Exacerbated High‐Temperature Calendar Aging of SiOx‐Graphite Electrode Induced by Interparticle Lithium Crosstalk

Silicon oxide‐graphite (SiOx‐G) composites are promising anode materials for building practical high‐energy Li‐ion batteries. To acquire long and safe operation of battery, extensive efforts are made to maintain stable Li storage of SiOx‐G against materials aging and the accompanied performance fade...

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Published inAdvanced functional materials Vol. 34; no. 2
Main Authors Zhang, Yu, Wen‐Peng Wang, Zhao, Yao, Zhang, Xing, Guo, Hua, Gao, Hongcai, Di‐Xin Xu, Yu‐Ming Zhao, Li, Ge, Jia‐Yan Liang, Sen, Xin, Yu‐Guo Guo
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc 09.01.2024
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Abstract Silicon oxide‐graphite (SiOx‐G) composites are promising anode materials for building practical high‐energy Li‐ion batteries. To acquire long and safe operation of battery, extensive efforts are made to maintain stable Li storage of SiOx‐G against materials aging and the accompanied performance fade. While previous studies mostly focus on the cycling aging, the calendar aging occurred during battery storage at a high state of charge or high temperature has not received sufficient attention. In this work, a mechanism study on the calendar aging chemistry of fully lithiated SiOx‐G electrodes in half‐cells both at ambient and high temperature (60 °C) is performed. Unmodified SiOx is employed as active materials to inspect the change of thermodynamics properties in the bulk and at interfaces. By excluding the interference from cathode, it is revealed that besides aggravated parasitic reactions happening at interface, Li migration from the lithiated graphite to the vicinal SiOx particles is also responsible for calendar aging of SiOx‐G electrodes, and high‐temperature storage notably accelerates the aging process. This work enriches the fundamental understandings about the multifactor‐coupled aging process of anode materials and sheds lights on rational materials design toward improved calendar life of a high‐energy rechargeable battery.
AbstractList Silicon oxide‐graphite (SiOx‐G) composites are promising anode materials for building practical high‐energy Li‐ion batteries. To acquire long and safe operation of battery, extensive efforts are made to maintain stable Li storage of SiOx‐G against materials aging and the accompanied performance fade. While previous studies mostly focus on the cycling aging, the calendar aging occurred during battery storage at a high state of charge or high temperature has not received sufficient attention. In this work, a mechanism study on the calendar aging chemistry of fully lithiated SiOx‐G electrodes in half‐cells both at ambient and high temperature (60 °C) is performed. Unmodified SiOx is employed as active materials to inspect the change of thermodynamics properties in the bulk and at interfaces. By excluding the interference from cathode, it is revealed that besides aggravated parasitic reactions happening at interface, Li migration from the lithiated graphite to the vicinal SiOx particles is also responsible for calendar aging of SiOx‐G electrodes, and high‐temperature storage notably accelerates the aging process. This work enriches the fundamental understandings about the multifactor‐coupled aging process of anode materials and sheds lights on rational materials design toward improved calendar life of a high‐energy rechargeable battery.
Author Jia‐Yan Liang
Di‐Xin Xu
Yu‐Ming Zhao
Li, Ge
Gao, Hongcai
Zhang, Xing
Yu‐Guo Guo
Zhang, Yu
Wen‐Peng Wang
Sen, Xin
Zhao, Yao
Guo, Hua
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Snippet Silicon oxide‐graphite (SiOx‐G) composites are promising anode materials for building practical high‐energy Li‐ion batteries. To acquire long and safe...
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SubjectTerms Aging
Aging (materials)
Anodes
Batteries
Calendars
Crosstalk
Electrode materials
Electrodes
Energy storage
Graphite
High temperature
Lithium-ion batteries
Rechargeable batteries
Silicon oxides
Title Exacerbated High‐Temperature Calendar Aging of SiOx‐Graphite Electrode Induced by Interparticle Lithium Crosstalk
URI https://www.proquest.com/docview/2912166441
Volume 34
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