材料科学
阳极
一氧化硅
硅酸盐
一氧化碳
锂(药物)
硅
化学工程
氧气
析氧
相(物质)
桥接(联网)
离子
纳米技术
工作(物理)
基质(化学分析)
锂离子电池
氧化物
原硅酸盐
电极
电流密度
作者
H Chen,Di-Xin Xu,Ge Li,Shu-Hao Xiao,Zhuo-Ya Lu,Wanli Wang,Wenpeng Wang,Ji-Lei Shi,Juan Zhang,Yu-guo GUO
标识
DOI:10.1021/acsami.5c22957
摘要
The development of high-energy-density anodes capable of withstanding fast-charging conditions remains a significant challenge for lithium-ion batteries. Silicon monoxide (SiOx) is a promising candidate, yet its performance intrinsically depends on the structure of the lithium silicate matrix formed during the initial lithiation. Herein, we demonstrate that the lithiation method, chemical versus electrochemical, serves as a powerful tool for the precise phase engineering of this silicate component. We selectively synthesized Li2Si2O5, Li2SiO3, and Li4SiO4, establishing that the [NBO]/[Si] ratio is the key descriptor for Li-ion transport kinetics. Multiscale simulations confirm that nonbridging oxygen (NBO) sites provide low-energy migration pathways, whereas bridging oxygen (BO) sites impede ion mobility. The electrochemically derived Li4SiO4 phase, which possesses the highest [NBO]/[Si] ratio, consequently enables a superior fast-charging performance. Practical validation using 2-Ah pouch cells demonstrates 85% capacity retention after 300 cycles at 4C (15-min charging). This work establishes lithiation engineering as a fundamental strategy for developing high-performance SiOx anodes, transforming it from a simple pretreatment into a critical design parameter for fast-charging batteries.
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