电解质
锂(药物)
无机化学
镁
化学
钴
阴极
四氢呋喃
盐(化学)
硫化物
氧化还原
电极
电化学
阳极
有机化学
溶剂
物理化学
内分泌学
医学
作者
Xu Zhang,Hao Xu,Jisheng Yang,Yuxiao Zhu,Chong Lu,Kemin Zhang,Guo‐Ming Weng,Jianxin Zou
出处
期刊:ChemNanoMat
[Wiley]
日期:2021-04-29
卷期号:7 (6): 641-650
被引量:14
标识
DOI:10.1002/cnma.202100024
摘要
Abstract Magnesium lithium dual ion batteries (MLIBs) possess the advantages of Mg anodes with low dendrite formation tendency, high volumetric capacity and abundant resources. The fast reaction kinetics of Li + ions for the whole electrochemical redox processes contribute to provide high reversible capacity and long cycle life. In this study, we propose one type of MLIBs coupled with Mg anodes, flower‐like cobalt sulfide (CoS) cathodes, all‐phenyl complex (APC) and lithium chloride dissolved in tetrahydrofuran (THF) derived APC‐ x LiCl/THF ( x =0–0.8 mol L −1 ) electrolytes. By virtue of APC‐0.8 LiCl/THF electrolyte, the capacity of MLIB increases gradually to a high capacity of 507 mAh g −1 at 0.1 A g −1 and maintains a reversible capacity of 219 mAh g −1 at 0.5 A g −1 after 500 cycles. More significantly, Mg 2+ and Li + ions co‐conversion mechanism on the CoS cathodes is demonstrated for MLIBs. The systems studied here may offer insights in the design of MLIBs.
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