Improving Sodium Storage Performance of Hard Carbon Anodes in Cyclic Ether Electrolytes by an Anion Receptor Additive

被引:12
作者
Lin, Ya [1 ]
Yang, Chao [1 ]
You, Ya [1 ,2 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[2] Wuhan Univ Technol, Int Sch Mat Sci & Engn, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
GLYME-BASED ELECTROLYTE; ION BATTERIES; ELECTROCHEMICAL PERFORMANCE; LITHIUM-ION; METAL; INTERCALATION; INTERPHASE; TRANSPORT; CATHODE; DESIGN;
D O I
10.1149/1945-7111/ac534e
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The intrinsic ring-opening polymerization of five-membered cyclic ether induced by Lewis acid hinder its practical application as electrolyte solvents in sodium-ion batteries. In this work, we find that introducing tris (2,2,2-trifluoroethyl) borate (TTFEB), an anion acceptor additive, into cyclic ether-based electrolyte solution effectively inhibits its polymerization by tethering the PF6 (-) anion. In addition, a stable inorganics-rich SEI layer is formed in TTFEB-containing electrolyte solution, which ensures fast Na+ transport kinetics upon extensive cycles. As a result, the cycle stability and rate capability of HC anodes in 1,3-dioxolane-based electrolyte solutions are evidently improved by TTFEB additive. Our study paves the way for the application of cyclic ethers in sodium-ion batteries.
引用
收藏
页数:7
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