电解质
离子液体
双功能
二甲氧基乙烷
阳极
化学工程
阴极
离子电导率
化学
锂(药物)
材料科学
溶剂
无机化学
有机化学
电极
物理化学
工程类
内分泌学
医学
催化作用
作者
Sufu Liu,Sufu Liu,Tao Deng,Fuqiang Huang,Jiaxun Zhang,Xinzi He,Xiao Ji,Xiayin Yao,Chunsheng Wang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2021-02-05
卷期号:6 (3): 862-868
被引量:136
标识
DOI:10.1021/acsenergylett.0c02617
摘要
Li10GeP2S12 (LGPS) has a high ionic conductivity and compatibility with sulfur cathodes; however, the instability of LGPS against Li and Li dendrite growth still remains unsolved. Here, we solved these two challenges by forming a lithiophilic–lithiophobic gradient interlayer interphase layer between Li and LGPS through the sequential reduction of salts and solvent in Mg(TFSI)2-LiTFSI-DME liquid electrolyte at the LGPS/Li interface (TFSI = bis(trifluoromethanesulfonyl)imide; DME = dimethoxyethane). Mg(TFSI)2-LiTFSI is first reduced, forming a lithiophilic LixMg alloy-rich layer on the lithium surface and a lithiophobic LiF-rich layer on top of LixMg due to the lithiophobicity difference. The later reduced DME solvent forms a flexible organic polymer between the LiF-rich layer and LGPS. After evaporation of DME solvent, the Li/LGPS/Ni-Li2S-LiTiS2 all-solid-state battery shows a reversible capacity of 699.7 mAh g–1 (1.07 mAh cm–2) based on the mass of Ni-Li2S-LiTiS2 at 100 mA g–1 (0.26 mA cm–2). The rational design of a solid electrolyte interface between a Li anode and LGPS electrolyte opens a new opportunity to develop high-performance all-solid-state lithium batteries.
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