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Structural Changes in Alloy Anodes for Li-Ion Batteries

[+] Author Affiliations
Jacob N. Adams, Logan J. Ausderau, George J. Nelson

University of Alabama in Huntsville, Huntsville, AL

Paper No. ES2018-7539, pp. V001T07A009; 8 pages
doi:10.1115/ES2018-7539
From:
  • ASME 2018 12th International Conference on Energy Sustainability collocated with the ASME 2018 Power Conference and the ASME 2018 Nuclear Forum
  • ASME 2018 12th International Conference on Energy Sustainability
  • Lake Buena Vista, Florida, USA, June 24–28, 2018
  • Conference Sponsors: Advanced Energy Systems Division, Solar Energy Division
  • ISBN: 978-0-7918-5141-8
  • Copyright © 2018 by ASME

abstract

Tin (Sn) alloy electrodes show great potential for advancing battery performance due to the high capacity of tin. To realize this potential, the volumetric expansion during the lithiation process must be mitigated. One means of mitigating volumetric expansion of tin is to alloy it with copper to create Cu6Sn5. Such alloy electrodes retain some of the high capacity of tin, while attempting to accommodate volumetric changes with the addition of the malleable copper. Lithiation and delithiation tests were conducted with the Cu6Sn5 pellet electrodes to produce microstructural changes at the electrode surface. To observe and quantify these microstructural changes, x-ray microtomography was performed on electrode samples after electrochemical testing. The microtomography data was reconstructed into a 3D image, segmented, and the continuous phase size distribution (PSD) of each electrode sample was analyzed. The electrodes lithiated to 0 V vs Li/Li+ and then delithiated to 0.2 V vs. Li/Li+ showed the most substantial reduction in overall PSD compared to the other samples. This suggests that full lithiation of the Sn present in the alloy electrodes followed by partial delithiation of the Li4.4Sn to Li2CuSn can cause substantial microstructural changes related to volume expansion on lithiation and structural collapse upon delithiation. The electrodes fully lithiated to 0 V vs Li/Li+ and not delithiated show a higher overall phase size distribution, including all solid phases, than the pristine sample and the electrode samples that were partially lithiated to 0.2 V vs. Li/Li+ and delithiated to 1.5 V vs. Li/Li+. The higher overall phase size distribution that is shown by the sample that was fully lithiated and not delithiated is evidence of the significant volumetric expansion of the Cu6Sn5 compound due to lithiation. During this process of volumetric expansion, the phase size distribution of the Cu6Sn5/Sn phase is shown to decrease. When the volumetric expansion of the lithiated electrode samples and the volumetric contraction of the delithiated electrode sample are considered together, it can be inferred that the microstructural changes that are observed, such as the decrease in phase size distribution of the Cu6Sn5/Sn phase, can be attributed to the volumetric expansion and contraction of the compound during the lithiation and delithiation process.

Copyright © 2018 by ASME

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