Enabling Dual-Ion Batteries via the Reversible Storage of Pyr14+ Cations into Coronene Crystal

被引:6
|
作者
Fang, Yaobing [1 ]
Bi, Wanying [1 ]
Wang, Aiye [1 ]
Zheng, Wen [1 ]
Yuan, Wenhui [1 ]
Li, Li [2 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, Guangdong Engn Technol Res Ctr Effect Storage & U, Guangzhou 510640, Peoples R China
[2] South China Univ Technol, Sch Environm & Energy, Guangzhou 510006, Peoples R China
关键词
cations storage; dual-ion batteries; graphite cathodes; ionic liquid electrolytes; organic electrodes; ORGANIC CATHODE; GRAPHITE; LIQUID; INTERCALATION; IMIDE;
D O I
10.1002/ente.202000223
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Dual-ion batteries with pure ionic liquid electrolyte (IL-DIBs) have received increasing interest due to their sustainability, high operating voltage, and environmental friendliness. However, owing to the insertion/extraction of large-size ionic liquid cations, the conventional IL-DIBs with a graphite anode suffer from severe volume expansion and graphite exfoliation on the anode, causing a poor cycling performance. Herein, a novel IL-DIB is constructed by introducing a bulk organic material (coronene) as the anode, against a natural graphite cathode. The results show that, in a voltage window range from 1.0 to 4.4 V, the battery has a high discharge specific capacity of approximate to 73.3 mA h g(-1) and exhibits a good cycling performance for 450 cycles with a lower capacity loss of 0.061 mA h g(-1) per cycle at a current density of 300 mA g(-1) (3 C). Notably, it still maintains a considerable capacity of approximate to 55.8 mA h g(-1) at a high rate of 10 C. In addition, the reversible intercalation/de-intercalation of the Pyr(14)(+) cations into/from the coronene anode is investigated by ex situ X-ray diffraction and Fourier transform infrared spectroscopy, showing an excellent structure stability of the coronene crystal during the charge-discharge process.
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页数:7
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