Tailoring solid-electrolyte interphase and solvation structure for subzero temperature, fast-charging, and long-cycle-life sodium-ion batteries

被引:30
作者
Tao, Lei [1 ]
Sittisomwong, Poom [2 ]
Ma, Bingyuan [2 ]
Hu, Anyang [1 ]
Xia, Dawei [1 ]
Hwang, Sooyeon [3 ]
Huang, Haibo [4 ]
Bai, Peng [2 ]
Lin, Feng [1 ]
机构
[1] Virginia Tech, Dept Chem, Blacksburg, VA 24061 USA
[2] Washington Univ, Dept Energy Environm & Chem Engn, St Louis, MO 63130 USA
[3] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[4] Virginia Tech, Dept Food Sci & Technol, Blacksburg, VA 24061 USA
基金
美国食品与农业研究所;
关键词
Carbon materials; Pseudo-SEI; Co; -intercalation; Fast charging; Low temperature; HARD CARBON; ANODE;
D O I
10.1016/j.ensm.2022.12.042
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 sluggish Na+ reaction kinetics with carbon materials limits the fast-charging capability, Coulombic effi-ciency, and cycle life of sodium-ion batteries, especially at low temperatures. Herein, free-standing carbon nanofiber films, with controllable crystallinity and surface chemistry, are used as a platform to investigate the correlation between Na+ reaction kinetics, storage mechanism, and electrolyte environment. The ion solvation effect and solid-electrolyte interphase (SEI) properties determine the kinetics and storage mechanism. A strong Na+-solvent interaction, such as Na+-diglyme, tends to form a "pseudo-SEI" layer dominated by anion decom-position, enabling fast Na+-solvent co-intercalation kinetics. Tuning the SEI chemistries by pre-cycling in the weakly solvated electrolyte (e.g., ester electrolyte), the intercalation capacity rapidly disappears due to the high energy barrier for Na+ transport. Such mechanistic insights allow us to develop the optimal combination of electrode materials and electrolyte chemistry to achieve high initial Coulombic efficiency, ultra-long cycle life under fast charging, and excellent low-temperature performance.
引用
收藏
页码:826 / 835
页数:10
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