Computationally Accelerated Discovery of High Entropy Pyrochlore Oxides
Source abstract
Abstract
High entropy ceramics provide enhanced flexibility for tailoring a wide range of physical properties, emerging from the diverse chemical and configurational degrees of freedom. Expanding upon the endeavors of recently synthesized high entropy ceramics in rock salt, fluorite, spinel, and perovskite structures, we explore the relative feasibility of formation of high entropy pyrochlore oxides, A2B2O7, with multication occupancy of the B-site, estimated from first-principles-based thermodynamic descriptors. Subsequently, we used Monte Carlo simulations to estimate the phase composition, oxygen vacancy concentration, and local ionic segregation as a function of temperature and oxygen partial pressure. In synergy with the theoretical calculations, we have investigated the synthesis of several multicomponent oxides with a pyrochlore composition, related to our computational investigations, resulting in four phase pure and one 97.4% pure high entropy pyrochlore oxides. Ultimately, our approach allows us to evaluate potential impurity phases, ionic disorder, and oxygen vacancy concentration in response to the experimental variables, thereby making realistic predictions that can direct and accelerate experimental synthesis of novel multicomponent ceramics.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nuclear materials and radiation effects · High Entropy Alloys Studies · High-pressure geophysics and materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States
Department of Chemistry, University of California, Berkeley, California 94720, United States
National Center for Computational Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States
Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States
Funding
Oak Ridge National Laboratory · Basic Energy Sciences · U.S. Department of Energy
References (59)
Show source-provided references
1. 10.1038/ncomms948510.1038/ncomms9485 ↗
2. 10.1038/s41578-019-0170-810.1038/s41578-019-0170-8 ↗
3. Bergerhoff, G.; Brown, I.; Allen, F. In Crystallographic databases ; International Union of Crystallography: Chester, England, 1987; Vol. 360; pp 77–95.
4. 10.1146/annurev.pc.40.100189.00145110.1146/annurev.pc.40.100189.001451 ↗
5. 10.1021/acs.chemmater.7b0076610.1021/acs.chemmater.7b00766 ↗
6. 10.1021/acsami.9b1322010.1021/acsami.9b13220 ↗
7. 10.1088/0953-8984/11/36/31410.1088/0953-8984/11/36/314 ↗
8. Taira N. · J. Phys.: Condens. Matter · 2001 · 13 · 5527
9. 10.1126/science.289.5480.74810.1126/science.289.5480.748 ↗
10. 10.1038/nmat184210.1038/nmat1842 ↗
11. 10.1021/acs.jpcc.6b1252210.1021/acs.jpcc.6b12522 ↗
12. 10.1111/jace.1297910.1111/jace.12979 ↗
13. 10.1007/s40145-019-0342-410.1007/s40145-019-0342-4 ↗
14. 10.1002/adma.20180500410.1002/adma.201805004 ↗
15. 10.1039/C6TA03249D10.1039/C6TA03249D ↗
16. 10.1038/s41467-018-05774-510.1038/s41467-018-05774-5 ↗
17. 10.1021/acsami.0c0356210.1021/acsami.0c03562 ↗
18. 10.1021/acs.chemmater.9b0062410.1021/acs.chemmater.9b00624 ↗
19. 10.1103/PhysRevMaterials.4.07440510.1103/PhysRevMaterials.4.074405 ↗
20. 10.1063/5.001135210.1063/5.0011352 ↗
21. 10.1039/C9TA12846H10.1039/C9TA12846H ↗
22. 10.1021/acs.chemmater.0c0155510.1021/acs.chemmater.0c01555 ↗
23. 10.1016/j.jmst.2019.05.05410.1016/j.jmst.2019.05.054 ↗
24. 10.1021/jacs.0c1073910.1021/jacs.0c10739 ↗
25. 10.1021/acs.chemmater.0c0270210.1021/acs.chemmater.0c02702 ↗
26. 10.1107/S056773947600155110.1107/S0567739476001551 ↗
27. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
28. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
29. 10.1103/PhysRevLett.100.13640610.1103/PhysRevLett.100.136406 ↗
30. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
31. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
32. 10.1038/s41524-018-0144-110.1038/s41524-018-0144-1 ↗
33. 10.1016/j.jssc.2008.11.00810.1016/j.jssc.2008.11.008 ↗
34. 10.1111/jace.1309510.1111/jace.13095 ↗
35. 10.1016/j.jssc.2004.02.02510.1016/j.jssc.2004.02.025 ↗
36. 10.1139/p01-11810.1139/p01-118 ↗
37. 10.4028/www.scientific.net/MSF.228-231.75310.4028/www.scientific.net/MSF.228-231.753 ↗
38. Kurova T. · Doklady Akademii Nauk SSSR · 1971 · 201 · 1095
39. 10.1107/S056774087500700510.1107/S0567740875007005 ↗
40. 10.1006/jssc.2000.871210.1006/jssc.2000.8712 ↗
41. 10.1103/PhysRevB.92.18441810.1103/PhysRevB.92.184418 ↗
42. 10.1107/S010876739201303510.1107/S0108767392013035 ↗
43. 10.1016/S0925-8388(00)01043-410.1016/S0925-8388(00)01043-4 ↗
44. 10.1107/S160053681300549710.1107/S1600536813005497 ↗
45. 10.1016/0025-5408(84)90065-510.1016/0025-5408(84)90065-5 ↗
46. 10.1006/jssc.2000.914210.1006/jssc.2000.9142 ↗
47. Gao, Z.; Liu, Y.; Lu, C.; Ma, Y.; Xia, Y.; Fang, L.; He, Q.; Liu, Y.; Liu, G.; Yang, J.; He, H.; He, D. Origin of the phase change from pyrochlore to perovskite-like layered structure and a new lead free ferroelectric. arXiv 2017, arXiv:1703.01016v1, https://arxiv.org/abs/1703.01016 (accessed 2021–04–15).
48. Stull D. R. · 1971
49. 10.1103/PhysRevB.65.03540610.1103/PhysRevB.65.035406 ↗
50. 10.1051/jphysrad:01962002301008350010.1051/jphysrad:019620023010083500 ↗
51. 10.1038/s41467-018-06757-210.1038/s41467-018-06757-2 ↗
52. 10.1088/1742-6596/144/1/01202110.1088/1742-6596/144/1/012021 ↗
53. 10.1007/s10832-004-5153-410.1007/s10832-004-5153-4 ↗
54. 10.1002/adfm.20150316910.1002/adfm.201503169 ↗
55. 10.1063/5.000794410.1063/5.0007944 ↗
56. 10.1557/JMR.1999.046210.1557/JMR.1999.0462 ↗
57. 10.1111/j.1551-2916.2010.03945.x10.1111/j.1551-2916.2010.03945.x ↗
58. 10.3390/ma1303055810.3390/ma13030558 ↗
59. 10.1007/s10853-018-2168-910.1007/s10853-018-2168-9 ↗