材料科学
石墨
电解质
相间
兴奋剂
纳米技术
格子(音乐)
相变
离子键合
可扩展性
化学工程
碳纤维
降级(电信)
相(物质)
复合材料
化学物理
动力学
作者
Lei Wang,Can Wang,Fu‐Da Yu,Lan‐Fang Que,Xiang‐Gong Zhang,Ke-Yu Xie
摘要
ABSTRACT Low‐temperature fast charging of lithium‐ion batteries is primarily constrained by sluggish reaction kinetics and mechanical degradation of graphite anodes. Here, a kinetic–structural coordination strategy based on a 15 wt.% hard carbon (HC) percolating network embedded within the graphite matrix is proposed. This HC network functions as an ionic flux redistributor, effectively suppressing the high‐strain phase transition to stage 1 (LiC 6 ) and reducing lattice strain, thereby protecting the graphite from mechanical pulverization. Moreover, the coordinated lithiation promotes the formation of a robust, LiF‐rich inorganic solid electrolyte interphase (SEI), which facilitates fast desolvation and prevents interfacial delamination. As a result, NCM523‖Graphite/HC pouch cells deliver 2250 cycles at −20°C under a 4C rate with 88% capacity retention, and maintain stable operation at 8C and −40°C. This network doping approach thus provides a scalable design principle for all‐climate, high‐power batteries intended for electric vehicle applications.
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