Abstract

Lithium-ion batteries are expected to serve as a key technology for large-scale energy storage systems (ESSs), which will help satisfy recent increasing demands for renewable energy utilization. Besides their promising electrochemical performance, the low self-discharge rate (<5% of the stored capacity over 1 month) of lithium-ion batteries is one of their most significant advantages for ESSs. Herein, contrary to conventional belief, we report that the self-discharge of LIBs can be abnormally accelerated when the battery had been exposed even to a routine short-term thermal exposure. We demonstrate that, this thermal ‘history’ in addition to the temperature itself is memorized in the battery and accelerates the self-discharge rate. The series of characterizations performed in our work reveal that the electrolyte salt acts as a strong oxidizing agent by vigorously damaging the surface of the cathode, producing an internal ‘parasitic’ lithium source that continuously supplies lithium for the self-discharge. Although it is widely known that battery operation at elevated temperature generally induces faster degradation of capacity over cycles, the key finding here is that not only the operation temperature but also the ‘thermal history’ of the battery should be carefully considered because this history remains and continues to affect the self-discharge rate afterwards. The self-discharge of LIBs has remained largely neglected; however, our findings suggest that close attention must be paid to the self-discharge of LIBs applied to large-scale ESSs, which, unlike mobile electronic devices, would be exposed to various outdoor temperature conditions.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.