journal article·2025-05-13Open access

Origin of Stability in the Solid Electrolyte Interphase formed between Lithium and Lithium Phosphorus Oxynitride

Stephen J. Turrell, Yi Liang, Tiancheng Cai, Ben Jagger, Mauro Pasta

Chemistry of Materials· Volume 37· Issue 9

Abstract

High Resolution Image Download MS PowerPoint Slide Lithium phosphorus oxynitride (LiPON) is one of the few solid electrolytes that form a truly passivating solid electrolyte interphase (SEI) when in contact with metallic lithium. Investigations into the origin of this stability may provide the insights needed to replicate it in the SEIs of alternative solid electrolyte materials. In this study, we used in situ lithium plating X-ray photoelectron spectroscopy (XPS) to investigate the formation and evolution of the Li-LiPON SEI. We show that the SEI is chemically and structurally inhomogeneous, with the fully reduced compounds identified in previous studies (Li 2 O, Li 3 N, and Li 3 P) concentrated near the lithium metal side and partially lithiated species, including Li x P, predominant closer to the LiPON side. Li 3 P and Li x P have recently been suggested as enablers of continuous SEI growth in thiophosphate solid electrolytes. We suggest that the stability of the Li-LiPON SEI is derived from a combination of the LiPON reduction potential (0.68 V vs Li + /Li), which is below the oxidation potentials of the fully reduced SEI compounds, and the graded structure of the SEI, which ensures that the most reduced species are not in physical or electrical contact with the LiPON layer.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Solid-state spectroscopy and crystallography

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

Affiliations

Department of Materials, University of Oxford, Parks Road, Oxford OX1 3PH, U.K.

The Faraday Institution, Quad One, Becquerel Avenue, Harwell Campus, Didcot OX11 0RA, U.K.

Funding

Henry Royce Institute · Clarendon Fund · Faraday Institution

References (64)

Show source-provided references
1. 10.1021/acs.chemrev.7b0011510.1021/acs.chemrev.7b00115 ↗
2. 10.1038/3510464410.1038/35104644 ↗
3. 10.3390/ma1308188410.3390/ma13081884 ↗
4. 10.1038/nmat306610.1038/nmat3066 ↗
5. 10.1038/nenergy.2016.3010.1038/nenergy.2016.30 ↗
6. 10.1021/jacs.8b1028210.1021/jacs.8b10282 ↗
7. 10.1021/jacs.9b0835710.1021/jacs.9b08357 ↗
8. 10.1038/s41560-023-01208-910.1038/s41560-023-01208-9 ↗
9. 10.1088/2515-7655/ab95f410.1088/2515-7655/ab95f4 ↗
10. 10.1016/0022-3093(83)90464-710.1016/0022-3093(83)90464-7 ↗
11. 10.1016/0167-2738(92)90442-R10.1016/0167-2738(92)90442-R ↗
12. 10.1149/1.183718810.1149/1.1837188 ↗
13. 10.1002/aenm.20220175010.1002/aenm.202201750 ↗
14. 10.1002/aenm.20140140810.1002/aenm.201401408 ↗
15. 10.1149/1.139322610.1149/1.1393226 ↗
16. 10.1021/acs.chemmater.6b0061010.1021/acs.chemmater.6b00610 ↗
17. 10.1021/jp405127510.1021/jp4051275 ↗
18. 10.1016/j.ssi.2015.06.00110.1016/j.ssi.2015.06.001 ↗
19. 10.1016/j.ssi.2015.11.03410.1016/j.ssi.2015.11.034 ↗
20. 10.1149/1.212885910.1149/1.2128859 ↗
21. 10.1016/j.ssi.2014.10.01710.1016/j.ssi.2014.10.017 ↗
22. 10.1016/j.jpowsour.2017.04.00510.1016/j.jpowsour.2017.04.005 ↗
23. 10.1021/acsami.5b0751710.1021/acsami.5b07517 ↗
24. 10.1016/j.joule.2020.08.01310.1016/j.joule.2020.08.013 ↗
25. 10.1021/acs.nanolett.0c0343810.1021/acs.nanolett.0c03438 ↗
26. 10.1021/acs.chemmater.4c0037710.1021/acs.chemmater.4c00377 ↗
27. 10.1021/acsenergylett.0c0184010.1021/acsenergylett.0c01840 ↗
28. 10.1021/acsenergylett.3c0048810.1021/acsenergylett.3c00488 ↗
29. 10.1002/aesr.20230000110.1002/aesr.202300001 ↗
30. 10.1038/s41467-018-04762-z10.1038/s41467-018-04762-z ↗
31. 10.1021/acs.chemmater.0c0386910.1021/acs.chemmater.0c03869 ↗
32. 10.1149/1945-7111/ac163d10.1149/1945-7111/ac163d ↗
33. 10.1038/s41467-022-34855-910.1038/s41467-022-34855-9 ↗
34. 10.1038/s41586-021-03584-210.1038/s41586-021-03584-2 ↗
35. 10.1016/0022-3093(94)00665-210.1016/0022-3093(94)00665-2 ↗
36. 10.1016/j.ssi.2008.04.00410.1016/j.ssi.2008.04.004 ↗
37. 10.1111/ijag.1350810.1111/ijag.13508 ↗
38. 10.1016/0022-1902(68)80109-510.1016/0022-1902(68)80109-5 ↗
39. 10.1016/j.apsadv.2021.10011210.1016/j.apsadv.2021.100112 ↗
40. 10.1007/s12034-008-0108-z10.1007/s12034-008-0108-z ↗
41. 10.1016/j.jpowsour.2014.10.20210.1016/j.jpowsour.2014.10.202 ↗
42. 10.1051/e3sconf/2018530100810.1051/e3sconf/20185301008 ↗
43. 10.1016/j.electacta.2017.12.02010.1016/j.electacta.2017.12.020 ↗
44. 10.1016/0378-7753(93)80106-Y10.1016/0378-7753(93)80106-Y ↗
45. 10.1016/j.ijhydene.2014.01.04310.1016/j.ijhydene.2014.01.043 ↗
46. 10.1016/0022-3093(88)90413-910.1016/0022-3093(88)90413-9 ↗
47. 10.1016/j.ssi.2012.12.01710.1016/j.ssi.2012.12.017 ↗
48. 10.1021/acs.chemmater.3c0209910.1021/acs.chemmater.3c02099 ↗
49. 10.1002/admi.20200027610.1002/admi.202000276 ↗
50. 10.1021/jacs.8b0519210.1021/jacs.8b05192 ↗
51. 10.1016/j.ssi.2020.11532910.1016/j.ssi.2020.115329 ↗
52. 10.1016/j.jpowsour.2016.09.05910.1016/j.jpowsour.2016.09.059 ↗
53. 10.1021/acsenergylett.4c0015310.1021/acsenergylett.4c00153 ↗
54. 10.1016/j.ssi.2011.04.00110.1016/j.ssi.2011.04.001 ↗
55. 10.1016/j.tsf.2011.08.10710.1016/j.tsf.2011.08.107 ↗
56. 10.1016/j.ssi.2016.01.04610.1016/j.ssi.2016.01.046 ↗
57. 10.1016/j.jpowsour.2018.05.02310.1016/j.jpowsour.2018.05.023 ↗
58. 10.1039/D3TA00386H10.1039/D3TA00386H ↗
59. 10.1002/sia.352210.1002/sia.3522 ↗
60. 10.1021/acs.nanolett.6b0475510.1021/acs.nanolett.6b04755 ↗
61. 10.1039/D4CC04462B10.1039/D4CC04462B ↗
62. 10.1002/smm2.120010.1002/smm2.1200 ↗
63. 10.1016/j.joule.2024.07.00610.1016/j.joule.2024.07.006 ↗
64. Burton, M.; Jagger, B.; Liang, Y.; Gibson, J. S.; Aspinall, J.; Swallow, J. E. N.; Weatherup, R. S.; Pasta, M. The Role of Phosphorous in the Solid Electrolyte Interphase of Argyrodite Solid Electrolytes, ChemRxiv Preprint Repository, Materials Chemistry Section, version 2, Preprint (not peer-reviewed). Submitted January 10, 2025. Accessed April 8, 2025.10.26434/chemrxiv-2024-1727n-v2 ↗