Adaptive Localized Ectopic Structure Enhances Regeneration of Spent Lithium‐Ion Battery Cathodes

S Siyu Zhang (Key Laboratory of Functional Polymer Materials of Ministry of Education, Institute of Polymer Chemistry, State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for New Organic Matter, Haihe Laboratory of Sustainable Chemical Transformations, College of Chemistry) Y Yangyang Liu (State Key Laboratory for Mechanical Behavior of Materials, School of Instrument Science and Technology) G Gen Chen Z Zeinhom M. El‐Bahy (Faculty of Science Department of Chemistry Al‐Azhar University Cairo Egypt) D Dalal A. Alshammari (Department of Chemistry College of Science University of Hafr Al Batin Hafr Al Batin P.O. Box 39524 Saudi Arabia) M Mohamed H. Helal (Center For Scientific Research and Entrepreneurship Northern Border University Arar Saudi Arabia) J Jiang Zhou (School of Materials Science and Engineering, Hunan Provincial Key Laboratory of Electronic Packaging and Advanced Functional Materials) J Junwei Han (Shandong Key Laboratory of Advanced Electrochemical Energy Storage Technologies, College of New Energy)

Abstract

Abstract Direct regeneration has emerged as a budding strategy for recycling spent lithium‐ion batteries, yet restoring the degraded crystal structure of the cathode remains a momentous handicap. Here, a novel deep eutectic solvent rich in lithium (Li) is developed that not only induces the formation of an adaptive local ectopic structure (ALES) characterized by disordered and localized cations, but also facilitates the separation of cathode sheets and replenishes depleted elements. Within ALES, ectopic cobalt (Co) sites boost Li + diffusion by expanding the Li slab and forming octahedral coordination with low‐spin Co 3+ , while ectopic Li modulates Co─O interactions, collaboratively impeding long‐range structural disorder, mitigating lattice stress, and reducing charge density fluctuations. The synergistic interaction between the ectopic Co and Li enables in situ structural repair of spent lithium cobalt oxide (LCO), thereby restoring crystallinity and enhancing electrochemical performance. The regenerated LCO delivers a reversible capacity of 183.08 mAh g −1 at 0.2 C, with 87.01% capacity retention after 200 cycles at 0.5 C, outperforming commercial counterparts. This study offers a new pathway for addressing an urgent bottleneck in structure‐targeted LIB regeneration.

Article Details

Volume / Issue Vol. 38, Issue 1
Published January 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (8)

S

Siyu Zhang

Key Laboratory of Functional Polymer Materials of Ministry of Education, Institute of Polymer Chemistry, State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for New Organic Matter, Haihe Laboratory of Sustainable Chemical Transformations, College of Chemistry

Y

Yangyang Liu

State Key Laboratory for Mechanical Behavior of Materials, School of Instrument Science and Technology

G

Gen Chen

Z

Zeinhom M. El‐Bahy

Faculty of Science Department of Chemistry Al‐Azhar University Cairo Egypt

D

Dalal A. Alshammari

Department of Chemistry College of Science University of Hafr Al Batin Hafr Al Batin P.O. Box 39524 Saudi Arabia

M

Mohamed H. Helal

Center For Scientific Research and Entrepreneurship Northern Border University Arar Saudi Arabia

J

Jiang Zhou

School of Materials Science and Engineering, Hunan Provincial Key Laboratory of Electronic Packaging and Advanced Functional Materials

J

Junwei Han

Shandong Key Laboratory of Advanced Electrochemical Energy Storage Technologies, College of New Energy