Combining Polyester-Based Solid Polymer Electrolytes with Lithiated Organic Cathodes for 3.5 V-Class Li-Organic Rechargeable Batteries
Source abstract
Abstract
Solid-state batteries have attracted intensive attention in recent years for their potential to overcome the limitations of conventional liquid-electrolyte batteries while allowing for compatibility with lithium metal electrodes and improving energy density. On the other hand, there is a growing interest in developing organic electrode materials to supplement existing technologies while offering sustainable, versatile, and potentially low-cost electrochemical storage devices. In this study, we report the first solid-state Li polymer batteries based on poly(ε-caprolactone- co -trimethylene carbonate) 80:20 random copolymer with 28 wt % LiTFSI as the electrolyte paired with high-potential lithiated organic insertion materials, namely, both magnesium and zinc (2,5-dilithium-oxy)-terephthalate compounds. This polymer electrolyte was shown to be compatible with the organic electrode, and functional cells could be constructed. The zinc derivative was selected due to the high ionic potential value of Zn 2+, similar to that of Mg 2+, and was synthesized in methanol using a scalable and efficient two-step chemical process. The electrochemical study pointed out an optimal operation temperature of 60 °C for such solid-state Li polymer batteries compared with the use of conventional carbonate-based liquid electrolytes at 23 °C. A better stability upon cycling was observed with the magnesium-based phase, while the zinc counterpart showed more pronounced capacity loss, requiring further investigations.
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.
Affiliations
Nantes Université, CNRS, Institut des Matériaux de Nantes Jean Rouxel, IMN, F-44000 Nantes, France
ALISTORE-European Research Institute, 80000 Amiens, France
Technocentre Renault, 1 Avenue du Golf, 78280 Guyancourt, France
Department of Chemistry−Ångström Laboratory, Uppsala University, SE-751 21 Uppsala, Sweden
Funding
Vetenskapsr?det · European Commission · H2020 Marie Sklodowska-Curie Actions
References (55)
Show source-provided references
1. 10.1039/C3EE42613K10.1039/C3EE42613K ↗
2. 10.1002/aenm.20120002810.1002/aenm.201200028 ↗
3. 10.1039/c0ee00731e10.1039/c0ee00731e ↗
4. 10.1080/10643389.2021.187485410.1080/10643389.2021.1874854 ↗
5. 10.1021/acs.chemrev.9b0048210.1021/acs.chemrev.9b00482 ↗
6. 10.1002/eem2.1245010.1002/eem2.12450 ↗
7. 10.1002/cssc.20070016110.1002/cssc.200700161 ↗
8. 10.1039/c3ee40878g10.1039/c3ee40878g ↗
9. 10.1021/am405470p10.1021/am405470p ↗
10. 10.1039/C6TA03166H10.1039/C6TA03166H ↗
11. 10.1016/j.joule.2017.10.01310.1016/j.joule.2017.10.013 ↗
12. 10.1039/D0SE01338B10.1039/D0SE01338B ↗
13. 10.1038/s41586-021-03399-110.1038/s41586-021-03399-1 ↗
14. 10.1002/eom2.1205510.1002/eom2.12055 ↗
15. 10.1016/j.jpowsour.2020.22881410.1016/j.jpowsour.2020.228814 ↗
16. 10.1038/s41570-020-0160-910.1038/s41570-020-0160-9 ↗
17. 10.1002/aenm.20210156210.1002/aenm.202101562 ↗
18. 10.1039/D0MH01391A10.1039/D0MH01391A ↗
19. 10.1016/j.progpolymsci.2021.10144910.1016/j.progpolymsci.2021.101449 ↗
20. 10.1021/acsenergylett.1c0136810.1021/acsenergylett.1c01368 ↗
21. 10.1002/aesr.20220003010.1002/aesr.202200030 ↗
22. 10.1002/aenm.20200198410.1002/aenm.202001984 ↗
23. 10.1002/adma.20230189810.1002/adma.202301898 ↗
24. 10.1016/j.mtener.2020.10054710.1016/j.mtener.2020.100547 ↗
25. Brandell D. · 202110.1515/9781501521140 ↗
26. 10.1039/C3EE40795K10.1039/C3EE40795K ↗
27. Armand, M.; Chabagno, J. M.; Duclot, M. J. Second international meeting on solid electrolytes; University of St Andrews, Scotland, September 20–22, 1978. https://search.worldcat.org/title/230397846 (accessed 2024–02–01).
28. 10.1088/0953-8984/7/34/00710.1088/0953-8984/7/34/007 ↗
29. 10.1021/ma00103a03410.1021/ma00103a034 ↗
30. 10.1016/0167-2738(94)90419-710.1016/0167-2738(94)90419-7 ↗
31. 10.1149/1945-7111/ab787a10.1149/1945-7111/ab787a ↗
32. 10.1016/j.progpolymsci.2017.12.00410.1016/j.progpolymsci.2017.12.004 ↗
33. 10.1016/0167-2738(83)90068-110.1016/0167-2738(83)90068-1 ↗
34. 10.1016/j.eurpolymj.2008.06.02210.1016/j.eurpolymj.2008.06.022 ↗
35. 10.1038/2881810.1038/28818 ↗
36. 10.1021/ma00182a04410.1021/ma00182a044 ↗
37. 10.1038/s41598-020-61373-910.1038/s41598-020-61373-9 ↗
38. 10.1016/j.polymdegradstab.2018.11.01310.1016/j.polymdegradstab.2018.11.013 ↗
39. 10.1016/j.elecom.2015.03.01010.1016/j.elecom.2015.03.010 ↗
40. 10.3390/molecules2611307910.3390/molecules26113079 ↗
41. 10.1016/j.polymer.2015.02.05210.1016/j.polymer.2015.02.052 ↗
42. 10.1016/j.jpowsour.2015.08.03510.1016/j.jpowsour.2015.08.035 ↗
43. 10.1038/s41467-018-06708-x10.1038/s41467-018-06708-x ↗
44. 10.1021/acsaem.2c0164110.1021/acsaem.2c01641 ↗
45. 10.1016/j.nanoen.2020.10469010.1016/j.nanoen.2020.104690 ↗
46. 10.1002/anie.20221604710.1002/anie.202216047 ↗
47. 10.1021/jacs.1c0459110.1021/jacs.1c04591 ↗
48. 10.1021/nl402239p10.1021/nl402239p ↗
49. 10.1149/1945-7111/ab7c6d10.1149/1945-7111/ab7c6d ↗
50. 10.3390/inorganics1005006210.3390/inorganics10050062 ↗
51. 10.1016/j.gca.2007.03.03810.1016/j.gca.2007.03.038 ↗
52. 10.1021/acs.chemmater.0c0298910.1021/acs.chemmater.0c02989 ↗
53. 10.1021/acsaem.0c0309810.1021/acsaem.0c03098 ↗
54. 10.1016/j.ssi.2013.08.01410.1016/j.ssi.2013.08.014 ↗
55. 10.1039/C6CP00757K10.1039/C6CP00757K ↗