过电位
法拉第效率
材料科学
成核
钠
碳纤维
纳米技术
枝晶(数学)
化学工程
电化学
碳纳米纤维
金属
储能
合金
纳米纤维
阳极
寄主(生物学)
多孔性
导电体
同种类的
剥离(纤维)
脚手架
碳纳米管
工作(物理)
作者
Bo Yan,Linxuan Liu,Xiaojing Liu,Yilong Yu,Wei Wang,Xiao Wei,Daping Qiu,Yahao Li,Lulu Zhang,Xuelin Yang,Xifei Li,Renheng Wang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-02-16
卷期号:20 (8): 7105-7116
被引量:1
标识
DOI:10.1021/acsnano.5c19488
摘要
Constructing self-supporting, sodiophilic scaffolds to suppress inactive "dead sodium" accumulation and subsequent dendrite growth is crucial for the advancement of rechargeable sodium metal batteries. However, uniformly incorporating sodiophilic species into conductive scaffolds while maintaining sufficient buffer space to spatially regulate Na plating/stripping reversibility remains a formidable challenge. Herein, we report a three-dimensional multifunctional host featuring cucurbit-shaped nitrogen-doped carbon nanofibers uniformly embedded within pomegranate-like porous ZnNi alloys (Zn/Ni@NCF). Benefiting from its precisely engineered structure and composition, the Zn/Ni@NCF host enables an ultralow nucleation overpotential (as low as 8 mV), a high average Coulombic efficiency (>99.6% over 1100 cycles), and stable long-term cycling performance (>3200 h in symmetric cells), showing favorable electrochemical behavior compared with representative reported sodium metal anodes. Combined theoretical calculations and in situ/exsitu visualizations reveal that the outstanding performance originates from the high Na-binding energy of the alloy seeds, homogeneous Na-ion flux, and spatial confinement effect, which synergistically suppress dead sodium formation and dendrite growth. When this tailored host is integrated into anode-less full cells, the cells achieve 90.4% capacity retention after 200 cycles at 1C (surpassing control cells by more than 8-fold), while anode-free pouch cells exhibit impressive capacity and stability even under high current densities, indicating its potential for practical application. This work highlights the role of host-structure engineering in mitigating dead sodium and provides design principles for developing high-energy sodium metal batteries.
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