Lithium salt-derived artificial near-surface reconfiguration to stabilize high-voltage LiCoO2†

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2024-12-20 Epub Date: 2025-01-06 DOI:10.1039/d4cc05449k
Jun-Ke Liu , Guo-Dong Bai , Zu-Wei Yin , Li Deng , Wen-Jing Sun , Zhen Wang , Gao-Yang Bai , Yu-Xi Luo , Zhi-Liang Jin , Yao Zhou , Jun-Tao Li , Shi-Gang Sun
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Abstract

Pushing the limit of the charging cut-off voltage inevitably leads to the instability of bulk and interfacial structures. Herein, one-step dual-modified LiCoO2 (LCO) is achieved by thermodynamic decomposition of lithiuim salts on the surface, featuring F-doped bulk and LiF & LixByOz coating layers. Notably, such artificial near-surface reconfiguration effectively suppresses Co dissolution, structural deconstruction and electrolyte side reactions during repeated lithiation/delithiation processes. As a result, the modified LCO delivers a high capacity retention of 81.4% after 150 cycles at 0.5C and 81.7% after 300 cycles at 2C in the voltage region of 3.0–4.6 V (vs. Li/Li+).

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锂盐衍生人工近表面重构稳定高压LiCoO2
突破充电截止电压的极限不可避免地会导致块体和界面结构的不稳定。在这里,通过热力学分解表面的锂盐,一步实现了双重改性钴酸锂(LCO),具有掺杂 F 的体层和 LiF & LixByOz 涂层层。值得注意的是,在反复的锂化/退锂过程中,这种人工近表面重构能有效抑制钴的溶解、结构解构和电解质副反应。因此,在 3.0-4.6 V 的电压范围内(相对于 Li/Li+),改性 LCO 在 0.5C 下循环 150 次后的容量保持率高达 81.4%,在 2C 下循环 300 次后的容量保持率高达 81.7%。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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