Clay Nanosheets in Skeletons of Controlled Phase Inversion Separators for Thermally Stable Li‐Ion Batteries
Source abstract
Abstract
Phase inversion is a powerful alternative process for preparing ultra‐thin separators for various secondary batteries. Unfortunately, separators prepared from phase inversion generally suffer from uneven pore size and pore size distribution, which frequently results in poor battery performance. Here, a straightforward route is demonstrated to solve the drawbacks of phase‐inversion‐based separators for Li‐ion batteries by means of directly incorporating 2D clay sheets in the skeleton of poly(vinylidene fluoride‐co‐hexafluoropropylene) (PVdF‐HFP) with multiscale pore generation from a simple one‐step solution coating method. Additionally generated pores by the inclusion of 2D nanosheets in PVdF‐HFP skeletons, combined with the multiscale pores (several micrometers + sub‐micrometers) originally generated by means of the controlled phase inversion, can generate additional ionic transport pathways, leading to Li‐ion battery performances better than those of commercialized polyethylene separators. Moreover, the addition of extremely low contents of 2D clay sheets in PVdF‐HFP separators allows thermally stable polymer separators to be realized.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical Engineering Sungkyunkwan University Suwon 440‐746 Republic of Korea
Department of Chemical and Biomolecular Engineering Yonsei University 50 Yonsei‐ro Seodaemun‐gu Seoul 120‐749 Republic of Korea
References (38)
Show source-provided references
1. 10.1039/c1ee01388b10.1039/c1ee01388b ↗
2. 10.1038/nnano.2007.31810.1038/nnano.2007.318 ↗
3. 10.1002/adma.20080062710.1002/adma.200800627 ↗
4. 10.1002/aenm.20120002810.1002/aenm.201200028 ↗
5. 10.1126/science.115183110.1126/science.1151831 ↗
6. 10.1038/nature0785310.1038/nature07853 ↗
7. 10.1038/3510464410.1038/35104644 ↗
8. 10.1016/j.jpowsour.2006.10.06510.1016/j.jpowsour.2006.10.065 ↗
9. 10.1021/cr020738u10.1021/cr020738u ↗
10. 10.1149/1.183953110.1149/1.1839531 ↗
11. 10.1016/j.progpolymsci.2013.07.00810.1016/j.progpolymsci.2013.07.008 ↗
12. 10.1016/j.memsci.2005.12.03810.1016/j.memsci.2005.12.038 ↗
13. 10.1016/S0167-2738(02)00090-510.1016/S0167-2738(02)00090-5 ↗
14. 10.1016/S0378-7753(99)00154-810.1016/S0378-7753(99)00154-8 ↗
15. Li Z. H. · Solid State Ionics · 2005 · 176 · 23
16. 10.1039/c0ee00348d10.1039/c0ee00348d ↗
17. 10.1016/j.apsusc.2006.03.09010.1016/j.apsusc.2006.03.090 ↗
18. Li Z. H. · Solid State Ionics · 2005 · 176 · 23
19. 10.1002/adma.20130307010.1002/adma.201303070 ↗
20. 10.1016/S0013-4686(02)00601-110.1016/S0013-4686(02)00601-1 ↗
21. 10.1002/aenm.20130023510.1002/aenm.201300235 ↗
22. 10.1557/JMR.1993.118510.1557/JMR.1993.1185 ↗
23. 10.1002/app.1993.07049071510.1002/app.1993.070490715 ↗
24. 10.1016/S0169-1317(99)00017-410.1016/S0169-1317(99)00017-4 ↗
25. 10.1180/claymin.1967.007.2.0310.1180/claymin.1967.007.2.03 ↗
26. 10.1016/S1005-0302(10)60098-910.1016/S1005-0302(10)60098-9 ↗
27. Reddy B. · 2014 · 113
28. 10.1002/polb.1035510.1002/polb.10355 ↗
29. 10.1002/pi.169210.1002/pi.1692 ↗
30. 10.1002/adma.1996008010410.1002/adma.19960080104 ↗
31. 10.1002/1521-3927(20011101)22:17<1422::AID-MARC1422>3.0.CO;2-V10.1002/1521-3927(20011101)22:17<1422::AID-MARC1422>3.0.CO;2-V ↗
32. 10.1002/pola.1993.08031100910.1002/pola.1993.080311009 ↗
33. 10.1016/j.polymer.2008.04.01710.1016/j.polymer.2008.04.017 ↗
34. 10.1016/S0169-1317(99)00019-810.1016/S0169-1317(99)00019-8 ↗
35. 10.1039/df954180012010.1039/df9541800120 ↗
36. 10.1016/0927-7757(93)02656-Y10.1016/0927-7757(93)02656-Y ↗
37. 10.1021/la981071310.1021/la9810713 ↗
38. 10.1039/c1jm12246k10.1039/c1jm12246k ↗