Insights into the Enhanced Reversibility of Graphite Anode Upon Fast Charging Through Li Reservoir
Source abstract
Abstract
Increasing the charging rate and reducing the charging time for Li-ion batteries are crucial to realize the mainstream of electric vehicles. However, it is formidable to avoid the Li plating on graphite anode upon fast charging. Despite the tremendous progress in Li detection techniques, the fundamental mechanism of Li plating and its chemical/electrochemical responses upon cycling still remains elusive. Herein, we present a comprehensive electrochemical method to investigate the fast charging behavior of graphite electrode. A detailed analysis is directed toward understanding the changes in phase, composition, and morphology of the fast-charged graphite. By applying a resting process, we scrutinize the further reactions of the plated Li, which readily transforms into irreversible (dead) Li. We further develop a modified graphite electrode with a thin Ag coating as the Li reservoir. The plated Li can be "absorbed" by the Ag layer to form the Li-Ag solid solution that suppresses the formation of dead Li and provides structural stability, thus promoting the further lithiation of graphite and enhancing the reversibility. This work not only provides additional insights into the fast charging behavior of graphite electrode but also demonstrates a potential strategy to improve the fast charging performance of graphite anode.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Energy Storage and Distributed Resources Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States
Funding
Basic Energy Sciences
References (34)
Show source-provided references
1. 10.1002/adma.20180056110.1002/adma.201800561 ↗
2. 10.1016/j.jpowsour.2017.06.05510.1016/j.jpowsour.2017.06.055 ↗
3. 10.1038/s41560-019-0405-310.1038/s41560-019-0405-3 ↗
4. 10.1016/j.etran.2019.10001110.1016/j.etran.2019.100011 ↗
5. 10.1149/1945-7111/abd3b810.1149/1945-7111/abd3b8 ↗
6. 10.1002/aenm.20210037210.1002/aenm.202100372 ↗
7. 10.1016/j.pecs.2021.10095310.1016/j.pecs.2021.100953 ↗
8. 10.1021/acsenergylett.0c0083110.1021/acsenergylett.0c00831 ↗
9. 10.1016/j.jpowsour.2015.11.04410.1016/j.jpowsour.2015.11.044 ↗
10. 10.1016/j.jpowsour.2013.12.06010.1016/j.jpowsour.2013.12.060 ↗
11. 10.1016/j.xcrp.2020.10011410.1016/j.xcrp.2020.100114 ↗
12. 10.1149/2.1581912jes10.1149/2.1581912jes ↗
13. 10.1149/2.0621506jes10.1149/2.0621506jes ↗
14. 10.1038/nenergy.2016.1010.1038/nenergy.2016.10 ↗
15. 10.1021/jacs.0c0181110.1021/jacs.0c01811 ↗
16. 10.1038/s41586-021-04168-w10.1038/s41586-021-04168-w ↗
17. 10.1039/D1TA06023F10.1039/D1TA06023F ↗
18. 10.1016/j.joule.2020.12.02010.1016/j.joule.2020.12.020 ↗
19. 10.1016/j.mattod.2017.11.00110.1016/j.mattod.2017.11.001 ↗
20. 10.1016/S0167-2738(02)00080-210.1016/S0167-2738(02)00080-2 ↗
21. 10.1016/j.electacta.2012.08.01610.1016/j.electacta.2012.08.016 ↗
22. 10.1021/acsenergylett.1c0055110.1021/acsenergylett.1c00551 ↗
23. 10.1002/adfm.20200695010.1002/adfm.202006950 ↗
24. 10.1021/jacs.9b1019510.1021/jacs.9b10195 ↗
25. 10.1016/j.nanoen.2018.06.00310.1016/j.nanoen.2018.06.003 ↗
26. 10.1038/s41560-021-00917-310.1038/s41560-021-00917-3 ↗
27. 10.1007/BF0286899310.1007/BF02868993 ↗
28. 10.1021/acsenergylett.1c0212710.1021/acsenergylett.1c02127 ↗
29. 10.1016/j.jallcom.2017.10.20610.1016/j.jallcom.2017.10.206 ↗
30. 10.1016/j.jpowsour.2003.07.00410.1016/j.jpowsour.2003.07.004 ↗
31. 10.1021/acsnano.1c0294210.1021/acsnano.1c02942 ↗
32. 10.1002/adfm.20180875610.1002/adfm.201808756 ↗
33. 10.1002/aenm.20190256810.1002/aenm.201902568 ↗
34. 10.1107/S002188981200403710.1107/S0021889812004037 ↗