Clarification of Solvent Effects on Discharge Products in Li–O2 Batteries through a Titration Method
Source abstract
Abstract
As a substitute for the current lithium-ion batteries, rechargeable lithium oxygen batteries have attracted much attention because of their theoretically high energy density, but many challenges continue to exist. For the development of these batteries, understanding and controlling the main discharge product Li 2 O 2 (lithium peroxide) are of paramount importance. Here, we comparatively analyzed the amount of Li 2 O 2 in the cathodes discharged at various discharge capacities and current densities in dimethyl sulfoxide (DMSO) and tetraethylene glycol dimethyl ether (TEGDME) solvents. The precise assessment entailed revisiting and revising the UV–vis titration analysis. The amount of Li 2 O 2 electrochemically formed in DMSO was less than that formed in TEGDME at the same capacity and even at a much higher full discharge capacity in DMSO than in TEGDME. On the basis of our analytical experimental results, this unexpected result was ascribed to the presence of soluble LiO 2 -like intermediates that remained in the DMSO solvent and the chemical transformation of Li 2 O 2 to LiOH, both of which originated from the inherent properties of the DMSO solvent.
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, Hanyang University, Seoul 04763, Republic of Korea
Funding
National Research Foundation of Korea · Korea Institute of Energy Technology Evaluation and Planning
References (38)
Show source-provided references
1. 10.1021/jz100538410.1021/jz1005384 ↗
2. 10.1002/aenm.20100001010.1002/aenm.201000010 ↗
3. 10.1149/1.183637810.1149/1.1836378 ↗
4. 10.1002/adma.20140306410.1002/adma.201403064 ↗
5. 10.1038/nature1648410.1038/nature16484 ↗
6. 10.1021/nl504425h10.1021/nl504425h ↗
7. 10.1021/nn400477d10.1021/nn400477d ↗
8. 10.1021/acscatal.7b0235910.1021/acscatal.7b02359 ↗
9. 10.1038/nenergy.2017.11810.1038/nenergy.2017.118 ↗
10. 10.1038/nenergy.20173610.1038/nenergy.2017.3610.1038/nenergy.20173610.1038/nenergy.2017.36 ↗
11. 10.1039/c7sc02519j10.1039/c7sc02519j ↗
12. 10.1038/nchem.210110.1038/nchem.2101 ↗
13. 10.1021/jz501382410.1021/jz5013824 ↗
14. 10.1021/acsami.5b0196910.1021/acsami.5b01969 ↗
15. 10.1021/jz401718810.1021/jz4017188 ↗
16. 10.1039/c2cc32844e10.1039/c2cc32844e ↗
17. 10.1149/2.118309jes10.1149/2.118309jes ↗
18. 10.1126/sciadv.160280910.1126/sciadv.1602809 ↗
19. 10.1021/jz500494s10.1021/jz500494s ↗
20. 10.1021/acs.nanolett.5b0351010.1021/acs.nanolett.5b03510 ↗
21. 10.1021/jz301784210.1021/jz3017842 ↗
22. 10.1149/2.0241506jes10.1149/2.0241506jes ↗
23. 10.1038/nmat462910.1038/nmat4629 ↗
24. 10.1021/jz401659f10.1021/jz401659f ↗
25. 10.1021/jz300430s10.1021/jz300430s ↗
26. 10.1149/2.0621409jes10.1149/2.0621409jes ↗
27. 10.1039/an980050095010.1039/an9800500950 ↗
28. 10.1002/kin.2025910.1002/kin.20259 ↗
29. 10.1021/acs.jpcc.6b1295010.1021/acs.jpcc.6b12950 ↗
30. 10.1134/s107036321202014410.1134/s1070363212020144 ↗
31. 10.1016/j.catcom.2006.03.01510.1016/j.catcom.2006.03.015 ↗
32. 10.1039/c3ee40998h10.1039/c3ee40998h ↗
33. 10.1039/c3cp00069a10.1039/c3cp00069a ↗
34. 10.1063/1.477324210.1063/1.4773242 ↗
35. 10.1002/ange.20110087910.1002/ange.201100879 ↗
36. 10.1021/acs.nanolett.6b0085610.1021/acs.nanolett.6b00856 ↗
37. 10.1038/nchem.137610.1038/nchem.1376 ↗
38. 10.1126/science.122398510.1126/science.1223985 ↗