通过溶解结构调整提高单晶钴酸锂阴极在 4.8 V 电压下的稳定性

IF 19 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Zhenjie Zhang, Jing Wang, Xinyi Sun, Chuanchao Sheng, Maozeng Cheng, Hang Liu, Yiting Wang, Haoshen Zhou, Ping He
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引用次数: 0

摘要

提高充电截止电压可显著提高钴酸锂阴极的容量。然而,当截止电压超过 4.5 V 时(相对于 Li/Li+),钴酸锂会发生不可逆的相变,导致颗粒开裂和结构失效。此外,电解质的分解会影响阴极/电解质界面的稳定性,从而导致电池容量降低。在此,我们在单晶钴酸锂中掺入了铝、镁和锆元素,以增强钴酸锂的结构稳定性。此外,还使用 3 Å 沸石薄膜来调节溶解结构,以增强电解质的抗氧化性。这种设计使阴极/电解质界面在高压循环期间更加稳定。在截止电压为 4.8 V 时,钴酸锂电池在 0.1 C 下的初始放电容量为 236.2 mAh g-1,在 1 C 下循环 100 次后,容量保持率为 86.6%。采用石墨阳极和钴酸锂阴极的袋式全电池在 2.8-4.65 V 的充放电范围内工作,比能量达到 276 Wh kg-1,循环 200 次后容量保持率为 81%。这项研究在钴酸锂电池系统中引入了脱溶电解质,为应对高压钴酸锂电池的挑战提供了一种专业方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Improved Stability of Single-Crystal LiCoO2 Cathodes at 4.8 V through Solvation Structure Regulation

Improved Stability of Single-Crystal LiCoO2 Cathodes at 4.8 V through Solvation Structure Regulation

Improved Stability of Single-Crystal LiCoO2 Cathodes at 4.8 V through Solvation Structure Regulation

Improved Stability of Single-Crystal LiCoO2 Cathodes at 4.8 V through Solvation Structure Regulation

Increasing the charging cut-off voltage can significantly improve the capacity of LiCoO2 cathode. However, when the cut-off voltage exceeds 4.5 V (vs Li/Li+), LiCoO2 undergoes irreversible phase transitions, leading to particle cracking and structural failure. Additionally, the decomposition of the electrolyte compromises the stability of the cathode/electrolyte interface, resulting in diminished battery capacity. Herein, the elements Al, Mg, and Zr are doped into single-crystal LiCoO2 to enhance the structural stability of LiCoO2. Moreover, a 3 Å zeolite film is used to regulate the solvation structure to enhance the oxidation resistance of the electrolyte. This design enables a more stable cathode/electrolyte interface during high-voltage cycling. At a cut-off voltage of 4.8 V, the Li||LiCoO2 battery exhibits an initial discharge capacity of 236.2 mAh g−1 at 0.1 C and maintains 86.6% capacity retention after 100 cycles at 1 C. The pouch full cell, which utilizes a graphite anode and LiCoO2 cathode, operating within a charge–discharge range of 2.8–4.65 V, achieves a specific energy of 276 Wh kg−1 with 81% capacity retention after 200 cycles. This work introduces a desolvated electrolyte into the LiCoO2 battery system, providing a professional approach to addressing the challenges of high-voltage LiCoO2.

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来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
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