分离器(采油)
材料科学
金属
对偶(语法数字)
金属有机骨架
极地的
双重角色
钠
纳米技术
化学工程
组合化学
有机化学
化学
吸附
冶金
工程类
热力学
艺术
物理
文学类
天文
作者
Jiaze Lv,Zhen Tang,Qiman Zhang,Han Sun,Mingwei Ouyang,Yan Cao
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-04-15
标识
DOI:10.1021/acsnano.5c04051
摘要
Sodium metal, regarded as an ideal anode material for high-energy-density rechargeable sodium metal batteries (SMBs), faces critical challenges, such as sluggish Na+ transport kinetics and uncontrolled dendritic growth, which severely hinder its cycling stability and practical applications. Herein, the well-designed, multifunctional separator, UFS2@GF, constructed using metal-organic frameworks functionalized with fluorinated (-F) and sulfonic acid (-SO3H) groups, synergistically provides more nucleation sites for Na+ deposition, thereby reducing the nucleation overpotential and achieving uniform deposition. The inorganic-rich solid electrolyte interphase induced by UFS2 facilitates a uniform Na+ flux and enhances charge transfer efficiency. Structural characterization and density functional theory calculations further demonstrate that the introduction of abundant sodiophilic sites provided by -F and -SO3H significantly enhances Na+ transport kinetics by reducing the energy barriers for Na+ migration within the UFS2 framework, leading to a higher Na+ transference number, superior ionic conductivity, and accelerated ion transport. Because of these synergistic effects, the symmetric cell with UFS2@GF achieves stable performance, enabling stable cycling for over 2500 h at 0.25 mA cm-2 while delivering an excellent specific capacity of 87.3 mA h g-1 at 10C in Na∥Na3V2(PO4)3 cells. These results highlight the critical role of synergistic functional group strategies in addressing the limitations of SMBs.
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