电解质
阳极
金属锂
锂(药物)
电化学
材料科学
金属
二甲醚
电极
化学工程
化学
有机化学
物理化学
催化作用
冶金
内分泌学
工程类
医学
作者
Changfei Zou,Li Yang,Kaili Luo,Lei Liu,Xiyuan Tao,Lingguang Yi,Xianhu Liu,Xiaoyan Zhang,Xianyou Wang
标识
DOI:10.1021/acsaem.2c00971
摘要
Due to the advantages of high safety and high energy density, solid-state lithium batteries (SSLBs) are promising competitors for next-generation batteries. Unfortunately, the growth of Li dendrites and irreversible capacity loss caused by the Li metal anode/solid electrolyte interfacial incompatibility remain challenges. Herein, an in situ formed artificial protective layer between the lithium metal anode and solid electrolyte Li6PS5Cl (LPSC) is introduced. A stable solid electrolyte interface (SEI) is in situ formed in the Li/Li6PS5Cl interface via the electrochemical reduction of the liquid electrolyte LiTFSI/tetraethylene glycol dimethyl ether (Li(G4)TFSI), which is beneficial for the improvement of the stability of interfacial chemistry and homogeneous lithium deposition behavior. The assembled Li/Li(G4)TFSI-assisted Li6PS5Cl/Li symmetric cells enable stable cycles for 850 and 400 h at a current density of 0.1 and 0.2 mA/cm2, respectively. Moreover, the LiNi0.6Co0.1Mn0.3O2(NCM613)/Li(G4)TFSI-assisted Li6PS5Cl/Li SSLBs can achieve prominent cycling stability at room temperature. This work provides a new insight into the interfacial modification to design SSLBs with high energy density.
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