阳极
电解质
相间
化学
电化学
电池(电)
催化作用
储能
枝晶(数学)
钠
金属
化学工程
纳米技术
材料科学
电极
有机化学
冶金
工程类
物理化学
功率(物理)
物理
生物
量子力学
遗传学
数学
几何学
作者
Wenping Sun,Chongyang Hao,Xiaomin Zhang,Zixu He,Mingxia Gao,Yongfeng Liu,Hongge Pan
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-03-27
卷期号:64 (23): e202503691-e202503691
被引量:22
标识
DOI:10.1002/anie.202503691
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 (∼ 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.
科研通智能强力驱动
Strongly Powered by AbleSci AI