journal article·2017-12-13

Strain-Induced Tailoring of Oxygen-Ion Transport in Highly Doped CeO2 Electrolyte: Effects of Biaxial Extrinsic and Local Lattice Strain

Junsung Ahn, Sungjun Choi, Kyung Joong Yoon, Ji-Won Son, Byung-Kook Kim, Jong-Ho Lee, Ho Won Jang, Hyoungchul Kim

Publisher page

Abstract

We explored oxygen-ion transport in highly doped CeO 2 through density-functional theory calculations. By applying biaxial strain to 18.75 mol % CeO 2:Gd, we predicted the average migration-barrier energy with six different pathways, with results in good agreement with those of experiments. Additionally, we found that the migration-barrier energy could be lowered by increasing the tetrahedron volume, including the space occupied by the oxygen vacancy. Our results indicate that the tetrahedron volume can be expanded by larger codopants, as well as biaxial tensile strain. Thus, the combination of thin-film structure and codoping could offer a new approach to accelerate oxygen-ion transport.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Catalytic Processes in Materials Science · Advancements in Solid Oxide Fuel Cells · Electronic and Structural Properties of Oxides

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

High-Temperature Energy Materials Research Center, Korea Institute of Science and Technology, 5 Hwarang-ro 14-gil, Seongbuk-gu, Seoul 02792, Republic of Korea

Department of Materials Science and Engineering, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea

Funding

Korea Institute of Energy Technology Evaluation and Planning

References (30)

Show source-provided references
1. 10.1557/mrs.2011.26510.1557/mrs.2011.265 ↗
2. 10.1126/science.115639310.1126/science.1156393 ↗
3. 10.1557/mrs.2014.810.1557/mrs.2014.8 ↗
4. 10.1038/nmat426610.1038/nmat4266 ↗
5. 10.1038/nmat427810.1038/nmat4278 ↗
6. 10.1038/ncomms1069210.1038/ncomms10692 ↗
7. 10.1039/C7TA00499K10.1039/C7TA00499K ↗
8. 10.1063/1.32164510.1063/1.321645 ↗
9. 10.1016/j.ssi.2010.03.01410.1016/j.ssi.2010.03.014 ↗
10. 10.1016/j.ssi.2011.07.00910.1016/j.ssi.2011.07.009 ↗
11. 10.1016/S0167-2738(00)00714-110.1016/S0167-2738(00)00714-1 ↗
12. 10.1103/PhysRevB.69.21420210.1103/PhysRevB.69.214202 ↗
13. 10.1103/PhysRevLett.65.35310.1103/PhysRevLett.65.353 ↗
14. 10.1063/1.12274910.1063/1.122749 ↗
15. 10.1063/1.483324810.1063/1.4833248 ↗
16. 10.1039/b900162j10.1039/b900162j ↗
17. 10.1149/2.0641707jes10.1149/2.0641707jes ↗
18. 10.7566/JPSJ.83.09470710.7566/JPSJ.83.094707 ↗
19. 10.1039/C2EE02508F10.1039/C2EE02508F ↗
20. 10.1039/b904583j10.1039/b904583j ↗
21. 10.1063/1.162937810.1063/1.1629378 ↗
22. 10.1016/j.jeurceramsoc.2007.02.13510.1016/j.jeurceramsoc.2007.02.135 ↗
23. 10.1016/0167-2738(82)90045-510.1016/0167-2738(82)90045-5 ↗
24. 10.1016/S0378-7753(00)00389-X10.1016/S0378-7753(00)00389-X ↗
25. 10.1111/j.1551-2916.2009.03273.x10.1111/j.1551-2916.2009.03273.x ↗
26. 10.1107/S056773947600155110.1107/S0567739476001551 ↗
27. 10.1016/j.jpowsour.2012.08.09510.1016/j.jpowsour.2012.08.095 ↗
28. 10.1016/j.ceramint.2012.10.23010.1016/j.ceramint.2012.10.230 ↗
29. 10.1016/j.jallcom.2015.10.27710.1016/j.jallcom.2015.10.277 ↗
30. 10.1088/0031-8949/2007/T129/06710.1088/0031-8949/2007/T129/067 ↗