Electrochemical Activation of Manganese-Based Cathode in Aqueous Zinc-Ion Electrolyte

被引:176
作者
Zhang, Tengsheng [1 ]
Tang, Yan [1 ,2 ]
Fang, Guozhao [1 ,2 ]
Zhang, Chenyang [3 ,4 ]
Zhang, Hongliang [3 ]
Guo, Xun [1 ,2 ]
Cao, Xinxin [1 ]
Zhou, Jiang [1 ,2 ]
Pan, Anqiang [1 ,2 ]
Liang, Shuquan [1 ,2 ]
机构
[1] Cent South Univ, Sch Mat Sci & Engn, Changsha 410083, Hunan, Peoples R China
[2] Cent South Univ, Key Lab Elect Packaging & Adv Funct Mat Hunan Pro, Changsha 410083, Hunan, Peoples R China
[3] Cent South Univ, Sch Minerals Proc & Bioengn, Changsha 410083, Hunan, Peoples R China
[4] Nanjing Univ, Sch Chem & Chem Engn, Inst Theoret & Computat Chem, Nanjing 210023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
desolvation; electrochemical activation; electrolyte; interfacial reaction; zinc-ion battery; HIGH-ENERGY; LITHIUM IONS; HIGH-POWER; LONG-LIFE; BATTERIES; PERFORMANCE; SOLVATION; CHEMISTRY; VOLTAGE;
D O I
10.1002/adfm.202002711
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Low-cost and highly safe zinc-manganese batteries are expected for practical energy storage and grid-scale application. The electrolyte adjustment is further combined to boost their performance output; however, the mechanism behind the electrochemical contrast caused by electrolyte composition remains unclear, which has held back the development of these systems. Hence, new insight into the electrochemical activation of manganese-based cathodes, which is induced by the aqueous zinc-ion electrolyte, is provided. The relationship between the desolvation of Zn2+ from [Zn(OH2)(6)](2+)-solvation shell and the electrolyte/electrode interfacial reaction to form Zn4SO4(OH)(6)center dot 4H(2)O phase or its analogues is established, which is the key for the electrochemical activation. Further electrolyte optimization promotes the cycling stability of Zn/LiMn2O4 battery with a long life span over 2000 cycles. This work illuminates the confused direction in exploring electrolyte for zinc-manganese batteries.
引用
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页数:7
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