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用于锂离子电池的纳米结构富锂锰基氧化物的表面氧空位调制

Surface Oxygen Vacancy Modulation of Nanostructured Li-Rich Mn-Based Oxides for Lithium-Ion Batteries.

作者信息

Nong Jinxia, Zhao Xiayan, Liang Fangan, Jia Shengkun, Zou Zhengguang

机构信息

College of Materials Science and Engineering, Guilin University of Technology, Guilin 541004, China.

出版信息

Materials (Basel). 2025 May 28;18(11):2537. doi: 10.3390/ma18112537.

Abstract

Li-rich Mn-based cathode materials are considered potential cathode materials for next-generation lithium-ion batteries due to their outstanding theoretical capacity and energy density. Nonetheless, challenges like oxygen loss, transition metal migration, and structural changes during cycling have limited their potential for commercialization. The work in this study employed a straightforward heat treatment to generate oxygen vacancies. This process led to the development of a spinel phase on the surface, which improved Li diffusion and boosted the electrochemical performance of Li-rich Mn-based oxides. The results demonstrate that the treated LiMnNiCoO exhibits an initial specific capacity of 247 mAh·g at 0.2C, as well as a reversible capacity of 224 mAh·g after 100 cycles, with a capacity retention of 90.7%. The voltage decay is 1.221 mV per cycle under 1C long-term cycling conditions, indicating excellent cycling stability and minimal voltage drop. Therefore, this strategy of engineering through nanoscale oxygen vacancies provides a new idea for the development of high-stability layered oxide anodes and provides a reference for the development and application of new energy materials.

摘要

富锂锰基正极材料因其出色的理论容量和能量密度,被认为是下一代锂离子电池的潜在正极材料。尽管如此,诸如氧损失、过渡金属迁移以及循环过程中的结构变化等挑战,限制了它们的商业化潜力。本研究中的工作采用了一种简单的热处理方法来产生氧空位。这一过程导致在表面形成了尖晶石相,改善了锂扩散并提高了富锂锰基氧化物的电化学性能。结果表明,经过处理的LiMnNiCoO在0.2C时的初始比容量为247 mAh·g,在100次循环后的可逆容量为224 mAh·g,容量保持率为90.7%。在1C长期循环条件下,电压衰减为每循环1.221 mV,表明具有出色的循环稳定性和最小的电压降。因此,这种通过纳米级氧空位进行工程设计的策略为高稳定性层状氧化物阳极的开发提供了新思路,并为新能源材料的开发与应用提供了参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b0d/12155591/80e346c1ecfb/materials-18-02537-g001.jpg

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