journal article·2019-04-22Open access

In Situ Focused Ion Beam-Scanning Electron Microscope Study of Crack and Nanopore Formation in Germanium Particle During (De)lithiation

Xinwei Zhou, Tianyi Li, Yi Cui, Melissa L. Meyerson, C. Buddie Mullins, Yuzi Liu, Likun Zhu

ACS Applied Energy Materials· Volume 2· Issue 4

Abstract

Germanium has emerged as a promising high-capacity anode material for lithium ion batteries. To understand the microstructure evolution of germanium under different cycling rates, we monitored single germanium particle batteries using an in situ focused ion beam-scanning electron microscope. Our results show that both the lithium concentration and delithiation rate have an impact on nanopore formation. This study reveals that germanium electrodes with low and high cycling rates have better microstructure integrity, which leads to better cycling performance. The nanopores tend to aggregate into large porous structures during cycling which leads to particle pulverization and capacity fading of the electrode.
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Research context

OpenAlex topics: Advancements in Battery Materials · Semiconductor materials and devices · Semiconductor materials and interfaces

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Affiliations

Department of Mechanical and Energy Engineering, Indiana University Purdue University Indianapolis, Indianapolis, Indiana 46202, United States

Center for Nanoscale Materials, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, Illinois 60439, United States

Departments of Chemical Engineering and Chemistry, University of Texas at Austin, Austin, Texas 78712, United States

Funding

National Science Foundation · Welch Foundation

References (28)

Show source-provided references
1. 10.1038/451652a10.1038/451652a ↗
2. 10.1021/jz101542210.1021/jz1015422 ↗
3. 10.1039/C3EE42613K10.1039/C3EE42613K ↗
4. 10.1149/1.165242110.1149/1.1652421 ↗
5. 10.1002/ppsc.20130023110.1002/ppsc.201300231 ↗
6. 10.1016/j.jpowsour.2013.11.10310.1016/j.jpowsour.2013.11.103 ↗
7. 10.1016/j.jmat.2015.06.00210.1016/j.jmat.2015.06.002 ↗
8. 10.1149/1.169741210.1149/1.1697412 ↗
9. 10.1016/j.jpowsour.2014.04.01110.1016/j.jpowsour.2014.04.011 ↗
10. 10.1002/adma.20150397810.1002/adma.201503978 ↗
11. 10.1021/nl403979s10.1021/nl403979s ↗
12. 10.1021/nl072715710.1021/nl0727157 ↗
13. 10.1002/adma.20090184610.1002/adma.200901846 ↗
14. 10.1002/anie.20110306210.1002/anie.201103062 ↗
15. 10.1002/anie.20150965110.1002/anie.201509651 ↗
16. 10.1021/nl202411810.1021/nl2024118 ↗
17. 10.1021/jz201432d10.1021/jz201432d ↗
18. 10.1021/la504382q10.1021/la504382q ↗
19. 10.1021/acs.jpcc.5b0585710.1021/acs.jpcc.5b05857 ↗
20. 10.1021/cm504312x10.1021/cm504312x ↗
21. 10.1002/aenm.20150059910.1002/aenm.201500599 ↗
22. 10.1002/aenm.20120002410.1002/aenm.201200024 ↗
23. 10.1021/nn400330h10.1021/nn400330h ↗
24. 10.1002/celc.20130019510.1002/celc.201300195 ↗
25. 10.1039/C4EE01384K10.1039/C4EE01384K ↗
26. 10.1021/acsami.8b1398110.1021/acsami.8b13981 ↗
27. 10.1039/C5TA00319A10.1039/C5TA00319A ↗
28. 10.1038/nmat374110.1038/nmat3741 ↗