Effects of Methyl Acetate as a Co-Solvent in Carbonate-Based Electrolytes for Improved Lithium Metal Batteries
Source abstract
Abstract
In lithium metal batteries (LMBs), electrolytes composed of salts and organic solvents play a significant role in transporting Li+ ions and creating the surface film on Li-metal anodes. Herein, the effect of methyl acetate (MA) as a co-solvent is reported, which enables the facilitated Li+ transport and formation of a robust solid electrolyte interphase (SEI) on the Li-metal anode. The symmetrical Li//Li cell tests show remarkable cycle stability of MA-based electrolytes at 3 mA/cm2 without obvious voltage fluctuation. At 5 mA/cm2, the Li//Li cells in MA-based electrolytes can still run up to 110 h with lower overpotential, compared to the cell cycled with MA-free electrolytes. Furthermore, the LMBs consisting of the Li anode and LiNi0.8Co0.15Al0.05O2 (NCA) cathode deliver the high capacity (∼200 mA h/g), good cycling stability up to 300 cycles, excellent rate capability (10 C), and low self-discharging rates (8.5%) with MA-based electrolytes. Especially, the capacity of the Li//NCA cells with MA30 electrolytes at −35 °C is as high as 144 mA h/g, which is higher than that of the cells in MA-free electrolytes. It demonstrates that the MA is beneficial for the LMB operation at high rate and low temperature.
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
Department of Energy Engineering, Dankook University, Cheonan 31116, Republic of Korea
Dongnam Regional Division, Korea Institute of Industrial Technology (KITECH), Busan 46744, Republic of Korea
Funding
National Research Foundation of Korea
References (37)
Show source-provided references
1. 10.1038/3510464410.1038/35104644 ↗
2. 10.1038/s41565-018-0183-210.1038/s41565-018-0183-2 ↗
3. 10.1016/j.joule.2018.03.00810.1016/j.joule.2018.03.008 ↗
4. 10.1073/pnas.171289511510.1073/pnas.1712895115 ↗
5. 10.1149/1.139334910.1149/1.1393349 ↗
6. 10.1038/nenergy.2017.8310.1038/nenergy.2017.83 ↗
7. 10.1021/acs.chemrev.7b0011510.1021/acs.chemrev.7b00115 ↗
8. 10.1039/c8ta05069d10.1039/c8ta05069d ↗
9. 10.1038/s41467-018-06126-z10.1038/s41467-018-06126-z ↗
10. 10.1038/nnano.2014.15210.1038/nnano.2014.152 ↗
11. 10.1073/pnas.151818811310.1073/pnas.1518188113 ↗
12. 10.1016/j.nanoen.2017.05.01510.1016/j.nanoen.2017.05.015 ↗
13. 10.1002/aenm.20170148210.1002/aenm.201701482 ↗
14. 10.1021/acs.chemmater.7b0149610.1021/acs.chemmater.7b01496 ↗
15. 10.1002/adfm.20160598910.1002/adfm.201605989 ↗
16. 10.1016/j.nanoen.2017.04.05610.1016/j.nanoen.2017.04.056 ↗
17. 10.1002/anie.20170930510.1002/anie.201709305 ↗
18. 10.1016/j.jpowsour.2008.04.09410.1016/j.jpowsour.2008.04.094 ↗
19. 10.1038/s41524-018-0064-010.1038/s41524-018-0064-0 ↗
20. 10.1021/acsaem.8b0070510.1021/acsaem.8b00705 ↗
21. 10.1021/acsenergylett.7b0030010.1021/acsenergylett.7b00300 ↗
22. 10.1149/2.0011507jes10.1149/2.0011507jes ↗
23. 10.1021/acsenergylett.7b0098210.1021/acsenergylett.7b00982 ↗
24. 10.1016/j.jpowsour.2016.08.02310.1016/j.jpowsour.2016.08.023 ↗
25. 10.1016/j.jpowsour.2019.01.08510.1016/j.jpowsour.2019.01.085 ↗
26. 10.1149/2.0861805jes10.1149/2.0861805jes ↗
27. 10.1002/anie.20160593110.1002/anie.201605931 ↗
28. 10.1039/c7ta01564j10.1039/c7ta01564j ↗
29. 10.1016/j.trechm.2019.02.01510.1016/j.trechm.2019.02.015 ↗
30. 10.1149/2.0981803jes10.1149/2.0981803jes ↗
31. 10.1126/sciadv.aar441010.1126/sciadv.aar4410 ↗
32. 10.1016/j.electacta.2014.05.12010.1016/j.electacta.2014.05.120 ↗
33. 10.1002/aenm.20150215110.1002/aenm.201502151 ↗
34. 10.1149/2.0541410jes10.1149/2.0541410jes ↗
35. 10.1149/2.0451805jes10.1149/2.0451805jes ↗
36. 10.1149/2.0071509jes10.1149/2.0071509jes ↗
37. 10.1016/j.electacta.2016.12.12610.1016/j.electacta.2016.12.126 ↗