School of Chemistry and Environment, South China Normal University , Guangzhou 510631, China.
Engineering Research Center of MTEES (Ministry of Education), Research Center of BMET (Guangdong Province), Engineering Laboratory of OFMHEB (Guangdong Province), Key Laboratory of ETESPG (GHEI), and Innovative Platform for ITBMD (Guangzhou Municipality), South China Normal University , Guangzhou 510006, China.
ACS Appl Mater Interfaces. 2017 Apr 5;9(13):12021-12034. doi: 10.1021/acsami.7b00032. Epub 2017 Mar 24.
Layered cathodes for lithium-ion battery, including LiCoNiMnO and xLiMnO·(1-x)LiMO (M = Mn, Ni, and Co), are attractive for large-scale applications such as electric vehicles, because they can deliver additional specific capacity when the end of charge voltage is improved to over 4.2 V. However, operation under a high voltage might cause capacity decaying of layered cathodes during cycling. The failure mechanisms that have been given, up to date, include the electrolyte oxidation decomposition, the Ni, Co, or Mn ion dissolution, and the phase transformation. In this work, we report a new mechanism involving the exfoliation of layered cathodes when the cathodes are performed with deep cycling under 4.5 V in the electrolyte consisting of carbonate solvents and LiPF salt. Additionally, an electrolyte additive that can form a cathode interface film is applied to suppress this exfoliation. A representative layered cathode, LiCoO, and an interface film-forming additive, dimethyl phenylphosphonite (DMPP), are selected to demonstrate the exfoliation and the protection of layered structure. When evaluated in half-cells, LiCoO exhibits a capacity retention of 24% after 500 cycles in base electrolyte, but this value is improved to 73% in the DMPP-containing electrolyte. LiCoO/graphite full cell using DMPP behaves better than the Li/LiCoO half-cell, delivering an initial energy density of 700 Wh kg with an energy density retention of 82% after 100 cycles at 0.2 C between 3 and 4.5 V, as compared to 45% for the cell without using DMPP.
锂离子电池的层状阴极,包括 LiCoNiMnO 和 xLiMnO·(1-x)LiMO(M = Mn、Ni 和 Co),因其在充电截止电压提高到 4.2 V 以上时可提供额外的比容量,而在电动汽车等大型应用中具有吸引力。然而,在高电压下运行可能会导致层状阴极在循环过程中容量衰减。迄今为止,已经提出了几种失效机制,包括电解质氧化分解、Ni、Co 或 Mn 离子溶解和相转变。在这项工作中,我们报告了一种新的机制,即在含有碳酸盐溶剂和 LiPF 盐的电解质中,在 4.5 V 下进行深度循环时,层状阴极会发生剥落。此外,还应用了一种可以形成阴极界面膜的电解质添加剂来抑制这种剥落。选择了一种代表性的层状阴极 LiCoO 和一种界面成膜添加剂二甲基苯基膦(DMPP)来演示剥落和对层状结构的保护。在半电池中评估时,LiCoO 在基础电解质中经过 500 次循环后容量保持率为 24%,但在含有 DMPP 的电解质中,这一值提高到 73%。使用 DMPP 的 LiCoO/石墨全电池的性能优于 Li/LiCoO 半电池,在 3 至 4.5 V 之间以 0.2 C 的倍率循环 100 次后,初始能量密度为 700 Wh kg,能量密度保持率为 82%,而不使用 DMPP 的电池则为 45%。