journal article·2016Open access

Probing the Electrode-Electrolyte Interface in Cycled LiNi0.5Mn1.5O4by XPS Using Mg and Synchrotron X-rays

Azzam N. Mansour, David G. Kwabi, Ronald A. Quinlan, Yi-Chun Lu, Yang Shao-Horn

Abstract

X-ray photoelectron spectroscopy (XPS) was used to investigate the surface chemistry of high voltage spinel, LiNi 0.5 Mn 1.5 O 4 (LNMO) positive electrodes cycled 5 and 10 times in Li-cells with 1 M LiPF 6 in (3:7) EC:DMC. The XPS spectra were collected using conventional Mg X-rays with energy of 1253.6 eV as well as synchrotron X-rays with energies of 2493.6 and 3498.4 eV in order to examine the depth distribution of various surface chemical species induced during cycling. The XPS spectra revealed a 5 – 10 nm surface layer of organic and Li x PF y O z -type species formed as result of electrolyte decomposition, and a comparatively thinner layer composed of transition metal fluorides and LiF. These results suggest that electrolyte decomposition is a major contributor to parasitic reactions in LNMO battery electrochemistry. Limiting electrolyte decomposition with the use of solvents with wide electrochemical stability windows thus comprises a promising strategy for ensuring the practical feasibility of high voltage spinel materials in future Li-ion systems.
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Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Extraction and Separation Processes

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References (35)

Show source-provided references
1. 10.1149/1.320659010.1149/1.3206590 ↗
2. 10.1016/j.jpowsour.2014.08.01510.1016/j.jpowsour.2014.08.015 ↗
3. 10.1021/acs.jpclett.5b0172710.1021/acs.jpclett.5b01727 ↗
4. 10.1021/cm301148d10.1021/cm301148d ↗
5. 10.1021/cm401496k10.1021/cm401496k ↗
6. 10.1016/j.jallcom.2006.10.15310.1016/j.jallcom.2006.10.153 ↗
7. 10.1039/c2jm33338d10.1039/c2jm33338d ↗
8. 10.1021/nl303619s10.1021/nl303619s ↗
9. 10.1016/j.jpowsour.2006.10.02510.1016/j.jpowsour.2006.10.025 ↗
10. 10.1149/1.342851510.1149/1.3428515 ↗
11. 10.1039/c3ee24414h10.1039/c3ee24414h ↗
12. 10.1016/j.elecom.2013.08.00910.1016/j.elecom.2013.08.009 ↗
13. 10.1021/jp102650910.1021/jp1026509 ↗
14. 10.1021/acs.analchem.5b0469610.1021/acs.analchem.5b04696 ↗
15. 10.1021/ja511669810.1021/ja5116698 ↗
16. 10.1021/jp405158m10.1021/jp405158m ↗
17. 10.1016/j.electacta.2013.03.01010.1016/j.electacta.2013.03.010 ↗
18. 10.1021/cm035050s10.1021/cm035050s ↗
19. 10.1149/1.183730010.1149/1.1837300 ↗
20. 10.1016/j.apsusc.2006.10.07110.1016/j.apsusc.2006.10.071 ↗
21. 10.1002/sia.200510.1002/sia.2005 ↗
22. 10.1002/sia.74020011210.1002/sia.740200112 ↗
23. 10.1021/ac00039a01810.1021/ac00039a018 ↗
24. 10.1021/ac00059a00610.1021/ac00059a006 ↗
25. 10.1016/j.electacta.2004.03.04910.1016/j.electacta.2004.03.049 ↗
26. 10.1149/1.142639810.1149/1.1426398 ↗
27. 10.1021/la011354m10.1021/la011354m ↗
28. 10.1149/1.150563610.1149/1.1505636 ↗
29. 10.1149/1.352630910.1149/1.3526309 ↗
30. 10.1149/2.069304jes10.1149/2.069304jes ↗
31. 10.1149/1.347966410.1149/1.3479664 ↗
32. 10.1016/0368-2048(95)02374-710.1016/0368-2048(95)02374-7 ↗
33. 10.1021/jp051626k10.1021/jp051626k ↗
34. 10.1002/cphc.20140007010.1002/cphc.201400070 ↗
35. 10.1021/cm504753410.1021/cm5047534 ↗