"Preferential adsorption-decomposition and strong binding" strategy-derived interphase enabling fast-charging and wide-temperature sodium metal batteries

被引:0
|
作者
Wang, Qian [1 ]
Cheng, Fangyuan [1 ]
Chen, Xuezhen [1 ]
Cao, Meilian [1 ]
Qin, Daomin [1 ]
Yan, Feiyang [1 ]
Li, Qing [1 ]
Fang, Chun [1 ]
Han, Jiantao [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Mat Sci & Engn, State Key Lab Mat Proc & Die & Mould Technol, Wuhan 430074, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Additive; Electrolyte; Interphase; High rate; Wide-temperature; ION; ELECTROLYTES; NA4FE3(PO4)(2)(P2O7);
D O I
10.1016/j.ensm.2024.103922
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The interface reaction that occurs between electrodes and electrolyte is a significant factor to the degradation of batteries' electrochemical performance. One crucial avenue to enhance the electrochemical performance of sodium metal batteries (SMBs) is to construct robust inorganic-rich interphases that can effectively inhibit interface side reactions. Herein, we report and demonstrate a collaborative strategy called "Preferential AdsorptionDecomposition and Strong Binding" (ADSB) that is based on sodium fluorophosphate (Na2PO3F, safe and nontoxic, can be utilized as an anti-caries agent in toothpaste.), a multifunctional anionic additive that preferentially adsorbs on the inner Helmholtz plane (IHP), preferentially decomposes, and contributes to the solvation structure to form a multi-anion solvated sheath. Based on the ADSB strategy, the robust electrode electrolyte interphases are successfully constructed on the surface of Na4Fe3(PO4)2P2O7 (NFPP) and sodium-metal. Consequently, at an extremely high rate of 50 C, the NFPP||Na cell with Na2PO3F modified electrolyte achieves a high capacity of 60.9 mAh g-1. Furthermore, the stable interphases derived from Na2PO3F are resistant to widetemperature. At -40 degrees C, the NFPP||Na cell demonstrates a high capacity of 73.0 mAh g-1, and after 200 cycles at 60 degrees C, it achieves 84.2% capacity retention.
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页数:10
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