材料科学
硅
电池(电)
锂(药物)
阳极
多酚
自愈
纳米技术
锂离子电池
离子
功率(物理)
光电子学
有机化学
电极
抗氧化剂
物理化学
化学
病理
替代医学
内分泌学
物理
医学
量子力学
作者
Hao-wen Jiang,Zuxue Mo,Xiao‐Liang Xie,Yi‐Long Wu,Xue‐Yi Xue
标识
DOI:10.1021/acsami.4c12880
摘要
This study introduces an anode material for lithium-ion batteries, achieved by integrating tea polyphenols (TP) with the widely utilized polyacrylic acid (PAA) binder. The composite material capitalizes on the intrinsic self-healing properties of TP, enhancing the anode's durability and adhesiveness without the need for additional organic synthesis. The incorporation of TP has been demonstrated to significantly elevate ionic conductivity and expedite lithium ion diffusion, thereby reducing interfacial resistance and decelerating the rate of capacity fade due to electrolyte decomposition and silicon particle expansion. Employing a comprehensive analytical toolkit, including Fourier transform infrared spectroscopy, thermogravimetric analysis, peel strength measurements, and density functional theory calculations, we elucidated the physicochemical properties of the Si@PAA-TP anode. The anode's electrochemical performance was systematically assessed through galvanostatic charge-discharge, cyclic voltammetry, and electrochemical impedance spectroscopy, with scanning electron microscopy providing insights into postcycling mechanical property alterations. This research advances a cost-effective, high-performance adhesive strategy for silicon anodes and contributes to the development.
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