journal article·2020-09-22

Zwitterionic Copolymer-Supported Ionogel Electrolytes Featuring a Sodium Salt/Ionic Liquid Solution

Huan Qin, Matthew J. Panzer

Chemistry of Materials· Volume 32· Issue 18
Publisher page

Abstract

A series of zwitterionic (ZI) copolymers, including both binary, fully-ZI and ternary, partially-ZI copolymer variations, have been successfully employed as scaffolds to support mechanically robust ionic liquid-based gel (ionogel) electrolytes containing sodium bis(trifluoromethylsulfonyl)imide salt. All of the synthesized ionogels, which were optically transparent and freestanding without any covalent cross-links, contained 15 mol % copolymer and displayed room-temperature ionic conductivities above 1 mS cm–1 while also exhibiting high compressive elastic modulus values (0.7–11 MPa). The activation energy of ionic conductivity of an ionogel with a fully-ZI copolymer scaffold (18 kJ mol–1) was found to be noticeably lower than that of the ionic liquid electrolyte solution itself (23 kJ mol–1), highlighting the positive role that ZI moieties may play in aiding ion transport. NMR chemical shift analysis revealed favorable interactions between sodium cations and both types of ZI motifs employed here (sulfobetaine and phosphorylcholine). In addition, the sodium-ion transference number value of a ternary copolymer-supported ionogel electrolyte was determined to be larger compared to that of the ionic liquid solution (0.19 vs 0.10, respectively).
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Ionic liquids properties and applications · Conducting polymers and applications

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Affiliations

Department of Chemical and Biological Engineering, Tufts University, 4 Colby Street, Medford, Massachusetts 02155, United States

Funding

Tufts University · Division of Chemical, Bioengineering, Environmental, and Transport Systems

References (38)

Show source-provided references
1. 10.1039/B820660K10.1039/B820660K ↗
2. 10.1038/nchem.208510.1038/nchem.2085 ↗
3. 10.1038/nmat319110.1038/nmat3191 ↗
4. 10.1002/adma.20160343610.1002/adma.201603436 ↗
5. 10.1126/science.121274110.1126/science.1212741 ↗
6. 10.1039/c1ee01598b10.1039/c1ee01598b ↗
7. 10.1038/nchem.68010.1038/nchem.680 ↗
8. 10.1039/C6CS00776G10.1039/C6CS00776G ↗
9. 10.1039/C4TA04428B10.1039/C4TA04428B ↗
10. 10.1039/c3ee40847g10.1039/c3ee40847g ↗
11. 10.1021/acs.jpcc.5b1174610.1021/acs.jpcc.5b11746 ↗
12. 10.1039/C4CP00746H10.1039/C4CP00746H ↗
13. 10.1002/anie.20141037610.1002/anie.201410376 ↗
14. 10.1002/smll.20197007210.1002/smll.201970072 ↗
15. 10.1016/j.joule.2018.07.02810.1016/j.joule.2018.07.028 ↗
16. 10.1002/celc.20190010110.1002/celc.201900101 ↗
17. 10.1021/acssuschemeng.8b0621210.1021/acssuschemeng.8b06212 ↗
18. 10.1021/acs.accounts.8b0056610.1021/acs.accounts.8b00566 ↗
19. 10.1021/acs.chemrev.6b0050410.1021/acs.chemrev.6b00504 ↗
20. 10.1016/j.electacta.2006.03.01610.1016/j.electacta.2006.03.016 ↗
21. 10.1039/C9EE02041A10.1039/C9EE02041A ↗
22. 10.1039/c3ta15273a10.1039/c3ta15273a ↗
23. 10.1039/C0CS00059K10.1039/C0CS00059K ↗
24. 10.1038/natrevmats.2015.510.1038/natrevmats.2015.5 ↗
25. 10.1039/C4TA06062H10.1039/C4TA06062H ↗
26. 10.1039/C6TA04767J10.1039/C6TA04767J ↗
27. 10.1021/acsami.9b0218210.1021/acsami.9b02182 ↗
28. 10.1016/j.electacta.2016.08.08410.1016/j.electacta.2016.08.084 ↗
29. 10.1016/j.electacta.2015.03.02410.1016/j.electacta.2015.03.024 ↗
30. 10.1021/acsaem.9b0123410.1021/acsaem.9b01234 ↗
31. 10.1021/acs.jpclett.9b0294710.1021/acs.jpclett.9b02947 ↗
32. 10.1021/acs.chemmater.6b0445610.1021/acs.chemmater.6b04456 ↗
33. 10.1021/acsmaterialslett.9b0050010.1021/acsmaterialslett.9b00500 ↗
34. 10.1021/acs.jpcb.8b0598510.1021/acs.jpcb.8b05985 ↗
35. 10.1021/acs.chemmater.9b0017210.1021/acs.chemmater.9b00172 ↗
36. 10.1002/aenm.20180164610.1002/aenm.201801646 ↗
37. 10.1016/0032-3861(87)90394-610.1016/0032-3861(87)90394-6 ↗
38. 10.1021/acs.jpcb.5b0825010.1021/acs.jpcb.5b08250 ↗