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Revealing the Role of Fluoride‐Rich Battery Electrode Interphases by Operando Transmission Electron Microscopy
Author(s) -
Gong Chen,
Pu Shengda D.,
Gao Xiangwen,
Yang Sixie,
Liu Junliang,
Ning Ziyang,
Rees Gregory J.,
Capone Isaac,
Pi Liquan,
Liu Boyang,
Hartley Gareth O.,
Fawdon Jack,
Luo Jun,
Pasta Mauro,
Grovenor Chris R. M.,
Bruce Peter G.,
Robertson Alex W.
Publication year - 2021
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.202003118
Subject(s) - lithium fluoride , electrolyte , materials science , fluoride , electrode , dissolution , transmission electron microscopy , lithium (medication) , stripping (fiber) , chemical engineering , battery (electricity) , inorganic chemistry , nanotechnology , chemistry , composite material , medicine , power (physics) , physics , quantum mechanics , endocrinology , engineering
The solid electrolyte interphase (SEI), a complex layer that forms over the surface of electrodes exposed to battery electrolyte, has a central influence on the structural evolution of the electrode during battery operation. For lithium metallic anodes, tailoring this SEI is regarded as one of the most effective avenues for ensuring consistent cycling behavior, and thus practical efficiencies. While fluoride‐rich interphases in particular seem beneficial, how they alter the structural dynamics of lithium plating and stripping to promote efficiency remains only partly understood. Here, operando liquid‐cell transmission electron microscopy is used to investigate the nanoscale structural evolution of lithium electrodeposition and dissolution at the electrode surface across fluoride‐poor and fluoride‐rich interphases. The in situ imaging of lithium cycling reveals that a fluoride‐rich SEI yields a denser Li structure that is particularly amenable to uniform stripping, thus suppressing lithium detachment and isolation. By combination with quantitative composition analysis via mass spectrometry, it is identified that the fluoride‐rich SEI suppresses overall lithium loss through drastically reducing the quantity of dead Li formation and preventing electrolyte decomposition. These findings highlight the importance of appropriately tailoring the SEI for facilitating consistent and uniform lithium dissolution, and its potent role in governing the plated lithium's structure.

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