journal article·2024-09-13Open access

Rethinking Oxygen Redox: Does Oxygen Dimerization Occur without Oxidation in Li 2 NiO 3 ?

Matthew J. W. Ogley, Ashok S. Menon, Beth J. Johnston, Gaurav Pandey, Innes McClelland, Xiaoqun Shi, Stefano Agrestini, Veronica Celorrio, Gabriel E. Pérez, Samuel G. Booth, Jordi Cabana, Serena A. Cussen, Louis F. J. Piper

ACS Energy Letters· Volume 9· Issue 9

Abstract

High Resolution Image Download MS PowerPoint Slide In layered lithium transition metal oxide cathodes, high-voltage operation is accompanied by the formation of oxygen dimers, which are widely used as an indicator of oxygen-redox activity. However, understanding the role that oxygen dimerization plays in facilitating charge compensation is still needed. Li 2 NiO 3 (a 3d 8 L 2 -containing compound, where L is a ligand hole) is studied as a model system, where oxygen dimerization is shown to occur without cathode oxidation. Electrochemical cycling results in a net reduction of the cathode, accompanied by structural transformations, despite spectroscopic features of oxygen dimers arising at the top-of-charge. Here, oxygen dimerization is shown to coexist alongside a structurally transformed and electronically reduced cathode structure, thus highlighting that O dimerization is independent of bulk redox processes. This makes it clear that a thermodynamically derived transformation toward a reduced phase remains the only variable capable of generating O–O dimers in Li 2 NiO 3 .
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Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Semiconductor materials and devices

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Affiliations

Warwick Manufacturing Group, University of Warwick, Coventry, CV4 7AL, U.K.

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

Department of Materials Science and Engineering, The University of Sheffield, Sheffield, S1 3JD, U.K.

Diamond Light Source Ltd, Harwell Science and Innovation Campus, Didcot, OX11 0DE, U.K.

ISIS Neutron and Muon Source, Rutherford Appleton Laboratory, Harwell Science and Innovation Campus, Didcot, OX11 0QX, U.K.

Department of Chemistry, University of Illinois at Chicago, Chicago, Illinois 60607, United States

School of Chemistry, University College Dublin, Belfield, Dublin 4, Ireland

Funding

Faraday Institution

References (51)

Show source-provided references
1. 10.1021/acsenergylett.2c0172210.1021/acsenergylett.2c01722 ↗
2. 10.1021/acs.chemrev.1c0032710.1021/acs.chemrev.1c00327 ↗
3. 10.1016/j.ensm.2019.08.01310.1016/j.ensm.2019.08.013 ↗
4. 10.1038/s41578-022-00416-110.1038/s41578-022-00416-1 ↗
5. 10.1016/j.joule.2020.05.00410.1016/j.joule.2020.05.004 ↗
6. 10.1146/annurev-matsci-080222-03553310.1146/annurev-matsci-080222-035533 ↗
7. 10.1016/j.joule.2023.06.01710.1016/j.joule.2023.06.017 ↗
8. 10.1038/ncomms1301710.1038/ncomms13017 ↗
9. 10.1016/0038-1098(91)90600-Z10.1016/0038-1098(91)90600-Z ↗
10. 10.1103/PhysRevB.50.1132610.1103/PhysRevB.50.11326 ↗
11. 10.1103/PhysRevB.45.161210.1103/PhysRevB.45.1612 ↗
12. 10.1038/s41467-023-37775-410.1038/s41467-023-37775-4 ↗
13. Ogley, M. J. W.; Menon, A. S.; Pandey, G.; Fajardo, G. J. P.; Johnston, B. J.; McClelland, I.; Majherova, V.; Huband, S.; Tripathy, D.; Temprano, I.; Agrestini, S.; Celorrio, V.; Pérez, G. E.; Booth, S. G.; Grey, C. P.; Cussen, S. A.; Piper, L. F. J. Metal–Ligand Redox in Layered Oxide Cathodes for Li-Ion Batteries. ChemRXiv 2024,10.26434/chemrxiv-2024-w906n.10.26434/chemrxiv-2024-w906n ↗
14. 10.1103/PRXEnergy.2.01300510.1103/PRXEnergy.2.013005 ↗
15. 10.1021/acsenergylett.9b0214710.1021/acsenergylett.9b02147 ↗
16. 10.1021/jacs.8b1379810.1021/jacs.8b13798 ↗
17. 10.1021/acs.jpcc.7b0659810.1021/acs.jpcc.7b06598 ↗
18. 10.1039/D3TA05516G10.1039/D3TA05516G ↗
19. 10.1039/D3EE04354A10.1039/D3EE04354A ↗
20. 10.1103/PhysRevLett.104.19300210.1103/PhysRevLett.104.193002 ↗
21. 10.1038/s41560-020-00697-210.1038/s41560-020-00697-2 ↗
22. 10.1021/cm062094310.1021/cm0620943 ↗
23. 10.1088/2515-7655/acdd9c10.1088/2515-7655/acdd9c ↗
24. 10.1103/PhysRevB.59.74210.1103/PhysRevB.59.742 ↗
25. 10.1016/S0167-2738(98)00075-710.1016/S0167-2738(98)00075-7 ↗
26. 10.1021/cm030340u10.1021/cm030340u ↗
27. 10.1016/j.matt.2021.03.01210.1016/j.matt.2021.03.012 ↗
28. 10.1021/cm303096e10.1021/cm303096e ↗
29. 10.1002/cssc.20190003210.1002/cssc.201900032 ↗
30. 10.1016/0167-2738(94)90415-410.1016/0167-2738(94)90415-4 ↗
31. 10.1007/BF0191549410.1007/BF01915494 ↗
32. 10.1006/jssc.2001.942810.1006/jssc.2001.9428 ↗
33. 10.1021/acsenergylett.4c0130710.1021/acsenergylett.4c01307 ↗
34. 10.1021/acs.chemmater.0c0288010.1021/acs.chemmater.0c02880 ↗
35. 10.1149/2.0861610jes10.1149/2.0861610jes ↗
36. 10.1021/ic970927910.1021/ic9709279 ↗
37. 10.1021/acsenergylett.9b0279910.1021/acsenergylett.9b02799 ↗
38. 10.1021/acsenergylett.0c0241810.1021/acsenergylett.0c02418 ↗
39. 10.1038/nchem.252410.1038/nchem.2524 ↗
40. 10.1038/s41467-017-02041-x10.1038/s41467-017-02041-x ↗
41. 10.1038/s41560-021-00780-210.1038/s41560-021-00780-2 ↗
42. 10.1149/1.139349210.1149/1.1393492 ↗
43. 10.1371/journal.pone.004918210.1371/journal.pone.0049182 ↗
44. 10.1038/srep0044210.1038/srep00442 ↗
45. 10.1021/acs.langmuir.6b0148310.1021/acs.langmuir.6b01483 ↗
46. 10.1038/s41586-019-1854-310.1038/s41586-019-1854-3 ↗
47. 10.1021/acs.jpcc.5b0747910.1021/acs.jpcc.5b07479 ↗
48. 10.1021/acs.chemmater.2c0136010.1021/acs.chemmater.2c01360 ↗
49. 10.1021/cm035050s10.1021/cm035050s ↗
50. 10.1149/2.0021707jes10.1149/2.0021707jes ↗
51. 10.1039/D2YA00321J10.1039/D2YA00321J ↗