A Polysulfide-Trapping Interface for Electrochemically Stable Sulfur Cathode Development
Source abstract
Abstract
Lithium-sulfur (Li-S) cells have a strong edge to become an inexpensive, high-capacity rechargeable battery system. However, currently, several prohibitive challenges occur within the sulfur core, especially the polysulfide-diffusion problem. To address these scientific issues, we present here a boron-doped multiwalled carbon nanotube coated separator (B-CNT-coated separator). The B-CNT-coated separator creates a polysulfide trap between the pure sulfur cathode and the polymeric separator as a "polysulfide-trapping interface," stabilizing the active material and allowing the dissolved polysulfides to activate the bulk sulfur cores. Therefore, the dissolved polysulfides change from causing fast capacity fade to assisting with the activation of bulk sulfur clusters in pure sulfur cathodes. Moreover, the heteroatom-doped polysulfide-trapping interface is currently one of the missing pieces of carbon-coated separators, which might inspire further studies in its effect and battery chemistry. Li-S cells employing B-CNT-coated separators (i) exhibit improved cyclability at various cycling rates from 0.2C to 1.0C rate and (ii) attain a high capacity retention rate of 60% with a low capacity fade rate of 0.04% cycle(-1) after 500 cycles. We believe that our B-CNT-coated separator could light up a new research area for integrating heteroatom-doped carbon into the flexible, lightweight, carbon-coated separator.
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
Materials Science and Engineering Program & Texas Materials Institute, The University of Texas at Austin, Austin, Texas 78712, United States
Funding
Division of Engineering Education and Centers
References (39)
Show source-provided references
1. 10.1021/ar300179v10.1021/ar300179v ↗
2. 10.1002/adma.20140511510.1002/adma.201405115 ↗
3. 10.1002/aenm.20150021210.1002/aenm.201500212 ↗
4. 10.1002/aenm.20150011810.1002/aenm.201500118 ↗
5. 10.1002/aenm.20150011710.1002/aenm.201500117 ↗
6. 10.1149/1.180639410.1149/1.1806394 ↗
7. 10.1021/ac203224410.1021/ac2032244 ↗
8. 10.1039/b925751a10.1039/b925751a ↗
9. 10.1039/c3ta11045a10.1039/c3ta11045a ↗
10. 10.1002/aenm.20140198610.1002/aenm.201401986 ↗
11. 10.1002/admi.20140022710.1002/admi.201400227 ↗
12. 10.1021/am501627f10.1021/am501627f ↗
13. 10.1002/adma.20140124310.1002/adma.201401243 ↗
14. 10.1002/anie.20141110910.1002/anie.201411109 ↗
15. 10.1002/adma.20130157910.1002/adma.201301579 ↗
16. 10.1002/adfm.20130329610.1002/adfm.201303296 ↗
17. 10.1021/acs.jpcc.5b0259610.1021/acs.jpcc.5b02596 ↗
18. 10.1039/C5TA00651A10.1039/C5TA00651A ↗
19. 10.1016/j.elecom.2013.02.02110.1016/j.elecom.2013.02.021 ↗
20. 10.1016/j.jpowsour.2014.05.11110.1016/j.jpowsour.2014.05.111 ↗
21. 10.1002/aenm.20150012410.1002/aenm.201500124 ↗
22. 10.1016/j.jpowsour.2011.10.07610.1016/j.jpowsour.2011.10.076 ↗
23. 10.1002/adfm.20140084510.1002/adfm.201400845 ↗
24. 10.1002/adma.20140289310.1002/adma.201402893 ↗
25. 10.1002/adma.20130436510.1002/adma.201304365 ↗
26. 10.1021/acs.jpclett.5b0092710.1021/acs.jpclett.5b00927 ↗
27. 10.1002/cssc.20130128710.1002/cssc.201301287 ↗
28. 10.1039/C5TA05374A10.1039/C5TA05374A ↗
29. 10.1021/jp512062t10.1021/jp512062t ↗
30. 10.1002/adma.20140563710.1002/adma.201405637 ↗
31. 10.1002/aenm.20150073810.1002/aenm.201500738 ↗
32. 10.1002/adfm.20150225110.1002/adfm.201502251 ↗
33. 10.1039/c3ee41444b10.1039/c3ee41444b ↗
34. 10.1002/anie.20110128710.1002/anie.201101287 ↗
35. 10.1016/j.electacta.2014.02.07710.1016/j.electacta.2014.02.077 ↗
36. 10.1039/C5TA01378J10.1039/C5TA01378J ↗
37. 10.1016/j.jpowsour.2013.11.09010.1016/j.jpowsour.2013.11.090 ↗
38. 10.1039/C3EE42223B10.1039/C3EE42223B ↗
39. 10.1021/nn507178a10.1021/nn507178a ↗