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Fast‐Charging and Ultrahigh‐Capacity Lithium Metal Anode Enabled by Surface Alloying
Author(s) -
Xu Tianhui,
Gao Peng,
Li Peirong,
Xia Kai,
Han Na,
Deng Jun,
Li Yanguang,
Lu Jun
Publication year - 2020
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.201902343
Subject(s) - anode , materials science , cathode , metal , current density , alloy , amorphous solid , foil method , chemical engineering , lithium (medication) , lithium metal , nanotechnology , composite material , metallurgy , electrode , crystallography , electrical engineering , medicine , chemistry , physics , quantum mechanics , endocrinology , engineering
Li metal anodes are going through a great revival but they still encounter grand challenges. One often neglected issue is that most reported Li metal anodes are only cyclable under relatively low current density (<5 mA cm −2 ) and small areal capacity (<5 mAh cm −2 ), which essentially limits their high‐power applications and results in ineffective Li utilization (<1%). Herein, it is reported that surface alloyed Li metal anodes can enable reversible cycling with ultrafast rate and ultralarge areal capacity. Low‐cost Si wafers are used and are chemically etched down to 20–30 µm membranes. Simply laminating a Si membrane onto Li foil results in the formation of Li x Si alloy film fused onto Li metal with mechanical robustness and high Li‐ion conductivity. Symmetric cell measurements show that the surface alloyed Li anode has excellent cycling stability, even under high current density up to 25 mA cm −2 and unprecedented areal capacity up to 100 mAh cm −2 . Furthermore, the surface alloyed Li anode is paired with amorphous MoS 3 cathode and achieves remarkable full‐cell performance.