This research develops a self-healing binder for SiOx anodes, improving ion conduction and mechanical stability.
Volume expansion during repeated cycling is the primary cause of degradation of SiOx 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 SiOx 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 SiOx 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 SiOx electrode with the PPC binder demonstrates a decent performance with a specific discharge capacity of 998.6 mAh g-1 after 200 cycles at 2000 mA g-1, corresponding to a capacity retention of 85%. Meanwhile, the binder enabled the SiOx||NCM622 full cell to achieve remarkable capacity retention of 95.1% after 100 cycles at 0.5 C.
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Long et al. (2025) studied this question.
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