Thermal stability of Ce0.5Gd0.5O1.75 nanoparticles in contact with an amorphous SiO2
Source abstract
Abstract
Abstract Morphology, microstructure and phase evolution of nanocrystalline Ce 0.5 Gd 0.5 O 1.75 mixed oxide supported on amorphous SiO 2 were studied in oxidizing and reducing atmosphere by XRD, TEM and SEM-EDS. The Ce 0.5 Gd 0.5 O 1.75 /SiO 2 samples were prepared by two methods: impregnation of the support with an aqueous solution of nitrates and deposition of homogeneous Ce 0.5 Gd 0.5 O 1.75 nanoparticles synthesized using the microemulsion method. The latter system is structurally and chemically stable in the oxidizing atmosphere up to 1000 °C, exhibiting only a small increase of the mean crystallite size of the mixed oxide from 2 to 3 nm. Prolonged heating at 1100 °C for 24 h caused partial decomposition of the mixed oxide and formation of small amount of B-Gd 2 Si 2 O 7 . In the reducing atmosphere the Ce 0.5 Gd 0.5 O 1.75 underwent amorphization and spreading over SiO 2 already at 900 °C to form an amorphous silicate. Most of the silicate remained amorphous even after reduction at 1100 °C, but certain amount crystallized into particles with strongly defected structure. The system prepared by impregnation exhibited significantly worse thermal stability due to chemical inhomogeneity. The complex systems synthesized in this work, containing nanocrystalline particles of mixed silicate with high concentration of Ce 3 + ions, may be interesting as scintillating materials.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Nuclear materials and radiation effects · Electronic and Structural Properties of Oxides · Luminescence Properties of Advanced Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (23)
Show source-provided references
1. Mogensen · Solid State Ionics · 2000 · 129 · 6310.1016/S0167-2738(99)00318-5 ↗
2. Inaba · Solid State Ionics · 1996 · 83 · 110.1016/0167-2738(95)00229-4 ↗
3. Artini · J. Solid State Chem. · 2012 · 190 · 2410.1016/j.jssc.2012.01.056 ↗
4. Kossoy · Phys. Rev. B · 2013 · 87 · 05410110.1103/PhysRevB.87.054101 ↗
5. Grover · Mater. Res. Bull. · 2004 · 39 · 85910.1016/j.materresbull.2004.01.007 ↗
6. Peng · Ceram. Int. · 2007 · 33 · 113310.1016/j.ceramint.2006.03.004 ↗
7. Katta · Catal. Sci. Technol. · 2012 · 2 · 99510.1039/c2cy00551d ↗
8. Malecka · J. Solid State Chem. · 2012 · 192 · 22110.1016/j.jssc.2012.04.020 ↗
9. Kepinski · J. Solid State Chem. · 2014 · 209 · 4210.1016/j.jssc.2013.10.025 ↗
10. Malecka · Appl. Catal. B · 2007 · 74 · 29010.1016/j.apcatb.2007.02.021 ↗
11. Solovyov · J. Appl. Crystallogr. · 2004 · 37 · 74310.1107/S0021889804015638 ↗
12. Felsche · J. Less-Common Met. · 1970 · 21 · 110.1016/0022-5088(70)90159-1 ↗
13. Fleet · Z. Kristallogr. · 2003 · 218 · 79510.1524/zkri.218.12.795.20550 ↗
14. Kepinski · J. Solid State Chem. · 2002 · 168 · 11010.1006/jssc.2002.9697 ↗
15. Baumer · J. Alloys Compd. · 2011 · 509 · 847810.1016/j.jallcom.2011.06.016 ↗
16. Landheer · Appl. Phys. Lett. · 2001 · 79 · 261810.1063/1.1412284 ↗
17. Sahoo · Appl. Opt. · 2006 · 45 · 324310.1364/AO.45.003243 ↗
18. Das · J. Appl. Phys. · 2011 · 110 · 06352710.1063/1.3642083 ↗
19. Ballem · Microporous Mesoporous Mater. · 2013 · 168 · 22110.1016/j.micromeso.2012.10.009 ↗
20. Hardy · Appl. Surf. Sci. · 2009 · 255 · 781210.1016/j.apsusc.2009.04.184 ↗
21. Su · Appl. Surf. Sci. · 2011 · 257 · 252610.1016/j.apsusc.2010.10.016 ↗
22. DiMartino · J. Non-Cryst. Solids · 2008 · 354 · 381710.1016/j.jnoncrysol.2008.05.027 ↗
23. Moretti · J. Lumin. · 2012 · 132 · 46110.1016/j.jlumin.2011.09.016 ↗