journal article·2024-02-23

Peristaltic Ion-Conduction Mechanism in Sodium Polymer Electrolytes Based on Perfluoropolyethers, DMSO, and Sodium Bis(trifluoromethanesulfonyl)imide

Sumit Kumar, Rajesh Raghupathy, Michele Vittadello

ACS Applied Polymer Materials· Volume 6· Issue 4
Publisher page

Abstract

The promise of sodium-ion conducting polymer electrolytes in rechargeable power sources is yet to be fulfilled. The possibility to combine the very attractive physical–chemical properties of perfluorinated polyethers (PFPEs) with sodium salts has not thus far been considered. Here we investigate a series of eight plasticized polymer electrolytes based on an α,ω-OH-terminated poly[PFPE- block -PEO] (hereafter called PEG-PFPE-PEG), sodium bis(trifluoromethanesulfonyl)imide (NaTFSI), and dimethyl sulfoxide (DMSO) as plasticizer, having general formula PEG-PFPE-PEG/(NaTFSI) x (DMSO) y (0.004 ≤ x ≤ 0.610, 3.205 ≤ y ≤ 3.794). The thermal analysis results, carried out by means of DSC, indicate that the plasticizer remains intimately integrated in the polymer electrolytes up to the decomposition temperature of PEG-PFPE-PEG (180 °C ca.) and is not significantly released out of the polymer hosts in closed cells. The vibrational investigation, carried out by FT-IR spectroscopy in the medium IR region, shed light on NaTFSI–PEG-PFPE-PEG–DMSO interactions. In particular, the role of the OH functional groups in facilitating salt dissolution was elucidated, along with that of the CO and CF moieties. The ionic conductivity was investigated by impedance spectroscopy, in the frequency interval 100 mHz to 1 MHz. The conductivity at 25 °C is as high as 8.0 × 10 –4 S·cm –1 . Three of at least five polarization events (one electrode and four interdomain polarizations in total) were fully resolved and were associated with different interfacing domains in the polymer electrolytes with increasing DMSO content. The behavior of the corresponding conductivities and frequencies were fitted with Vogel–Tamman–Fulcher (VTF) and Arrhenius equations, respectively, highlighting the concomitant roles of segmental motion and ionic hopping in these hybrid systems. Furthermore, it was shown that the presence of DMSO, a well-known cryodepressant, significantly decreases the glass transition temperature of the electrolytes.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Conducting polymers and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry and Environmental Science, Medgar Evers College of the City University of New York (CUNY), 1638 Bedford Avenue, Brooklyn, New York 11225, United States

Bioorganic Research Laboratory, Department of Chemistry, University of Delhi, University Enclave, Delhi 110007, India

Nano and Bioelectrochemistry Research Laboratory and Carbon Dioxide Research and Green Technology Centre, Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Turuvalam Road, Vellore 632014, India

Ph.D. Program in Chemistry and M.S. Program in Nanoscience, The Graduate Center of CUNY, 365 5th Avenue, New York, New York 10016, United States

Funding

City University of New York · Natrion Incorporated

References (50)

Show source-provided references
1. 10.1039/c3ee24086j10.1039/c3ee24086j ↗
2. 10.1002/aenm.20120002610.1002/aenm.201200026 ↗
3. 10.1038/3510464410.1038/35104644 ↗
4. Gray F. M. · 1997
5. Scrosati B. · 199310.1007/978-94-011-1568-1 ↗
6. 10.1016/S0013-4686(97)10023-810.1016/S0013-4686(97)10023-8 ↗
7. 10.1021/jp983764y10.1021/jp983764y ↗
8. 10.1149/1.177448810.1149/1.1774488 ↗
9. 10.1016/j.electacta.2011.07.13310.1016/j.electacta.2011.07.133 ↗
10. 10.1149/1.212885910.1149/1.2128859 ↗
11. 10.1016/0022-0728(87)80001-310.1016/0022-0728(87)80001-3 ↗
12. 10.1073/pnas.131461511110.1073/pnas.1314615111 ↗
13. 10.1021/acs.macromol.9b0163710.1021/acs.macromol.9b01637 ↗
14. 10.1016/j.jiec.2018.04.00610.1016/j.jiec.2018.04.006 ↗
15. 10.1016/j.ssi.2017.08.00710.1016/j.ssi.2017.08.007 ↗
16. 10.1021/acs.macromol.6b0041210.1021/acs.macromol.6b00412 ↗
17. 10.1021/cm504228a10.1021/cm504228a ↗
18. 10.1088/2053-1591/ab103210.1088/2053-1591/ab1032 ↗
19. 10.1016/j.electacta.2021.13798410.1016/j.electacta.2021.137984 ↗
20. 10.1038/2201315a010.1038/2201315a0 ↗
21. 10.1038/s41598-019-51412-510.1038/s41598-019-51412-5 ↗
22. 10.1002/ange.20190891310.1002/ange.201908913 ↗
23. 10.1177/096368972199961710.1177/0963689721999617 ↗
24. 10.1039/B413486A10.1039/B413486A ↗
25. 10.1016/S0013-4686(96)00440-910.1016/S0013-4686(96)00440-9 ↗
26. 10.1002/jrs.125020030810.1002/jrs.1250200308 ↗
27. Xuan X.-P. · Acta Chimica Sinica · 2004 · 62 · 940
28. 10.1139/v79-11410.1139/v79-114 ↗
29. Dykyj, J.; Svoboda, J.; Wilhoit, R. C.; Frenkel, M. L.; Hall, K. R. Vapor Pressure of Chemicals: Part A. Vapor Pressure and Antoine Constants for Hydrocarbons and Sulfur, Selenium, Tellurium and Hydrogen Containing Organic Compounds; Springer, 1999; p 373.
30. 10.1021/acs.oprd.0c0015910.1021/acs.oprd.0c00159 ↗
31. 10.1016/j.jpowsour.2005.05.08510.1016/j.jpowsour.2005.05.085 ↗
32. Bertie J. E. · 2006 · 88
33. 10.1366/000370285424857510.1366/0003702854248575 ↗
34. 10.1016/S0924-2031(98)00033-210.1016/S0924-2031(98)00033-2 ↗
35. 10.1021/jp983764y10.1021/jp983764y ↗
36. 10.1016/S0167-2738(02)00030-910.1016/S0167-2738(02)00030-9 ↗
37. 10.1021/jp101840f10.1021/jp101840f ↗
38. 10.1021/acs.jpca.8b0114810.1021/acs.jpca.8b01148 ↗
39. 10.1246/bcsj.41.179810.1246/bcsj.41.1798 ↗
40. 10.1021/jp301967e10.1021/jp301967e ↗
41. Ratner M. · 1989
42. 10.1063/1.166215810.1063/1.1662158 ↗
43. 10.1021/jp010393410.1021/jp0103934 ↗
44. 10.1143/JJAP.36.111910.1143/JJAP.36.1119 ↗
45. 10.1016/j.jpowsour.2022.23108410.1016/j.jpowsour.2022.231084 ↗
46. 10.1016/j.jpowsour.2008.10.06610.1016/j.jpowsour.2008.10.066 ↗
47. 10.1002/polb.2453310.1002/polb.24533 ↗
48. 10.1007/s10965-020-2016-x10.1007/s10965-020-2016-x ↗
49. 10.1366/13-0722910.1366/13-07229 ↗
50. Lin-Vien D. · 1991