Regulating the Mott–Hubbard Splitting for High‐Performance Co‐Free Li‐Rich Mn‐Based Oxide Cathode

Abstract Co‐free Li‐rich Mn‐based layered oxides attract great attention as next‐generation cathodes due to high specific capacity and low cost. However, their practical applications are hindered by the structural damage and poor cycling stability caused by the irreversible oxygen anion redox (OAR). Herein, a distinct strategy for regulating Mott–Hubbard splitting to address the detrimental issues is proposed. Introducing cations with specific electronic properties into the Li layer and transition metal (TM) layer decreases the Mott–Hubbard splitting energy (U) of TM cations, which promotes the electron removal and optimizes the band structure. This causes the antibonding band (M─O)* to rise and reduces its overlap with O2p band, thereby simultaneously enhancing the redox activity of TMs and the reversibility of OAR. The specific capacity, rate capability, and capacity retention are all significantly improved (255 mAh g −1 vs 223 mAh g −1 at 0.1C;197 mAh g −1 vs168 mAh g −1 at 1C;147 mAh g −1 vs115 mAh g −1 at 5 C; 93.2% vs 75.5% at 1C after 400 cycles). The oxygen release and voltage decay are also mitigated (92.4% vs 85.6% at 1C after 400 cycles). Moreover, a quantitative method to estimate U value is established for the first time. These findings provide insights into the intrinsic interaction mechanism of anions and cations redox and provide guidance for designing high‐performance cathodes.

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Publication Details

Journal
Advanced Functional Materials
Published
2025-02-16
DOI
https://doi.org/10.1002/adfm.202423843
Citations
10
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
7.30

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article

Regulating the Mott–Hubbard Splitting for High‐Performance Co‐Free Li‐Rich Mn‐Based Oxide Cathode

Lirong Zheng, Xiangfeng Liu, Guangxue Zhao, Tianyu Wang et al.
10 citations
Advanced Functional Materials
Advancements in Battery Materials
7.30
article

Regulating the Mott–Hubbard Splitting for High‐Performance Co‐Free Li‐Rich Mn‐Based Oxide Cathode

Lirong Zheng, Xiangfeng Liu, Guangxue Zhao, Tianyu Wang, Ruoyu Wang, Wen Hui Yin, Jicheng Zhang, Nian Zhang
article en
10 citations

Abstract

Abstract Co‐free Li‐rich Mn‐based layered oxides attract great attention as next‐generation cathodes due to high specific capacity and low cost. However, their practical applications are hindered by the structural damage and poor cycling stability caused by the irreversible oxygen anion redox (OAR). Herein, a distinct strategy for regulating Mott–Hubbard splitting to address the detrimental issues is proposed. Introducing cations with specific electronic properties into the Li layer and transition metal (TM) layer decreases the Mott–Hubbard splitting energy (U) of TM cations, which promotes the electron removal and optimizes the band structure. This causes the antibonding band (M─O)* to rise and reduces its overlap with O2p band, thereby simultaneously enhancing the redox activity of TMs and the reversibility of OAR. The specific capacity, rate capability, and capacity retention are all significantly improved (255 mAh g −1 vs 223 mAh g −1 at 0.1C;197 mAh g −1 vs168 mAh g −1 at 1C;147 mAh g −1 vs115 mAh g −1 at 5 C; 93.2% vs 75.5% at 1C after 400 cycles). The oxygen release and voltage decay are also mitigated (92.4% vs 85.6% at 1C after 400 cycles). Moreover, a quantitative method to estimate U value is established for the first time. These findings provide insights into the intrinsic interaction mechanism of anions and cations redox and provide guidance for designing high‐performance cathodes.

Advanced Functional MaterialsVol. 35(28)
Chinese Academy of Sciences (CN), China Spallation Neutron Source (CN), Sino-Danish Centre for Education and Research (CN), Institute of High Energy Physics (CN), Shanghai Institute of Microsystem and Information Technology (CN), University of Chinese Academy of Sciences (CN)
Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 3%
Advancements in Battery Materials
7.30
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