泥浆
电池(电)
电阻抗
阴极
介电谱
电容
电极
极化(电化学)
泰文定理
流变学
材料科学
电介质
微观结构
阳极
等效电路
粘度
可扩展性
内阻
导电体
电子工程
光电子学
电化学
微波食品加热
输出阻抗
电化学电池
模数
放松(心理学)
流变仪
相对介电常数
复合材料
作者
Hyeseong Oh,Changhoon Park,Seung Ho Park,Kyeong‐Min Jeong
标识
DOI:10.1016/j.jpowsour.2025.238658
摘要
Understanding the internal microstructure of lithium-ion battery slurries is essential for achieving high-performance electrodes. However, conventional rheological metrics such as viscosity and modulus offer only indirect insight into the electrically active network formed by conductive agents. Here, we present a standardized coin cell-based impedance spectroscopy framework that directly quantifies the internal structure of lithium-ion battery slurries. By applying the distribution of relaxation times analysis, we resolve distinct dielectric responses attributed to interfacial polarization and electrical conduction, and propose a unified equivalent circuit model. The extracted resistance and capacitance exhibit strong correlations with electrode-level electrical conductivity, microstructural tortuosity, and cell-level electrochemical performance metrics including initial capacity and rate capability. This scalable and reproducible approach enables predictive evaluation of slurry quality using only a coin cell and potentiostat, offering a practical tool for process monitoring and optimization in both lithium-ion and emerging battery systems. • Standardized coin cell enables reproducible slurry impedance analysis. • DRT analysis deconvolutes interfacial polarizations regarding homogeneity. • RC parameters of slurries correlate with electrode parameters and cell performance.
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