Glycolic Acid-Induced Surface Reconstruction and In Situ Carbon Coating for High-Electrochemical-Performance Lithium-Rich Manganese-Based Cathodes

Lithium-rich manganese-based cathode materials (LRMs, Li1.2Mn0.54Ni0.13Co0.13O2) are promising prospects for subsequent-generation lithium-ion batteries owing to their elevated operating voltage, large specific capacity, and affordability. Nonetheless, their actual implementation is significantly impeded by irreversible lattice-oxygen redox reactions, surface structural disorder, and interfacial phase collapse, leading to low initial Coulombic efficiency (ICE), inadequate rate capability, and sluggish Li+ transport. Herein, we report a simple and mild glycolic acid-assisted surface-engineering strategy to enhance the electrochemical performance of LRM. Glycolic acid treatment induces controlled H+/Li+ ion exchange at the particle surface and anchors surface transition metals through the formation of transition metals (TM)–OH and TM–O–C=O bonds. Subsequent calcination constructs an in situ carbon layer-spinel-layered heterostructure, accompanied by the generation of coupled anionic and cationic vacancies. This reconstructed surface provides fast Li+ diffusion pathways and stabilized ion-transport channels, while the dual-vacancy configuration enhances lattice-oxygen reversibility and suppresses structural disorder. Consequently, the modified LRM delivers a high initial discharge capacity of 285.3 mAh⋅g−1 with an ICE of 89.9%, while maintaining 81% capacity retention after 100 cycles. Notably, it exhibits a significantly suppressed voltage decay of only 1.7 mV/cycle at 3C, markedly outperforming the pristine LRM. Density Functional Theory (DFT) calculations reveal that the surface-modified sample possesses enhanced electronic conductivity, as evidenced by the improved Density of States (DOS), and achieves superior structural stability through increased binding energies. This environmentally benign surface-engineering strategy offers a practical and efficient route toward the industrial application of LRM.

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Journal
Batteries
Published
2026-02-15
DOI
https://doi.org/10.3390/batteries12020070
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Glycolic Acid-Induced Surface Reconstruction and In Situ Carbon Coating for High-Electrochemical-Performance Lithium-Rich Manganese-Based Cathodes

Yaoxun Fang, Xichen Yang, Gongchang Peng, Jin Miao et al.
Batteries
Advancements in Battery Materials
article

Glycolic Acid-Induced Surface Reconstruction and In Situ Carbon Coating for High-Electrochemical-Performance Lithium-Rich Manganese-Based Cathodes

Yaoxun Fang, Xichen Yang, Gongchang Peng, Jin Miao, Ying Chen, Hao Wang
article en

Abstract

Lithium-rich manganese-based cathode materials (LRMs, Li1.2Mn0.54Ni0.13Co0.13O2) are promising prospects for subsequent-generation lithium-ion batteries owing to their elevated operating voltage, large specific capacity, and affordability. Nonetheless, their actual implementation is significantly impeded by irreversible lattice-oxygen redox reactions, surface structural disorder, and interfacial phase collapse, leading to low initial Coulombic efficiency (ICE), inadequate rate capability, and sluggish Li+ transport. Herein, we report a simple and mild glycolic acid-assisted surface-engineering strategy to enhance the electrochemical performance of LRM. Glycolic acid treatment induces controlled H+/Li+ ion exchange at the particle surface and anchors surface transition metals through the formation of transition metals (TM)–OH and TM–O–C=O bonds. Subsequent calcination constructs an in situ carbon layer-spinel-layered heterostructure, accompanied by the generation of coupled anionic and cationic vacancies. This reconstructed surface provides fast Li+ diffusion pathways and stabilized ion-transport channels, while the dual-vacancy configuration enhances lattice-oxygen reversibility and suppresses structural disorder. Consequently, the modified LRM delivers a high initial discharge capacity of 285.3 mAh⋅g−1 with an ICE of 89.9%, while maintaining 81% capacity retention after 100 cycles. Notably, it exhibits a significantly suppressed voltage decay of only 1.7 mV/cycle at 3C, markedly outperforming the pristine LRM. Density Functional Theory (DFT) calculations reveal that the surface-modified sample possesses enhanced electronic conductivity, as evidenced by the improved Density of States (DOS), and achieves superior structural stability through increased binding energies. This environmentally benign surface-engineering strategy offers a practical and efficient route toward the industrial application of LRM.

BatteriesVol. 12(2)
Chinese Academy of Sciences (CN), Chengdu Organic Chemicals (China) (CN), University of Chinese Academy of Sciences (CN)
Natural Science Foundation of Henan Province
Openalex Percentile: Top 54%
Advancements in Battery Materials
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