High Performance 4.6 V LiCoO <sub>2</sub> Cathode Materials Enabled by Surface Lattice Modulation

Charging the cathode of LiCoO<sub>2</sub> (LCO) to higher voltages, typically 4.6 V, is able to increase reversible capacity, but meanwhile raises serious stability issues. Here, through a decomposition-induced reconstruction (DIR) process, we demonstrate the possibility of modulating the surface lattice of LCO with high precision in depth control, thereby enabling the 4.6 V LCO cathode to have both high capacity and structural integrity. Following the precise construction of a conformal Y(OH)CO<sub>3</sub> nanoshell, a sintering process induces the hydrocarbonate decomposition, which releases CO<sub>2</sub> to transform the layered structure of the LCO crust into rock-salt-like lattices, forming a renovated surface with high electrochemical and mechanical stability. The prepared LCO cathode delivers a high reversible capacity of 215.8 mAh g<sup>-1</sup> at 0.1 C with an extraordinary capacity retention of 93.0% after 100 cycles at 4.6 V. The much-improved stability is meanwhile manifested by cyclability test at 1 C (85.5% vs 13.6% of pristine LCO after 500 cycles), as well as tests at harsh conditions. Our results highlight the essential role played by the surface chemistry in addressing the stability issue of high voltage LCO cathode, and provide useful guidelines for the development of lithium-ion batteries with higher energy density.

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Publication Details

Journal
Advanced Materials
Published
2025-12-26
DOI
https://doi.org/10.1002/adma.202521637
Citations
1
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
0.73

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High Performance 4.6 V LiCoO 2 Cathode Materials Enabled by Surface Lattice Modulation

Qi‐wen Liu, Siqi Lu, Si‐Dong Zhang, Wei Zhou et al.
1 citations
Advanced Materials
Advancements in Battery Materials
0.73
article

High Performance 4.6 V LiCoO 2 Cathode Materials Enabled by Surface Lattice Modulation

Qi‐wen Liu, Siqi Lu, Si‐Dong Zhang, Wei Zhou, Wenbo Ma, Xincheng Lei, Hao Huang, Sijie Guo, Ting‐Ting Wu, An‐Min Cao, Dong Su
article en
1 citations

Abstract

Charging the cathode of LiCoO<sub>2</sub> (LCO) to higher voltages, typically 4.6 V, is able to increase reversible capacity, but meanwhile raises serious stability issues. Here, through a decomposition-induced reconstruction (DIR) process, we demonstrate the possibility of modulating the surface lattice of LCO with high precision in depth control, thereby enabling the 4.6 V LCO cathode to have both high capacity and structural integrity. Following the precise construction of a conformal Y(OH)CO<sub>3</sub> nanoshell, a sintering process induces the hydrocarbonate decomposition, which releases CO<sub>2</sub> to transform the layered structure of the LCO crust into rock-salt-like lattices, forming a renovated surface with high electrochemical and mechanical stability. The prepared LCO cathode delivers a high reversible capacity of 215.8 mAh g<sup>-1</sup> at 0.1 C with an extraordinary capacity retention of 93.0% after 100 cycles at 4.6 V. The much-improved stability is meanwhile manifested by cyclability test at 1 C (85.5% vs 13.6% of pristine LCO after 500 cycles), as well as tests at harsh conditions. Our results highlight the essential role played by the surface chemistry in addressing the stability issue of high voltage LCO cathode, and provide useful guidelines for the development of lithium-ion batteries with higher energy density.

Advanced MaterialsVol. 38(10)
Beijing National Laboratory for Molecular Sciences (CN), FZU ‒ Institute of Physics of the Academy of Sciences of the Czech Republic (CZ), University of Chinese Academy of Sciences (CN), Beijing University of Chemical Technology (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences
Affordable and clean energy
Openalex Percentile: Top 20%
Advancements in Battery Materials
0.73
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