材料科学
阳极
介电谱
石墨烯
氧化物
电解质
渗透(认知心理学)
电极
电化学
放松(心理学)
导电体
化学工程
相间
原位
纳米技术
工作(物理)
壳体(结构)
电阻抗
渗流理论
化学物理
复合材料
图层(电子)
碳纳米管
作者
Min Ju Oh,Jong Hyeok Park,Kwang Chul Roh
标识
DOI:10.1002/sstr.202500689
摘要
Si is a promising anode material for lithium‐ion batteries due to its high theoretical capacity, but its practical use is hindered by severe volume changes, unstable solid electrolyte interphase (SEI) formation, and poor intrinsic conductivity. To address these limitations, Si/SiO X /reduced graphene oxide (rGO) composites were synthesized, in which the in situ grown SiO X layer stabilizes interfacial reactions and the rGO network enhances electronic conductivity. Here, electrochemical impedance spectroscopy combined with distribution of relaxation times (DRT) analysis was employed to disentangle the overlapping contributions of the SEI, charge transfer, and diffusion. Importantly, the DRT analysis resolved the dynamic SEI responses, revealing that SiO X predominantly governs interfacial stability by mitigating volume change induced stress, while rGO ensures continuous electron percolation and suppresses excessive SEI growth. As a result, the composites demonstrated superior cycling stability and rate capability compared with pristine Si. This work provides mechanistic insights into how interfacial and conductive layers cooperatively govern resistance evolution in Si‐based electrodes and offers guidance for the rational design of high‐performance Si anodes.
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