法拉第效率
成核
材料科学
阴极
剥离(纤维)
阳极
纳米技术
动力学
化学工程
无定形固体
双金属片
钠
电极
金属
电流密度
储能
可扩展性
能量密度
寄主(生物学)
降级(电信)
功率密度
碳纤维
纳米颗粒
锂离子电池的纳米结构
氧化还原
电化学
能量转换
作者
Chenglin Li,Yiyang Tang,Xucheng Wang,Yong Cheng,Ming‐Sheng Wang
摘要
ABSTRACT Anode‐free sodium metal batteries (AFSMBs) promise high energy density and simplified fabrication, yet require repeated sodium nucleation on the current collector surface after the complete stripping in each cycle. Here, we present a strategy utilizing sodiophilic hosts with pseudocapacitive kinetics to realize durable and efficient nucleation processes in AFSMBs, together with a scalable synthesis route for these hosts. To illustrate, a highly sodiophilic host was constructed by integrating pseudocapacitive T‐Nb 2 O 5 into amorphous carbon nanotubes (aCNTs) through in situ self‐assembly. Experimental and theoretical results reveal that T‐Nb 2 O 5 domains can simultaneously preserve their structural integrity, minimize Na consumption, accelerate Na transport, and ensure reversible redox reactions, thereby establishing robust nucleation sites. Consequently, the T‐Nb 2 O 5 @aCNTs host achieves highly reversible and uniform Na deposition, delivering an ultrahigh average Coulombic efficiency of 99.98% over 800 cycles in half‐cells and long cycling over 900 h in symmetric cells under harsh conditions. When paired with a high‐mass‐loading Na 3 V 2 (PO 4 ) 3 cathode (15 or 30 mg cm −2 ), the full cells exhibit high energy density and stable cycling performance. Moreover, the anode‐free pouch cell maintains favorable capacity retention over 100 cycles at 2 C. The proposed host design concept with scalable manufacturing capability opens a universal pathway toward practical high‐performance AFSMBs.
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