材料科学
法拉第效率
阳极
电解质
锂(药物)
离子电导率
阴极
二甲氧基乙烷
金属
无机化学
化学工程
电极
冶金
化学
物理化学
内分泌学
工程类
医学
作者
Kaiqiang Qin,Jacqueline V. Nguyen,Zhenzhen Yang,Chao Luo
标识
DOI:10.1016/j.mtener.2022.101199
摘要
The durability of anode-free Li metal batteries is largely limited by the undesired Li plating/stripping irreversibility on the current collector due to the infinite volume change, uncontrollable Li dendrite growth, and continuous parasitic reactions between Li metal and the electrolyte. To address these challenges, the formation of a stable and robust solid electrolyte interphase (SEI) with high ionic conductivity and strong mechanical strength is critical. Here, we developed an advanced electrolyte by introducing LiNO3 into the localized high concentration electrolyte (LHCE) with lithium bis(fluorosulfonyl)imide (LiFSI) salt, 1,2-dimethoxyethane (DME) solvent, and 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropylether (TFTE) diluent to in situ construct a LiF and LixNyOz co-enriched passivation layer on the Cu current collector. The synergetic effect of the high mechanical strength of LiF and high ionic conductivity of LixNyOz endows the Li metal anode with a high Coulombic efficiency (CE) of 99.35%. An anode-free Li metal pouch cell using LiFePO4 (LFP) as a cathode holds an exceptionally improved capacity retention under the charging/discharging rate of 1/3 C, demonstrating great promise for developing dendrite-free and safe Li metal batteries.
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