Formation and control of mechanism for the preparation of ultra-fine barium strontium titanate powders by the citrate precursor method
Source abstract
Abstract
A modified citrate precursor method, combining the advantages of the nitrate autocombustion method by introducing the nitric acid, was successfully used to synthesize ultrafine Ba{sub 0.70}Sr{sub 0.30}TiO{sub 3} powders. Slight agglomerated and homogenized BST powders, with an average particle size of 20 nm, were obtained at 800 deg. C. Combining the results of TG/DTA and XRD, it can be concluded that the formation of BST powders takes place via two reaction mechanisms: decomposition of an intermediate oxycarbonate mechanism (DIOm) at low temperature, and solid-state reaction mechanism (SSRm) between nanocrystalline carbonates and amorphous TiO{sub 2} at high temperature. TEM shows higher amount of CA led to BST powders of better quality in morphology. Based on results of chemical analysis, it is suggested that higher amount of CA drives the mechanism to tend to DIOm. By simply adjusting the ratio of reagents, the reaction mechanism can be dominated and we can greatly control the final morphology of the powders.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Ferroelectric and Piezoelectric Materials · Advanced ceramic materials synthesis · Microwave Dielectric Ceramics Synthesis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (28)
Show source-provided references
1. Davis · J. Appl. Phys. · 1953 · 24 · 119410.1063/1.1721469 ↗
2. Bethe · Mater. Res. Bull. · 1971 · 6 · 20910.1016/0025-5408(71)90032-8 ↗
3. Dietz · J. Appl. Phys. · 1995 · 78 · 611310.1063/1.360553 ↗
4. Frey · Mater. Res. Bull. · 2005 · 40 · 128610.1016/j.materresbull.2005.04.006 ↗
5. Whatmore · Ferroelectrics · 1987 · 76 · 35110.1080/00150198708016956 ↗
6. Zhang · Mater. Res. Bull. · 2005 · 40 · 149010.1016/j.materresbull.2005.04.029 ↗
7. Sharma · Chem. Mater. · 2000 · 12 · 259010.1021/cm000041u ↗
8. Schrey · J. Am. Ceram. Soc. · 1965 · 48 · 40110.1111/j.1151-2916.1965.tb14776.x ↗
9. Roeder · J. Am. Ceram. Soc. · 1999 · 82 · 166510.1111/j.1151-2916.1999.tb01984.x ↗
10. Rajendran · J. Solid State Chem. · 1994 · 113 · 23910.1006/jssc.1994.1366 ↗
11. Kumar · J. Am. Ceram. Soc. · 1993 · 76 · 61710.1111/j.1151-2916.1993.tb03650.x ↗
12. Arima · J. Am. Ceram. Soc. · 1996 · 79 · 284710.1111/j.1151-2916.1996.tb08718.x ↗
13. Hennings · J. Solid State Chem. · 1978 · 16 · 32910.1016/0022-4596(78)90167-6 ↗
14. Mosset · J. Non-Cryst. Solids · 1988 · 100 · 33910.1016/0022-3093(88)90043-9 ↗
15. Durán · J. Mater. Chem. · 2001 · 11 · 182810.1039/b010172i ↗
16. Arya · J. Mater. Chem. · 2003 · 13 · 41510.1039/b205087k ↗
17. M.P. Pechini, U.S. Patent 330(3) (1967) 697;10.13182/NT67-A27852 ↗
18. N. Chakrabarti, H.S. Maiti, Indian Patent Application 435/DEL (1995).
19. Wang · 2002
20. Tsay · J. Mater. Sci. · 1998 · 33 · 372110.1023/A:1004636219542 ↗
21. Coutures · J. Mater. Sci. · 1992 · 27 · 184910.1007/BF01107212 ↗
22. Bellamy · 1958
23. Cho · J. Mater. Sci. · 1990 · 25 · 473810.1007/BF01129934 ↗
24. Nakamoto · 1986
25. Stokehuber · J. Am. Ceram. Soc. · 1993 · 76 · 118510.1111/j.1151-2916.1993.tb03738.x ↗
26. Bellamy · 1958
27. Tian · Nanotechnology · 2005 · 16 · 4710.1088/0957-4484/16/1/011 ↗
28. Kakihana · Chem. Mater. · 1997 · 9 · 45110.1021/cm9602353 ↗