This randomized trial demonstrates enhanced cycling stability and rate performance in silicon anodes, implying a new design strategy.
As promising high‐energy density anodes for lithium‐ion batteries, the Si electrodes face critical challenges from severe volume expansion and poor electrical conductivity. Herein, we report a dual‐layer protective structure (Si@MnSiO 3 @C) constructed through an in‐situ conversion reaction followed by chemical vapor deposition carbon coating. The inner MnSiO 3 layer is derived from the native SiO 2 layer on Si, forming robust Si─O─Mn covalent bonds that ensure strong interfacial adhesion. The outer carbon layer provides a conductive network and additional structural confinement. This architecture effectively buffers volume expansion, enhances electron transport, and facilitates Li + diffusion kinetics. As a result, the Si@MnSiO 3 @C composite delivers a high initial Coulombic efficiency of 80.1%, retains 86.1% of its capacity after 100 cycles at 0.5 A g −1 , and maintains a specific capacity of 1334 mA h g −1 after 600 cycles at 1 A g −1 , demonstrating excellent cycling stability and rate performance. This work presents a promising strategy for designing high‐performance Si‐based anodes through interfacial engineering.
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Gu et al. (2026) studied this question.
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