Robust Solid Electrolyte Interphase Engineered by Catalysis Chemistry Toward Durable Anode-Free Sodium Metal Batteries

被引:0
|
作者
Hao, Chongyang [1 ]
Zhang, Xiaomin [1 ]
He, Zixu [2 ]
Gao, Mingxia [1 ]
Liu, Yongfeng [1 ]
Pan, Hongge [1 ,3 ]
Sun, Wenping [1 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, Hangzhou 310058, Peoples R China
[2] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Sch Chem & Mat Sci, Hefei 230026, Peoples R China
[3] Xian Technol Univ, Inst Sci & Technol New Energy, Xian 710021, Peoples R China
基金
中国国家自然科学基金;
关键词
Catalysis chemistry; Dendrite; Sodium deposition; Sodium metal batteries; Solid electrolyte interphase;
D O I
10.1002/anie.202503691
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 (similar to 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.
引用
收藏
页数:10
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