电解质
稀释剂
二甲氧基乙烷
法拉第效率
阳极
钝化
材料科学
金属
惰性
阴极
化学工程
化学
纳米技术
冶金
电极
物理化学
核化学
有机化学
工程类
图层(电子)
作者
Junbo Zhang,Haikuo Zhang,Ruhong Li,Ling Lv,Di Lu,Shuo‐Qing Zhang,Xuezhang Xiao,Shujiang Geng,Fuhui Wang,Tao Deng,Lixin Chen,Xiulin Fan
标识
DOI:10.1016/j.jechem.2022.11.013
摘要
Passivation by the inorganic-rich solid electrolyte interphase (SEI), especially the LiF-rich SEI, is highly desirable to guarantee the durable lifespan of Li metal batteries (LMBs). Here, we report a diluent with the capability to facilitate the formation of LiF-rich SEI while avoiding the excess consumption of Li salts. Dissimilar to most of reported inert diluents, heptafluoro-1-methoxypropane (HM) is firstly demonstrated to cooperate with the decomposition of anions to generate LiF-rich SEI via releasing F-containing species near Li surface. The designed electrolyte consisting of 1.8 M LiFSI in the mixture of 1,2-dimethoxyethane (DME)/HM (2:1 by vol.) achieves excellent compatibility with both Li metal anodes (Coulombic efficiency ∼ 99.8%) and high-voltage cathodes (4.4 V LiNi0.8Mn0.1Co0.1O2 (NMC811) and 4.5 V LiCoO2 (LCO) vs Li+/Li). The 4.4 V Li (20 μm)||NMC811 (2.5 mA h cm−2) and 4.5 V Li (20 μm)||LCO (2.5 mA h cm−2) cells achieve capacity retentions of 80% over 560 cycles and 80% over 505 cycles, respectively. Meanwhile, the anode-free pouch cell delivers an energy density of ∼293 W h kg−1 initially and retains 70% of capacity after 100 deep cycles. This work highlights the critical impact of diluent on the SEI formation, and opens up a new direction for designing desirable interfacial chemistries to enable high-performance LMBs.
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