TY - JOUR
T1 - Ultra-thin and Mechanically Stable LiCoO2-Electrolyte Interphase Enabled by Mg2+ Involved Electrolyte
AU - Liu, Pei
AU - Huang, Tao
AU - Xiao, Biwei
AU - Zou, Lianfeng
AU - Wang, Kai
AU - Wang, Kuan
AU - Wang, Kai
AU - Yao, Xiangming
AU - Liu, Yuying
AU - Huang, Zhencheng
AU - Wang, Hongbin
AU - Liu, Mijie
AU - Ren, Xiaodi
AU - Ren, Xiangzhong
AU - Ouyang, Xiaoping
AU - Liu, Jianhong
AU - zhang, Qianling
AU - Hu, Jiangtao
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2024/7/11
Y1 - 2024/7/11
N2 - LiCoO2 (LCO) cathode materials have attracted significant attention for its potential to provide higher energy density in current Lithium-ion batteries (LIBs). However, the structure and performance degradation are exacerbated by increasing voltage due to the catastrophic reaction between the applied electrolyte and delithiated LCO. The present study focuses on the construction of physically and chemically robust Mg-integrated cathode-electrolyte interface (MCEI) to address this issue, by incorporating Magnesium bis(trifluoromethanesulfonyl)imide (Mg[TFSI]2) as an electrolyte additive. During formation cycles, the strong MCEI is formed and maintained its 2 nm thickness throughout long-term cycling. Notably, Mg is detected not only in the robust MCEI, but also imbedded in the surface of the LCO lattice. As a result, the parasitic interfacial side reactions, surface phase reconstruction, particle cracking, Co dissolution and shuttling are considerably suppressed, resulting in long-term cycling stability of LCO up to 4.5 V. Therefore, benefit from the double protection of the strong MCEI, the Li||LCO coin cell and the Ah-level Graphite||LCO pouch cell exhibit high capacity retention by using Mg-electrolyte, which are 88.13% after 200 cycles and 90.4% after 300 cycles, respectively. This work provides a novel approach for the rational design of traditional electrolyte additives.
AB - LiCoO2 (LCO) cathode materials have attracted significant attention for its potential to provide higher energy density in current Lithium-ion batteries (LIBs). However, the structure and performance degradation are exacerbated by increasing voltage due to the catastrophic reaction between the applied electrolyte and delithiated LCO. The present study focuses on the construction of physically and chemically robust Mg-integrated cathode-electrolyte interface (MCEI) to address this issue, by incorporating Magnesium bis(trifluoromethanesulfonyl)imide (Mg[TFSI]2) as an electrolyte additive. During formation cycles, the strong MCEI is formed and maintained its 2 nm thickness throughout long-term cycling. Notably, Mg is detected not only in the robust MCEI, but also imbedded in the surface of the LCO lattice. As a result, the parasitic interfacial side reactions, surface phase reconstruction, particle cracking, Co dissolution and shuttling are considerably suppressed, resulting in long-term cycling stability of LCO up to 4.5 V. Therefore, benefit from the double protection of the strong MCEI, the Li||LCO coin cell and the Ah-level Graphite||LCO pouch cell exhibit high capacity retention by using Mg-electrolyte, which are 88.13% after 200 cycles and 90.4% after 300 cycles, respectively. This work provides a novel approach for the rational design of traditional electrolyte additives.
KW - LiCoO cathode
KW - electrolyte additives
KW - high energy density
KW - magnesium-integrated CEI
KW - pouch cell
UR - https://www.scopus.com/pages/publications/85183890189
U2 - 10.1002/smll.202311520
DO - 10.1002/smll.202311520
M3 - 文章
AN - SCOPUS:85183890189
SN - 1613-6810
VL - 20
JO - Small
JF - Small
IS - 28
M1 - 2311520
ER -