Rapidly-Formed Interphase Facilitating Fast-Charging Lithium-Ion Batteries

Sluggish lithium-ion (Li+) transport through the electrode–electrolyte interface hinders fast charging of lithium-ion batteries. Contrary to the conventionally slow-formed solid electrolyte interphase (SEI), fast-formed SEI is proposed and evidenced to be beneficial in enhancing the interfacial Li+ transport and thus the fast-charging of the graphite anode. Various characterization techniques including cryogenic transmission electron microscopy, in situ Raman spectroscopy, and gas chromatography are applied to uncover the nanostructure, formation pathways, and stability of SEI layers formed at varied current densities during the formation process. The results show that the rapidly formed SEI layer has more crystalline inorganic components with reduced size (4.4 nm at 5C vs. 8.0 nm at 0.2C), elevated stacking density (33% vs. 12%), thinner (∼7 nm vs. 18 nm), and faster Li+ diffusion. With such a preformed SEI layer, the capacity retention of the LiFePO4||graphite cell is dramatically improved from 65% to 98% at 1C after 400 cycles.

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Publication Details

Journal
ACS Energy Letters
Published
2025-08-30
DOI
https://doi.org/10.1021/acsenergylett.5c02398
Citations
9
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
6.57
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article

Rapidly-Formed Interphase Facilitating Fast-Charging Lithium-Ion Batteries

Chun Zhan, Zhaoxiang Wang, Suting Weng, Lifan Wang et al.
9 citations
ACS Energy Letters
Advancements in Battery Materials
6.57
article

Rapidly-Formed Interphase Facilitating Fast-Charging Lithium-Ion Batteries

Chun Zhan, Zhaoxiang Wang, Suting Weng, Lifan Wang, Yejing Li, Cong Zhong, Xuefeng Wang, Xiaoyun Li, Jiacheng Zhu
article en
9 citations

Abstract

Sluggish lithium-ion (Li+) transport through the electrode–electrolyte interface hinders fast charging of lithium-ion batteries. Contrary to the conventionally slow-formed solid electrolyte interphase (SEI), fast-formed SEI is proposed and evidenced to be beneficial in enhancing the interfacial Li+ transport and thus the fast-charging of the graphite anode. Various characterization techniques including cryogenic transmission electron microscopy, in situ Raman spectroscopy, and gas chromatography are applied to uncover the nanostructure, formation pathways, and stability of SEI layers formed at varied current densities during the formation process. The results show that the rapidly formed SEI layer has more crystalline inorganic components with reduced size (4.4 nm at 5C vs. 8.0 nm at 0.2C), elevated stacking density (33% vs. 12%), thinner (∼7 nm vs. 18 nm), and faster Li+ diffusion. With such a preformed SEI layer, the capacity retention of the LiFePO4||graphite cell is dramatically improved from 65% to 98% at 1C after 400 cycles.

ACS Energy LettersVol. 10(9)
Chinese Academy of Sciences (CN), Energy Storage Systems (United States) (US), FZU ‒ Institute of Physics of the Academy of Sciences of the Czech Republic (CZ), Institute of Metallurgy (RU), Institute of Physics (CN), National Laboratory for Superconductivity (CN), University of Chinese Academy of Sciences (CN), University of Science and Technology Beijing (CN)
Affordable and clean energy
Openalex Percentile: Top 3%
Advancements in Battery Materials
6.57
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