Enhancing Anionic Redox Reversibility and Structural Stability of Li-Rich Mn-Based Cathodes via Tuning Band Structure by Sn Doping

Li-rich Mn-based cathodes (LRMs) demonstrate exceptionally high specific capacity due to the anionic redox reaction. However, the irreversibility of anionic redox leads to lattice oxygen release; meanwhile, Mn-ion migration causes structural phase transitions and dissolution, resulting in severe capacity decay and voltage drop. Herein, we propose Sn doping at Mn sites to modulate the relative positions and overlap of energy bands, thereby enabling anionic redox reversibility and enhancing the structural stability. Compared with non-doped LRM, the Sn-doped LRM downshifts the energy of the O 2p non-bonding orbital and enhances its overlap with the (TM-O) antibonding orbital, preventing excessive oxygen oxidation and improving the reversibility of anionic redox. Meanwhile, it reduces the content of Mn<sup>3+</sup> and alleviates the distortion of MnO<sub>6</sub> octahedra, resulting in the improved structural stability. Therefore, the Sn-doped LRM exhibits outstanding cycling stability and high-rate capability at high voltages. This work offers insights into improving the reversibility of the anionic redox reaction and structural stability of LRMs through energy band engineering.

Authors

Institutions

Publication Details

Journal
ACS Nano
Published
2025-11-25
DOI
https://doi.org/10.1021/acsnano.5c14872
Citations
3
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
2.19
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Enhancing Anionic Redox Reversibility and Structural Stability of Li-Rich Mn-Based Cathodes via Tuning Band Structure by Sn Doping

Jie Sun, Huaqiang Chen, Haochen Gong, Tian Qiu et al.
3 citations
ACS Nano
Advancements in Battery Materials
2.19
article

Enhancing Anionic Redox Reversibility and Structural Stability of Li-Rich Mn-Based Cathodes via Tuning Band Structure by Sn Doping

Jie Sun, Huaqiang Chen, Haochen Gong, Tian Qiu, Xiaoyi Wang, Haiping Zhang, Shaowei Wang, Wei Liu, Minghua Yang, Wei Xu, Kang Ma
article en
3 citations

Abstract

Li-rich Mn-based cathodes (LRMs) demonstrate exceptionally high specific capacity due to the anionic redox reaction. However, the irreversibility of anionic redox leads to lattice oxygen release; meanwhile, Mn-ion migration causes structural phase transitions and dissolution, resulting in severe capacity decay and voltage drop. Herein, we propose Sn doping at Mn sites to modulate the relative positions and overlap of energy bands, thereby enabling anionic redox reversibility and enhancing the structural stability. Compared with non-doped LRM, the Sn-doped LRM downshifts the energy of the O 2p non-bonding orbital and enhances its overlap with the (TM-O) antibonding orbital, preventing excessive oxygen oxidation and improving the reversibility of anionic redox. Meanwhile, it reduces the content of Mn<sup>3+</sup> and alleviates the distortion of MnO<sub>6</sub> octahedra, resulting in the improved structural stability. Therefore, the Sn-doped LRM exhibits outstanding cycling stability and high-rate capability at high voltages. This work offers insights into improving the reversibility of the anionic redox reaction and structural stability of LRMs through energy band engineering.

ACS NanoVol. 19(48)
Tianjin University (CN), Nankai University (CN), Quzhou College of Technology (CN), Institute for Learning Innovation (US), Quzhou University (CN), Shanghai Huayi Group (China) (CN)
Openalex Percentile: Top 11%
Advancements in Battery Materials
2.19
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.