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复合表面重构富锂正极降解的软X射线叠层成像化学分析

Soft X-ray Ptychography Chemical Imaging of Degradation in a Composite Surface-Reconstructed Li-Rich Cathode.

作者信息

Sun Tianxiao, Sun Gang, Yu Fuda, Mao Yongzhi, Tai Renzhong, Zhang Xiangzhi, Shao Guangjie, Wang Zhenbo, Wang Jian, Zhou Jigang

机构信息

Canadian Light Source Inc., University of Saskatchewan, Saskatoon, SK S7N 2V3, Canada.

Shanghai Institute of Applied Physics, Chinese Academy of Sciences, 2019 Jialuo Highway, Jiading District, Shanghai 201800, China.

出版信息

ACS Nano. 2021 Jan 26;15(1):1475-1485. doi: 10.1021/acsnano.0c08891. Epub 2020 Dec 23.

Abstract

The capability in spatially resolving the interactions between components in lithium (Li)-ion battery cathodes, especially correlating chemistry and electronic structure, is challenging but critical for a better understanding of complex degradation mechanisms for rational developments. X-ray spectro-ptychography and conventional synchrotron-based scanning transmission X-ray microscopy image stacks are the most powerful probes for studying the distribution and chemical state of cations in degraded Li-rich cathodes. Herein, we propose a chemical approach with a spatial resolution of around 5.6 nm to imaging degradation heterogeneities and interplay among components in degraded Li-rich cathodes. Through the chemical imaging reconstruction of the degraded Li-rich cathodes, fluorine (F) ions incorporated into the lattice during charging/discharging processes are proved and strongly correlate with the manganese (Mn) dissolution and oxygen loss within the secondary particles and impact the electronic structure. Otherwise, the electrode-electrolyte interphase component, scattered LiF particles (100-500 nm) along with the MnF layer, is also visualized between the primary particles inside the secondary particles of the degraded cathodes. The results provide direct visual evidence for the Li-rich cathode degradation mechanisms and demonstrate that the low-energy ptychography technique offers a superior approach for high-resolution battery material characterization.

摘要

在空间上解析锂离子电池阴极中各组分之间的相互作用,尤其是关联化学性质和电子结构,这一能力具有挑战性,但对于更好地理解复杂的降解机制以进行合理开发至关重要。X射线光谱叠层成像技术和传统的基于同步加速器的扫描透射X射线显微镜图像堆栈是研究富锂阴极降解过程中阳离子分布和化学状态的最强大探针。在此,我们提出一种化学方法,其空间分辨率约为5.6纳米,用于成像富锂阴极降解过程中的不均匀性以及各组分之间的相互作用。通过对富锂阴极降解情况进行化学成像重建,证实了在充电/放电过程中掺入晶格的氟(F)离子,并且这些离子与二次颗粒内的锰(Mn)溶解和氧损失密切相关,并影响电子结构。此外,在降解阴极二次颗粒内部的一次颗粒之间,还可视化了电极-电解质界面组分,即散布着的LiF颗粒(100 - 500纳米)以及MnF层。这些结果为富锂阴极降解机制提供了直接的可视化证据,并表明低能叠层成像技术为高分辨率电池材料表征提供了一种优越的方法。

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