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Robust Solid Electrolyte Interphase Engineered by Catalysis Chemistry Toward Durable Anode‐Free Sodium Metal Batteries
Author(s) -
Hao Chongyang,
Zhang Xiaomin,
He Zixu,
Gao Mingxia,
Liu Yongfeng,
Pan Hongge,
Sun Wenping
Publication year - 2025
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202503691
Subject(s) - anode , electrolyte , interphase , catalysis , electrochemistry , battery (electricity) , chemical engineering , materials science , energy storage , dendrite (mathematics) , sodium , nanotechnology , metal , chemistry , electrode , metallurgy , organic chemistry , power (physics) , physics , geometry , mathematics , quantum mechanics , genetics , engineering , biology
Abstract Anode‐free sodium metal batteries (AFSMBs) are considered one of the most promising large‐scale energy storage systems due to their extremely high energy density. Nonetheless, their practical application is hindered by the uncontrolled growth of sodium dendrites. Constructing a mechanically robust solid electrolyte interphase (SEI) is an effective strategy to suppress dendrite formation. Herein, we report a catalysis chemistry approach to construct an ultra‐thin (∼ 5 nm), NaF‐rich and high‐strength (203 MPa) SEI layer by introducing Ru catalytic sites on the current collector, which promotes rapid Na⁺ diffusion and effectively inhibits dendrite growth. Benefiting from this design, the Ru modified‐Cu//Na asymmetric cells exhibit exceptional cycling stability over 2000 h (1000 cycles at 2 mA cm −2 , 2 mAh cm −2 ). Furthermore, the AFSMBs with Ru modified‐Cu current collector also deliver excellent cycling performance and maintains nearly 98.1% capacity retention after 100 cycles at 0.5 C. The results demonstrate great potential of catalysis chemistry in developing advanced sodium metal anodes and provide a new perspective to engineering efficient SEI toward battery applications.
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