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Tailoring Lithium Deposition via an SEI‐Functionalized Membrane Derived from LiF Decorated Layered Carbon Structure
Author(s) -
Wang Muqin,
Peng Zhe,
Luo Wenwei,
Ren Feihong,
Li Zhendong,
Zhang Qiang,
He Haiyong,
Ouyang Chuying,
Wang Deyu
Publication year - 2019
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.201802912
Subject(s) - materials science , anode , chemical engineering , electrolyte , lithium (medication) , graphene , plating (geology) , deposition (geology) , carbon fibers , surface modification , membrane , coating , nanotechnology , electrode , composite number , composite material , chemistry , medicine , paleontology , biochemistry , sediment , geophysics , geology , engineering , biology , endocrinology
Lithium (Li) metal is a key anode material for constructing next generation high energy density batteries. However, dendritic Li deposition and unstable solid electrolyte interphase (SEI) layers still prevent practical application of Li metal anodes. In this work, it is demonstrated that an uniform Li coating can be achieved in a lithium fluoride (LiF) decorated layered structure of stacked graphene (SG), leading to the formation of an SEI‐functionalized membrane that retards electron transfer by three orders of magnitude to avoid undesirable Li deposition on the top surface, and ameliorates Li + ion migration to enable uniform and dendrite‐free Li deposition beneath such an interlayer. Surface chemistry analysis and density functional theory calculations demonstrate that these beneficial features arise from the formation of C–F x surface components on the SG sheets during the Li coating process. Based on such an SEI‐functionalized membrane, stable cycling at high current densities up to 3 mA cm −2 and Li plating capacities up to 4 mAh cm −2 can be realized in LiPF 6 /carbonate electrolytes. This work elucidates the promising strategy of modifying Li plating behavior through the SEI‐functionalized carbon structure, with significantly improved cycling stability of rechargeable Li metal anodes.