Thermally and Electrochemically Driven Topotactical Transformations in Sodium Layered Oxides NaxVO2
Source abstract
Abstract
Phase diagrams and structural transformations in the complex Na x VO 2 system have been studied using electrochemical (de)intercalation and in situ and operando high resolution synchrotron powder diffraction. Starting from O′3-Na 1/2 VO 2 obtained by sodium electrochemical deintercalation of O3-NaVO 2, the structural details of irreversible and reversible thermally driven transformations to P′3 and P3 type structures are presented. Subsequently, these P′3-Na x VO 2 phases provide a platform for operando studies exploring the Na x VO 2 phase diagram as a function of sodium electrochemical (de)intercalation. In this system, three single phase domains have been found: a line phase P′3-Na 1/2 VO 2, one solid solution for 0.53 ≤ x ≤ 0.55 characterized by an incommensurate modulated structure, and a second solid solution for 0.63 ≤ x ≤ 0.65 with a defective structure resulting from a random stack of O′3 and P′3 layers. With further sodium intercalation ( x > 0.65), the structure irreversibly transforms to the starting parent phase O3-NaVO 2 . This work reveals new details about the diverse structural polymorphs found in sodium layered oxides used as electrode battery materials and the transitional pathways between them as a function of temperature and composition.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Transition Metal Oxide Nanomaterials · Thermal Expansion and Ionic Conductivity · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Advanced Photon Source, Argonne National Laboratory, Lemont, Illinois 60439, United States
Funding
Centre National de la Recherche Scientifique · U.S. Department of Energy · R?gion Aquitaine
References (35)
Show source-provided references
1. 10.1088/0953-8984/16/32/01610.1088/0953-8984/16/32/016 ↗
2. 10.1103/PhysRevB.70.02410110.1103/PhysRevB.70.024101 ↗
3. 10.1103/PhysRevB.73.17410410.1103/PhysRevB.73.174104 ↗
4. 10.1038/nmat292010.1038/nmat2920 ↗
5. 10.1021/cm502178810.1021/cm5021788 ↗
6. 10.1088/0953-8984/20/14/14520510.1088/0953-8984/20/14/145205 ↗
7. 10.1103/PhysRevLett.101.16640210.1103/PhysRevLett.101.166402 ↗
8. 10.1103/PhysRevB.80.04510310.1103/PhysRevB.80.045103 ↗
9. 10.1103/PhysRevB.83.09441710.1103/PhysRevB.83.094417 ↗
10. 10.1149/1.355510210.1149/1.3555102 ↗
11. 10.1016/j.elecom.2011.06.00510.1016/j.elecom.2011.06.005 ↗
12. 10.1038/nmat347810.1038/nmat3478 ↗
13. Rüdorff W. · Z. Naturforsch., B: Chem. Sci. · 1954 · 9 · 61410.1515/znb-1954-0911 ↗
14. 10.1016/0378-4363(80)90214-410.1016/0378-4363(80)90214-4 ↗
15. 10.1016/0167-2738(81)90076-X10.1016/0167-2738(81)90076-X ↗
16. 10.1016/0025-5408(82)90124-610.1016/0025-5408(82)90124-6 ↗
17. 10.1149/1.311272710.1149/1.3112727 ↗
18. 10.1016/j.jpowsour.2014.02.04810.1016/j.jpowsour.2014.02.048 ↗
19. 10.1038/2021000a010.1038/2021000a0 ↗
20. 10.1021/ic300357d10.1021/ic300357d ↗
21. 10.1016/j.elecom.2013.05.01210.1016/j.elecom.2013.05.012 ↗
22. 10.1021/jp411382r10.1021/jp411382r ↗
23. 10.1021/cm300466b10.1021/cm300466b ↗
24. 10.1016/j.elecom.2014.10.00310.1016/j.elecom.2014.10.003 ↗
25. 10.1007/BF0065801410.1007/BF00658014 ↗
26. 10.1039/c2cp43377j10.1039/c2cp43377j ↗
27. 10.1021/ic900865310.1021/ic9008653 ↗
28. 10.1021/ic301505e10.1021/ic301505e ↗
29. 10.1515/zkri-2014-173710.1515/zkri-2014-1737 ↗
30. 10.1006/jssc.1996.009010.1006/jssc.1996.0090 ↗
31. 10.1103/PhysRevB.78.15511610.1103/PhysRevB.78.155116 ↗
32. 10.1103/PhysRevB.82.02410310.1103/PhysRevB.82.024103 ↗
33. van Smaalen S. · 200710.1093/acprof:oso/9780198570820.001.0001 ↗
34. 10.1103/PhysRevB.77.18411610.1103/PhysRevB.77.184116 ↗
35. Treacy M. M. J. · Proc. R. Soc. London, Ser. A · 1991 · 433 · 49910.1098/rspa.1991.0062 ↗