锂(药物)
电极
盐(化学)
离子
材料科学
能量密度
化学
工程物理
物理
医学
有机化学
内分泌学
物理化学
作者
Yangtao Ou,Bao Zhang,Renming Zhan,Shiyu Liu,Wenyu Wang,Shuibin Tu,Yang Hu,Zihe Chen,Xiangrui Duan,Xiancheng Wang,Li Wang,Yongming Sun
标识
DOI:10.1038/s41467-025-63257-w
摘要
The substantial consumption of lithium ions and sluggish reaction kinetics at the anode detrimentally impact the deliverable energy and fast-charging capability of lithium-ion batteries with silicon-based anodes. The prevailing contact prelithiation method using an electrolyte medium can replenish the active lithium, but it may cause materials/electrode instability and bring barrier for lithium-ion transport. Here we explore a contact prelithiation methodology employing cyclic carbonate mediums that can enable spatially and temporally uniform prelithiation reaction. These mediums enable a delicate equilibrium between a lithium-ion diffusion and the intrinsic prelithiation reaction rate throughout the electrode depth. Not only does this prelithiation method serve the fundamental purpose of tackling lithium loss issue, but it also fosters the creation of a solid electrolyte interphase with favorable lithium-ion transport properties. By utilizing fluoroethylene carbonate as the medium for anode contact prelithiation, an Ah-level laminated Si/C||LiCoO2 pouch cell shows a significant enhancement in cell-level energy density by 42.7%. Moreover, a Si/C||LiCoO2 pouch cell achieves an 80.9% capacity utilization at a fast-charging rate of 10 C (6 min) and exhibits a low capacity decay rate of 0.047% per cycle. Such a prelithiation method demonstrates versatility across various cyclic carbonate mediums, electrodes, and scalability for industrial applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI