材料科学
硅
离子电导率
阳极
电解质
复合材料
电导率
复合数
丙烯酸酯
电极
化学工程
极限抗拉强度
离子键合
纳米技术
纤维素
石墨
聚合物
纳米颗粒
相间
水溶液
纳米复合材料
作者
Lirong Tang,Lan Zhao,Zhiyi Cao,Fengcai Lin,Biao Huang,Haijun Li,Lingling Qian,Yingshan Shi,Yaohang Weng,Xuan Yang,Hanyang Liu,Beili Lu,Jianhua Lv,Xinda You,Jiayu Tao,Zhenwei Wu
标识
DOI:10.1002/advs.202522802
摘要
ABSTRACT Silicon anodes require binders that not only buffer volume changes but also preserve interfacial integrity. However, excessive encapsulation limits ion transport and long–term stability. Here, we develop a lipoic acid–rosin acrylate (LRA) binder via thiol–ene click chemistry. LRA exhibits high stretchability (4154%) and self–assembles into chain motifs, forming microphase arrangements in aqueous media. Incorporated into hinged–tethering phosphorylated cellulose nanocrystals (HT–PCNCs) and ionically crosslinked alginate–Ba 2 + scaffolds, these motifs cluster into mesoscale domains, reminiscent of the armor plates of Phloeodes diabolicus . This hybrid structure integrates rigid backbones with deformable rosin–rich beads, enabling localized strain dissipation, self–repair, and regulated ion conduction for stable solid electrolyte interphase (SEI) formation. The elastic mosaic dispersed within HT–PCNCs/SA–Ba 2 + provides mechanical robustness and ionic accessibility. The composite binder achieves a tensile strength of 308.52 MPa, fracture energy of 3288.48 MJ m − 3 , and ionic conductivity of 33.607 mS cm − 1 , while effectively suppressing interfacial cracks. Silicon electrodes deliver 83.25% capacity retention after 100 cycles, high rate capability (869.8 mAh g − 1 at 3C), and long‐term durability (1798 mAh g − 1 after 300 cycles), accompanied by an ultrathin (∼17 nm) LiF–rich SEI. This work highlights spatially resolved microphase engineering as a promising strategy for adaptive bio–based binders in silicon anodes.
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