电解质
分离器(采油)
电化学
石墨
介电谱
循环伏安法
材料科学
分析化学(期刊)
扩散
电极
阳极
锂离子电池
电化学电池
多孔性
滴定法
化学
电池(电)
极化(电化学)
离子
化学工程
伏安法
锂(药物)
浓差极化
锂电池
无机化学
线性扫描伏安法
作者
Çağatay Özada,Hatice Güngör,Neslihan Yuca
标识
DOI:10.1016/j.est.2026.122743
摘要
This study systematically investigates LiFePO 4 (LFP) and graphite half-cells using different separator-electrolyte configurations to explain their effects on lithium-ion transport and electrochemical performance. The electrodes are prepared from commercially available powders and characterized using XRD and SEM. Electrochemical analysis is performed using cyclic voltammetry (CV), galvanostatic intermittent titration technique (GITT), and electrochemical impedance spectroscopy (EIS). Lithium diffusion coefficients (D Li+ ) are determined from both CV and GITT data, allowing for comparison of transport kinetics. The results indicate that electrolyte viscosity and separator porosity are critical determinants of ion transport. The LFP and graphite cell configuration containing Electrolyte-B (1.08 M LiPF 6 in 1:3 EC:EMC) consistently provides the highest D Li+ values and the lowest charge transfer resistance. In graphite half-cells, the Electrolyte-B and Separator-2 (three-layer, PP, 54% porosity, 20 μm) configuration exhibits superior anodic kinetics, low polarization, and excellent capacity retention. Similarly, the same electrolyte and Separator-1 (single-layer, PP, 55% porosity, 25 μm) cell configuration exhibits the highest diffusion coefficient and specific discharge capacity among LFP systems. These results confirm a strong correlation between lithium-ion diffusion and long-term electrochemical stability.
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