金属锂
相间
锂(药物)
材料科学
电介质
离子
金属
纳米技术
电极
工程物理
光电子学
化学
电解质
物理
冶金
物理化学
内分泌学
生物
医学
有机化学
遗传学
作者
Guo Ai,Xiaojuan Lian,Zhipeng Hu,Yong Lyu,Tiande Mo,Xiaochen Zhao,Xinggang Hou,Meng Sun,Hui Zhao,Ting Zhang,Wenfeng Mao
标识
DOI:10.1016/j.jcis.2024.11.058
摘要
The poor stability and slow lithium ion (Li+) transfer kinetics of solid electrolyte interphase (SEI) pose significant challenges to lithium (Li) metal batteries. Although various SEI-related strategies have been developed, the Li+ transport properties and uniform Li deposition still require substantial improvement for fast-charging applications. Herein, we introduce a dielectric, single-ion-conductive artificial SEI (DS-SEI) composed of lithiated Nafion and BaTiO3 (BTO) nanoceramics to address these issues. The lithiated Nafion stabilizes the Li anode with its elastic F-rich components and facilitates fast, single Li+ conduction through its anion-anchored structure. The high-dielectric BTO dynamically homogenizes the electric field (E-field) to promote uniform Li deposition, synergistically enhancing intrinsic single Li+ conductivity and Li+ desolvation/diffusion kinetics, thereby enabling fast charging of the Li anode. Consequently, the DS-SEI protected Li anode can cycle over 6800 h in a Li||Li cell at 10 mA cm-2/5 mAh cm-2, over 400 cycles in a 2.75 mAh cm-2 Li||LiFePO4 cell at 1C, with 83.0 % capacity retention at 6C (16.5 mA cm-2), and maintain stable cycling in a 5.62 mAh cm-2 Li||Li6PS5Cl|| LiNi0.8Co0.1Mn0.1O2 all solid-state cell. Our findings provide insights into the interfacial regulation of Li anode, paving the way for fast-charging Li metal batteries.
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