Self-discharge in Li-ion aqueous batteries: A case study on LiMn2O4

Aqueous rechargeable lithium-ion batteries have attracted great attention as an alternative to traditional battery technologies, being able to overcome the issues caused by flammable and expensive organic electrolytes. In particular, LiMn2O4 has reached very fast second-level charge capability by the synthesis of unconventional morphology and particle sizes, allowing charging rates up to 600 C and 93% retention of the capacity after 10,0 0 0 cycles. However, the self-discharge process and aging mechanisms for aqueous batteries have been rarely studied, which contrasts with the extensive bibliography of the same phenomena in LMO cells based on organic electrolytes. In this article, the mechanisms involved in the loss of reversible specific charges were studied by diverse techniques like OCV, EIS, and In-situ Raman. The results revealed a more favorable self-discharge process compared with using organic electrolytes owing to the lower stability of water. The self-discharge process can be divided into three different regions with a sequential lower decay rate of voltage and capacity as well as two different evolutions of the electric parameters. This study opens new questions about the nature, composition, and mechanisms of the self discharge in aqueous media which will play a critical role in the electrochemical performance of novel aqueous Li-ion batteries. (C) 2021 Elsevier Ltd. All rights reserved.

Automated summary

This study investigated the self-discharge process in aqueous rechargeable lithium-ion batteries, revealing that the lower stability of water leads to more favorable self-discharge characteristics compared to organic electrolytes. The self-discharge process can be divided into three different regions with a sequential lower decay rate of voltage and capacity.