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。
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.
期刊介绍:
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