Qian Zhang, Chuang Sun, Kaiwen Yu, Tianpin Wu, Mengting Zheng, Junxiu Wu, Jun Lu
Silicon monoxide (SiO) has emerged as a promising high-capacity anode material for next-generation lithium-ion batteries. Nevertheless, the practical application of SiO anodes remains hindered by sluggish Li+ ion transport kinetics and persistent mechanical stress heterogeneity during deep lithiation. Here, we propose a piezoelectric functional-modification strategy that transforms the intrinsic expansion stress of SiO into a self-adaptive driving force for electrochemical regulation. By decorating SiO with piezoelectric LiTaO3 (SiO-P), the periodic volume fluctuation during cycling activates localized electric fields that accelerate Li+ ion migration, homogenize interfacial charge distribution, and promote the formation of a uniform, robust SEI. The resulting SiO-P composite delivers exceptional cycling stability, maintaining 380.8 mAh g-1 after 500 cycles at 2 C, with significantly enhanced durability validated in pouch-cell configurations. This work establishes a mechano-electrochemical paradigm that converts detrimental mechanical stress into a beneficial regulatory signal, offering a promising route toward high-energy, durable SiO-based anodes for practical LIBs.