二甲氧基乙烷
电解质
碱金属
四氢呋喃
材料科学
钠
金属
溶剂
电极
相间
无机化学
化学工程
化学
物理化学
有机化学
冶金
工程类
生物
遗传学
作者
Jing Zhou,Yingyu Wang,Jiawei Wang,Yu Liu,Yanmei Li,Liwei Cheng,Yang Ding,Shuai Dong,Qiaonan Zhu,Mengyao Tang,Yunzi Wang,Yushu Bi,Rong Sun,Zhongchang Wang,Hua Wang
标识
DOI:10.1016/j.ensm.2022.05.005
摘要
High-rate cycling of alkali metal batteries at subzero temperature is essential for their practical applications in extreme environments. Here, we realize high-rate low-temperature sodium metal batteries (LT SMBs) through modulating electrolyte chemistry. By introducing a weak Na+ solvating co-solvent, tetrahydrofuran/1,2-Dimethoxyethane (THF/DME), the kinetic barrier for Na+ desolvation is significantly mitigated. Furthermore, an anion-derived NaF-rich solid-electrolyte interphase (SEI) film generated on the sodium electrode suppresses the dendrite growth and guarantees stable cycling of SMBs down to -60°C. In consequence, the symmetric Na/Na batteries achieve a high current density of 3 mA cm−2 at -20°C and 2 mA cm−2 at -40°C. Meanwhile, they exhibit an outstanding cumulative cycling capacity of 1350 mAh cm−2 (-20°C) and 285.5 mAh cm−2 (-40°C), which outperforms the previously reported LT alkali metal symmetric batteries. Moreover, the Na-NaTi2(PO4)3 (NTP) full batteries exhibit a power density of 1396.5 W kg−1 at 46.2 Wh kg−1 (based on NTP) under -40°C.
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