NaF-Rich Multifunctional Layers toward Stable All-Solid-State Sodium Batteries

被引:9
作者
Liu, Tinghu [1 ,2 ]
Shen, Lin [2 ]
Li, Yunming [2 ]
Jiang, Kemin [2 ]
Song, Libo [1 ,2 ]
Jin, Yuming [2 ]
Yang, Jing [2 ]
Xin, Xing [1 ]
Yao, Xiayin [2 ]
机构
[1] Ningbo Univ, Sch Mat Sci & Chem Engn, Ningbo 315211, Peoples R China
[2] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Ningbo 315201, Peoples R China
基金
中国国家自然科学基金;
关键词
all-solid-state sodium batteries; dendrite suppression; NaF-rich interface layer; Na metal anode; Na3V2(PO4)(3) cathode; ELECTROLYTE; INTERFACE;
D O I
10.1021/acsami.3c10128
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
NASICON oxide solid electrolytes are considered promising candidates for all-solid-state sodium batteries due to their extremely high ionic conductivity and favorable electrochemical stability. However, the practical application of NASICON electrolytes is greatly impeded by poor electrolyte-electrode interfacial contact and continuous sodium dendrite propagation. Herein, a NaF-rich multifunctional interface layer on the surface of a Na anode (Na@NaF-rich), containing NaF, amorphous carbon, and an unreacted C-F bond species, is developed in situ by the reaction between Na and commercial poly(tetrafluoroethylene). This NaF-rich interface layer is proven to reduce the diffusion barriers at the Na/NASICON electrolyte interface and homogenize Na deposition as well as suppress Na dendrite growth, thus achieving a high critical current density of 4 mA cm(-2). The resultant Na3V2(PO4)(3)@C/Na@NaF-rich all-solid-state cell showed a high initial specific capacity of 117.6 mAh g(-1) at 0.1 C with a Coulombic efficiency of 94.8%. Even at 0.5 and 1 C, it still exhibited high capacity retentions of 83.3% and 80.4%, respectively, after 750 cycles.
引用
收藏
页码:45026 / 45034
页数:9
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