TY - JOUR
T1 - Self-terminating, heterogeneous solid–electrolyte interphase enables reversible Li–ether cointercalation in graphite anodes
AU - Xia, Dawei
AU - Jeong, Heonjae
AU - Hou, Dewen
AU - Tao, Lei
AU - Li, Tianyi
AU - Knight, Kristin
AU - Hu, Anyang
AU - Kamphaus, Ethan P.
AU - Nordlund, Dennis
AU - Sainio, Sami
AU - Liu, Yuzi
AU - Morris, John R.
AU - Xu, Wenqian
AU - Huang, Haibo
AU - Li, Luxi
AU - Xiong, Hui
AU - Cheng, Lei
AU - Lin, Feng
N1 - Publisher Copyright:
Copyright © 2024 the Author(s).
PY - 2024/1/30
Y1 - 2024/1/30
N2 - Ether solvents are suitable for formulating solid-electrolyte interphase (SEI)-less ion-solvent cointercalation electrolytes in graphite for Na-ion and K-ion batteries. However, ether-based electrolytes have been historically perceived to cause exfoliation of graphite and cell failure in Li-ion batteries. In this study, we develop strategies to achieve reversible Li–solvent cointercalation in graphite through combining appropriate Li salts and ether solvents. Specifically, we design 1M LiBF4 1,2-dimethoxyethane (G1), which enables natural graphite to deliver ~91% initial Coulombic efficiency and >88% capacity retention after 400 cycles. We captured the spatial distribution of LiF at various length scales and quantified its heterogeneity. The electrolyte shows self-terminated reactivity on graphite edge planes and results in a grainy, fluorinated pseudo-SEI. The molecular origin of the pseudo-SEI is elucidated by ab initio molecular dynamics (AIMD) simulations. The operando synchrotron analyses further demonstrate the reversible and monotonous phase transformation of cointercalated graphite. Our findings demonstrate the feasibility of Li cointercalation chemistry in graphite for extreme-condition batteries. The work also paves the foundation for understanding and modulating the interphase generated by ether electrolytes in a broad range of electrodes and batteries.
AB - Ether solvents are suitable for formulating solid-electrolyte interphase (SEI)-less ion-solvent cointercalation electrolytes in graphite for Na-ion and K-ion batteries. However, ether-based electrolytes have been historically perceived to cause exfoliation of graphite and cell failure in Li-ion batteries. In this study, we develop strategies to achieve reversible Li–solvent cointercalation in graphite through combining appropriate Li salts and ether solvents. Specifically, we design 1M LiBF4 1,2-dimethoxyethane (G1), which enables natural graphite to deliver ~91% initial Coulombic efficiency and >88% capacity retention after 400 cycles. We captured the spatial distribution of LiF at various length scales and quantified its heterogeneity. The electrolyte shows self-terminated reactivity on graphite edge planes and results in a grainy, fluorinated pseudo-SEI. The molecular origin of the pseudo-SEI is elucidated by ab initio molecular dynamics (AIMD) simulations. The operando synchrotron analyses further demonstrate the reversible and monotonous phase transformation of cointercalated graphite. Our findings demonstrate the feasibility of Li cointercalation chemistry in graphite for extreme-condition batteries. The work also paves the foundation for understanding and modulating the interphase generated by ether electrolytes in a broad range of electrodes and batteries.
KW - Li-ion batteries
KW - cointercalation
KW - ether electrolytes
KW - graphite anode
KW - solid-electrolyte interphase
UR - http://www.scopus.com/inward/record.url?scp=85183333340&partnerID=8YFLogxK
U2 - 10.1073/pnas.2313096121
DO - 10.1073/pnas.2313096121
M3 - Article
C2 - 38261613
AN - SCOPUS:85183333340
SN - 0027-8424
VL - 121
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 5
M1 - e2313096121
ER -