Additive-rejuvenated anions (De)intercalation into graphite cathode enables optimum dual-ion battery

被引:8
作者
Zheng, Ying [1 ]
Zhang, Wei [1 ]
Liu, Fuxi [1 ]
Liang, Qing [1 ]
Li, Wenwen [1 ]
Zhou, Xinyan [1 ]
Yue, Nailin [1 ]
Zheng, Weitao [1 ]
机构
[1] Jilin Univ, Electron Microscopy Ctr, Int Ctr Future Sci, Sch Mat Sci & Engn,Key Lab Automobile Mat MOE,Jili, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
Aqueous electrolyte; Graphite cathode; Dual-ion battery; Cathode electrolyte interphase; IN-SALT ELECTROLYTE;
D O I
10.1016/j.ensm.2024.103326
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
Cathode-electrolyte interphase (CEI) has particular function in maintaining electrolyte and cathode stability. However, the CEI will also cause some negative effects on ion transport. It is crucial for optimizing the structure of CEI through additives in the electrolyte to improve the electrode reaction. In this study, we proposed using C3H3FO3 (FEC) as an additive to optimize an aqueous LiTFSI (bistrifluoromethanesulfonimide lithium salt) electrolyte. The incorporation of FEC modified the solvation structure of TFSI-, inhibit the formation of CEI with thicker size, thereby facilitating the intercalation of TFSI- into the selected graphite cathode. Consequently, the graphite's discharge capacity was doubled, reaching 47 mAh g-1. The influence of TFSI- solvation structure on CEI formation was further studied by the emerging correlative SEM, Raman imaging and TOF-SIMS techniques and theoretical calculation techniques. Using this optimization strategy, we successfully constructed an aqueous dual -ion battery using C24H10N2O4 and graphite as the anode and cathode with an impressive potential window of 2.55 V, which delivered the energy density of 66 Wh kg -1 at the power density of 128 W kg-1.
引用
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页数:10
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