Insights into the Mechanisms Behind Structural Repair of Spent Layered Cathode Materials for Lithium‐Ion Batteries

S Shuaiwei Liu H Hao Liu A Arseniy Bokov (Institute for Applied Materials (IAM) Karlsruhe Institute of Technology (KIT) Hermann‐von‐Helmholtz‐Platz 1, D‐76344 Eggenstein‐Leopoldshafen Karlsruhe Germany) M Mohammad Jaleh (Institute for Applied Materials (IAM) Karlsruhe Institute of Technology (KIT) Hermann‐von‐Helmholtz‐Platz 1, D‐76344 Eggenstein‐Leopoldshafen Karlsruhe Germany) H Hang Li S Sylvio Indris O Oleksandr Dolotko (Institute for Applied Materials (IAM) Karlsruhe Institute of Technology (KIT) Hermann‐von‐Helmholtz‐Platz 1, D‐76344 Eggenstein‐Leopoldshafen Karlsruhe Germany) A Aleksandr Kalinko (Department of Chemistry and Center for Sustainable Systems Design (CSSD), University of Paderborn, Warburger Strasse 100, Paderborn D-33098, Germany) E Edgar Eduardo Villalobos Portillo (CELLS‐ALBA, Synchrotron Barcelona E‐08290 Spain) C Carlo Marini (ALBA Synchrotron Light Source) T Thomas Bergfeldt M Michael Knapp H Helmut Ehrenberg

Abstract

Abstract Structural repair is a vital step in the direct recycling of spent LiNi x Co y Mn z O 2 lithium‐ion batteries, yet its underlying mechanisms remain insufficiently clear. Herein, the thermal solid‐state structural repair of spent LiNi 0.6 Co 0.2 Mn 0.2 O 2 (NCM622) layered cathode material is systematically investigated. Through multiscale techniques combining XRD, XAS, and 6 Li solid‐state NMR, we identify the structural degradation in spent NCM622 and monitor both long‐ and short‐range structural evolution during repair. Our findings reveal that degradation predominantly occurs through Ni migration into Li octahedral sites, while Co and Mn demonstrate relatively lower occupancies in the Li layer. Such occupancies are primarily responsible for structural disorder and cubic‐symmetry domain formation within the spent material. The repair process is demonstrated to involve re‐lithiation, oxygen capture, increased transition metal (TM) oxidation states, and the migration of TM ions from the Li layer back to the TM layer, followed by cation diffusion. Both temperature and lithium compensation ratio are identified as critical factors promoting these processes. Capacity recovery studies show a strong correlation between reduced TM occupancy in the Li layer and improved electrochemical performances. These insights allow us to move beyond conventional phase‐transition perspectives, offering an atomic‐level understanding of structural degradation and repair mechanisms in spent layered cathode materials.

Article Details

Volume / Issue Vol. 64, Issue 32
Published August 04, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (13)

S

Shuaiwei Liu

H

Hao Liu

A

Arseniy Bokov

Institute for Applied Materials (IAM) Karlsruhe Institute of Technology (KIT) Hermann‐von‐Helmholtz‐Platz 1, D‐76344 Eggenstein‐Leopoldshafen Karlsruhe Germany

M

Mohammad Jaleh

Institute for Applied Materials (IAM) Karlsruhe Institute of Technology (KIT) Hermann‐von‐Helmholtz‐Platz 1, D‐76344 Eggenstein‐Leopoldshafen Karlsruhe Germany

H

Hang Li

S

Sylvio Indris

O

Oleksandr Dolotko

Institute for Applied Materials (IAM) Karlsruhe Institute of Technology (KIT) Hermann‐von‐Helmholtz‐Platz 1, D‐76344 Eggenstein‐Leopoldshafen Karlsruhe Germany

A

Aleksandr Kalinko

Department of Chemistry and Center for Sustainable Systems Design (CSSD), University of Paderborn, Warburger Strasse 100, Paderborn D-33098, Germany

E

Edgar Eduardo Villalobos Portillo

CELLS‐ALBA, Synchrotron Barcelona E‐08290 Spain

C

Carlo Marini

ALBA Synchrotron Light Source

T

Thomas Bergfeldt

M

Michael Knapp

H

Helmut Ehrenberg