journal article·2020-07-29

Functional Localized High-Concentration Ether-Based Electrolyte for Stabilizing High-Voltage Lithium-Metal Battery

Shuangshuang Lin, Haiming Hua, Zhisen Li, Jinbao Zhao

ACS Applied Materials & Interfaces· Volume 12· Issue 30
Publisher page

Abstract

Localized high-concentration electrolytes have attracted much attention of researchers due to their low viscosity, low cost, and relatively higher electrochemical performance than their low-concentration counterparts. In our work, 1.5 M (mol L–1) locally concentrated ether-based electrolyte has been obtained by adding 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether (HFE) into a 4 M LiFSI concentrated dimethoxyethane (DME)-based electrolyte. The optimal ratio is determined by density functional theory (DFT) calculation and experimental combination, and finally, DH(3/5)-1.5M-LiFSI (DME/HFE = 3:5 by volume) is obtained. The electrolyte not only has relatively good physical properties such as low viscosity and high conductivity but also shows decent electrochemical performance. Li∥Cu half-cells can maintain a coulombic efficiency of no less than 99% after circulating for 250 cycles under the condition of 1 mA cm–2 current density and 1 mAh cm–2 lithium deposition for each cycle, and the stable battery polarization voltage was about 50 mV. Furthermore, 0.15 M lithium trifluoromethyl acetate (LiCO2CF3) has been added as an additive to enhance the oxidation stability. The new electrolyte DH(3/5)-1.65M-LiFC (LiFC/LiFSI + LiCO2CF3) makes Li||NCM523 batteries maintain about 83% capacity after cycling for 250 times with a 0.5 C charge current density and a 1 C discharge current density of 160 mAh g–1 when charged to 4.3 V. Furthermore, this new additive has a little negative effect on the Li||Cu half-cell performance under the same condition as before, indicating this new type of localized high-concentration DME-based electrolyte benefits both high-voltage cathode and lithium-metal 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

State-Province Joint Engineering Laboratory of Power Source Technology for New Energy Vehicle, Engineering Research Center of Electrochemical Technology, Ministry of Education, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, P. R. China

Funding

Ministry of Education of the People's Republic of China · Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China

References (43)

Show source-provided references
1. 10.1016/j.trechm.2019.02.01510.1016/j.trechm.2019.02.015 ↗
2. 10.1002/advs.20197014710.1002/advs.201970147 ↗
3. 10.1021/acs.chemrev.8b0042210.1021/acs.chemrev.8b00422 ↗
4. 10.1039/C8CS00322J10.1039/C8CS00322J ↗
5. 10.1021/cm901452z10.1021/cm901452z ↗
6. 10.1038/451652a10.1038/451652a ↗
7. 10.1038/3510464410.1038/35104644 ↗
8. 10.1016/j.elecom.2010.05.01010.1016/j.elecom.2010.05.010 ↗
9. 10.1002/adma.20180654110.1002/adma.201806541 ↗
10. 10.1021/acsami.8b0518510.1021/acsami.8b05185 ↗
11. 10.1002/anie.20180703410.1002/anie.201807034 ↗
12. 10.1002/adma.20170762910.1002/adma.201707629 ↗
13. 10.1002/anie.20180173710.1002/anie.201801737 ↗
14. 10.1002/adma.20180647010.1002/adma.201806470 ↗
15. 10.1016/j.ssi.2018.06.01710.1016/j.ssi.2018.06.017 ↗
16. 10.1002/aenm.20170302210.1002/aenm.201703022 ↗
17. 10.1016/j.memsci.2018.03.03810.1016/j.memsci.2018.03.038 ↗
18. 10.1038/s41560-018-0237-610.1038/s41560-018-0237-6 ↗
19. 10.1038/s41560-018-0199-810.1038/s41560-018-0199-8 ↗
20. 10.1038/nenergy.2017.1210.1038/nenergy.2017.12 ↗
21. 10.1021/acsnano.7b0353010.1021/acsnano.7b03530 ↗
22. 10.1021/acsenergylett.6b0065010.1021/acsenergylett.6b00650 ↗
23. 10.1002/adma.20160446010.1002/adma.201604460 ↗
24. 10.1002/adma.20160553110.1002/adma.201605531 ↗
25. 10.1039/C8EE02601G10.1039/C8EE02601G ↗
26. 10.1002/celc.20180068610.1002/celc.201800686 ↗
27. 10.1016/j.chempr.2017.10.01710.1016/j.chempr.2017.10.017 ↗
28. 10.1002/aenm.20150215110.1002/aenm.201502151 ↗
29. 10.1038/ncomms736210.1038/ncomms7362 ↗
30. 10.1126/science.aap878710.1126/science.aap8787 ↗
31. 10.1016/j.elecom.2008.02.00610.1016/j.elecom.2008.02.006 ↗
32. 10.1038/ncomms251310.1038/ncomms2513 ↗
33. 10.1016/j.jpowsour.2012.12.02810.1016/j.jpowsour.2012.12.028 ↗
34. 10.1149/2.022310jes10.1149/2.022310jes ↗
35. 10.1016/j.jpowsour.2005.04.02310.1016/j.jpowsour.2005.04.023 ↗
36. 10.1016/j.chempr.2018.05.00210.1016/j.chempr.2018.05.002 ↗
37. 10.1002/aenm.20180377410.1002/aenm.201803774 ↗
38. 10.1002/adma.20170610210.1002/adma.201706102 ↗
39. 10.1021/acsenergylett.8b0093510.1021/acsenergylett.8b00935 ↗
40. 10.1016/j.joule.2019.05.00610.1016/j.joule.2019.05.006 ↗
41. 10.1002/advs.20170003210.1002/advs.201700032 ↗
42. 10.1002/advs.20190103610.1002/advs.201901036 ↗
43. 10.1002/aenm.20190384310.1002/aenm.201903843 ↗