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Discerning Roles of Interfacial Model and Solid Electrolyte Interphase Layer for Stabilizing Antimony Anode in Lithium-Ion Batteries

Authors
Sun, QujiangCao, ZhenMa, ZhengZhang, JunliWahyudi, WandiCai, TaoCheng, HaoranLi, QianKim, HunXie, ErqingCavallo, LuigiSun, Yang KookMing, Jun
Issue Date
Nov-2022
Publisher
American Chemical Society
Citation
ACS Materials Letters, v.4, no.11, pp.2233 - 2243
Indexed
SCIE
SCOPUS
Journal Title
ACS Materials Letters
Volume
4
Number
11
Start Page
2233
End Page
2243
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/185785
DOI
10.1021/acsmaterialslett.2c00679
ISSN
2639-4979
Abstract
Electrolyte solvation chemistry has attracted great attention since the recent discovery of its effect on the performances of metal-ion batteries. However, it is challenging to discern its decisive influence from the well-known effect of the solid electrolyte interphase (SEI) layer. This issue becomes more complex upon introducing additives into the electrolyte, as the key role of additives in forming the SEI layer or changing the electrolyte solvation structure also become hard to be discerned. Herein, we design a new dimethyl ether-based electrolyte, and then we unravel the effects of solvation chemistry and the SEI on determining electrode performances, such as the antimony (Sb) anode as a promising example for lithium-ion batteries (LIBs). We find that both the unique solvation structure-derived interfacial model and the SEI are necessary to stabilize the Sb anode. The influences of electrolyte components, particularly the lithium difluoro(oxalato)borate additive, were elucidated for the first time by the dynamic molecular behaviors ranging from solvation structure, interfacial model, to microstructure of the SEI. Finally, extremely high performance of the Sb anode with the capacity of 668 mAh g-1, high-rate performance over 5 A g-1, and long cycle life over 100 cycles are obtained, which is superior to that previously reported. This work provides a comprehensive guideline for designing electrolytes via a synergetic approach of solvation structure and the SEI aspects.
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