4D nano-tomography of electrochemical energy devices using lab-based X-ray imaging

被引:36
作者
Heenan, T. M. M. [1 ]
Finegan, D. P. [1 ,2 ]
Tjaden, B. [1 ]
Lu, X. [1 ]
Iacoviello, F. [1 ]
Millichamp, J. [1 ]
Brett, D. J. L. [1 ]
Shearing, P. R. [1 ]
机构
[1] UCL, Dept Chem Engn, Electrochem Innovat Lab, London WC1E 7JE, England
[2] Natl Renewable Energy Lab, Transportat & Hydrogen Syst Ctr, 1617 USA Cole Blvd, Lakewood, CO 80401 USA
基金
英国工程与自然科学研究理事会;
关键词
Li-ion batteries; Solid oxide fuel cells; 4D imaging; X-ray nano tomography; Degradation; FUEL-CELL ANODES; LITHIUM-ION BATTERIES; THERMAL RUNAWAY; FIB-SEM; ELECTRODES; MICROSTRUCTURE; RECONSTRUCTION; OXIDATION; STRESS; NICKEL;
D O I
10.1016/j.nanoen.2018.03.001
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrochemical energy devices offer a variety of alternate means for low-carbon, multi-scale energy conversion and storage. Reactions in these devices are supported by electrodes with characteristically complex microstructures. To meet the increasing capacity and lifetime demands across a range of applications, it is essential to understand microstructural evolutions at a cell and electrode level which are thought to be critical aspects influencing material and device lifetime and performance. X-ray computed tomography (CT) has become a highly employed method for non-destructive characterisation of such microstructures with high spatial resolution. However, sub-micron resolutions present significant challenges for sample preparation and handling particularly in 4D studies, (three spatial dimensions plus time). Here, microstructural information is collected from the same region of interest within two electrode materials: a solid oxide fuel cell and the positive electrode from a lithium-ion battery. Using a lab-based X-ray instrument, tomograms with sub-micron resolutions were obtained between thermal cycling. The intricate microstructural evolutions captured within these two materials provide model examples of 4D X-ray nano-CT capabilities in tracking challenging degradation mechanisms. This technique is valuable in the advancement of electrochemical research as well as broader applications for materials characterisation.
引用
收藏
页码:556 / 565
页数:10
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