材料科学
阴极
法拉第效率
溶剂
锂(药物)
电化学
阳极
化学反应
纳米技术
化学工程
有机化学
物理化学
电极
化学
工程类
医学
内分泌学
作者
Tassadit Ouaneche,Lorenzo Stievano,Laure Monconduit,Claude Guéry,Moulay Tahar Sougrati,Nadir Recham
标识
DOI:10.1016/j.ensm.2024.103507
摘要
The lithiation reaction holds immense significance across various branches of chemistry, particularly in the realm of electrochemical energy storage. Here, we report a new method that enables a solvent-free process at room temperature, exhibiting remarkably swift reaction kinetics. Through this process, the chemical integration of Li+ into charged materials based on transition metals is achieved using lithium iodide, LiI. An evident application of this method lies in advancing the direct recycling of cathode materials reclaimed from spent batteries. Notably, the process facilitates the efficient and direct recycling of spent Li(1-x)FePO4 cathode material, sourced from a commercial LIB, without the need for any solvents or heat treatments. The regenerated material exhibits a fully reversible capacity of approximately 168 mAh/g against Li metal, even under high current density conditions, with a consistently stable coulombic efficiency surpassing 99% over 45 cycles. This regenerative approach holds the potential for seamless extension to other LIB cathode materials, including but not limited to LMFP, LMO, LCO and NMC.
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