High-Performance Polycrystalline Ge Microwire Film Anodes for Li Ion Batteries
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide High-performance Li ion battery anodes have been made using Ge microwire films containing high levels of residual gallium (Ga). These materials were prepared by the electrochemical liquid–liquid–solid (ec-LLS) process with liquid metal alloy droplets containing Ga, indium (In), and copper (Cu) at T = 80 °C on Cu foil. The as-prepared Ge microwires yielded an initial discharge capacity of 1350 mA h g –1 and retained more than 80% of their original capacity after 80 cycles when subject to discharge–charge cycles at 0.1 C. Ge microwires where the residual metal content had been lowered still showed unusually large capacities and decent capacity retention, albeit less than those of the as-prepared materials. The cumulative data point to the premises that ec-LLS is amenable to making Ge microwires that are innately active as Li + battery anodes and that Ga incorporation in Ge is beneficial to countering the material stress incurred during Li + insertion.
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Research context
OpenAlex topics: Advancements in Battery Materials · Supercapacitor Materials and Fabrication · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Chemistry Department, ‡Department of Chemical Engineering, and §Applied Physics Program, University of Michigan, Ann Arbor, Michigan 48109, United States
Funding
Division of Chemistry
References (31)
Show source-provided references
1. 10.1038/nnano.2007.41110.1038/nnano.2007.411 ↗
2. 10.1021/nl072715710.1021/nl0727157 ↗
3. 10.1016/j.electacta.2012.10.15410.1016/j.electacta.2012.10.154 ↗
4. 10.1016/j.eml.2015.01.00910.1016/j.eml.2015.01.009 ↗
5. 10.1007/s10008-013-2148-610.1007/s10008-013-2148-6 ↗
6. 10.1038/nnano.2012.3510.1038/nnano.2012.35 ↗
7. 10.1038/nchem.180210.1038/nchem.1802 ↗
8. 10.1149/1.359109410.1149/1.3591094 ↗
9. 10.1016/j.ssi.2004.05.02110.1016/j.ssi.2004.05.021 ↗
10. 10.1063/1.175397510.1063/1.1753975 ↗
11. 10.1021/acs.accounts.5b0015810.1021/acs.accounts.5b00158 ↗
12. 10.1021/nl301912f10.1021/nl301912f ↗
13. 10.1016/j.tsf.2006.12.09010.1016/j.tsf.2006.12.090 ↗
14. 10.1107/S0365110X6200147410.1107/S0365110X62001474 ↗
15. 10.1021/acs.chemmater.5b0064410.1021/acs.chemmater.5b00644 ↗
16. 10.1007/BF0288041110.1007/BF02880411 ↗
17. 10.1038/nature1199910.1038/nature11999 ↗
18. 10.1021/acsami.5b0951110.1021/acsami.5b09511 ↗
19. 10.1149/2.0541514jes10.1149/2.0541514jes ↗
20. 10.1149/2.006407jes10.1149/2.006407jes ↗
21. 10.1039/C6RA13378A10.1039/C6RA13378A ↗
22. 10.1021/nl404228z10.1021/nl404228z ↗
23. 10.3762/bjnano.6.13910.3762/bjnano.6.139 ↗
24. 10.1016/j.nanoen.2015.03.03910.1016/j.nanoen.2015.03.039 ↗
25. 10.1063/1.172569710.1063/1.1725697 ↗
26. 10.1016/0375-9601(79)90886-710.1016/0375-9601(79)90886-7 ↗
27. Peisl H. · 1978 · 5310.1007/3540087052_42 ↗
28. 10.1016/j.jpowsour.2013.05.09810.1016/j.jpowsour.2013.05.098 ↗
29. 10.1063/1.315903110.1063/1.3159031 ↗
30. 10.1021/cm501233k10.1021/cm501233k ↗
31. 10.1021/nl403979s10.1021/nl403979s ↗