阳极
化学工程
金属
对偶(语法数字)
锂(药物)
材料科学
化学
金属锂
组合化学
图层(电子)
纳米技术
电极
生物
物理化学
有机化学
艺术
文学类
内分泌学
工程类
作者
Yue Ma,Feng Wu,Nan Chen,Tianyu Yang,Yaohui Liang,Zhaoyang Sun,Guangqiu Luo,Jianguo Du,Yanxin Shang,Mai Feng,Ziyue Wen,Li Li,Renjie Chen
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2022-08-15
卷期号:27 (16): 5199-5199
被引量:6
标识
DOI:10.3390/molecules27165199
摘要
Solid electrolyte interphase (SEI) on a Li anode is critical to the interface stability and cycle life of Li metal batteries. On the one hand, components of SEI with the passivation effect can effectively hinder the interfacial side reactions to promote long-term cycling stability. On the other hand, SEI species that exhibit the active site effect can reduce the Li nucleation barrier and guide Li deposition homogeneously. However, strategies that only focus on a separated effect make it difficult to realize an ideal overall performance of a Li anode. Herein, a dual functional artificial SEI layer simultaneously combining the passivation effect and the active site effect is proposed and constructed via a facial surface chemistry method. Simultaneously, the formed LiF component effectively passivates the anode/electrolyte interface and contributes to the long-term stable cycling performance, while the Li-Mg solid solution alloy with the active site effect promotes the transmission of Li+ and guides homogeneous Li deposition with a low energy barrier. Benefiting from these advantages, the Li||Li cell with the modified anode performs with a lower nucleation overpotential of 2.3 mV, and an ultralong cycling lifetime of over 2000 h at the current density of 1 mA cm-2, while the Li||LiFePO4 full battery maintains a capacity retention of 84.6% at rate of 1 C after 300 cycles.
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