Structure-Selective Operando X-ray Spectroscopy
Source abstract
Abstract
The relationship between charge transport and structural transformations dictates the properties of electrochemical systems. Despite their importance, the reduction–oxidation (redox) reactions within dynamically coexisting structures have so far eluded direct operando investigation. Here, we use resonant X-ray scattering to select X-ray spectra of a crystal structure coexisting with a different structure during a redox-induced phase transformation in P2-Na2/3Ni1/3Mn2/3O2. The spectra of the P2 structure become static midway through the sodium extraction in an operando coin cell, while the overall desodiation proceeds. The coincident emergence of the O2 structure reveals the rigid link between the local redox and the long-range order in this archetypal sodium-ion battery material. Structure-selective X-ray spectroscopy thus opens a powerful avenue for resolving the dynamic chemistry of different structural phases in multistructure electrochemical systems.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Supercapacitor Materials and Fabrication · Transition Metal Oxide Nanomaterials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, Cornell University, Ithaca, New York 14850, United States
Department of NanoEngineering, University of California San Diego, La Jolla, California 92093-0448, United States
Cornell High Energy Synchrotron Source, Cornell University, Ithaca, New York 14850, United States
Funding
U.S. Department of Energy · National Science Foundation
References (40)
Show source-provided references
1. Tarascon, J. M.; Armand, M. In Materials for Sustainable Energy: A Collection of Peer-Reviewed Research and Review Articles; Nature Publishing Group: 2010; pp 171–179.10.1142/9789814317665_0024 ↗
2. 10.1021/cs300400610.1021/cs3004006 ↗
3. 10.1126/science.121274110.1126/science.1212741 ↗
4. 10.1038/nature1147510.1038/nature11475 ↗
5. 10.1021/cr500192f10.1021/cr500192f ↗
6. 10.1002/aenm.20160288810.1002/aenm.201602888 ↗
7. 10.1016/0378-4363(80)90214-410.1016/0378-4363(80)90214-4 ↗
8. 10.1149/2.0201816jes10.1149/2.0201816jes ↗
9. 10.1021/acs.chemrev.7b0000710.1021/acs.chemrev.7b00007 ↗
10. 10.1021/jacs.7b0016410.1021/jacs.7b00164 ↗
11. 10.1021/jacs.8b1224310.1021/jacs.8b12243 ↗
12. 10.1038/ncomms1430910.1038/ncomms14309 ↗
13. 10.1016/j.joule.2017.12.00810.1016/j.joule.2017.12.008 ↗
14. 10.1126/science.aaf491410.1126/science.aaf4914 ↗
15. 10.1038/nature0966410.1038/nature09664 ↗
16. 10.1016/j.ultramic.2012.03.00210.1016/j.ultramic.2012.03.002 ↗
17. 10.1038/s41586-018-0397-310.1038/s41586-018-0397-3 ↗
18. 10.1021/acs.nanolett.8b0258710.1021/acs.nanolett.8b02587 ↗
19. Pickering I. J. · 1993
20. 10.1103/PhysRevB.93.21442010.1103/PhysRevB.93.214420 ↗
21. 10.1103/PhysRevLett.109.16700110.1103/PhysRevLett.109.167001 ↗
22. 10.1103/PhysRevLett.69.306410.1103/PhysRevLett.69.3064 ↗
23. 10.1038/s41467-019-09862-y10.1038/s41467-019-09862-y ↗
24. 10.1016/j.eurpolymj.2016.04.01410.1016/j.eurpolymj.2016.04.014 ↗
25. 10.7567/JJAPS.32S2.19810.7567/JJAPS.32S2.198 ↗
26. 10.1039/C5CP00940E10.1039/C5CP00940E ↗
27. 10.1021/acs.jpcc.8b0553910.1021/acs.jpcc.8b05539 ↗
28. Als-Nielsen J. · 201110.1002/9781119998365 ↗
29. 10.1107/S0365110X6500004X10.1107/S0365110X6500004X ↗
30. 10.1149/1.140724710.1149/1.1407247 ↗
31. 10.1149/1.137611610.1149/1.1376116 ↗
32. 10.1039/c2cp44467d10.1039/c2cp44467d ↗
33. 10.1021/nl502332b10.1021/nl502332b ↗
34. 10.1038/s41560-018-0184-210.1038/s41560-018-0184-2 ↗
35. Huggins R. · 2009
36. 10.1021/acscentsci.9b0116610.1021/acscentsci.9b01166 ↗
37. 10.3390/nano603004110.3390/nano6030041 ↗
38. 10.1039/c1cc15779e10.1039/c1cc15779e ↗
39. 10.1038/nmat345810.1038/nmat3458 ↗
40. 10.1016/j.coelec.2020.10065310.1016/j.coelec.2020.100653 ↗