TY - JOUR
T1 - Stabilizing a Lithium Metal Battery by an in Situ Li2S-modified Interfacial Layer via Amorphous-Sulfide Composite Solid Electrolyte
AU - Lai, Chen
AU - Shu, Chengyong
AU - Li, Wei
AU - Wang, Liu
AU - Wang, Xiaowei
AU - Zhang, Tianran
AU - Yin, Xuesong
AU - Ahmad, Iqbal
AU - Li, Mingtao
AU - Tian, Xiaolu
AU - Yang, Pu
AU - Tang, Wei
AU - Miao, Naihua
AU - Zheng, Guangyuan Wesley
N1 - Publisher Copyright:
© 2020 American Chemical Society. All rights reserved.
PY - 2020/11/11
Y1 - 2020/11/11
N2 - A novel strategy has been proposed to produce in situ Li2S at the interfacial layer between lithium anode and the solid electrolyte, by using an amorphous-sulfide-LiTFSI-poly(vinylidene difluoride) (PVDF) composite solid electrolyte (SLCSE). Besides retarding the decomposition of PVDF in CSE, the Li2S-modified interfacial layer (SMIL) also improves the wettability between lithium metal and SLCSE which in turn optimizes the lithium deposition process. Our density functional theory calculation results reveal that the migration energy barrier of Li passing through SMIL is much lower than that of Li passing through LiF-modified interfacial layer (FMIL) formed from the decomposition of PVDF. The as-prepared SLCSE shows a Li ionic transference number of 0.44 and Li ion conductivity of 3.42 × 10-4 S/cm at room temperature, and the Li||SLCSE||LiFePO4 cell exhibits an outstanding rate performance with a capacity of 153, 144, 131, and 101 mAh/g at a current density of 0.05, 0.10, 0.25, and 0.50 mA/cm2, respectively.
AB - A novel strategy has been proposed to produce in situ Li2S at the interfacial layer between lithium anode and the solid electrolyte, by using an amorphous-sulfide-LiTFSI-poly(vinylidene difluoride) (PVDF) composite solid electrolyte (SLCSE). Besides retarding the decomposition of PVDF in CSE, the Li2S-modified interfacial layer (SMIL) also improves the wettability between lithium metal and SLCSE which in turn optimizes the lithium deposition process. Our density functional theory calculation results reveal that the migration energy barrier of Li passing through SMIL is much lower than that of Li passing through LiF-modified interfacial layer (FMIL) formed from the decomposition of PVDF. The as-prepared SLCSE shows a Li ionic transference number of 0.44 and Li ion conductivity of 3.42 × 10-4 S/cm at room temperature, and the Li||SLCSE||LiFePO4 cell exhibits an outstanding rate performance with a capacity of 153, 144, 131, and 101 mAh/g at a current density of 0.05, 0.10, 0.25, and 0.50 mA/cm2, respectively.
KW - amorphous sulfide
KW - composite solid electrolyte
KW - interfacial layer
KW - lithium metal batteries
UR - https://www.scopus.com/pages/publications/85095819656
U2 - 10.1021/acs.nanolett.0c03395
DO - 10.1021/acs.nanolett.0c03395
M3 - 文章
C2 - 33108209
AN - SCOPUS:85095819656
SN - 1530-6984
VL - 20
SP - 8273
EP - 8281
JO - Nano Letters
JF - Nano Letters
IS - 11
ER -