Surface Engineering Enabling Efficient Upcycling of Highly Degraded Layered Cathodes

IF 26.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Advanced Materials Pub Date : 2025-03-06 DOI:10.1002/adma.202419872
Qingrong Huang, Xiaodong Zhang, Xiaowei Lv, Jiao Lin, Zhongsheng Dai, Ersha Fan, Renjie Chen, Feng Wu, Li Li
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Abstract

Direct recycling of cathode materials has attracted phenomenal attention due to its economic and eco-friendly advantages. However, existing direct recycling technologies are difficult to apply to highly degraded layered materials as the accumulation of thick rock-salt phases on their surfaces not only blocks lithiation channels but also is thermodynamically difficult to transform into layered phases. Here, a surface engineering-assisted direct upcycling strategy that reactivates the lithium diffusion channels at the highly degraded cathode surfaces using acid etching explored. Acid can selectively remove the electrochemically inert rock-salt phases on the surface while simultaneously dissociating the degraded polycrystalline structure to single crystals, thereby reducing the thermodynamic barrier of the relithiation process and enhancing the stability of the regenerated cathode. This strategy can restore the capacity of highly degraded LiNi0.5Co0.2Mn0.3O2 from 59.7 to 165.4 mAh g−1, comparable to that of commercialized ones. The regenerated cathode also exhibits excellent electrochemical stability with a capacity retention of 80.1% at 1 C after 500 cycles within 3.0–4.2 V (vs graphite) in pouch-type full cells. In addition, the generality of this strategy has also been validated on Ni-rich layered materials and LiCoO2. This work presents a promising approach for direct recycling of highly degraded cathode materials.

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表面工程实现高降解层状阴极的有效升级回收
正极材料的直接回收利用因其经济、环保等优点而备受关注。然而,现有的直接回收技术很难应用于高度降解的层状材料,因为厚岩盐相在其表面堆积不仅阻塞了锂化通道,而且在热力学上难以转化为层状相。在这里,研究人员探索了一种表面工程辅助的直接升级回收策略,该策略利用酸蚀刻技术在高度降解的阴极表面重新激活锂扩散通道。酸可以选择性地去除表面的电化学惰性岩盐相,同时将降解的多晶结构解离为单晶,从而降低了还原过程的热力学屏障,增强了再生阴极的稳定性。该策略可以将高度退化的LiNi0.5Co0.2Mn0.3O2的容量从59.7 mAh g−1恢复到165.4 mAh g−1,与商业化的电池容量相当。再生阴极还表现出优异的电化学稳定性,在3.0-4.2 V (vs石墨)下,在1℃下循环500次后,容量保持率为80.1%。此外,该策略的通用性也在富镍层状材料和LiCoO2上得到了验证。这项工作为直接回收高度降解的阴极材料提供了一种很有前途的方法。
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来源期刊
Advanced Materials
Advanced Materials 工程技术-材料科学:综合
CiteScore
43.00
自引率
4.10%
发文量
2182
审稿时长
2 months
期刊介绍: Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.
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