Cu pouch cells achieve an areal capacity of 7.25 mAh cm-2 and deliver an 80% capacity retention over 160 cycles. We show that the proposed approach is compatible with a range of different metal materials, offering a promising path toward next generation long-lasting, high-energy, initially active material-free anode based Li metal batteries.
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