Tuning cation ordering and Mn3+ content in non-stoichiometric LiNi0.5-Mn1.5+O4- (LNMO) for enhanced cathode stability in lithium-ion batteries

Rapidly increasing demand for high-energy, long-cycle-life lithium-ion batteries (LIBs), particularly in electric vehicles and grid-scale applications, has highlighted the need for advanced cathode materials. High-voltage LiNi 0.5 Mn 1.5 O 4 (LNMO) has attracted considerable attention owing to its elevated working potential, reduced reliance on nickel, and cobalt-free composition. In this work, a scalable co-precipitation method is employed to synthesize non-stoichiometry LNMO cathodes with varying particle size, enabling precise control over particle morphology, cation ordering and Mn 3+ content. Comprehensive structural and electrochemical evaluations reveal that reducing the Ni content in LNMO elevates the Mn 3+ concentration and promotes the degree if cation disorder, which facilitates a single-phase, solid-solution reaction mechanism during lithiation and de-lithiation. In such a mechanism, Li + are inserted and extracted uniformly throughout the material without the formation of distinct phase boundaries, thereby significantly reducing kinetic barriers and polarization. Furthermore, although Mn 3+ typically induces local Jahn-Teller distortions, in a highly disordered lattice these distortions are more uniformly distributed, which minimizes local stress accumulation and enhances structural stability during cycling. This uniform distribution not only supports rapid Li + diffusion through continuous and well-connected pathways but also improves electronic conductivity by optimizing the local electronic structure. Consequently, LNMO with the highest cation disorder and Mn 3+ content, exhibits superior electrochemical performance, delivering 119.6 mAh·g −1 at 2C, retaining 70.3 % of its capacity after 1000 cycles and demonstrating the best kinetics among the samples. • Non-Stoichiometric LNMO was synthesized through a scalable co-precipitation method. • The cation ordering and Mn 3+ content LNMO were precisely tuned by control of Ni/Mn ratio. • Optimized LNMO achieves reduced polarization and accelerated Li + kinetics. • LNMO-9 delivers 119.6 mAh·g −1 at 2C and 70.3 % retention after 1000 cycles at 1C.

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Journal
Journal of Energy Storage
Published
2025-10-31
DOI
https://doi.org/10.1016/j.est.2025.119200
Primary Topic
Advancements in Battery Materials
Type
article
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article

Tuning cation ordering and Mn3+ content in non-stoichiometric LiNi0.5-Mn1.5+O4- (LNMO) for enhanced cathode stability in lithium-ion batteries

Zhengying Wu, Gayathri Peta, Ulla M. Lassi, Pekka Tynjälä et al.
Journal of Energy Storage
Advancements in Battery Materials
article

Tuning cation ordering and Mn3+ content in non-stoichiometric LiNi0.5-Mn1.5+O4- (LNMO) for enhanced cathode stability in lithium-ion batteries

Zhengying Wu, Gayathri Peta, Ulla M. Lassi, Pekka Tynjälä, Tao Hu, Ruguang Ma, Shubo Wang, Hesu Mo, Doron Aurbach
article en

Abstract

Rapidly increasing demand for high-energy, long-cycle-life lithium-ion batteries (LIBs), particularly in electric vehicles and grid-scale applications, has highlighted the need for advanced cathode materials. High-voltage LiNi 0.5 Mn 1.5 O 4 (LNMO) has attracted considerable attention owing to its elevated working potential, reduced reliance on nickel, and cobalt-free composition. In this work, a scalable co-precipitation method is employed to synthesize non-stoichiometry LNMO cathodes with varying particle size, enabling precise control over particle morphology, cation ordering and Mn 3+ content. Comprehensive structural and electrochemical evaluations reveal that reducing the Ni content in LNMO elevates the Mn 3+ concentration and promotes the degree if cation disorder, which facilitates a single-phase, solid-solution reaction mechanism during lithiation and de-lithiation. In such a mechanism, Li + are inserted and extracted uniformly throughout the material without the formation of distinct phase boundaries, thereby significantly reducing kinetic barriers and polarization. Furthermore, although Mn 3+ typically induces local Jahn-Teller distortions, in a highly disordered lattice these distortions are more uniformly distributed, which minimizes local stress accumulation and enhances structural stability during cycling. This uniform distribution not only supports rapid Li + diffusion through continuous and well-connected pathways but also improves electronic conductivity by optimizing the local electronic structure. Consequently, LNMO with the highest cation disorder and Mn 3+ content, exhibits superior electrochemical performance, delivering 119.6 mAh·g −1 at 2C, retaining 70.3 % of its capacity after 1000 cycles and demonstrating the best kinetics among the samples. • Non-Stoichiometric LNMO was synthesized through a scalable co-precipitation method. • The cation ordering and Mn 3+ content LNMO were precisely tuned by control of Ni/Mn ratio. • Optimized LNMO achieves reduced polarization and accelerated Li + kinetics. • LNMO-9 delivers 119.6 mAh·g −1 at 2C and 70.3 % retention after 1000 cycles at 1C.

Journal of Energy StorageVol. 141
Bar-Ilan University (IL), Suzhou University of Science and Technology (CN), Keski-Pohjanmaan keskussairaala (FI), University of Oulu (FI)
Openalex Percentile: Top 68%
Advancements in Battery Materials
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