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Facile ex situ formation of a LiF-polymer composite layer as an artificial SEI layer on Li metal by simple roll-press processing for carbonate electrolyte-based Li metal batteries

Authors
Sun, SehoMyung, SeungcheolKim, GaeunLee, DongsooSon, HyunsuJang, MinchulPark, EunkyungSon, ByoungkukJung, Yeon-GilPaik, UngyuSong, Taeseup
Issue Date
Sep-2020
Publisher
ROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY A, v.8, no.33, pp.17229 - 17237
Journal Title
JOURNAL OF MATERIALS CHEMISTRY A
Volume
8
Number
33
Start Page
17229
End Page
17237
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/89280
DOI
10.1039/d0ta05372d
ISSN
2050-7488
Abstract
Lithium (Li) metal is considered an ideal anode for next-generation Li metal batteries (LMBs). However, Li dendrite formation and low coulombic efficiency (CE) are major obstacles for its practical use in LMBs. The engineering of the interface between Li metal and electrolytes is crucial for better Li ion kinetics and interface stability to overcome the above problems. In this study, we report a thin LiF/defluorinated polymer (LiF@Po) composite as an artificial SEI layer. The LiF@Po composite layer, formed by a facile and scalable roll-pressing process using polytetrafluoroethylene (PTFE) and Li metal, is composed of an inner (lithium side) LiF-rich layer and an outer (electrolyte side) polymer rich (polyene/fluoropolymer) layer. The free space between LiF particles could be conformally filled with a polymeric layer, improving the Li surface coverage properties of the protection layer. This novel LiF@Po protection layer enables highly stable cyclability even in a carbonate-based electrolyte for more than 1000 h at 1 mA cm(-2)in a Li||Li symmetric cell and a cycle retention of 80% capacity for >200 cycles with an extremely stable average CE of 99.7% in a Li||LiCoO(2)full cell. Furthermore, this LiF@Po protection layer could significantly enhance the cyclability and reversible capacity in a Li||LiNi0.8Co0.1Mn0.1O2(NCM-811) full cell.
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