Improved Cycling Performance of Lithium–Sulfur Cell through Supramolecular Interactions
Source abstract
Abstract
Commercialization of lithium–sulfur batteries is plagued by poor electronic conductivity of elemental sulfur, shuttling of polysulfides, and poor interfacial properties of lithium metal anodes with nonaqueous electrolytes. Although numerous attempts have been made to alleviate such challenges, trapping of polysulfides within sulfur composite cathodes appears as an efficient way to improve the cycling performance of Li–S cells. In the present work, naphthyl viologen was successfully synthesized and incorporated in a sulfur cathode in order to enhance the electrochemical performance of Li–S cells. Charge–discharge studies revealed that the viologen-added Li–S cell delivered higher discharge capacity than the unladen one. The enhanced performance of viologen-laden sulfur cathode was attributed to the electrostatic interaction between polysulfide and viologen, which was further substantiated by UV–vis spectroscopy.
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
CSIR—Central Electrochemical Research Institute, Karaikudi 630 003, India
Academy of Scientific and Innovative Research (AcSIR), CSIR—CECRI Campus, Karaikudi 630 003, India
Center for Materials Science, Zewail City of Science and Technology, October Gardens, 6th of October, 12578 Giza, Egypt
Funding
Department of Science and Technology, Ministry of Science and Technology · Department of Scientific and Industrial Research, Ministry of Science and Technology
References (38)
Show source-provided references
1. Tarascon J.-M. · 2010 · 17110.1142/9789814317665_0024 ↗
2. 10.1016/j.mattod.2014.02.01410.1016/j.mattod.2014.02.014 ↗
3. 10.1021/cr020731c10.1021/cr020731c ↗
4. 10.1039/b925751a10.1039/b925751a ↗
5. 10.1149/1.180639410.1149/1.1806394 ↗
6. 10.1149/1.150307610.1149/1.1503076 ↗
7. 10.1039/c2cs35256g10.1039/c2cs35256g ↗
8. 10.1002/anie.20070250510.1002/anie.200702505 ↗
9. 10.1021/jacs.5b0707110.1021/jacs.5b07071 ↗
10. 10.1007/s11581-018-2496-410.1007/s11581-018-2496-4 ↗
11. 10.1021/acs.chemmater.7b0116610.1021/acs.chemmater.7b01166 ↗
12. 10.1021/acsami.5b0702410.1021/acsami.5b07024 ↗
13. 10.1039/c6ta07337a10.1039/c6ta07337a ↗
14. 10.1016/j.electacta.2018.01.15510.1016/j.electacta.2018.01.155 ↗
15. 10.1039/c8ta02259c10.1039/c8ta02259c ↗
16. 10.1021/acs.chemmater.6b0547510.1021/acs.chemmater.6b05475 ↗
17. 10.1002/aenm.20150144910.1002/aenm.201501449 ↗
18. 10.1021/acsenergylett.7b0001910.1021/acsenergylett.7b00019 ↗
19. 10.1016/j.elecom.2012.10.00910.1016/j.elecom.2012.10.009 ↗
20. 10.1039/c4cc09208b10.1039/c4cc09208b ↗
21. 10.1039/c5ra25850b10.1039/c5ra25850b ↗
22. 10.1039/c3ta14459c10.1039/c3ta14459c ↗
23. 10.1002/aenm.20120001710.1002/aenm.201200017 ↗
24. 10.1002/ange.20110063710.1002/ange.201100637 ↗
25. 10.1149/1.347982810.1149/1.3479828 ↗
26. 10.1039/b813099j10.1039/b813099j ↗
27. 10.1002/pssb.20120012110.1002/pssb.201200121 ↗
28. 10.1103/physrevb.8.358310.1103/physrevb.8.3583 ↗
29. 10.1149/2.020211jes10.1149/2.020211jes ↗
30. 10.1149/1.314872110.1149/1.3148721 ↗
31. 10.1149/1.139162910.1149/1.1391629 ↗
32. 10.1016/j.jpowsour.2008.10.03310.1016/j.jpowsour.2008.10.033 ↗
33. 10.1016/j.jpowsour.2010.08.10510.1016/j.jpowsour.2010.08.105 ↗
34. 10.1016/j.jpowsour.2012.10.09210.1016/j.jpowsour.2012.10.092 ↗
35. 10.1016/j.jpowsour.2008.02.05310.1016/j.jpowsour.2008.02.053 ↗
36. 10.1016/j.electacta.2013.02.10110.1016/j.electacta.2013.02.101 ↗
37. 10.1134/s102319351107009310.1134/s1023193511070093 ↗
38. 10.1016/j.jpowsour.2011.07.02110.1016/j.jpowsour.2011.07.021 ↗