Redox Shuttles for Lithium-Ion Batteries at Concentrations up to 1 M Using an Electroactive Ionic Liquid Based on 2,5-di-tert-butyl-1,4-dimethoxybenzene
Source abstract
Abstract
In this work, we designed two redox shuttles with high solubility (up to 1 M) in conventional carbonate-based lithium-ion battery (LIB) electrolytes. At this high concentration, redox shuttles ensure improved overcharge protection than lower concentrations. We developed electroactive imidazolium salts by modifying imidazolium with 2,5-di- tert -butyl-1,4-dimethoxybenzene. Two salts with the cation 1-(3-(2,5-di- tert -butyl-1,4-methoxyphenoxy)propyl)-3-methyl-1 H -imidazol-3-ium (EMIm) were synthesized using either hexafluorophosphate (DDB-EMIm-PF 6 ) or bis(trifluromethanesulfonyl)amide (DDB-EMIm-TFSI)) anions. The electrochemical properties of DDB-EMIm-PF 6 and DDB-EMIm-TFSI dissolved in ethylene carbonate : diethyl carbonate (EC:DEC), in the presence of either LiPF 6 or LiTFSI, were evaluated. Cyclic voltammetry showed a compatible potential (∼3.85 V vs. Li/Li + ) for use in LIBs using LiFePO 4 as cathodes. Electrolytes using 0.1 M of DDB-EMIm-PF 6 or 0.3, 0.7 and 1 M of DDB-EMIm-TFSI were prepared and evaluated in Li/LiFePO 4 (LFP) test cells to demonstrate overcharge protection. Electrochemical cycling at C/10 showed an overcharge protection for all concentrations of the redox ionic salts under 100% overcharge conditions. Among these salts, DDB-EMIm-TFSI, at a concentration of 0.7 M, was effective in shuttling excess current for over 200 cycles, representing over 6000 operating hours, while maintaining nominal values for the discharge capacity of LiFePO 4 .
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.
References (32)
Show source-provided references
1. 10.1016/S0378-7753(01)00887-410.1016/S0378-7753(01)00887-4 ↗
2. 10.1016/j.jpowsour.2007.06.21710.1016/j.jpowsour.2007.06.217 ↗
3. 10.1038/451652a10.1038/451652a ↗
4. 10.1038/3510464410.1038/35104644 ↗
5. 10.1166/mex.2012.107510.1166/mex.2012.1075 ↗
6. 10.1016/j.jpowsour.2012.02.03810.1016/j.jpowsour.2012.02.038 ↗
7. 10.1016/j.electacta.2009.05.01710.1016/j.electacta.2009.05.017 ↗
8. 10.1149/1.137974010.1149/1.1379740 ↗
9. 10.1149/1.183611910.1149/1.1836119 ↗
10. 10.1016/j.jpowsour.2005.03.10510.1016/j.jpowsour.2005.03.105 ↗
11. 10.1149/1.139175510.1149/1.1391755 ↗
12. 10.1149/1.208681710.1149/1.2086817 ↗
13. 10.1149/1.183732610.1149/1.1837326 ↗
14. 10.1016/j.jpowsour.2005.12.00210.1016/j.jpowsour.2005.12.002 ↗
15. 10.1149/1.209826510.1149/1.2098265 ↗
16. 10.1016/j.electacta.2009.05.01710.1016/j.electacta.2009.05.017 ↗
17. 10.1016/j.jpowsour.2011.10.00510.1016/j.jpowsour.2011.10.005 ↗
18. 10.1016/j.jpowsour.2011.10.03610.1016/j.jpowsour.2011.10.036 ↗
19. 10.1016/j.electacta.2006.03.01610.1016/j.electacta.2006.03.016 ↗
20. 10.1016/j.jpowsour.2009.06.08910.1016/j.jpowsour.2009.06.089 ↗
21. 10.1016/j.electacta.2007.04.06710.1016/j.electacta.2007.04.067 ↗
22. 10.1016/j.jpowsour.2009.08.05610.1016/j.jpowsour.2009.08.056 ↗
23. 10.1016/j.jpowsour.2009.06.08910.1016/j.jpowsour.2009.06.089 ↗
24. 10.1007/s11581-006-0023-510.1007/s11581-006-0023-5 ↗
25. 10.1016/j.jpowsour.2011.06.00510.1016/j.jpowsour.2011.06.005 ↗
26. 10.1039/c3cp50560j10.1039/c3cp50560j ↗
27. 10.1149/1.190602510.1149/1.1906025 ↗
28. 10.1039/c2ee21977h10.1039/c2ee21977h ↗
29. 10.1039/c3ra41345d10.1039/c3ra41345d ↗
30. 10.1016/j.jpowsour.2005.12.00210.1016/j.jpowsour.2005.12.002 ↗
31. 10.1039/b615127b10.1039/b615127b ↗
32. 10.1007/s11581-012-0673-410.1007/s11581-012-0673-4 ↗