Chemical Environment and Structural Variations in High Entropy Oxide Thin Film Probed with Electron Microscopy
Source abstract
Abstract
O (J14), with two layers grown at different substrate temperatures (500 and 200 °C) using pulsed laser deposition (PLD). Electron diffraction and atomically resolved STEM imaging reveal the difference in out-of-plane lattice parameters in the stacked thin film, which is further quantified on a larger scale using four-dimensional STEM (4D-STEM). In the layer deposited at a lower temperature, electron energy loss spectroscopy (EELS) mapping indicates drastic changes in the oxidation states and bonding environment for Co ions, and energy-dispersive X-ray spectroscopy (EDX) mapping detects more significant cation deficiency. Ab initio density functional theory (DFT) calculations validate that vacancies on the cation sublattice of J14 result in significant electronic and structural changes. The experimental and computational analyses indicate that low temperatures during film growth result in cation deficiency, an altered chemical environment, and reduced lattice parameters while maintaining a single phase. Our results demonstrate that the complex correlation of configurational entropy, kinetics, and thermodynamics can be utilized for accessing a range of metastable configurations in HEO materials without altering cation proportions, enabling further engineering of functional properties of HEO materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: High Entropy Alloys Studies · Electronic and Structural Properties of Oxides · High-Temperature Coating Behaviors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, The Pennsylvania State University, University Park, Pennsylvania 16802, United States
Department of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802, United States
National Center for Electron Microscopy Facility, Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States
Funding
Air Force Office of Scientific Research · Office of Science · Division of Materials Research
References (54)
Show source-provided references
1. 10.1016/j.scriptamat.2020.05.01910.1016/j.scriptamat.2020.05.019 ↗
2. 10.1016/j.msea.2003.10.25710.1016/j.msea.2003.10.257 ↗
3. 10.1002/adem.20030056710.1002/adem.200300567 ↗
4. 10.1038/ncomms948510.1038/ncomms9485 ↗
5. 10.1016/j.matlet.2017.12.14810.1016/j.matlet.2017.12.148 ↗
6. 10.1016/j.scriptamat.2017.08.04010.1016/j.scriptamat.2017.08.040 ↗
7. 10.1016/j.jeurceramsoc.2018.04.06310.1016/j.jeurceramsoc.2018.04.063 ↗
8. 10.1016/j.ceramint.2018.08.10010.1016/j.ceramint.2018.08.100 ↗
9. 10.1038/s41598-020-76945-y10.1038/s41598-020-76945-y ↗
10. 10.1126/science.abe129210.1126/science.abe1292 ↗
11. 10.1038/s41467-018-05774-510.1038/s41467-018-05774-5 ↗
12. 10.1039/C6TA03249D10.1039/C6TA03249D ↗
13. 10.1016/j.jallcom.2018.11.04910.1016/j.jallcom.2018.11.049 ↗
14. 10.1002/adma.20210034710.1002/adma.202100347 ↗
15. 10.1016/j.actamat.2021.11673510.1016/j.actamat.2021.116735 ↗
16. 10.1111/jace.1475610.1111/jace.14756 ↗
17. 10.1080/21663831.2018.155460510.1080/21663831.2018.1554605 ↗
18. 10.1103/PhysRevMaterials.4.10040110.1103/PhysRevMaterials.4.100401 ↗
19. 10.1557/mrc.2018.18410.1557/mrc.2018.184 ↗
20. 10.1017/S143192762100180X10.1017/S143192762100180X ↗
21. Kotsonis, G. N. High-Entropy Oxides: Epitaxial Growth, Kinetic Dependencies, and Linear Optical Properties. PhD Thesis, The Pennsylvania State University: University Park, PA, U.S. 2022.
22. Rost, C. M. Entropy-Stabilized Oxides: Explorations of a Novel Class of Multicomponent Materials. PhD Thesis, North Carolina State University: Raleigh, NC, U.S., 2016.
23. 10.1021/acs.nanolett.6b0213010.1021/acs.nanolett.6b02130 ↗
24. 10.1186/s40679-018-0052-y10.1186/s40679-018-0052-y ↗
25. 10.1016/j.ultramic.2019.11289010.1016/j.ultramic.2019.112890 ↗
26. 10.1016/S0968-4328(99)00139-010.1016/S0968-4328(99)00139-0 ↗
27. 10.1088/1757-899X/109/1/01200710.1088/1757-899X/109/1/012007 ↗
28. 10.1016/0304-3991(89)90304-510.1016/0304-3991(89)90304-5 ↗
29. 10.1016/j.micron.2013.08.00510.1016/j.micron.2013.08.005 ↗
30. 10.1038/nature1246910.1038/nature12469 ↗
31. 10.1016/j.ultramic.2016.08.00610.1016/j.ultramic.2016.08.006 ↗
32. 10.1016/j.ultramic.2012.05.00610.1016/j.ultramic.2012.05.006 ↗
33. 10.1016/j.ultramic.2021.11331410.1016/j.ultramic.2021.113314 ↗
34. 10.1021/acs.chemrev.9b0043910.1021/acs.chemrev.9b00439 ↗
35. 10.1017/S143192761600017910.1017/S1431927616000179 ↗
36. 10.1361/10549710377033051410.1361/105497103770330514 ↗
37. 10.1107/S056773947600155110.1107/S0567739476001551 ↗
38. 10.1116/1.58031010.1116/1.580310 ↗
39. 10.1016/S0022-3697(72)80096-910.1016/S0022-3697(72)80096-9 ↗
40. 10.1103/PhysRevLett.65.35310.1103/PhysRevLett.65.353 ↗
41. 10.1088/0034-4885/56/8/00210.1088/0034-4885/56/8/002 ↗
42. 10.1007/s00339-008-4696-710.1007/s00339-008-4696-7 ↗
43. 10.1002/adma.20070191910.1002/adma.200701919 ↗
44. 10.1016/S0169-4332(00)00781-910.1016/S0169-4332(00)00781-9 ↗
45. 10.1016/j.matchemphys.2013.10.00510.1016/j.matchemphys.2013.10.005 ↗
46. 10.1107/S002188981103897010.1107/S0021889811038970 ↗
47. 10.1016/j.ultramic.2015.12.00210.1016/j.ultramic.2015.12.002 ↗
48. 10.1017/S143192762100047710.1017/S1431927621000477 ↗
49. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
50. 10.1103/PhysRevLett.100.13640610.1103/PhysRevLett.100.136406 ↗
51. 10.1103/PhysRevB.57.150510.1103/PhysRevB.57.1505 ↗
52. 10.1021/acs.chemmater.9b0062410.1021/acs.chemmater.9b00624 ↗
53. 10.1016/j.commatsci.2005.04.01010.1016/j.commatsci.2005.04.010 ↗
54. 10.1002/adts.20190001510.1002/adts.201900015 ↗