阴极
材料科学
焦耳加热
烧结
纳米技术
降级(电信)
腐蚀
化学稳定性
兴奋剂
电池(电)
联轴节(管道)
阳极
热液循环
化学工程
储能
乏核燃料
格子(音乐)
量子隧道
纳米材料
纳米结构
闪光灯(摄影)
金属
作者
Yinhai Liu,Binglei Jiao,Beikai Zhang,Xingyu Guo,Liang Zhang,Guiling Wang,Jinxing Chen,Jiadong Yu,Panpan Xu,Qiao Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-01-14
卷期号:20 (3): 2830-2841
被引量:3
标识
DOI:10.1021/acsnano.5c17921
摘要
The direct regeneration of spent lithium-ion batteries has attracted considerable attention due to its potential to maximize economic benefits while minimizing environmental impacts. However, fluorine-containing contaminants severely interfere with the regeneration process through chemical interactions, often resulting in the cathode fluorination. Moreover, constrained by the technical limitations inherent in the original synthesis processes of waste electrodes, the cycling stability of regenerated cathode materials struggles to meet the current technical standards. Herein, we elucidate the underlying mechanisms of F-induced degradation in spent cathode materials and develop a flash Joule heating (FJH) technique with a Ca(OH)2 medium to achieve the coupling effect of fluorination inhibition and lattice stabilization in a single processing step. The addition of Ca(OH)2 can effectively capture the secondary HF, mitigating its corrosion of the cathodes to form a metal fluoride. Furthermore, the high temperature during FJH treatment facilitates in situ Ca doping into the LiCoO2 lattice, enhancing its electronic and ionic conductivity. Following hydrothermal relithiation and a brief sintering regeneration process, the regenerated Ca-doped LiCoO2 demonstrates a high capacity of 150.2 mAh/g (0.1 C) and enhanced cycling stability from 64.3 to 91.2% compared to that without Ca doping. This work provides a mechanistically guided and industrially adaptable strategy for the efficient regeneration of fluorinated cathodes, advancing the practical implementation of sustainable battery recycling.
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