Single‐Crystalline Ultrahigh‐Ni Co‐free Cathode with Magnetic Control as an Alternative to Commercial Cobalt‐containing LiNi <sub>0.88</sub> Mn <sub>0.08</sub> Co <sub>0.04</sub> O <sub>2</sub>

J Jixue Shen (College of Chemistry and Materials Science The Flame Retardant Material and Processing Technology Engineering Research Center of Hebei Province Hebei University Baoding P. R. China) L Lipeng Yang (School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, China) J Jing Meng Z Zhongkai Cao (College of Chemistry and Materials Science The Flame Retardant Material and Processing Technology Engineering Research Center of Hebei Province Hebei University Baoding P. R. China) X Xiaoyu Zhao L Liubin Wang (College of Chemistry &amp; Materials Science The Flame Retardant Material and Processing Technology Engineering Research Center of Hebei Province Hebei Research Center of the Basic Discipline of Synthetic Chemistry Hebei University Baoding China) N Ning Qin (Institute of Gene Science and Industrialization for Bamboo and Rattan Resources, International Centre for Bamboo and Rattan) Z Zeheng Li J Jianzhong Xu (College of Chemistry and Materials Science The Flame Retardant Material and Processing Technology Engineering Research Center of Hebei Province Hebei University Baoding P. R. China) J Jun Lu

Abstract

ABSTRACT The development of high‐energy low‐cost lithium‐ion batteries has sparked interest in ultrahigh‐Ni Co‐free layered cathodes that offer high capacity, low cost, and environmental friendliness. Yet, their widespread deployment is impeded by the challenges posed by the large magnetic moments of Ni and Mn, as well as the aggregation of the highly spin‐unstable high‐spin state of Ni 3+ at the interface. Herein, an efficient three‐in‐one strategy of internal Al and external Zr is proposed to achieve an ultrastable single‐crystal ultrahigh‐Ni Co‐free cathode, Li(Ni 0.90 Mn 0.08 Al 0.02 ) 0.98 Zr 0.02 O 2 (NMAZ). The strong AlO 6 ligands prevent the formation of high‐spin Ni 3+ . Surface‐enriched Zr restricts the diffusion of Ni within the NiO 6 octahedron. The single‐crystal structure reduces unwanted reactions with the electrolyte. Consequently, NMAZ achieves a favorable unity of material cost and electrochemical performance by reducing the resource expense by &gt;7.5% than conventional Co‐containing single‐crystal LiNi 0.88 Mn 0.08 Co 0.04 O 2 (NMC) and demonstrating excellent calendar lifespan performance. Moreover, it shows better phase stability under high dissociation conditions, alleviates the harmful H2‐H3 phase transformation, and avoids the release of lattice oxygen due to the overlap of Co 3+/4+ 3d and O 2− 2p orbitals upon deep delithiation.

Article Details

Volume / Issue Vol. 38, Issue 25
Published May 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

J

Jixue Shen

College of Chemistry and Materials Science The Flame Retardant Material and Processing Technology Engineering Research Center of Hebei Province Hebei University Baoding P. R. China

L

Lipeng Yang

School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, China

J

Jing Meng

Z

Zhongkai Cao

College of Chemistry and Materials Science The Flame Retardant Material and Processing Technology Engineering Research Center of Hebei Province Hebei University Baoding P. R. China

X

Xiaoyu Zhao

L

Liubin Wang

College of Chemistry &amp; Materials Science The Flame Retardant Material and Processing Technology Engineering Research Center of Hebei Province Hebei Research Center of the Basic Discipline of Synthetic Chemistry Hebei University Baoding China

N

Ning Qin

Institute of Gene Science and Industrialization for Bamboo and Rattan Resources, International Centre for Bamboo and Rattan

Z

Zeheng Li

J

Jianzhong Xu

College of Chemistry and Materials Science The Flame Retardant Material and Processing Technology Engineering Research Center of Hebei Province Hebei University Baoding P. R. China

J

Jun Lu