A robust interface enabled by electrospun membrane with optimal resistance in lithium metal batteries

被引:18
作者
Dong, Chen [1 ]
Lin, Zhenkang [1 ]
Yin, Yuxin [1 ]
Qiao, Yaoxuan [1 ]
Wang, Wei [1 ]
Wu, Qibing [2 ]
Yang, Chengxiang [2 ]
Rooney, David [1 ,3 ]
Fan, Cheng [1 ]
Sun, Kening [1 ,2 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, Beijing Key Lab Chem Power Source & Green Catalys, Beijing 100081, Peoples R China
[2] Guizhou Meiling Power Sources Co Ltd, State Key Lab Adv Chem Power Sources, Zunyi 563003, Guizhou, Peoples R China
[3] Queens Univ Belfast, Sch Chem & Chem Engn, Belfast BT9 5AG, Antrim, North Ireland
来源
JOURNAL OF ENERGY CHEMISTRY | 2021年 / 55卷 / 55期
关键词
Lithium metal battery; Dendrite-free; Interfacial stability; Uniform diffusion layer; Deposition site; SOLID-ELECTROLYTE INTERPHASE; DENDRITE GROWTH; ION BATTERIES; RECHARGEABLE BATTERIES; ANODE; LAYER; MATRIX; FABRICATION; DEPOSITION; FILM;
D O I
10.1016/j.jechem.2020.06.060
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A uniform diffusion layer is essential for non-dendritic deposition of lithium in high-density lithium batteries. However, natural pristine solid electrolyte interface (SEI) is always porous and inhomogeneous because of repeated breakdown and repair cycles, whereas ideal materials with excellent mechanical property for artificial SEIs remain a challenge. Herein, a robust and stable interface is achieved by spinning soft polymer associated with few MoO3 into fibers, and thus mechanical property of fibers other than materials determines mechanical performance of the interface which can be optimized by adjusting parameters. Furthermore, lithium deposited underneath the layer is enabled by constructing an optimal resistance to make the membrane serve as an artificial SEI rather than lithium host. As a result, dendrite-free lithium was observed underneath the membrane, and stable interface for long-term cycling was also indicated by EIS measurements. The lithium iron phosphate (LiFePO4) full-cell with coated electrode demonstrated an initial capacity of 155.2 mAh g(-1), and 80% of its original capacity was retained after 500 cycles at 2.0 degrees C without any additive in carbonate-based electrolyte. (C) 2020 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
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