Surface Engineering Enabling Efficient Upcycling of Highly Degraded Layered Cathodes

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 LiNi<sub>0.5</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub>O<sub>2</sub> from 59.7 to 165.4 mAh g<sup>-1</sup>, 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 LiCoO<sub>2</sub>. This work presents a promising approach for direct recycling of highly degraded cathode materials.

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Publication Details

Journal
Advanced Materials
Published
2025-03-06
DOI
https://doi.org/10.1002/adma.202419872
Citations
17
Primary Topic
Extraction and Separation Processes
Type
article
Field-Weighted Citation Impact
12.13

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article

Surface Engineering Enabling Efficient Upcycling of Highly Degraded Layered Cathodes

Ersha Fan, Zhongsheng Dai, Qingrong Huang, Jiao Lin et al.
17 citations
Advanced Materials
Extraction and Separation Processes
12.13
article

Surface Engineering Enabling Efficient Upcycling of Highly Degraded Layered Cathodes

Ersha Fan, Zhongsheng Dai, Qingrong Huang, Jiao Lin, Xiaowei Lv, Li Li, Xiaodong Zhang, Feng Wu, Renjie Chen
article en
17 citations

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 LiNi<sub>0.5</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub>O<sub>2</sub> from 59.7 to 165.4 mAh g<sup>-1</sup>, 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 LiCoO<sub>2</sub>. This work presents a promising approach for direct recycling of highly degraded cathode materials.

Advanced MaterialsVol. 37(15)
Beijing Institute of Technology (CN), Jinan Institute of Quantum Technology (CN)
National Natural Science Foundation of China, Natural Science Foundation of Beijing Municipality, National Key Research and Development Program of China
Openalex Percentile: Top 1%
Extraction and Separation Processes
12.13
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