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通过阴离子-阳离子共掺杂缓解应力集中以实现高稳定性富镍阴极

Relieving Stress Concentration through Anion-Cation Codoping toward Highly Stable Nickel-Rich Cathode.

作者信息

Zhou Yu, Zhang Hanwei, Wang Yinglei, Wan Tao, Guan Peiyuan, Zhou Xindong, Wang Xuri, Chen Yichang, Shi Hancheng, Dou Aichun, Su Mingru, Guo Ruiqiang, Liu Yunjian, Dai Liming, Chu Dewei

机构信息

School of Material science and Engineering, Jiangsu University, Zhenjiang 212013, China.

Thermal Science Research Center, Shandong Institute of Advanced Technology, Jinan, Shandong Province 250103, China.

出版信息

ACS Nano. 2023 Oct 24;17(20):20621-20633. doi: 10.1021/acsnano.3c07655. Epub 2023 Oct 4.

DOI:10.1021/acsnano.3c07655
PMID:37791899
Abstract

Nickel-rich LiNiCoAlO (NCA) with excellent energy density is considered one of the most promising cathodes for lithium-ion batteries. Nevertheless, the stress concentration caused by Li/Ni mixing and oxygen vacancies leads to the structural collapse and obvious capacity degradation of NCA. Herein, a facile codoping of anion (F)-cation (Mg) strategy is proposed to address these problems. Benefiting from the synergistic effect of F and Mg, the codoped material exhibits alleviated Li/Ni mixing and demonstrates enhanced electrochemical performance at high voltage (≥4.5 V), outperformed the pristine and F/Mg single-doped counterparts. Combined experimental and theoretical studies reveal that Mg and F codoping decreases the Li diffusion energy barrier and enhances the Li transport kinetics. In particular, the codoping synergistically suppresses the Li/Ni mixing and lattice oxygen escape, and alleviates the stress-strain accumulation, thereby inhibiting crack propagation and improving the electrochemical performance of the NCA. As a consequence, the designed LiMgNiCoAlOF (Mg1+F2) demonstrates a much higher capacity retention of 82.65% than NCA (55.69%) even after 200 cycles at 2.8-4.5 V under 1 C. Furthermore, the capacity retention rate of the Mg1+F2||graphite pouch cell after 500 cycles is 89.6% compared to that of the NCA (only 79.4%).

摘要

具有优异能量密度的富镍LiNiCoAlO(NCA)被认为是锂离子电池最有前景的阴极材料之一。然而,Li/Ni混合和氧空位导致的应力集中会致使NCA结构崩塌和容量明显下降。在此,我们提出一种简单的阴离子(F)-阳离子(Mg)共掺杂策略来解决这些问题。得益于F和Mg的协同效应,共掺杂材料的Li/Ni混合现象得到缓解,并在高电压(≥4.5 V)下展现出增强的电化学性能,优于原始材料以及F/Mg单掺杂的对应材料。结合实验和理论研究表明,Mg和F共掺杂降低了Li扩散能垒并增强了Li传输动力学。特别地,共掺杂协同抑制了Li/Ni混合和晶格氧逸出,并减轻了应力-应变积累,从而抑制裂纹扩展并改善了NCA的电化学性能。因此,即使在1 C下于2.8-4.5 V循环200次后,设计的LiMgNiCoAlOF(Mg1+F2)的容量保持率也比NCA(55.69%)高得多,达到82.65%。此外,Mg1+F2||石墨软包电池在500次循环后的容量保持率为89.6%,而NCA(仅79.4%)。

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