journal article·2020-01-08

Dioxolanone-Anchored Poly(allyl ether)-Based Cross-Linked Dual-Salt Polymer Electrolytes for High-Voltage Lithium Metal Batteries

Vidyanand Vijayakumar, Diddo Diddens, Andreas Heuer, Sreekumar Kurungot, Martin Winter, Jijeesh Ravi Nair

Publisher page

Abstract

Novel cross-linked polymer electrolytes (XPEs) are synthesized by free-radical copolymerization induced by ultraviolet (UV)-light irradiation of a reactive solution, which is composed of a difunctional poly(ethylene glycol) diallyl ether oligomer (PEGDAE), a monofunctional reactive diluent 4-vinyl-1,3-dioxolan-2-one (VEC), and a stock solution containing lithium salt (lithium bis(trifluoromethanesulfonyl)imide, LiTFSI) in a carbonate-free nonvolatile plasticizer, poly(ethylene glycol) dimethyl ether (PEGDME). The resulting polymer matrix can be represented as a linear polyethylene chain functionalized with cyclic carbonate (dioxolanone) moieties and cross-linked by ethylene oxide units. A series of XPEs are prepared by varying the [O]/[Li] ratio (24 to 3) of the stock solution and thoroughly characterized using physicochemical (thermogravimetric analysis–mass spectrometry, differential scanning calorimetry, NMR, etc.) and electrochemical techniques. In addition, quantum chemical calculations are performed to elucidate the correlation between the electrochemical oxidation potential and the lithium ion–ethylene oxide coordination in the stock solution. Later, lithium bis(fluorosulfonyl)imide (LiFSI) salt is incorporated into the electrolyte system to produce a dual-salt XPE that exhibits improved electrochemical performance, a stable interface against lithium metal, and enhanced physical and chemical characteristics to be employed against high-voltage cathodes. The XPE membranes demonstrated excellent resistance against lithium dendrite growth even after reversibly plating and stripping lithium ions for more than 1000 h with a total capacity of 0.5 mAh cm–2. Finally, the XPE films are assembled in a lab-scale lithium metal battery configuration by using carbon-coated LiFePO4 (LFP) or LiNi0.8Co0.15Al0.05O2 (NCA) as a cathode and galvanostatically cycled at 20, 40, and 60 °C. Remarkably, at 20 °C, the NCA-based lithium metal cells displayed excellent cycling stability and good capacity retention (>50%) even after 1000 cycles.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research

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

Affiliations

IEK-12, Forschungszentrum Jülich GmbH, Helmholtz Institute Münster, Corrensstraße 46, 48149 Münster, Germany

Physical and Materials Chemistry Division, CSIR-National Chemical Laboratory, 411008 Pune, Maharashtra, India

Academy of Scientific and Innovative Research (AcSIR), Sector 19, Kamla Nehru Nagar, 201002 Ghaziabad, Uttar Pradesh, India

Institute of Physical Chemistry, University of Münster, Corrensstraße 28/30, 48149 Münster, Germany

MEET Battery Research Center, Corrensstraße 46, 48149 Münster, Germany

Funding

Bundesministerium für Bildung und Forschung

References (70)

Show source-provided references
1. 10.1021/acs.chemrev.8b0042210.1021/acs.chemrev.8b00422 ↗
2. 10.1007/s10008-017-3610-710.1007/s10008-017-3610-7 ↗
3. 10.1002/adfm.20140295310.1002/adfm.201402953 ↗
4. 10.1039/C8CC02280A10.1039/C8CC02280A ↗
5. 10.1002/aenm.20190057410.1002/aenm.201900574 ↗
6. 10.1149/2.F05192if10.1149/2.F05192if ↗
7. 10.1039/C5TA03471J10.1039/C5TA03471J ↗
8. 10.1002/aenm.20170218410.1002/aenm.201702184 ↗
9. 10.1021/acsenergylett.6b0021610.1021/acsenergylett.6b00216 ↗
10. 10.1016/j.ssi.2017.12.02310.1016/j.ssi.2017.12.023 ↗
11. 10.1016/j.jpowsour.2007.08.00410.1016/j.jpowsour.2007.08.004 ↗
12. 10.1039/C7TA01514C10.1039/C7TA01514C ↗
13. 10.1016/j.electacta.2009.05.05510.1016/j.electacta.2009.05.055 ↗
14. 10.1021/acs.chemmater.8b0417210.1021/acs.chemmater.8b04172 ↗
15. 10.1002/adma.20180490910.1002/adma.201804909 ↗
16. 10.1016/j.joule.2018.06.00810.1016/j.joule.2018.06.008 ↗
17. 10.1007/s10800-004-2726-510.1007/s10800-004-2726-5 ↗
18. 10.1021/acsami.7b0284410.1021/acsami.7b02844 ↗
19. 10.1002/advs.20160037710.1002/advs.201600377 ↗
20. 10.1002/marc.20160065210.1002/marc.201600652 ↗
21. 10.1016/j.electacta.2019.02.05810.1016/j.electacta.2019.02.058 ↗
22. 10.1038/srep1989210.1038/srep19892 ↗
23. 10.1021/ma401267w10.1021/ma401267w ↗
24. 10.1021/acs.macromol.6b0085110.1021/acs.macromol.6b00851 ↗
25. 10.1016/j.electacta.2013.08.12410.1016/j.electacta.2013.08.124 ↗
26. 10.1002/pola.2870410.1002/pola.28704 ↗
27. 10.1295/polymj.PJ200817410.1295/polymj.PJ2008174 ↗
28. 10.1021/jp056249q10.1021/jp056249q ↗
29. 10.1149/2.0211502jes10.1149/2.0211502jes ↗
30. 10.1016/j.saa.2009.09.03110.1016/j.saa.2009.09.031 ↗
31. 10.1016/j.seppur.2018.03.06210.1016/j.seppur.2018.03.062 ↗
32. 10.1016/0584-8539(73)80044-310.1016/0584-8539(73)80044-3 ↗
33. 10.1007/BF0304767510.1007/BF03047675 ↗
34. 10.1039/C4CP05943C10.1039/C4CP05943C ↗
35. 10.1039/C5CP02033F10.1039/C5CP02033F ↗
36. 10.1016/j.jcp.2008.06.00610.1016/j.jcp.2008.06.006 ↗
37. 10.1021/am300991e10.1021/am300991e ↗
38. 10.1016/j.xphs.2016.06.00410.1016/j.xphs.2016.06.004 ↗
39. 10.1021/ma901893h10.1021/ma901893h ↗
40. 10.1063/1.486121910.1063/1.4861219 ↗
41. 10.1002/(SICI)1521-4095(199804)10:6<439::AID-ADMA439>3.0.CO;2-I10.1002/(SICI)1521-4095(199804)10:6<439::AID-ADMA439>3.0.CO;2-I ↗
42. 10.1039/C6TA02621D10.1039/C6TA02621D ↗
43. 10.1088/0953-8984/7/39/00310.1088/0953-8984/7/39/003 ↗
44. 10.1021/acs.macromol.8b0175310.1021/acs.macromol.8b01753 ↗
45. 10.1039/C9ME00038K10.1039/C9ME00038K ↗
46. 10.1021/ma200109610.1021/ma2001096 ↗
47. 10.1021/cm970075a10.1021/cm970075a ↗
48. 10.1149/1.204420610.1149/1.2044206 ↗
49. 10.1088/0957-4484/26/35/35400310.1088/0957-4484/26/35/354003 ↗
50. 10.1021/acs.accounts.7b0048610.1021/acs.accounts.7b00486 ↗
51. 10.1126/science.aab159510.1126/science.aab1595 ↗
52. 10.1002/advs.20170003210.1002/advs.201700032 ↗
53. 10.1039/C3EE42351D10.1039/C3EE42351D ↗
54. 10.1038/ncomms1203210.1038/ncomms12032 ↗
55. 10.1002/cssc.20160163610.1002/cssc.201601636 ↗
56. 10.1016/j.electacta.2017.12.09910.1016/j.electacta.2017.12.099 ↗
57. 10.1016/S0378-7753(02)00110-610.1016/S0378-7753(02)00110-6 ↗
58. 10.1149/2.004205eel10.1149/2.004205eel ↗
59. 10.1002/celc.20150023510.1002/celc.201500235 ↗
60. 10.1002/polb.2423510.1002/polb.24235 ↗
61. 10.1002/anie.20190878410.1002/anie.201908784 ↗
62. 10.1039/C5CP01891A10.1039/C5CP01891A ↗
63. 10.1002/advs.20180055910.1002/advs.201800559 ↗
64. 10.1039/C8TA12008K10.1039/C8TA12008K ↗
65. 10.1524/zpch.2009.608610.1524/zpch.2009.6086 ↗
66. 10.1038/ncomms251310.1038/ncomms2513 ↗
67. 10.1016/j.elecom.2008.02.00610.1016/j.elecom.2008.02.006 ↗
68. 10.1088/1674-1056/25/7/07820310.1088/1674-1056/25/7/078203 ↗
69. 10.1039/C7CP06485C10.1039/C7CP06485C ↗
70. 10.1021/ja403082s10.1021/ja403082s ↗