Surface Reconstruction and Lattice Oxygen Modulation of 4.6 V LiCoO2 Cathode for Enhanced Fast-Charging Durability

IF 4.6 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Inorganic Chemistry Pub Date : 2026-05-11 Epub Date: 2026-04-29 DOI:10.1021/acs.inorgchem.6c00692
Zhuo Peng, , , Chengyu Li, , , Yan Pu, , , Yi Yang*, , , Wenge Yang*, , and , Yongjin Chen*, 
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引用次数: 0

Abstract

Increasing the charging cutoff voltage is the most direct way to enhance the energy density of LiCoO2, but it brings severe adverse effects. Here we propose a synergistic strategy of surface reconstruction and lattice oxygen modulation by Ba-doping to improve structural stability and electrochemical performance. Ba-doped LiCoO2 presents fast-charging durability at 4.6 V, and enhanced capacity retention of 69.4% after 200 cycles at 1 C compared to 16.8% for pristine LiCoO2. Introducing both the large ionic radius of Ba and lattice oxygen vacancies facilitates lithium-ion transport. The surface construction tailors the residual alkali layer and rocksalt phase. Two-phase hybrids with heterogeneous Li+ (de)lithiation were observed in pristine LiCoO2 during cycling, while a spinel phase with 3D lithium-ion diffusion channels was observed in Ba-doped LiCoO2. Our strategy suppresses lattice strain, structural degradation, and microcracks, and alleviates gas release during fast charging at high voltage, revealing the potential of lattice engineering to meet the demands of high-voltage batteries.

Abstract Image

Abstract Image

4.6 V LiCoO2阴极的表面重构和点阵氧调制提高了快速充电耐久性
提高充电截止电压是提高LiCoO2能量密度最直接的方法,但会带来严重的不良影响。在此,我们提出了一种表面重建和ba掺杂晶格氧调制的协同策略,以提高结构稳定性和电化学性能。ba掺杂的LiCoO2具有4.6 V的快速充电耐久性,在1℃下200次循环后的容量保留率提高了69.4%,而原始LiCoO2的容量保留率为16.8%。引入Ba的大离子半径和晶格氧空位有利于锂离子的输运。地表构造裁剪残碱层和岩盐相。在循环过程中,原始LiCoO2中观察到具有非均相Li+ (de)锂化的两相杂化物,而在ba掺杂LiCoO2中观察到具有3D锂离子扩散通道的尖晶石相。我们的策略抑制了晶格应变、结构退化和微裂纹,并缓解了高压快速充电过程中的气体释放,揭示了晶格工程满足高压电池需求的潜力。
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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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