Construction of an ultra-stable mixed conductive layer to stabilize the solid-state electrolyte/Na interface by in-situ interface chemistry

被引:9
|
作者
Yang, Yujie [1 ]
Hao, Yisu [1 ]
Zhang, Yan [1 ]
Huang, Cong [1 ]
Yao, Bin [1 ]
Qian, Yang [1 ]
Chang, Ge [1 ]
Liu, Zhixiao [1 ]
Tang, Qunli [1 ]
Hu, Aiping [1 ]
Chen, Xiaohua [1 ]
机构
[1] Hunan Univ, Coll Mat Sci & Engn, Hunan Prov Key Lab Adv Carbon Mat & Appl Technol, Changsha 410082, Peoples R China
基金
中国国家自然科学基金;
关键词
Solid -state electrolyte; Mixed conductive layer; Na dendrites; Interface issue; Solid -state sodium metal batteries; INTERPHASE; RESISTANCE; DENDRITES;
D O I
10.1016/j.cej.2023.146728
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The quest for high energy density, essentially safe, and cost-effective energy storing systems is powering the evolution of solid-state sodium metal batteries (SSSMBs). However, insufficient Na/solid-state electrolyte (SSE) interface contact leads to the formation of sodium dendrites, causing premature cell failure and safety issues that limit their practical application. Here, a novel ultra-stable mixed conductive layer (MCL) composed of Na15Sn4 and NaF is introduced at the Na|Na3Zr2Si2PO12 (NZSP) interface through in-situ interface chemistry. Such an MCL not only enables the transformation of the NZSP surface from sodiophobic to sodiophilic to achieve intimate contact with Na but also homogenizes the Na+ flux without dendritic sodium. Benefiting from the construction of the multifunctional interface, a high critical current density (CCD) of 1.3 mA cm-2 and an exceptionally long cycle life of 6000 h at 0.3 mA cm-2 are achieved for the Na|SnF2@NZSP|Na cell at room temperature (RT). Furthermore, the Na|SnF2@NZSP|Na3V2(PO4)3 full cell shows excellent cycling performance (91 % of maintained capacity for over 500 cycles at 1 C) and rate capability (101.4 mAh/g at 5 C) at RT. This work presents a validated method for the coordinated regulation of interfacial transfer kinetics and inhibition of sodium dendrite growth.
引用
收藏
页数:11
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