Lithium Sulfonate/Carboxylate-Anchored Polyvinyl Alcohol Separators for Lithium Sulfur Batteries
Source abstract
Abstract
A monolayer poly(vinyl alcohol) (PVA)-based separator with pendant sulfonate/carboxylate groups and compact morphology is synthesized to suppress the essential lithium polysulfide permeation in lithium sulfur batteries (LSBs). The Li+ transference number is significantly increased to 0.8, much higher than that of a commercial separator (0.43). The polysulfide retention is verified by idle test in a polysulfide-rich electrolyte under the internal electric field of the cell. The LSB with an additive-free electrolyte attains a Coulombic efficiency around 98% and delivered capacity of 804 mA h g–1 at 2.5 A g–1. After 500 cycles, it retains 901 mA h g–1 at 1.5 A g–1 with extra low fading rate of 0.016% per cycle. Overall, this monolayer PVA-based separator provides a facile and effective technique to assemble highly stable LSBs.
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.
References (33)
Show source-provided references
1. 10.1039/c5ta04289e10.1039/c5ta04289e ↗
2. 10.1021/acsami.6b0798910.1021/acsami.6b07989 ↗
3. 10.1039/c5ee01985k10.1039/c5ee01985k ↗
4. 10.1016/j.nanoen.2015.12.00510.1016/j.nanoen.2015.12.005 ↗
5. 10.1021/acsami.6b0257610.1021/acsami.6b02576 ↗
6. 10.1038/ncomms1120310.1038/ncomms11203 ↗
7. 10.1039/c7ta05145j10.1039/c7ta05145j ↗
8. 10.1021/nn507178a10.1021/nn507178a ↗
9. 10.1039/c7ta00290d10.1039/c7ta00290d ↗
10. 10.1039/c7ta03552g10.1039/c7ta03552g ↗
11. 10.1002/adfm.20140084510.1002/adfm.201400845 ↗
12. 10.1016/j.electacta.2016.01.22510.1016/j.electacta.2016.01.225 ↗
13. 10.1039/c7nr04320a10.1039/c7nr04320a ↗
14. 10.1002/adma.20160217210.1002/adma.201602172 ↗
15. 10.1021/acsami.5b1201210.1021/acsami.5b12012 ↗
16. 10.1021/acsami.6b0466210.1021/acsami.6b04662 ↗
17. 10.1016/j.ensm.2016.12.00410.1016/j.ensm.2016.12.004 ↗
18. 10.1016/j.jpowsour.2013.11.09010.1016/j.jpowsour.2013.11.090 ↗
19. 10.1039/c3ee42223b10.1039/c3ee42223b ↗
20. 10.1021/acs.chemmater.6b0219010.1021/acs.chemmater.6b02190 ↗
21. 10.1021/acsenergylett.7b0028910.1021/acsenergylett.7b00289 ↗
22. 10.1016/j.electacta.2012.08.11410.1016/j.electacta.2012.08.114 ↗
23. 10.1016/j.electacta.2013.10.16910.1016/j.electacta.2013.10.169 ↗
24. 10.1149/2.0921607jes10.1149/2.0921607jes ↗
25. 10.1016/j.memsci.2015.04.00410.1016/j.memsci.2015.04.004 ↗
26. 10.1016/j.memsci.2004.03.03010.1016/j.memsci.2004.03.030 ↗
27. 10.1016/j.memsci.2004.04.01010.1016/j.memsci.2004.04.010 ↗
28. 10.1038/ncomms251310.1038/ncomms2513 ↗
29. 10.1016/j.nanoen.2016.02.00810.1016/j.nanoen.2016.02.008 ↗
30. 10.1021/nl200658a10.1021/nl200658a ↗
31. 10.1038/nenergy.2016.9410.1038/nenergy.2016.94 ↗
32. 10.1002/smll.20150313310.1002/smll.201503133 ↗
33. 10.1021/acsami.7b0214210.1021/acsami.7b02142 ↗