journal article·2017-09-26

Highly Effective Solid Electrolyte Interphase-Forming Electrolyte Additive Enabling High Voltage Lithium-Ion Batteries

Stephan Röser, Andreas Lerchen, Lukas Ibing, Xia Cao, Johannes Kasnatscheew, Frank Glorius, Martin Winter, Ralf Wagner

Chemistry of Materials· Volume 29· Issue 18
Publisher page

Abstract

The electrochemical and thermal stabilities of commonly used LiPF 6 /organic carbonate-based electrolytes are still a bottleneck for the development of high energy density lithium-ion batteries (LIBs) operating at elevated cell voltage and elevated temperature. The use of intrinsic electrochemically stable electrolyte solvents, e.g. sulfones or dinitriles, has been reported as one approach to enable high voltage LIBs. However, the major challenge of these solvents is related to their poor reductive stability and lack of solid electrolyte interphase (SEI)-forming ability on the graphite electrode. Here, 3-methyl-1,4,2-dioxazol-5-one (MDO) is synthesized and investigated as new highly effective SEI-forming electrolyte additive which can sufficiently suppress electrolyte reduction and graphite exfoliation in propylene carbonate (PC)-based electrolytes. With the addition of only 2 wt % MDO, LiNi 0.5 Mn 0.3 Co 0.2 O 2 (NMC532)/graphite full cells containing a 1 M LiPF 6 in PC electrolyte reach a cycle life of more than 450 cycles while still having a capacity retention of 80%. In addition, MDO has proven to be oxidatively stable until potentials as high as 5.3 V vs Li/Li + . Further development of MDO and its derivatives as electrolyte additives is a step forward to high voltage stable electrolyte formulations based on alternative electrolyte solvents and high energy density LIBs.
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

MEET Battery Research Center/Institute of Physical Chemistry, University of Münster, Corrensstrasse 46, 48149 Münster, Germany

Institute of Organic Chemistry, University of Münster, Corrensstrasse 40, 48149 Münster, Germany

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

Funding

Bundesministerium f?r Bildung und Forschung · Deutsche Forschungsgemeinschaft

References (51)

Show source-provided references
1. 10.1039/C5TA00361J10.1039/C5TA00361J ↗
2. 10.1021/ja309143810.1021/ja3091438 ↗
3. 10.1149/2.0461614jes10.1149/2.0461614jes ↗
4. 10.1002/ente.20170006810.1002/ente.201700068 ↗
5. 10.1016/j.jpowsour.2012.01.12210.1016/j.jpowsour.2012.01.122 ↗
6. 10.1016/j.electacta.2003.09.00910.1016/j.electacta.2003.09.009 ↗
7. 10.1002/chem.20110148610.1002/chem.201101486 ↗
8. 10.1149/1.342851510.1149/1.3428515 ↗
9. 10.1149/2.0121514jes10.1149/2.0121514jes ↗
10. 10.1021/acsami.6b0916410.1021/acsami.6b09164 ↗
11. 10.1016/j.jpowsour.2015.12.02510.1016/j.jpowsour.2015.12.025 ↗
12. 10.1039/C5RA23624J10.1039/C5RA23624J ↗
13. 10.1021/acsami.6b0768710.1021/acsami.6b07687 ↗
14. 10.1016/j.progsolidstchem.2014.04.00310.1016/j.progsolidstchem.2014.04.003 ↗
15. 10.1016/j.jpowsour.2013.03.02410.1016/j.jpowsour.2013.03.024 ↗
16. 10.1002/admi.20160009610.1002/admi.201600096 ↗
17. 10.1016/j.electacta.2017.01.02910.1016/j.electacta.2017.01.029 ↗
18. 10.1016/j.electacta.2015.10.00210.1016/j.electacta.2015.10.002 ↗
19. 10.1007/s10800-013-0533-610.1007/s10800-013-0533-6 ↗
20. 10.1039/C4RA11575A10.1039/C4RA11575A ↗
21. 10.1021/cr500003w10.1021/cr500003w ↗
22. 10.1002/cphc.20140217510.1002/cphc.201402175 ↗
23. 10.1021/jp204401t10.1021/jp204401t ↗
24. 10.1016/j.elecom.2009.03.02010.1016/j.elecom.2009.03.020 ↗
25. 10.1149/2.088306jes10.1149/2.088306jes ↗
26. 10.1039/c3ee24414h10.1039/c3ee24414h ↗
27. 10.1524/zpch.2009.608610.1524/zpch.2009.6086 ↗
28. 10.1149/1.148386610.1149/1.1483866 ↗
29. 10.1016/j.elecom.2009.05.02010.1016/j.elecom.2009.05.020 ↗
30. 10.1149/1.302308410.1149/1.3023084 ↗
31. 10.1149/2.016204jes10.1149/2.016204jes ↗
32. 10.1016/j.jpowsour.2006.07.07410.1016/j.jpowsour.2006.07.074 ↗
33. 10.1016/j.elecom.2014.01.00410.1016/j.elecom.2014.01.004 ↗
34. 10.1149/2.009309jes10.1149/2.009309jes ↗
35. 10.1021/cr030203g10.1021/cr030203g ↗
36. 10.1149/1.302967410.1149/1.3029674 ↗
37. 10.1021/acs.chemmater.5b0162710.1021/acs.chemmater.5b01627 ↗
38. 10.1021/acs.chemmater.5b0033910.1021/acs.chemmater.5b00339 ↗
39. 10.1039/C5CP07583A10.1039/C5CP07583A ↗
40. 10.1021/acsnano.7b0092210.1021/acsnano.7b00922 ↗
41. 10.1149/2.0231509jes10.1149/2.0231509jes ↗
42. 10.1016/j.electacta.2016.12.12610.1016/j.electacta.2016.12.126 ↗
43. 10.1016/j.elecom.2005.06.00910.1016/j.elecom.2005.06.009 ↗
44. 10.1021/jacs.5b0132410.1021/jacs.5b01324 ↗
45. 10.1016/j.jpowsour.2013.11.06410.1016/j.jpowsour.2013.11.064 ↗
46. 10.1016/j.jpowsour.2012.01.02710.1016/j.jpowsour.2012.01.027 ↗
47. 10.1021/acs.chemmater.6b0289510.1021/acs.chemmater.6b02895 ↗
48. 10.1016/j.jpowsour.2016.09.10010.1016/j.jpowsour.2016.09.100 ↗
49. 10.1149/1.139260910.1149/1.1392609 ↗
50. 10.1149/1.183841910.1149/1.1838419 ↗
51. 10.1039/C6CS00875E10.1039/C6CS00875E ↗