Guided Lithium Metal Deposition and Improved Lithium Coulombic Efficiency through Synergistic Effects of LiAsF6 and Cyclic Carbonate Additives
Source abstract
Abstract
Spatial and morphology control over lithium (Li) metal nucleation and growth, as well as improving Li Coulombic efficiency (CE), are among the most challenging issues for rechargeable Li metal batteries. Here, we report that LiAsF6 and cyclic carbonate additives such as vinylene carbonate (VC) or fluoroethylene carbonate (FEC) can work synergistically to address these challenges. It is revealed that LiAsF6 can be reduced to LixAs alloy and LiF, which act as nanosized seeds for Li growth and form a robust solid electrolyte interface layer. The addition of VC or FEC not only enables the uniform distribution of LixAs seeds but also improves the flexibility of the solid electrolyte interface layer. As a result, highly compact, uniform, and dendrite-free Li film with vertically aligned column structure can be obtained with increased Li CE, and the Li metal batteries using the electrolyte with both LiAsF6 and cyclic carbonate additives can have improved cycle life.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Energy and Environment Directorate, Pacific Northwest National Laboratory, Richland, Washington 99354, United States
Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Washington 99354, United States
Funding
Vehicle Technologies Program · National Natural Science Foundation of China
References (28)
Show source-provided references
1. 10.1016/S0167-2738(02)00080-210.1016/S0167-2738(02)00080-2 ↗
2. 10.1038/nnano.2014.15210.1038/nnano.2014.152 ↗
3. 10.1039/C3EE40795K10.1039/C3EE40795K ↗
4. 10.1021/acs.chemrev.7b0011510.1021/acs.chemrev.7b00115 ↗
5. 10.1002/aenm.20140099310.1002/aenm.201400993 ↗
6. 10.1021/acscentsci.6b0026010.1021/acscentsci.6b00260 ↗
7. 10.1038/nenergy.2016.1010.1038/nenergy.2016.10 ↗
8. 10.1002/adma.20170271410.1002/adma.201702714 ↗
9. 10.1149/1.204865810.1149/1.2048658 ↗
10. 10.1149/2.100310jes10.1149/2.100310jes ↗
11. 10.1364/JOSA.41.00021510.1364/JOSA.41.000215 ↗
12. 10.1038/nmat404110.1038/nmat4041 ↗
13. 10.1088/0965-0393/21/7/07400510.1088/0965-0393/21/7/074005 ↗
14. 10.1021/ja312241y10.1021/ja312241y ↗
15. 10.1021/nl503911710.1021/nl5039117 ↗
16. 10.1016/j.nanoen.2015.04.00910.1016/j.nanoen.2015.04.009 ↗
17. 10.1149/1.302967410.1149/1.3029674 ↗
18. 10.1021/acs.chemmater.6b0228210.1021/acs.chemmater.6b02282 ↗
19. 10.1002/adfm.20160598910.1002/adfm.201605989 ↗
20. 10.1021/acsenergylett.7b0016310.1021/acsenergylett.7b00163 ↗
21. 10.1021/la203712s10.1021/la203712s ↗
22. 10.1149/1.209546210.1149/1.2095462 ↗
23. 10.1016/0169-4332(90)90042-X10.1016/0169-4332(90)90042-X ↗
24. 10.1109/TED.2014.232947910.1109/TED.2014.2329479 ↗
25. 10.1016/0368-2048(91)80017-O10.1016/0368-2048(91)80017-O ↗
26. 10.1007/s10008-015-3068-410.1007/s10008-015-3068-4 ↗
27. 10.1038/nenergy.2017.11910.1038/nenergy.2017.119 ↗
28. 10.1021/acs.jpcc.5b0007210.1021/acs.jpcc.5b00072 ↗