Department of Materials Science and Engineering, University of Illinois , Urbana-Champaign, Urbana, Illinois 61801, United States.
ACS Appl Mater Interfaces. 2016 Jun 8;8(22):14244-51. doi: 10.1021/acsami.6b02061. Epub 2016 May 26.
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.
近年来,基于锰的正极材料的锂离子电池因其成本更低、对环境更友好,相对于钴基电池受到了广泛关注。然而,使用这些正极材料与石墨负极结合的锂离子电池在高温下会严重衰减容量。在本文中,我们报告了锰的溶解如何影响锂离子电池的容量衰减。我们的研究表明,锰从正极溶解,迁移到石墨电极,并在最内层的固体电解质界面层的外表面上沉积,该界面层通常是无机盐(例如 Li2CO3、LiF 和 Li2O)的混合物。在这个位置,锰促进了电解质的还原以及随后在石墨上形成含锂产物,这会从电池的正常运行中除去锂离子,从而导致严重的容量衰减。