Water Radiolysis Enables CO <sub>2</sub> ‐Activated Radical Recycling of Spent Lithium‐Ion Cathodes

H Hang Zhang Z Zhiwen Jiang (School of Nuclear Science and Technology) P Pengfei Zheng (School of Nuclear Science and Technology) L Li Zhai (City University of Hong Kong , , , ,) C Changjiang Hu (School of Nuclear Science and Technology) Y Yue Wang H Hanzhi Yu S Shuo Yan (School of Applied Chemistry and Engineering) R Ruihang Shang (School of Nuclear Science and Technology University of Science and Technology of China Hefei P. R. China) L Liang Mao (State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University) S Shuao Wang (State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection, Collaborative Innovation Center of Radiological Medicine of Jiangsu Higher Education Institutions, Biomedical Basic Research Center (BBRC) of Jiangsu) Y Yuxiang Bu (School of Chemistry and Chemical Engineering) J Jun Ma

Abstract

ABSTRACT Conventional recycling of spent lithium‐ion batteries (LIBs) relies on energy‐intensive and complex processes that hinder sustainability. Here, we report a mild, efficient recycling strategy using programmable water radiolysis with CO 2 to establish an aqueous reductive radical platform. This radiolytic approach enables simultaneous cathode peeling, metal leaching, and component separation under ambient conditions, which is inaccessible to existing methods. Within minutes, high‐dose‐rate irradiation degrades the polymeric binder, enabling ∼99.5% active material recovery. Radiolytically generated CO 2 •− radicals reduce and leach transition metals (Co, Ni, Mn) and lithium with &gt;96% efficiency. The dynamic pH evolution during irradiation precipitates transition metals in situ as carbonates while retaining Li + in solution, accomplishing one‐step separation. Regenerated cathodes deliver electrochemical performance comparable to commercial benchmarks. Techno‐economic analysis indicates this CO 2 ‐mediated radiolytic pathway offers a more sustainable, energy‐efficient, and cost‐effective route for battery recycling.

Article Details

Volume / Issue Vol. 65, Issue 31
Published July 27, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (13)

H

Hang Zhang

Z

Zhiwen Jiang

School of Nuclear Science and Technology

P

Pengfei Zheng

School of Nuclear Science and Technology

L

Li Zhai

City University of Hong Kong , , , ,

C

Changjiang Hu

School of Nuclear Science and Technology

Y

Yue Wang

H

Hanzhi Yu

S

Shuo Yan

School of Applied Chemistry and Engineering

R

Ruihang Shang

School of Nuclear Science and Technology University of Science and Technology of China Hefei P. R. China

L

Liang Mao

State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University

S

Shuao Wang

State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection, Collaborative Innovation Center of Radiological Medicine of Jiangsu Higher Education Institutions, Biomedical Basic Research Center (BBRC) of Jiangsu

Y

Yuxiang Bu

School of Chemistry and Chemical Engineering

J

Jun Ma