journal article·2019-04-11

Effects of Neighboring Polyhedron Competition on the 5d Level of Ce3+ in Lanthanide Garnets

Zhen Song, Quanlin Liu

The Journal of Physical Chemistry C· Volume 123· Issue 14
Publisher page

Abstract

Herein, we provide a direct explanation for the reverse garnet effect based on polyhedron competition. On multisite substitution, the deformation of the dodecahedron which will accommodate Ce 3+ meets suppression from a neighboring octahedron and tetrahedron. This makes the dodecahedral deformation nonisotropic. Further, it is found that the lowest 5d state of Ce 3+ in garnet is closely related to the tetragonal distortion of the dodecahedron, which is characterized by a simplified cuboid model. Crystal-field calculations reveal how the edge-ratio of the cuboid affects energy levels. This model gives a satisfactory explanation for the reverse garnet effect and is helpful for seeking novel garnet-based luminescent materials.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Luminescence Properties of Advanced Materials · Crystal Structures and Properties · Lanthanide and Transition Metal Complexes

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

Affiliations

Beijing Key Laboratory for New Energy Materials and Technologies, School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083, China

Departamento de Química, Universidad Autónoma de Madrid, Madrid 28049, Spain

Funding

National Natural Science Foundation of China · China Scholarship Council · Ministry of Education of the People's Republic of China · Ministry of Science and Technology of the People's Republic of China

References (39)

Show source-provided references
1. 10.1039/c6cs00551a10.1039/c6cs00551a ↗
2. 10.1146/annurev-matsci-073012-12570210.1146/annurev-matsci-073012-125702 ↗
3. 10.1088/1468-6996/16/1/01490210.1088/1468-6996/16/1/014902 ↗
4. 10.1016/j.jlumin.2015.01.03410.1016/j.jlumin.2015.01.034 ↗
5. 10.1021/acsami.5b0841110.1021/acsami.5b08411 ↗
6. 10.1021/acsami.8b0275810.1021/acsami.8b02758 ↗
7. 10.1021/acs.inorgchem.8b0327010.1021/acs.inorgchem.8b03270 ↗
8. 10.1126/science.110871210.1126/science.1108712 ↗
9. 10.1016/j.jlumin.2017.09.00810.1016/j.jlumin.2017.09.008 ↗
10. 10.1021/cm060898c10.1021/cm060898c ↗
11. 10.1149/1.240343610.1149/1.2403436 ↗
12. 10.1063/1.170177110.1063/1.1701771 ↗
13. 10.1016/j.cplett.2007.05.02310.1016/j.cplett.2007.05.023 ↗
14. 10.1016/s0925-3467(03)00231-310.1016/s0925-3467(03)00231-3 ↗
15. 10.1039/c6tc00966b10.1039/c6tc00966b ↗
16. 10.1107/s0365110x6500474710.1107/s0365110x65004747 ↗
17. 10.1524/zkri.1967.125.125.110.1524/zkri.1967.125.125.1 ↗
18. Novak G. A. · Am. Sci. · 1971 · 56 · 791
19. Bagdasarov K. S. · Sov. Phys. Crystallogr. · 1991 · 36 · 398
20. 10.1021/acs.jpcc.7b1282610.1021/acs.jpcc.7b12826 ↗
21. 10.1021/cm401598n10.1021/cm401598n ↗
22. 10.1103/physrevb.80.01410510.1103/physrevb.80.014105 ↗
23. 10.1039/c2jm34479c10.1039/c2jm34479c ↗
24. 10.1021/acs.jpcc.6b0859310.1021/acs.jpcc.6b08593 ↗
25. 10.1016/s0022-2313(00)00229-510.1016/s0022-2313(00)00229-5 ↗
26. 10.1016/j.jlumin.2017.10.07310.1016/j.jlumin.2017.10.073 ↗
27. Dunn T. M. · 1965
28. 10.1016/j.ceramint.2017.05.22110.1016/j.ceramint.2017.05.221 ↗
29. 10.1016/j.jlumin.2012.08.02810.1016/j.jlumin.2012.08.028 ↗
30. 10.1021/acsomega.7b0030410.1021/acsomega.7b00304 ↗
31. 10.1016/j.optmat.2012.12.00710.1016/j.optmat.2012.12.007 ↗
32. 10.1088/0953-8984/26/11/11600110.1088/0953-8984/26/11/116001 ↗
33. 10.1021/jp301337f10.1021/jp301337f ↗
34. 10.1021/cm803076810.1021/cm8030768 ↗
35. 10.2109/jcersj2.123.105910.2109/jcersj2.123.1059 ↗
36. 10.1038/srep1151410.1038/srep11514 ↗
37. 10.1021/jp309572p10.1021/jp309572p ↗
38. Rotenberg M. · 1959
39. Nielson C. W. · 1963