Self-terminating, heterogeneous solid–electrolyte interphase enables reversible Li–ether cointercalation in graphite anodes

Author:

Xia Dawei1,Jeong Heonjae234,Hou Dewen56,Tao Lei1ORCID,Li Tianyi7ORCID,Knight Kristin1,Hu Anyang1,Kamphaus Ethan P.3,Nordlund Dennis8,Sainio Sami8,Liu Yuzi6,Morris John R.1ORCID,Xu Wenqian7,Huang Haibo9,Li Luxi7,Xiong Hui5ORCID,Cheng Lei23ORCID,Lin Feng110ORCID

Affiliation:

1. Department of Chemistry, Virginia Tech, Blacksburg, VA 24061

2. Joint Center for Energy Storage Research, Argonne National Laboratory, Lemont, IL 60439

3. Materials Science Division, Argonne National Laboratory, Lemont, IL 60439

4. Department of Electronic Engineering, Gachon University, Sujeong-gu, Seongnam-si, Gyeonggi-do 13120, South Korea

5. Micron School of Materials Science and Engineering, Boise State University, Boise, ID 83725

6. Center for Nanoscale Materials, Argonne National Laboratory, Lemont, IL 60439

7. X-ray Science Division, Argonne National Laboratory, Lemont, IL 60439

8. Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, Menlo Park, CA 94025

9. Department of Food Science and Technology, Virginia Tech, Blacksburg, VA 24061

10. Department of Materials Science and Engineering, Virginia Tech, Blacksburg, VA 24061

Abstract

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 LiBF 4 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.

Funder

USDA | National Institute of Food and Agriculture

U.S. Department of Energy

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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