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单晶高镍阴极中动力学反应路径与表面结构降解的协同调控

Synergistic regulation of kinetic reaction pathway and surface structure degradation in single-crystal high-nickel cathodes.

作者信息

Shen Jixue, Zhang Bao, He Xinyou, Xiao Biaobiao, Xiao Zhiming, Li Xiao, Ou Xing

机构信息

Engineering Research Center of the Ministry of Education for Advanced Battery Materials, School of Metallurgy and Environment, Central South University, Changsha 410083, PR China.

Wuhan University of Technology, Wuhan 430070, PR China.

出版信息

J Colloid Interface Sci. 2023 Jan;629(Pt A):388-398. doi: 10.1016/j.jcis.2022.08.184. Epub 2022 Sep 5.

DOI:10.1016/j.jcis.2022.08.184
PMID:36087554
Abstract

As a promising high energy density cathode, single-crystal Ni-rich cathode face poor diffusion dynamics, which leads to poor structural evolution, poor cyclic stability and unfavorable rate performance, thus impeding its wider application. Herein, the strategy of synergistic surface modification by ionic conductor coating and trace element doping is delicately designed. The surface protective LiBO layer is wrapped on the single-crystal LiNiCoMnO (NCM83), which can improve the compatibility of cathode/electrolyte with reduced interface resistance. While Zr is incorporated into bulk to stabilize the crystal structure and migration channel. This synergistic strategy achieves the improvement of ionic transport and structural stability of single-crystal NCM83 (Zr-NCM83@B) from the outer surface to the inner body. As expected, the modified cathode Zr-NCM83@B demonstrates a satisfying electrochemical performance. It delivers a high reversible capacity of 169 mAh g in coin-type half-cell at 4C within 3.0-4.3 V. Remarkably, it displays excellent capacity retention of 83.5 % in Zr-NCM83@B || graphite pouch-type full-cell over 1400 cycles at 1C with high voltage range of 2.8-4.4 V. This synergistic surface modification provides a reference for commercial development of advanced single-crystal Ni-rich cathode under harsh testing conditions.

摘要

作为一种很有前景的高能量密度正极材料,单晶富镍正极面临着扩散动力学较差的问题,这导致其结构演变不佳、循环稳定性差和倍率性能不理想,从而阻碍了其更广泛的应用。在此,精心设计了通过离子导体涂层和微量元素掺杂进行协同表面改性的策略。在单晶LiNiCoMnO(NCM83)上包裹表面保护LiBO层,这可以通过降低界面电阻来提高正极/电解质的兼容性。同时,将Zr掺入体相中以稳定晶体结构和迁移通道。这种协同策略实现了从单晶NCM83(Zr-NCM83@B)的外表面到内部体相的离子传输和结构稳定性的改善。正如预期的那样,改性后的正极Zr-NCM83@B表现出令人满意的电化学性能。在硬币型半电池中,在3.0-4.3 V范围内,4C时它具有169 mAh g的高可逆容量。值得注意的是,在Zr-NCM83@B||石墨软包型全电池中,在1C、2.8-4.4 V的高电压范围内,经过1400次循环后,它表现出83.5%的优异容量保持率。这种协同表面改性为苛刻测试条件下先进单晶富镍正极的商业开发提供了参考。

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引用本文的文献

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Challenges and approaches of single-crystal Ni-rich layered cathodes in lithium batteries.锂电池中富镍单晶层状正极的挑战与方法
Natl Sci Rev. 2023 Sep 22;10(12):nwad252. doi: 10.1093/nsr/nwad252. eCollection 2023 Dec.