A Desolvation-Free Sodium Dual-Ion Chemistry for High Power Density and Extremely Low Temperature

被引:96
作者
Chen, Jiawei [1 ,2 ]
Peng, Yu [1 ,2 ]
Yin, Yue [1 ,2 ]
Fang, Zhong [1 ,2 ]
Cao, Yongjie [1 ,2 ]
Wang, Yonggang [1 ,2 ]
Dong, Xiaoli [1 ,2 ]
Xia, Yongyao [1 ,2 ]
机构
[1] Fudan Univ, Dept Chem, Inst New Energy, iChEM Collaborat Innovat Ctr Chem Energy Mat, Shanghai 200433, Peoples R China
[2] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Inst New Energy, iChEM Collaborat Innovat Ctr Chem Energy Mat, Shanghai 200433, Peoples R China
关键词
desolvation process; fast kinetics; low-temperature performance; Sodium dual-ion battery; CO-INTERCALATION; GRAPHITE; ELECTROLYTE; BATTERIES; INTERFACE; BEHAVIOR; CATHODE;
D O I
10.1002/anie.202110501
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of conventional rechargeable batteries based on intercalation chemistry in the fields of fast charge and low temperature is generally hindered by the sluggish cation-desolvation process at the electrolyte/electrode interphase. To address this issue, a novel desolvation-free sodium dual-ion battery (SDIB) has been proposed by using artificial graphite (AG) as anode and polytriphenylamine (PTPAn) as cathode. Combining the cation solvent co-intercalation and anion storage chemistry, such a SDIB operated with ether-based electrolyte can intrinsically eliminate the sluggish desolvation process. Hence, it can exhibit an extremely fast kinetics of 10 Ag-1 (corresponding to 100C-rate) with a high capacity retention of 45 %. Moreover, the desolvation-free mechanism endows the battery with 61 % of its room-temperature capacity at an ultra-low temperature of -70 degrees C. This advanced battery system will open a door for designing energy storage devices that require high power density and a wide operational temperature range.
引用
收藏
页码:23858 / 23862
页数:5
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