journal article·2000-11

Preparation of nanosized LaCoO3 perovskite oxide using amorphous heteronuclear complex as a precursor at low temperature

Yongfa Zhu, Ruiqin Tan, Tao Yi, Shishan Ji, Xiaoyan Ye, Lili Cao

Journal of Materials Science· Volume 35· Issue 21
Publisher page

Abstract

Nanosized LaCoO3 cobaltite oxide powder with perovskite structure was successfully synthesized at a relatively low calcination temperature using an amorphous heteronuclear complex, LaCo(DTPA)·6H2O, as a precursor. The precursor decomposed completely into cobaltite oxide above 400 °C according to the DTA and TGA results. XPS revealed that the decomposed species was composed of LaCoO3 cobaltite oxide after the precursor was calcined at 500 °C for 2 hours. XRD demonstrated that nanosized LaCoO3 crystalline powder with perovskite structure was formed after the calcination temperature increased to 600 °C. The grain size and the crystal size of LaCoO3 increased with the calcination temperature from 500 °C to 800 °C, and the heat-treatment time has a less obvious effect on the grain size and the crystal size. It is a useful way to synthesize nanosized perovskite oxides using an amorphous complex as a precursor. This method can be easily quantitatively controlled.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Magnetic and transport properties of perovskites and related materials · Catalytic Processes in Materials Science · Layered Double Hydroxides Synthesis and Applications

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

References (16)

Show source-provided references
1. J. P. ATTFIELD, A. L. KHARLANOV and J. A. MCALLISTER, Nature 394 (1998) 157.10.1038/28120 ↗
2. K. ASAI et al., Phys. Rev. B 50 (1994) 3025.10.1103/PhysRevB.50.3025 ↗
3. S. YAMAGUCHI, Y. OKIMOTO and Y. TOKURA, ibid. 54 (1996) 11022.10.1103/PhysRevB.54.R11022 ↗
4. L. G. TEJUCA, J. L. G. FIERRO and J. M. D. TASCON, "Advanced Catalysis" (Academic Press, San Diego, 1998) p. 237.
5. D. B. MEADOWCROFT, Nature 226 (1970) 847.10.1038/226847a0 ↗
6. N. MIZUNO and M. YAMATO et al., J. Catal. 132 (1991) 560.10.1016/0021-9517(91)90171-Y ↗
7. J. A. ANDERSON and J. L. G. FIERRO, J. Solid State Chem. 108 (1994) 305.10.1006/jssc.1994.1047 ↗
8. S. B. ADLER, J. A. LANE and B. C. H. STEELE, J. Electrochem. Soc. 143(11) (1996) 3554.10.1149/1.1837252 ↗
9. D. W. JOHNSON, JR., P. K. GALLAGHER, F. SCHREY and W. W. RHODES, Am. Ceram. Soc. Bull. 55 (1976) 520.
10. L. SIMONOT, F. GARIN and G. MAIRE, Applied Catalysis B: Environmental 11 (1997) 181.10.1016/S0926-3373(96)00047-1 ↗
11. G. XIONG, ZHENG-LIANG ZHI and XUJIE YANG et al., J. Mater. Scien. Lett. 16 (1997) 1064.10.1023/A:1018586927079 ↗
12. N. MIZUNO et al., Catalysis Today 8 (1990) 221.10.1016/0920-5861(90)87019-Y ↗
13. M. GUGLIELMI and G. CARTURAN, Joural of Non-Crystalline Solids 100 (1988) 16.10.1016/0022-3093(88)90004-X ↗
14. J. F. MOULDER, W. F. STICKLE, P. E. SOBOL and K. D. BOMBEN, in "Handbook of X-ray Photoelectron Spectroscopy," edited by J. Chastain (Perkin-Elmer Corporation, Eden Prairie, MN, 1992).
15. N. S. MCLNTYRE and M. G. COOK, Analytical Chemistry 47(13) (1975) 2208.10.1021/ac60363a034 ↗
16. QIAN YITAI, "Crystallization Chemistry" (The Science andTechnology University of China Publishing House, Beijing, 1988) p. 140.