In situ magnetometry study on the origin of anomalously capacity in transition metal sulfides

Abstract

Cobalt sulfides are considered as promising candidates for lithium-ion battery (LIB) anode materials with high energy densities. Their energy storage mechanism is widely understood to involve the traditional intercalation and conversion reaction. However, these conventional mechanisms are unable to explain the storage capacities of certain materials which exceed the theoretical limit. Here, utilizing advanced in situ magnetometry to detect the magnetization evolution of Co1-xS LIBs in real time, it is demonstrated that the Co-catalytic lithium storage process and interfacial space charge storage mechanism are strongly related to the additional capacity of cobalt sulfides. During discharge, a Co/Li2S interface is formed, wherein the Co nanoparticles and Li2S could store a large amount of polarized electrons Li+, respectively. Subsequently, the electrons stored in Co are transferred to the polymeric film, forming radical anions and contributing extra capacity. These findings reveal the charge storage mechanisms of transition metal sulfides and highlight the critical role of magnetic testing in the investigation of energy storage mechanisms.

Keywords

• Lithium-ion batteries
• Co1-xS nanocomposites
• Additional capacity
• Energy storage mechanism