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Self-Healing Ion-Conductive Binder for High-Performance SiO Anodes in Lithium-Ion Batteries.

作者信息

Long Xianhao, Xie Liangxin, Huang Chuxiong, Ye Zhihuan, Wu Shuxing, Wei Xiujuan, Luo Yang, Ye Kai-Hang, Lin Zhan

机构信息

School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China.

Central Research Institute, EVE Energy Co., Ltd, NO. 38, Huifeng seventh Road, Zhongkai Hi-Tech Zone, Huizhou, Guangdong 516006, China.

出版信息

ACS Appl Mater Interfaces. 2025 Sep 24;17(38):53402-53412. doi: 10.1021/acsami.5c11054. Epub 2025 Sep 12.

DOI:10.1021/acsami.5c11054
PMID:40937702
Abstract

Volume expansion during repeated cycling is the primary cause of degradation of SiO anodes, impeding their practical application in next-generation high-energy-density lithium-ion batteries. Herein, a self-healing polymer binder incorporating both dynamic covalent and hydrogen bonding interactions is developed to accommodate volume changes and enhance the stability of SiO anodes. This self-healing binder (PPC) is prepared through the physical cross-linking of poly(α-lipoic acid) (PLA) and poly(acrylic acid) (PAA), together with the ion-conducting choline chloride (ChCl), which induces the formation of a network structure. Physical cross-linking effectively dissipates the stress and strain induced by the SiO expansion. And in this self-healing network, rigid PAA provides structural integrity, whereas elastic PTA with dynamic S-S bonds serves as a buffer, enabling a tunable balance between mechanical strength and flexibility to accommodate lithiation-induced volume expansion. As expected, the SiO electrode with the PPC binder demonstrates a decent performance with a specific discharge capacity of 998.6 mAh g after 200 cycles at 2000 mA g, corresponding to a capacity retention of 85%. Meanwhile, the binder enabled the SiO||NCM622 full cell to achieve remarkable capacity retention of 95.1% after 100 cycles at 0.5 C.

摘要

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