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具有密度梯度的垂直取向电极微结构中锂离子浓度的三维关联成像

3D Correlative Imaging of Lithium Ion Concentration in a Vertically Oriented Electrode Microstructure with a Density Gradient.

作者信息

Huang Chun, Wilson Matthew D, Suzuki Kosuke, Liotti Enzo, Connolley Thomas, Magdysyuk Oxana V, Collins Stephen, Van Assche Frederic, Boone Matthieu N, Veale Matthew C, Lui Andrew, Wheater Rhian-Mair, Leung Chu Lun Alex

机构信息

Department of Materials, Imperial College London, London, SW7 2AZ, UK.

The Faraday Institution, Quad One, Becquerel Ave, Harwell Campus, Didcot, OX11 0RA, UK.

出版信息

Adv Sci (Weinh). 2022 May;9(16):e2105723. doi: 10.1002/advs.202105723. Epub 2022 Apr 11.

DOI:10.1002/advs.202105723
PMID:35404540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9165496/
Abstract

The performance of Li ion batteries (LIBs) is hindered by steep Li ion concentration gradients in the electrodes. Although thick electrodes (≥300 µm) have the potential for reducing the proportion of inactive components inside LIBs and increasing battery energy density, the Li ion concentration gradient problem is exacerbated. Most understanding of Li ion diffusion in the electrodes is based on computational modeling because of the low atomic number (Z) of Li. There are few experimental methods to visualize Li ion concentration distribution of the electrode within a battery of typical configurations, for example, coin cells with stainless steel casing. Here, for the first time, an interrupted in situ correlative imaging technique is developed, combining novel, full-field X-ray Compton scattering imaging with X-ray computed tomography that allows 3D pixel-by-pixel mapping of both Li stoichiometry and electrode microstructure of a LiNi Mn Co O cathode to correlate the chemical and physical properties of the electrode inside a working coin cell battery. An electrode microstructure containing vertically oriented pore arrays and a density gradient is fabricated. It is shown how the designed electrode microstructure improves Li ion diffusivity, homogenizes Li ion concentration through the ultra-thick electrode (1 mm), and improves utilization of electrode active materials.

摘要

锂离子电池(LIBs)的性能受到电极中陡峭的锂离子浓度梯度的阻碍。尽管厚电极(≥300 µm)有潜力降低锂离子电池内部非活性成分的比例并提高电池能量密度,但锂离子浓度梯度问题却加剧了。由于锂的原子序数(Z)较低,大多数对电极中锂离子扩散的理解基于计算模型。几乎没有实验方法可以可视化典型配置电池(例如带不锈钢外壳的硬币电池)内电极的锂离子浓度分布。在此,首次开发了一种中断原位关联成像技术,将新型全场X射线康普顿散射成像与X射线计算机断层扫描相结合,可对LiNiMnCoO阴极的锂化学计量和电极微观结构进行逐像素三维映射,以关联工作硬币电池内电极的化学和物理性质。制备了一种包含垂直取向孔阵列和密度梯度的电极微观结构。展示了所设计的电极微观结构如何提高锂离子扩散率、使锂离子浓度在超厚电极(1 mm)中均匀化以及提高电极活性材料的利用率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a8b/9165496/a84069d54309/ADVS-9-2105723-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a8b/9165496/375cb3ba851c/ADVS-9-2105723-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a8b/9165496/4b1feab0210c/ADVS-9-2105723-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a8b/9165496/f3a5ef3c9aeb/ADVS-9-2105723-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a8b/9165496/a84069d54309/ADVS-9-2105723-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a8b/9165496/375cb3ba851c/ADVS-9-2105723-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a8b/9165496/4b1feab0210c/ADVS-9-2105723-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a8b/9165496/f3a5ef3c9aeb/ADVS-9-2105723-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a8b/9165496/a84069d54309/ADVS-9-2105723-g001.jpg

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