锂离子电池负极材料LiCoO2的电化学性能:废材料回收再利用的实现

IF 1.8 Q3 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS
Mikhail Kamenskii, Alexey Volkov, Valentin Romanovski, Evgenii Beletskii
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引用次数: 0

摘要

系统地研究了正极材料LiCoO2在阳极电位范围内的电化学行为,以探索其作为锂离子电池正极材料的可行性。观察到可逆锂离子嵌入是低电位极限的函数,表明其具有高容量储能的潜力。研究表明,当每配方单元插入1.25 Li+时,材料的电化学性能稳定,平均容量为350 mA·h·g−1。详细的恒流充放电和循环伏安试验表明,LiCoO2可以可逆地插入锂离子而不发生明显的结构降解,每个配方单位可达到1.5 Li+。在这种最佳锂含量下,材料在比容量和长期循环稳定性之间表现出良好的平衡性能。然而,在较高锂浓度下,由于结构不稳定和相变,电池容量衰减等问题也受到了挑战。尽管存在这些限制,LiCoO2作为一种转换型阳极材料表现出了良好的性能,使其成为先进锂离子电池传统阳极的可行替代品。该研究强调了精确控制锂嵌入水平对优化LiCoO2电化学性能的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrochemical Properties of LiCoO2 as Anode Material of Lithium-Ion Batteries: Implementation for Recycling and Reuse of Spent Material

The electrochemical behavior of the cathode material LiCoO2 was systematically investigated within the anodic potential range to explore its feasibility as an anode material for lithium-ion batteries (LIBs). Reversible lithium-ion intercalation was observed as a function of the low potential limit, demonstrating its potential for high-capacity energy storage. The study revealed that stable electrochemical performance was achieved when 1.25 Li+ per formula unit was inserted into the material, yielding an average capacity of 350 mA·h·g−1. Detailed galvanostatic charge/discharge and cyclic voltammetry tests indicated that LiCoO2 could intercalate lithium ions reversibly without significant structural degradation up to 1.5 Li+ per formula unit. At this optimal lithium content, the material exhibited a well-balanced performance between specific capacity and long-term cycling stability. However, challenges such as capacity fading at higher lithium concentrations were noted, which were attributed to structural instability and phase transformations. Despite these limitations, LiCoO2 demonstrated promising properties as a conversion-type anode material, making it a viable alternative to conventional anodes for advanced LIBs. This study underscores the importance of precise control over lithium intercalation levels to optimize the electrochemical performance of LiCoO2.

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