Electrical Conductivity, Self-Diffusivity and Electrolyte Performance of a Quasi-Solid-State Pseudo-Ternary System, Bis(trifluoromethanesulfonyl)amide-Based Room Temperature Ionic Liquid–Lithium Bis(trifluoromethanesulfonyl)amide–Fumed Silica Nanoparticles
Source abstract
Abstract
Quasi-solid-state electrolyte consisting of a pseudo-ternary system, RTILs – Li-TFSA – fumed silica nanoparticles, were prepared for use as electrolytes of the all-solid-state lithium rechargeable battery. EMI-TFSA, DEME-TFSA and PP13-TFSA were chosen as RTIL solvents. It was found that the pseudo-ternary composites had liquid-like high ionic conductivity as well as self-diffusion coefficients in spite of the solid-like appearances regardless of RTIL solvent species. Stability of the quasi-solid-state electrolytes to lithium electrodes was investigated by lithium symmetric cells with ac and dc techniques. All-solid-state bulk cells were assembled and the charge – discharge characteristics were evaluated. A stable charge – discharge cycles could be performed with high cathode utilization ratios such as above 85% with comparatively lower c-rates. At higher c-rates, the discharge capacities of our all-solid-state cells using the quasi-solid-state electrolytes are smaller than that using a conventional organic electrolyte with a separator. This suggests that the power density of our all-solid-state cells is essentially limited by slow lithium-ion transport similarly to RTIL – Li-salt mixtures. Based on the above results, the correlation between the charge – discharge cycling performance of our all-solid-state cells and the stabilities of the quasi-solid-state electrolytes were discussed.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Ionic liquids properties and applications · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (36)
Show source-provided references
1. 10.1016/j.jpowsour.2010.01.07610.1016/j.jpowsour.2010.01.076 ↗
2. 10.1038/nmat306610.1038/nmat3066 ↗
3. 10.1126/science.108228910.1126/science.1082289 ↗
4. 10.1149/1.200118710.1149/1.2001187 ↗
5. 10.1016/j.progsolidstchem.2005.11.04910.1016/j.progsolidstchem.2005.11.049 ↗
6. 10.1021/cm060656c10.1021/cm060656c ↗
7. 10.1149/1.272063610.1149/1.2720636 ↗
8. 10.1021/cm070781410.1021/cm0707814 ↗
9. 10.1021/jp072998r10.1021/jp072998r ↗
10. 10.1039/b903034d10.1039/b903034d ↗
11. 10.1021/cm900518410.1021/cm9005184 ↗
12. 10.1016/j.ssi.2011.08.00810.1016/j.ssi.2011.08.008 ↗
13. 10.1016/j.ssi.2012.01.02010.1016/j.ssi.2012.01.020 ↗
14. 10.1016/j.jpowsour.2012.02.04910.1016/j.jpowsour.2012.02.049 ↗
15. 10.5796/electrochemistry.80.76510.5796/electrochemistry.80.765 ↗
16. 10.1126/science.116450210.1126/science.1164502 ↗
17. 10.1039/b923571j10.1039/b923571j ↗
18. 10.1016/S0022-1139(99)00267-510.1016/S0022-1139(99)00267-5 ↗
19. 10.5796/electrochemistry.75.2310.5796/electrochemistry.75.23 ↗
20. 10.1063/1.350530710.1063/1.3505307 ↗
21. 10.1016/S1388-2481(03)00137-110.1016/S1388-2481(03)00137-1 ↗
22. 10.1016/j.jpowsour.2005.03.07110.1016/j.jpowsour.2005.03.071 ↗
23. 10.1016/j.jpowsour.2004.06.02710.1016/j.jpowsour.2004.06.027 ↗
24. 10.1149/1.204133010.1149/1.2041330 ↗
25. 10.1039/b514681j10.1039/b514681j ↗
26. 10.1063/1.169569010.1063/1.1695690 ↗
27. 10.1016/0022-2364(91)90252-O10.1016/0022-2364(91)90252-O ↗
28. Vogel · Phys. Z. · 1921 · 22 · 645
29. 10.1111/j.1151-2916.1925.tb16731.x10.1111/j.1151-2916.1925.tb16731.x ↗
30. 10.1021/jp711625r10.1021/jp711625r ↗
31. 10.1016/S0378-7753(98)00232-810.1016/S0378-7753(98)00232-8 ↗
32. 10.1016/S0032-3861(98)00859-310.1016/S0032-3861(98)00859-3 ↗
33. 10.1149/1.277996210.1149/1.2779962 ↗
34. 10.1063/1.350530710.1063/1.3505307 ↗
35. 10.1016/j.jpowsour.2006.02.01810.1016/j.jpowsour.2006.02.018 ↗
36. 10.1016/j.jpowsour.2009.08.05610.1016/j.jpowsour.2009.08.056 ↗