Hybrid-Solvent Electrolytes for Enhanced Potassium–Oxygen Battery Performance
Source abstract
Abstract
Rechargeable potassium–oxygen batteries (KOB) are promising next-generation energy storage devices because of the highly reversible O2/O2– redox reactions during battery charge and discharge. However, the complicated cathode reaction processes seriously jeopardize the battery reaction kinetics and discharge capacity. Herein, we propose a hybrid-solvent strategy to effectively tune the K+ solvation structure, which demonstrates a critical influence on the charge-transfer kinetics and cathode reaction mechanism. The cosolvation of K+ by 1,2-dimethoxyethane (DME) and dimethyl sulfoxide (DMSO) could greatly decrease overpotentials for the cathode processes and increase the cathode discharge capacity. Furthermore, the Coulombic efficiency for the cathode could be significantly improved with the enhanced solution-mediated KO2 growth and stripping during cycling. This work provides a promising electrolyte design approach to improve the electrochemical performance of the KOB.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advanced battery technologies research · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemistry and Materials Science, University of Science and Technology of China, Hefei230026, China
Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio43210, United States
Funding
National Key Research and Development Program of China · Central University Basic Research Fund of China · National Natural Science Foundation of China
References (28)
Show source-provided references
1. 10.1149/1.183637810.1149/1.1836378 ↗
2. 10.1126/science.122398510.1126/science.1223985 ↗
3. 10.1038/nmat373710.1038/nmat3737 ↗
4. 10.1038/nchem.213210.1038/nchem.2132 ↗
5. 10.1021/acs.chemrev.9b0060910.1021/acs.chemrev.9b00609 ↗
6. 10.1021/ja056811q10.1021/ja056811q ↗
7. 10.1002/anie.20110235710.1002/anie.201102357 ↗
8. 10.1021/ja310258x10.1021/ja310258x ↗
9. 10.1038/nmat348610.1038/nmat3486 ↗
10. 10.1021/ja312059q10.1021/ja312059q ↗
11. 10.1002/anie.20171045410.1002/anie.201710454 ↗
12. 10.1038/nchem.226010.1038/nchem.2260 ↗
13. 10.1021/acsami.6b0628010.1021/acsami.6b06280 ↗
14. 10.1021/am505351s10.1021/am505351s ↗
15. 10.1002/anie.20180134410.1002/anie.201801344 ↗
16. 10.1021/acs.jpcc.8b0375510.1021/acs.jpcc.8b03755 ↗
17. 10.1038/nchem.210110.1038/nchem.2101 ↗
18. 10.1021/jp102019y10.1021/jp102019y ↗
19. 10.1021/ja00905a00110.1021/ja00905a001 ↗
20. 10.1021/acs.jpcc.6b0765910.1021/acs.jpcc.6b07659 ↗
21. 10.1021/accountsmr.1c0006110.1021/accountsmr.1c00061 ↗
22. 10.1149/1.353198110.1149/1.3531981 ↗
23. 10.1023/A:102260940756010.1023/A:1022609407560 ↗
24. 10.1016/j.jct.2010.09.00810.1016/j.jct.2010.09.008 ↗
25. 10.1002/app.3191210.1002/app.31912 ↗
26. 10.1002/adfm.20210183110.1002/adfm.202101831 ↗
27. 10.1073/pnas.190132911610.1073/pnas.1901329116 ↗
28. 10.1038/s41563-019-0286-710.1038/s41563-019-0286-7 ↗