锰
材料科学
电解质
石墨
锂(药物)
阴极
衰退
阳极
化学工程
溶解
电极
无机化学
磷酸钒锂电池
沉积(地质)
锂离子电池的纳米结构
离子
冶金
化学
电气工程
有机化学
医学
频道(广播)
工程类
物理化学
内分泌学
古生物学
沉积物
生物
作者
Daniel R. Vissers,Zonghai Chen,Yuyan Shao,Mark Engelhard,Ujjal Das,Paul C. Redfern,Larry A. Curtiss,Baofei Pan,Jun Liu,Khalil Amine
标识
DOI:10.1021/acsami.6b02061
摘要
Lithium ion batteries utilizing manganese-based cathodes have received considerable interest in recent years for their lower cost and more favorable environmental friendliness relative to their cobalt counterparts. However, Li ion batteries using these cathodes combined with graphite anodes suffer from severe capacity fading at high operating temperatures. In this paper, we report on how the dissolution of manganese impacts the capacity fading within the Li ion batteries. Our investigation reveals that the manganese dissolves from the cathode, transports to the graphite electrode, and deposits onto the outer surface of the innermost solid-electrolyte interphase layer, which is known to be a mixture of inorganic salts (e.g., Li2CO3, LiF, and Li2O). In this location, the manganese facilitates the reduction of the electrolyte and the subsequent formation of lithium-containing products on the graphite, which removes lithium ions from the normal operation of the cell and thereby induces the severe capacity fade.
科研通智能强力驱动
Strongly Powered by AbleSci AI