Low-temperature sintering of dense lanthanum silicate electrolytes with apatite-type structure using an organic precipitant synthesized nanopowder
Source abstract
Abstract
Highly sinterable La10Si6O27 and La10Si5.5M0.5O27 (M = Mg, and Al) nanopowders with apatite-type structure have been synthesized via a homogeneous precipitation method using diethylamine (DEA) as a precipitant. The synthetic approach using an organic precipitant with dispersant characteristics is advantageous in configuring weakly agglomerated nanopowders, leading to desirable sintering activity. X-ray diffraction powder patterns confirmed the single-phase crystalline lanthanum silicate of hexagonal apatite structure at 800 °C, which is a relatively lower calcination temperature compared to conventionally prepared samples. Transmission electron microscopy images revealed particles ∼30 nm in size with a high degree of crystallinity. A dense grain morphology was recognized from the scanning electron microscopy images of the polished surface of the pellets that were sintered at 1400 and 1500 °C for 10 h. This low-temperature sintering is significant because conventional powder processing requires a temperature above 1700 °C to obtain the same dense electrolyte. The doped-lanthanum silicate electrolyte prepared by the DEA process and sintered at 1500 °C for 10 h exhibited electrical conductivity comparable with samples prepared at much higher sintering temperature (>1700 °C).
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Electronic and Structural Properties of Oxides · Catalysis and Oxidation Reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (31)
Show source-provided references
1. 10.1016/S0025-5408(01)00625-010.1016/S0025-5408(01)00625-0 ↗
2. 10.1038/nature0286310.1038/nature02863 ↗
3. 10.1023/A:101791422992310.1023/A:1017914229923 ↗
4. Physicochemical analysis of oxide systems based on a new class of chemical compounds-rare earth element germinates.
5. 10.1016/j.ssi.2005.05.01610.1016/j.ssi.2005.05.016 ↗
6. 10.1016/S0167-2738(98)00188-X10.1016/S0167-2738(98)00188-X ↗
7. 10.1111/j.1151-2916.1990.tb09787.x10.1111/j.1151-2916.1990.tb09787.x ↗
8. 10.1016/S0955-2219(99)00009-610.1016/S0955-2219(99)00009-6 ↗
9. 10.1016/S0022-0248(99)00374-710.1016/S0022-0248(99)00374-7 ↗
10. 10.1016/j.jpowsour.2007.05.08510.1016/j.jpowsour.2007.05.085 ↗
11. 10.1016/j.jpowsour.2007.06.06110.1016/j.jpowsour.2007.06.061 ↗
12. 10.1557/jmr.2004.19.2.47410.1557/jmr.2004.19.2.474 ↗
13. 10.1016/S0167-2738(00)00386-610.1016/S0167-2738(00)00386-6 ↗
14. 10.1557/JMR.2005.010110.1557/JMR.2005.0101 ↗
15. 10.1016/j.actamat.2003.08.00410.1016/j.actamat.2003.08.004 ↗
16. 10.1016/j.jpowsour.2007.07.07110.1016/j.jpowsour.2007.07.071 ↗
17. 10.1016/S0167-2738(99)00319-710.1016/S0167-2738(99)00319-7 ↗
18. 10.1002/1521-4095(200107)13:12/13<993::AID-ADMA993>3.0.CO;2-#10.1002/1521-4095(200107)13:12/13<993::AID-ADMA993>3.0.CO;2-# ↗
19. 10.1021/ja00088a01610.1021/ja00088a016 ↗
20. 10.1016/S0955-2219(98)00032-610.1016/S0955-2219(98)00032-6 ↗
21. 10.1016/S0955-2219(98)00215-510.1016/S0955-2219(98)00215-5 ↗
22. 10.1016/j.ssi.2005.06.02610.1016/j.ssi.2005.06.026 ↗
23. 10.1016/j.ssi.2005.11.02310.1016/j.ssi.2005.11.023 ↗
24. 10.1007/s10008-006-0129-810.1007/s10008-006-0129-8 ↗
25. 10.1016/j.jallcom.2007.03.12810.1016/j.jallcom.2007.03.128 ↗
26. 10.1063/1.169965810.1063/1.1699658 ↗
27. 10.1111/j.1151-2916.1988.tb06417.x10.1111/j.1151-2916.1988.tb06417.x ↗
28. 10.1016/j.jeurceramsoc.2006.09.00410.1016/j.jeurceramsoc.2006.09.004 ↗
29. 10.1016/S1359-6454(00)00327-X10.1016/S1359-6454(00)00327-X ↗
30. 10.1111/j.1151-2916.1994.tb07124.x10.1111/j.1151-2916.1994.tb07124.x ↗
31. 10.1039/b104006p10.1039/b104006p ↗